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Disparities in Amblyopia Treatment Outcomes: The Impact of Sociodemographic Factors, Treatment Compliance, and Age of Diagnosis. Ophthalmology. 2024 Sep 23.
Matsunaga K, Rajagopalan A, Nallasamy S, Nguyen A, de Castro-Abeger A, Borchert MS, Chang MY. PMID: 39321931.
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Autosomal Recessive Leber Hereditary Optic Neuropathy Triggered by Superior Mesenteric Artery Syndrome. J Neuroophthalmol. 2024 Apr 02.
Rajagopalan A, Jeste S, Borchert MS, Chang MY. PMID: 38564278; PMCID: PMC11445391.
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Aberrant gene expression yet undiminished retinal ganglion cell genesis in iPSC-derived models of optic nerve hypoplasia. Ophthalmic Genet. 2024 Feb; 45(1):1-15.
Aparicio JG, Hopp H, Harutyunyan N, Stewart C, Cobrinik D, Borchert M. PMID: 37807874; PMCID: PMC10841193.
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2 Fields:
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HumansCells
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An unexpected turn: a case of torsional anomalous retinal correspondence after myectomy of previously anteriorized inferior oblique muscles in a child. J AAPOS. 2024 02; 28(1):103820.
Phillips MJ, Nguyen AM, Borchert MS, Nallasamy S. PMID: 38242227.
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Humans
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Supracerebellar infratentorial resection of a torcular lesion causing fulminant intracranial hypertension: illustrative case. J Neurosurg Case Lessons. 2023 Dec 18; 6(25).
Dallas J, Lane JR, Hopkins BS, Chang M, Borchert M, Gonzalez NR, Chiarelli PA, Chu JK. PMID: 38109719; PMCID: PMC10732318.
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Comparison of Eye Tracking and Teller Acuity Cards for Visual Acuity Assessment in Pediatric Cortical/Cerebral Visual Impairment. Am J Ophthalmol. 2024 04; 260:115-121.
Chang MY, Borchert MS. PMID: 38065248; PMCID: PMC10981560.
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1 Fields:
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Humans
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Preretinal Hemorrhage in Myelin Oligodendrocyte Glycoprotein-Associated Disease. Ophthalmol Retina. 2023 Dec; 7(12):1108.
Sudharshan R, Borchert MS, Chang MY. PMID: 37642629; PMCID: PMC10793853.
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1 Fields:
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Humans
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Giant Dacryops in a 4-year-old Child. Ophthalmology. 2024 Jul; 131(7):835.
Jess A, Borchert MS, Chang MY. PMID: 37480911; PMCID: PMC10796837.
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Humans
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The Nictavi Tarsus Patch: A New Device for Achieving Temporary Eyelid Closure in Lagophthalmos. Clin Ophthalmol. 2023; 17:1877-1884.
Guo S, Borchert MS, Chang M, Nallasamy S, Reid MW, Zhang-Nunes S, Chang JR, Nguyen AM. PMID: 37425025; PMCID: PMC10327908.
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Association of prepregnancy body mass index and gestational weight gain on severity of optic nerve hypoplasia. Birth Defects Res. 2023 04 15; 115(7):753-763.
Situ BA, Borchert MS, Brown B, Garcia-Filion P. PMID: 36916489; PMCID: PMC10125100.
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1 Fields:
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Humans
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Full-field Scotopic Threshold Improvement after Voretigene Neparvovec-rzyl Treatment Correlates with Chorioretinal Atrophy. Ophthalmology. 2023 Jul; 130(7):764-770.
Stingl K, Stingl K, Schwartz H, Reid MW, Kempf M, Dimopoulos S, Kortuem F, Borchert MS, Lee TC, Nagiel A. PMID: 36822437; PMCID: PMC10293034.
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11 Fields:
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Humans
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Subretinal deposits in young patients treated with voretigene neparvovec-rzyl for RPE65-mediated retinal dystrophy. Br J Ophthalmol. 2023 03; 107(3):299-301.
Lopez J, Borchert M, Lee TC, Nagiel A. PMID: 35835501; PMCID: PMC9839889.
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9 Fields:
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HumansCells
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The Pediatric Optic Neuritis Prospective Outcomes Study: Two-Year Results. Ophthalmology. 2022 08; 129(8):856-864.
Pineles SL, Henderson RJ, Repka MX, Heidary G, Liu GT, Waldman AT, Borchert MS, Khanna S, Graves JS, Collinge JE, Conley JA, Davis PL, Kraker RT, Cotter SA, Holmes JM, Pediatric Eye Disease Investigator Group. PMID: 35364222; PMCID: PMC10357378.
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2 Fields:
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Humans
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Neovascularization of the optic disc and peripheral retinal ischemia in a child with a novel variant in ALMS1 (Alström syndrome). Am J Ophthalmol Case Rep. 2022 Jun; 26:101506.
Chang MY, Borchert MS, Schmidt R, Nagiel A. PMID: 35355858; PMCID: PMC8958466.
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Characteristics and Outcomes of Idiopathic and Non-idiopathic Ocular Motor Apraxia in Children. J Pediatr Ophthalmol Strabismus. 2022 Sep-Oct; 59(5):326-331.
