Catherine Argyriou

Title(s)Assistant Professor of Research Ophthalmology
SchoolKeck School of Medicine of Usc
Address4650 Sunset Blvd.
Off Campus
Los Angeles CA 90027
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Zellweger Spectrum Disorder: Ophthalmic Findings from a New Natural History Study Cohort and Scoping Literature Review. Ophthalmology. 2023 Dec; 130(12):1313-1326. Yergeau C, Coussa RG, Antaki F, Argyriou C, Koenekoop RK, Braverman NE. PMID: 37541626.
      View in: PubMed   Mentions:    Fields:    
    2. Peroxisomes : novel findings and future directions. Histochem Cell Biol. 2023 May; 159(5):379-387. Pedrosa AG, Reglinski K, Lismont C, Kors S, Costello J, Rodrigues TA, Marques M, Linka N, Argyriou C, Weinhofer I, Kocherlakota S, Riccio V, Ferreira V, Di Cara F, Ferreira AR, Francisco T, Azevedo JE, Ribeiro D. PMID: 37160800; PMCID: PMC10170047.
      View in: PubMed   Mentions: 1     Fields:    
    3. Clinical, neuroradiological, and molecular characterization of patients with atypical Zellweger spectrum disorder caused by PEX16 mutations: a case series. Neurogenetics. 2022 04; 23(2):115-127. Cheung A, Argyriou C, Yergeau C, D'Souza Y, Riou É, Lévesque S, Raymond G, Daba M, Rtskhiladze I, Tkemaladze T, Adang L, La Piana R, Bernard G, Braverman N. PMID: 35106698.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    4. AAV-mediated PEX1 gene augmentation improves visual function in the PEX1-Gly844Asp mouse model for mild Zellweger spectrum disorder. Mol Ther Methods Clin Dev. 2021 Dec 10; 23:225-240. Argyriou C, Polosa A, Song JY, Omri S, Steele B, Cécyre B, McDougald DS, Di Pietro E, Bouchard JF, Bennett J, Hacia JG, Lachapelle P, Braverman NE. PMID: 34703844; PMCID: PMC8516995.
      View in: PubMed   Mentions: 7  
    5. The biochemical basis of mitochondrial dysfunction in Zellweger Spectrum Disorder. EMBO Rep. 2021 10 05; 22(10):e51991. Nuebel E, Morgan JT, Fogarty S, Winter JM, Lettlova S, Berg JA, Chen YC, Kidwell CU, Maschek JA, Clowers KJ, Argyriou C, Chen L, Wittig I, Cox JE, Roh-Johnson M, Braverman N, Bonkowsky J, Gygi SP, Rutter J. PMID: 34351705; PMCID: PMC8490991.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansCells
    6. A longitudinal study of retinopathy in the PEX1-Gly844Asp mouse model for mild Zellweger Spectrum Disorder. Exp Eye Res. 2019 09; 186:107713. Argyriou C, Polosa A, Cecyre B, Hsieh M, Di Pietro E, Cui W, Bouchard JF, Lachapelle P, Braverman N. PMID: 31254513.
      View in: PubMed   Mentions: 9     Fields:    Translation:AnimalsCells
    7. Zellweger spectrum disorder patient-derived fibroblasts with the PEX1-Gly843Asp allele recover peroxisome functions in response to flavonoids. J Cell Biochem. 2019 03; 120(3):3243-3258. MacLean GE, Argyriou C, Di Pietro E, Sun X, Birjandian S, Saberian P, Hacia JG, Braverman NE. PMID: 30362618.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    8. Peroxisome biogenesis disorders. Transl Sci Rare Dis. 2016 Nov 07; 1(2):111-144. Argyriou C, D'Agostino MD, Braverman N. PMID: 29152457; PMCID: PMC5678237.
      View in: PubMed   Mentions: 30  
    9. An enhanced immune response of Mclk1⁺/⁻ mutant mice is associated with partial protection from fibrosis, cancer and the development of biomarkers of aging. PLoS One. 2012; 7(11):e49606. Wang D, Wang Y, Argyriou C, Carrière A, Malo D, Hekimi S. PMID: 23166727; PMCID: PMC3498213.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansAnimalsCells
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    NIH Funding Acknowledgment: Important - All publications resulting from the utilization of SC CTSI resources are required to credit the SC CTSI grant by including the NIH funding acknowledgment and must comply with the NIH Public Access Policy.

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