Chang MY, Grosrenaud P, Borchert MS. PMID: 35192381; PMCID: PMC9840404.
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Humans
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Delayed Diagnosis of Childhood-Onset Huntington Disease in an 8-Year-Old Boy With Ocular Motor Apraxia. J Neuroophthalmol. 2023 Dec 01; 43(4):e304-e305.
Im DH, Borchert MS, Chang MY. PMID: 34924521.
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Humans
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Increase in Pediatric Pseudotumor Cerebri Syndrome Emergency Department Visits, Inpatient Admissions, and Surgeries During the COVID-19 Pandemic. J Neuroophthalmol. 2022 03 01; 42(1):e87-e92.
Chang MY, Yim CK, Borchert MS. PMID: 34803141; PMCID: PMC9842394.
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PubMed Mentions:
1 Fields:
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HumansPHPublic Health
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Paroxysmal tonic upgaze (PTU) associated with CACNA1A mutation and gross motor delay. J AAPOS. 2021 12; 25(6):353-353.e1.
Chang MY, Yuen T, Vyas A, Borchert MS. PMID: 34775063.
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1 Fields:
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Humans
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Validity and reliability of eye tracking for visual acuity assessment in children with cortical visual impairment. J AAPOS. 2021 12; 25(6):334.e1-334.e5.
Chang MY, Borchert MS. PMID: 34687876.
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7 Fields:
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Humans
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Etiology and Outcomes of Acquired Pediatric Sixth Nerve Palsies. J Neuroophthalmol. 2022 03 01; 42(1):e254-e259.
Chang MY, Borchert MS. PMID: 34417775.
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2 Fields:
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Humans
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Ophthalmologic characteristics and outcomes of children with cortical visual impairment and cerebral palsy. J AAPOS. 2021 08; 25(4):223.e1-223.e6.
West MR, Borchert MS, Chang MY. PMID: 34271208.
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7 Fields:
Translation:
Humans
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Perifoveal Chorioretinal Atrophy after Subretinal Voretigene Neparvovec-rzyl for RPE65-Mediated Leber Congenital Amaurosis. Ophthalmol Retina. 2022 01; 6(1):58-64.
Gange WS, Sisk RA, Besirli CG, Lee TC, Havunjian M, Schwartz H, Borchert M, Sengillo JD, Mendoza C, Berrocal AM, Nagiel A. PMID: 33838313; PMCID: PMC8497635.
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39 Fields:
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Humans
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Repeated measurements of ERGs and VEPs using chloral hydrate sedation and propofol anesthesia in young children. Doc Ophthalmol. 2021 10; 143(2):141-153.
McCulloch DL, Garcia-Filion P, Matar M, Stewart C, Borchert MS. PMID: 33778913.
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2 Fields:
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Humans
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Cortical Visual Impairment Treated by Plasmapheresis in a Child With Metronidazole-Induced Encephalopathy. J Neuroophthalmol. 2021 03 01; 41(1):e66-e68.
Chang MY, Borchert MS. PMID: 31834198.
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3 Fields:
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Humans
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Methods of visual assessment in children with cortical visual impairment. Curr Opin Neurol. 2021 02 01; 34(1):89-96.
Chang MY, Borchert MS. PMID: 33230032.
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8 Fields:
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Humans
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Assessment of Pediatric Optic Neuritis Visual Acuity Outcomes at 6 Months. JAMA Ophthalmol. 2020 12 01; 138(12):1253-1261.
Writing Committee for the Pediatric Eye Disease Investigator Group (PEDIG), Pineles SL, Repka MX, Liu GT, Waldman AT, Borchert MS, Khanna S, Heidary G, Graves JS, Shah VS, Kupersmith MJ, Kraker RT, Wallace DK, Cotter SA, Holmes JM. PMID: 33057592; PMCID: PMC7563662.
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6 Fields:
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Humans
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Advances in the evaluation and management of cortical/cerebral visual impairment in children. Surv Ophthalmol. 2020 Nov - Dec; 65(6):708-724.
Chang MY, Borchert MS. PMID: 32199940.
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22 Fields:
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Humans
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Orbital MRI versus fundus photography in the diagnosis of optic nerve hypoplasia and prediction of vision. Br J Ophthalmol. 2020 10; 104(10):1458-1461.
Kruglyakova J, Garcia-Filion P, Nelson M, Borchert M. PMID: 32024653.
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3 Fields:
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Humans
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Utility of In Vitro Mutagenesis of RPE65 Protein for Verification of Mutational Pathogenicity Before Gene Therapy. JAMA Ophthalmol. 2019 12 01; 137(12):1381-1388.
Yang U, Gentleman S, Gai X, Gorin MB, Borchert MS, Lee TC, Villanueva A, Koenekoop R, Maguire AM, Bennett J, Redmond TM, Nagiel A. PMID: 31580392; PMCID: PMC6777234.
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6 Fields:
Translation:
HumansCells
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Papilledema Treated by Cranial Expansion in a 5-Year-Old Boy with Camurati-Engelmann Syndrome. Ophthalmology. 2019 11; 126(11):1579.
Chang MY, Borchert MS. PMID: 31635703.
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Humans
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Factors Associated With Lack of Vision Improvement in Children With Cortical Visual Impairment. J Neuroophthalmol. 2018 12; 38(4):429-433.
Handa S, Saffari SE, Borchert M. PMID: 29232345.
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9 Fields:
Translation:
Humans
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Decreased severity of age-related macular degeneration in amblyopic eyes. Br J Ophthalmol. 2018 11; 102(11):1575-1578.
Storey PP, Aziz HA, O'Keefe GAD, Borchert M, Lam LA, Puliafito CA, Olmos de Koo LC. PMID: 29437581.
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Humans
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Pediatric Optic Neuritis: What Is New. J Neuroophthalmol. 2017 09; 37 Suppl 1:S14-S22.
Borchert M, Liu GT, Pineles S, Waldman AT. PMID: 28806345; PMCID: PMC6149212.
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PubMed Mentions:
9 Fields:
Translation:
Humans
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Brain Malformations Do Not Predict Hypopituitarism in Young Children with Optic Nerve Hypoplasia. Horm Res Paediatr. 2017; 88(3-4):251-257.
Garcia-Filion P, Almarzouki H, Fink C, Geffner M, Nelson M, Borchert M. PMID: 28848142; PMCID: PMC5647222.
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3 Fields:
Translation:
Humans
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Predictive value of N95 waveforms of pattern electroretinograms (PERGs) in children with optic nerve hypoplasia (ONH). Doc Ophthalmol. 2017 10; 135(2):97-106.
McCulloch D, Garcia-Filion P, Fink C, Fisher AC, Eleuteri A, Borchert MS. PMID: 28795295; PMCID: PMC10085523.
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1 Fields:
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HumansCells
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The Optic Nerve Hypoplasia Spectrum: Review of the Literature and Clinical Guidelines. Adv Pediatr. 2016 08; 63(1):127-46.
Ryabets-Lienhard A, Stewart C, Borchert M, Geffner ME. PMID: 27426898.
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17 Fields:
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Humans
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Strabismus in patients with cortical visual impairment: outcomes of surgery and observations of spontaneous resolution. J AAPOS. 2016 Apr; 20(2):121-5.
Binder NR, Kruglyakova J, Borchert MS. PMID: 27079591.
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3 Fields:
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Humans
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An evaluation of the safety and efficacy of bimatoprost for eyelash growth in pediatric subjects. Clin Ophthalmol. 2016; 10:419-29.
Borchert M, Bruce S, Wirta D, Yoelin SG, Lee S, Mao C, VanDenburgh A. PMID: 27022239; PMCID: PMC4792214.
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12
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Efficacy of growth hormone replacement on anthropometric outcomes, obesity, and lipids in children with optic nerve hypoplasia and growth hormone deficiency. Int J Pediatr Endocrinol. 2016; 2016:5.
Stewart C, Garcia-Filion P, Fink C, Ryabets-Lienhard A, Geffner ME, Borchert M. PMID: 26937243; PMCID: PMC4774157.
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4
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Fanfare for the Uncommon Neuro-Ophthalmologist: A Tribute to Irma Miller Lessell. J Neuroophthalmol. 2015 Sep; 35(3):e24-5.
Borchert MS, Lessell S. PMID: 26505049.
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Humans
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Comparison of human expert and computer-automated systems using magnitude-squared coherence (MSC) and bootstrap distribution statistics for the interpretation of pattern electroretinograms (PERGs) in infants with optic nerve hypoplasia (ONH). Doc Ophthalmol. 2015 Aug; 131(1):25-34.
Fisher AC, McCulloch DL, Borchert MS, Garcia-Filion P, Fink C, Eleuteri A, Simpson DM. PMID: 25761929.
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4 Fields:
Translation:
HumansCells
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Hypothalamic dysfunction without hamartomas causing gelastic seizures in optic nerve hypoplasia. J Child Neurol. 2015 Feb; 30(2):233-7.
Fink C, Borchert M, Simon CZ, Saper C. PMID: 24700666.
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Humans
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Re: Ramakrishnaiah et al.: Reliability of magnetic resonance imaging for the detection of hypopituitarism in children with optic nerve hypoplasia (Ophthalmology 2014;121:387-91). Ophthalmology. 2014 May; 121(5):e26-7.
Borchert M, Garcia-Filion P, Fink C, Geffner M, Nelson M. PMID: 24565741.
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1 Fields:
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Humans
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Absence of age-related optic disk changes in young children with optic nerve hypoplasia. Eye (Lond). 2014 May; 28(5):562-6.
Sutedja J, Garcia-Filion P, Fink C, Borchert M. PMID: 24556885; PMCID: PMC4017100.
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Humans
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Prenatal determinants of optic nerve hypoplasia: review of suggested correlates and future focus. Surv Ophthalmol. 2013 Nov-Dec; 58(6):610-9.
Garcia-Filion P, Borchert M. PMID: 24160732; PMCID: PMC3879141.
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12 Fields:
Translation:
Humans
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Failure of stem cell therapy to improve visual acuity in children with optic nerve hypoplasia. J AAPOS. 2013 Oct; 17(5):490-3.
Fink C, Garcia-Filion P, Borchert M. PMID: 24160969.
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1 Fields:
Translation:
Humans
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Autism assessment in children with optic nerve hypoplasia and other vision impairments. Dev Med Child Neurol. 2014 Jan; 56(1):66-72.
Williams ME, Fink C, Zamora I, Borchert M. PMID: 24000901.
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PubMed Mentions:
13 Fields:
Translation:
HumansCells
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Prevalence of myopia, hyperopia, and astigmatism in non-Hispanic white and Asian children: multi-ethnic pediatric eye disease study. Ophthalmology. 2013 Oct; 120(10):2109-16.
Wen G, Tarczy-Hornoch K, McKean-Cowdin R, Cotter SA, Borchert M, Lin J, Kim J, Varma R, Multi-Ethnic Pediatric Eye Disease Study Group. PMID: 23953098; PMCID: PMC3902090.
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PubMed Mentions:
75 Fields:
Translation:
Humans
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Prevalence of amblyopia or strabismus in asian and non-Hispanic white preschool children: multi-ethnic pediatric eye disease study. Ophthalmology. 2013 Oct; 120(10):2117-24.
McKean-Cowdin R, Cotter SA, Tarczy-Hornoch K, Wen G, Kim J, Borchert M, Varma R, Multi-Ethnic Pediatric Eye Disease Study Group. PMID: 23697956; PMCID: PMC4848013.
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PubMed Mentions:
130 Fields:
Translation:
Humans
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Prevalence and causes of visual impairment in Asian and non-Hispanic white preschool children: Multi-ethnic Pediatric Eye Disease Study. Ophthalmology. 2013 Jun; 120(6):1220-6.
Tarczy-Hornoch K, Cotter SA, Borchert M, McKean-Cowdin R, Lin J, Wen G, Kim J, Varma R, Multi-Ethnic Pediatric Eye Disease Study Group. PMID: 23561327; PMCID: PMC4848010.
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21 Fields:
Translation:
Humans
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Optic nerve hypoplasia syndrome: a review of the epidemiology and clinical associations. Curr Treat Options Neurol. 2013 Feb; 15(1):78-89.
Garcia-Filion P, Borchert M. PMID: 23233151; PMCID: PMC3576022.
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29
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Newborn thyroid-stimulating hormone in children with optic nerve hypoplasia: associations with hypothyroidism and vision. J AAPOS. 2012 Oct; 16(5):418-23.
Fink C, Vedin AM, Garcia-Filion P, Ma NS, Geffner ME, Borchert M. PMID: 23084376; PMCID: PMC3481172.
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PubMed Mentions:
4 Fields:
Translation:
HumansPHPublic Health
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ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous. Hum Mol Genet. 2012 Aug 15; 21(16):3681-94.
Prasov L, Masud T, Khaliq S, Mehdi SQ, Abid A, Oliver ER, Silva ED, Lewanda A, Brodsky MC, Borchert M, Kelberman D, Sowden JC, Dattani MT, Glaser T. PMID: 22645276; PMCID: PMC3406761.
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37 Fields:
Translation:
HumansAnimalsCells
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Serum prolactin concentrations in relation to hypopituitarism and obesity in children with optic nerve hypoplasia. Horm Res Paediatr. 2012; 77(5):277-80.
Vedin AM, Garcia-Filion P, Fink C, Borchert M, Geffner ME. PMID: 22572701; PMCID: PMC3578391.
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5 Fields:
Translation:
Humans
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Reappraisal of the optic nerve hypoplasia syndrome. J Neuroophthalmol. 2012 Mar; 32(1):58-67.
Borchert M. PMID: 22330852.
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18 Fields:
Translation:
Humans
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Presenting features and long-term effects of growth hormone treatment of children with optic nerve hypoplasia/septo-optic dysplasia. Int J Pediatr Endocrinol. 2011 Nov 15; 2011(1):17.
Vedin AM, Karlsson H, Fink C, Borchert M, Geffner ME. PMID: 22085631; PMCID: PMC3256097.
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4
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Risk factors for astigmatism in preschool children: the multi-ethnic pediatric eye disease and Baltimore pediatric eye disease studies. Ophthalmology. 2011 Oct; 118(10):1974-81.
McKean-Cowdin R, Varma R, Cotter SA, Tarczy-Hornoch K, Borchert MS, Lin JH, Wen G, Azen SP, Torres M, Tielsch JM, Friedman DS, Repka MX, Katz J, Ibironke J, Giordano L, Multi-Ethnic Pediatric Eye Disease Study and the Baltimore Pediatric Eye Disease Study Groups. PMID: 21856010; PMCID: PMC3186875.
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PubMed Mentions:
26 Fields:
Translation:
Humans
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Risk factors for hyperopia and myopia in preschool children the multi-ethnic pediatric eye disease and Baltimore pediatric eye disease studies. Ophthalmology. 2011 Oct; 118(10):1966-73.
Borchert MS, Varma R, Cotter SA, Tarczy-Hornoch K, McKean-Cowdin R, Lin JH, Wen G, Azen SP, Torres M, Tielsch JM, Friedman DS, Repka MX, Katz J, Ibironke J, Giordano L, Multi-Ethnic Pediatric Eye Disease Study and the Baltimore Pediatric Eye Disease Study Groups. PMID: 21856013; PMCID: PMC3186878.
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40 Fields:
Translation:
Humans
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Risk factors for decreased visual acuity in preschool children: the multi-ethnic pediatric eye disease and Baltimore pediatric eye disease studies. Ophthalmology. 2011 Nov; 118(11):2262-73.
Tarczy-Hornoch K, Varma R, Cotter SA, McKean-Cowdin R, Lin JH, Borchert MS, Torres M, Wen G, Azen SP, Tielsch JM, Friedman DS, Repka MX, Katz J, Ibironke J, Giordano L, Joint Writing Committee for the Multi-Ethnic Pediatric Eye Disease Study and the Baltimore Pediatric. PMID: 21856014; PMCID: PMC3208077.
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PubMed Mentions:
38 Fields:
Translation:
Humans
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Risk factors associated with childhood strabismus: the multi-ethnic pediatric eye disease and Baltimore pediatric eye disease studies. Ophthalmology. 2011 Nov; 118(11):2251-61.
Cotter SA, Varma R, Tarczy-Hornoch K, McKean-Cowdin R, Lin J, Wen G, Wei J, Borchert M, Azen SP, Torres M, Tielsch JM, Friedman DS, Repka MX, Katz J, Ibironke J, Giordano L, Joint Writing Committee for the Multi-Ethnic Pediatric Eye Disease Study and the Baltimore Pediatric. PMID: 21856012; PMCID: PMC3208120.
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65 Fields:
Translation:
Humans
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Neurocognitive outcomes in pediatric and adolescent patients with central nervous system germinoma treated with a strategy of chemotherapy followed by reduced-dose and volume irradiation. Pediatr Blood Cancer. 2011 Oct; 57(4):669-73.
O'Neil S, Ji L, Buranahirun C, Azoff J, Dhall G, Khatua S, Patel S, Panigrahy A, Borchert M, Sposto R, Finlay J. PMID: 21495164.
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PubMed Mentions:
18 Fields:
Translation:
Humans
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Prevalence of astigmatism in 6- to 72-month-old African American and Hispanic children: the Multi-ethnic Pediatric Eye Disease Study. Ophthalmology. 2011 Feb; 118(2):284-93.
Fozailoff A, Tarczy-Hornoch K, Cotter S, Wen G, Lin J, Borchert M, Azen S, Varma R, Writing Committee for the MEPEDS Study Group. PMID: 20888047; PMCID: PMC3017730.
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PubMed Mentions:
28 Fields:
Translation:
Humans
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General health-related quality of life in preschool children with strabismus or amblyopia. Ophthalmology. 2011 Mar; 118(3):574-80.
Wen G, McKean-Cowdin R, Varma R, Tarczy-Hornoch K, Cotter SA, Borchert M, Azen S, Multi-ethnic Pediatric Eye Disease Study Group. PMID: 20884059; PMCID: PMC3017225.
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PubMed Mentions:
29 Fields:
Translation:
Humans
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Prevalence and risk factors for disrupted circadian rhythmicity in children with optic nerve hypoplasia. Br J Ophthalmol. 2010 Oct; 94(10):1358-62.
Rivkees SA, Fink C, Nelson M, Borchert M. PMID: 20576785.
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6 Fields:
Translation:
Humans
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Evolving central hypothyroidism in children with optic nerve hypoplasia. J Pediatr Endocrinol Metab. 2010 Jan-Feb; 23(1-2):53-8.
Ma NS, Fink C, Geffner ME, Borchert M. PMID: 20432806.
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PubMed Mentions:
6 Fields:
Translation:
Humans
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Clinical electrophysiology and visual outcome in optic nerve hypoplasia. Br J Ophthalmol. 2010 Aug; 94(8):1017-23.
McCulloch DL, Garcia-Filion P, Fink C, Chaplin CA, Borchert MS. PMID: 19955198.
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PubMed Mentions:
10 Fields:
Translation:
HumansCells
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Anisometropia in Hispanic and african american infants and young children the multi-ethnic pediatric eye disease study. Ophthalmology. 2010 Jan; 117(1):148-153.e1.
Borchert M, Tarczy-Hornoch K, Cotter SA, Liu N, Azen SP, Varma R, MEPEDS Group. PMID: 19818509; PMCID: PMC2814917.
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25 Fields:
Translation:
Humans
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Light-adapted electroretinograms in optic nerve hypoplasia. Doc Ophthalmol. 2009 Oct; 119(2):123-32.
Chaplin C, Borchert MS, Fink C, Garcia-Filion P, McCulloch DL. PMID: 19669817.
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PubMed Mentions:
5 Fields:
Translation:
HumansCells
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Visual acuity norms in pre-school children: the Multi-Ethnic Pediatric Eye Disease Study. Optom Vis Sci. 2009 Jun; 86(6):607-12.
Pan Y, Tarczy-Hornoch K, Cotter SA, Wen G, Borchert MS, Azen SP, Varma R, Multi-Ethnic Pediatric Eye Disease Study Group. PMID: 19430325; PMCID: PMC2742505.
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PubMed Mentions:
54 Fields:
Translation:
Humans
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Successful switch from insulin therapy to treatment with pioglitazone in type 2 diabetes patients with residual beta-cell function: results from the PioSwitch study. Diabetes Obes Metab. 2009 May; 11(5):464-71.
Hohberg C, Pfützner A, Forst T, Lübben G, Karagiannis E, Borchert M, Schöndorf T. PMID: 19422402.
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PubMed Mentions:
8 Fields:
Translation:
Humans
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Optic nerve hypoplasia in North America: a re-appraisal of perinatal risk factors. Acta Ophthalmol. 2010 Aug; 88(5):527-34.
Garcia-Filion P, Fink C, Geffner ME, Borchert M. PMID: 19141149; PMCID: PMC3319088.
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PubMed Mentions:
13 Fields:
Translation:
Humans
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Fixation preference and visual acuity testing in a population-based cohort of preschool children with amblyopia risk factors. Ophthalmology. 2009 Jan; 116(1):145-53.
Cotter SA, Tarczy-Hornoch K, Song E, Lin J, Borchert M, Azen SP, Varma R, Multi-Ethnic Pediatric Eye Disease Study Group. PMID: 18962921; PMCID: PMC2699252.
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PubMed Mentions:
26 Fields:
Translation:
Humans
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The syndrome of optic nerve hypoplasia. Curr Neurol Neurosci Rep. 2008 Sep; 8(5):395-403.
Borchert M, Garcia-Filion P. PMID: 18713575.
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PubMed Mentions:
18 Fields:
Translation:
HumansAnimalsCells
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Pediatric optic neuritis. J Med Assoc Thai. 2008 Mar; 91(3):323-30.
Chirapapaisan N, Borchert MS. PMID: 18575284.
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PubMed Mentions:
4 Fields:
Translation:
Humans
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Stereoacuity testability in African-American and Hispanic pre-school children. Optom Vis Sci. 2008 Mar; 85(3):158-63.
Tarczy-Hornoch K, Lin J, Deneen J, Cotter SA, Azen SP, Borchert MS, Wang Y, Varma R, Multi-Ethnic Pediatric Eye Disease Study Group. PMID: 18317330.
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PubMed Mentions:
7 Fields:
Translation:
Humans
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Optic nerve hypoplasia and hypopituitarism. Pediatr Endocrinol Rev. 2008 Mar; 5(3):772-7.
Ahmad T, Borchert M, Geffner M. PMID: 18367998.
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PubMed Mentions:
3 Fields:
Translation:
Humans
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Neuroradiographic, endocrinologic, and ophthalmic correlates of adverse developmental outcomes in children with optic nerve hypoplasia: a prospective study. Pediatrics. 2008 Mar; 121(3):e653-9.
Garcia-Filion P, Epport K, Nelson M, Azen C, Geffner ME, Fink C, Borchert M. PMID: 18250116.
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PubMed Mentions:
33 Fields:
Translation:
Humans
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Testability of the Retinomax autorefractor and IOLMaster in preschool children: the Multi-ethnic Pediatric Eye Disease Study. Ophthalmology. 2008 Aug; 115(8):1422-5, 1425.e1.
Borchert M, Wang Y, Tarczy-Hornoch K, Cotter S, Deneen J, Azen S, Varma R, MEPEDS Study Group. PMID: 18164067; PMCID: PMC4848014.
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PubMed Mentions:
14 Fields:
Translation:
HumansPHPublic Health
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Long-term outcomes of pediatric ocular myasthenia gravis. Ophthalmology. 2008 Jul; 115(7):1245-1248.e1.
Ortiz S, Borchert M. PMID: 18155768.
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PubMed Mentions:
14 Fields:
Translation:
Humans
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Review of the pleiotropic effects of peroxisome proliferator-activated receptor gamma agonists on platelet function. Diabetes Technol Ther. 2007 Oct; 9(5):410-20.
Borchert M, Schöndorf T, Lübben G, Forst T, Pfützner A. PMID: 17931049.
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PubMed Mentions:
4 Fields:
Translation:
HumansAnimalsCells
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Visual acuity testability in African-American and Hispanic children: the multi-ethnic pediatric eye disease study. Am J Ophthalmol. 2007 Nov; 144(5):663-7.
Cotter SA, Tarczy-Hornoch K, Wang Y, Azen SP, Dilauro A, Borchert M, Varma R, Multi-Ethnic Pediatric Eye Disease Study Group. PMID: 17868633; PMCID: PMC2099260.
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PubMed Mentions:
23 Fields:
Translation:
Humans
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Prolonged pancytopenia in a gene therapy patient with ADA-deficient SCID and trisomy 8 mosaicism: a case report. Blood. 2007 Jan 15; 109(2):503-6.
Engel BC, Podsakoff GM, Ireland JL, Smogorzewska EM, Carbonaro DA, Wilson K, Shah A, Kapoor N, Sweeney M, Borchert M, Crooks GM, Weinberg KI, Parkman R, Rosenblatt HM, Wu SQ, Hershfield MS, Candotti F, Kohn DB. PMID: 16973956; PMCID: PMC1785101.
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PubMed Mentions:
9 Fields:
Translation:
HumansCells
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Retinal function in infants with optic nerve hypoplasia: electroretinograms to large patterns and photopic flash. Eye (Lond). 2007 Jun; 21(6):712-20.
McCulloch DL, Garcia-Filion P, Garcia-Fillion P, van Boemel GB, Borchert MS. PMID: 16601748.
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PubMed Mentions:
6 Fields:
Translation:
HumansCells
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Measurement of amphotericin B concentration by resonant Raman spectroscopy--a novel technique that may be useful for non-invasive monitoring. Med Mycol. 2006 Mar; 44(2):169-74.
La Via WV, Lambert JL, Pelletier MJ, Morookian JM, Sirk SJ, Mickiene D, Walsh TJ, Borchert MS. PMID: 16519020.
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PubMed Mentions:
2 Fields:
Translation:
Animals
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Validation of ICNIRP estimates of toxicity thresholds for NIR (785 nm) light in the retinas of pigmented rabbits. Health Phys. 2006 Jan; 90(1):3-10.
Borchert M, Lambert J, Sliney D. PMID: 16340602.
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PubMed Mentions:
1 Fields:
Translation:
Animals
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Endocrinological and auxological abnormalities in young children with optic nerve hypoplasia: a prospective study. J Pediatr. 2006 Jan; 148(1):78-84.
Ahmad T, Garcia-Filion P, Borchert M, Kaufman F, Burkett L, Geffner M. PMID: 16423602.
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PubMed Mentions:
22 Fields:
Translation:
Humans
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Determination of glucose in human aqueous humor using Raman spectroscopy and designed-solution calibration. Appl Spectrosc. 2005 Aug; 59(8):1024-31.
Pelletier CC, Lambert JL, Borchert M. PMID: 16105211.
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PubMed Mentions:
11 Fields:
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Glucose determination in human aqueous humor with Raman spectroscopy. J Biomed Opt. 2005 May-Jun; 10(3):031110.
Lambert JL, Pelletier CC, Borchert M. PMID: 16229635.
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PubMed Mentions:
19 Fields:
Translation:
Humans
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Opsoclonus-ataxia caused by childhood neuroblastoma: developmental and neurologic sequelae. Pediatrics. 2002 Jan; 109(1):86-98.
Mitchell WG, Davalos-Gonzalez Y, Brumm VL, Aller SK, Burger E, Turkel SB, Borchert MS, Hollar S, Padilla S. PMID: 11773546.
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PubMed Mentions:
19 Fields:
Translation:
Humans
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Clinical diversity of hereditary Duane's retraction syndrome. Ophthalmology. 2000 Mar; 107(3):500-3.
Chung M, Stout JT, Borchert MS. PMID: 10711888.
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PubMed Mentions:
21 Fields:
Translation:
Humans
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Localization of a gene for Duane retraction syndrome to chromosome 2q31. Am J Hum Genet. 1999 Dec; 65(6):1639-46.
Appukuttan B, Gillanders E, Juo SH, Freas-Lutz D, Ott S, Sood R, Van Auken A, Bailey-Wilson J, Wang X, Patel RJ, Robbins CM, Chung M, Annett G, Weinberg K, Borchert MS, Trent JM, Brownstein MJ, Stout JT. PMID: 10577917; PMCID: PMC1288374.
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PubMed Mentions:
27 Fields:
Translation:
HumansCells
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The relationship between stereopsis and monocular optokinetic optokinetic nystagmus after infantile cataracts. J AAPOS. 1999 Aug; 3(4):221-6.
Hwang JM, Matsumoto ER, Borchert MS. PMID: 10477224.
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PubMed Mentions:
3 Fields:
Translation:
Humans
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Exclusion of candidate genetic loci for Duane retraction syndrome. Am J Ophthalmol. 1999 Mar; 127(3):358-60.
Ott S, Borchert M, Chung M, Appukuttan B, Wang X, Weinberg K, Stout JT. PMID: 10088756.
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Translation:
HumansCells
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Idiopathic intracranial hypertension in prepubertal pediatric patients: characteristics, treatment, and outcome. Am J Ophthalmol. 1999 Feb; 127(2):178-82.
Cinciripini GS, Donahue S, Borchert MS. PMID: 10030560.
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PubMed Mentions:
61 Fields:
Translation:
Humans
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Grand rounds #53: A case of small angle strabismus, torsion, aniseikonia and diplopia associated with epiretinal membranes [clincical conference]. Binocul Vis Strabismus Q. 1999; 14(1):46-51; discussion 51-2.
Kushner BJ, Alvares MG, Paysse EA, Brooks SE, Borchert M. PMID: 10076106.
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PubMed Mentions: Fields:
Translation:
Humans
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A noninvasive glucose monitor: preliminary results in rabbits. Diabetes Technol Ther. 1999; 1(2):145-51.
Borchert MS, Storrie-Lombardi MC, Lambert JL. PMID: 11475286.
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PubMed Mentions:
3 Fields:
Translation:
Animals
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Open globe injuries in children. J AAPOS. 1998 Aug; 2(4):234-8.
Rostomian K, Thach AB, Isfahani A, Pakkar A, Pakkar R, Borchert M. PMID: 10532742.
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PubMed Mentions:
13 Fields:
Translation:
Humans
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Visual outcome in high hypermetropia. J AAPOS. 1997 Sep; 1(3):147-50.
Edelman PM, Borchert MS. PMID: 10532776.
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PubMed Mentions:
6 Fields:
Translation:
Humans
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Etiology and prognosis of acute, late-onset esotropia. Ophthalmology. 1997 Aug; 104(8):1348-52.
Legmann Simon A, Borchert M. PMID: 9261325.
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PubMed Mentions:
21 Fields:
Translation:
Humans
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Comparisons of contact lens, foil, fiber and skin electrodes for patterns electroretinograms. Doc Ophthalmol. 1997-1998; 94(4):327-40.
McCulloch DL, Van Boemel GB, Borchert MS. PMID: 9858093.
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PubMed Mentions:
18 Fields:
Translation:
Humans
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Hemifield slide diplopia from altitudinal visual field defects. J Neuroophthalmol. 1996 Jun; 16(2):107-9.
Borchert MS, Lessell S, Hoyt WF. PMID: 8797166.
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PubMed Mentions:
5 Fields:
Translation:
Humans
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Clinical assessment, optic disk measurements, and visual-evoked potential in optic nerve hypoplasia. Am J Ophthalmol. 1995 Nov; 120(5):605-12.
Borchert M, McCulloch D, Rother C, Stout AU. PMID: 7485362.
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PubMed Mentions:
21 Fields:
Translation:
Humans
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Independence of optokinetic nystagmus asymmetry and binocularity in infantile esotropia. Arch Ophthalmol. 1994 Dec; 112(12):1580-3.
Aiello A, Wright KW, Borchert M. PMID: 7993213.
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PubMed Mentions: Fields:
Translation:
Humans
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Etiology of eyelid retraction in children: a retrospective study. J Pediatr Ophthalmol Strabismus. 1993 Mar-Apr; 30(2):96-9.
Stout AU, Borchert M. PMID: 8501625.
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PubMed Mentions:
3 Fields:
Translation:
Humans
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Ocular findings in neonates after extracorporeal membrane oxygenation. Retina. 1993; 13(3):202-7.
Gonzalez VH, Ober RR, Borchert MS, Bui KC, Ramos AD, Stout AU. PMID: 8235100.
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PubMed Mentions:
2 Fields:
Translation:
Humans
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Position-dependent Parinaud's syndrome. Am J Ophthalmol. 1992 Jul 15; 114(1):107-8.
Rismondo V, Borchert M. PMID: 1621779.
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Translation:
Humans
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Third nerve palsy due to cerebral artery aneurysm in a child. Aust N Z J Ophthalmol. 1992 May; 20(2):137-40.
Branley MG, Wright KW, Borchert MS. PMID: 1389132.
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Translation:
Humans
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Chronic ocular ischemia and neovascular glaucoma: a result of extracranial carotid artery disease. J Vasc Surg. 1988 Nov; 8(5):551-7.
Wagner WH, Weaver FA, Brinkley JR, Borchert M, Lindsay SF. PMID: 3184312.
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PubMed Mentions:
5 Fields:
Translation:
Humans
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Progressive and recurrent nonarteritic anterior ischemic optic neuropathy. Am J Ophthalmol. 1988 Oct 15; 106(4):443-9.
Borchert M, Lessell S. PMID: 3177563.
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PubMed Mentions:
14 Fields:
Translation:
Humans
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Bright light stimuli as a mask of relative afferent pupillary defects. Am J Ophthalmol. 1988 Jul 15; 106(1):98-9.
Borchert M, Sadun AA. PMID: 3394776.
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PubMed Mentions:
1 Fields:
Translation:
Humans
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Hypopyon keratouveitis in acute angle-closure glaucoma. Am J Ophthalmol. 1987 Oct 15; 104(4):430-1.
Schwartz SD, Borchert M, Oberman A. PMID: 3661656.
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PubMed Mentions:
3 Fields:
Translation:
Humans
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Assessment of visual impairment in patients with Alzheimer's disease. Am J Ophthalmol. 1987 Aug 15; 104(2):113-20.
Sadun AA, Borchert M, DeVita E, Hinton DR, Bassi CJ. PMID: 3618708.
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PubMed Mentions:
82 Fields:
Translation:
HumansCells
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Congenital ocular motor apraxia in twins. Findings with magnetic resonance imaging. J Clin Neuroophthalmol. 1987 Jun; 7(2):104-7.
Borchert MS, Sadun AA, Sommers JD, Wright KW. PMID: 2956282.
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PubMed Mentions:
1 Fields:
Translation:
Humans