Publications by authors named "Ronald Ja Wanders"

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Vision on gyrate atrophy: why treat the eye?
Arthur A Bergen, Mark Jn Buijs, Anneloor Lma Ten Asbroek, Berith M Balfoort, Camiel Jf Boon, Ronald Ja Wanders

EMBO Mol Med· January 2024

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Metabolic rerouting via SCD1 induction impacts X-linked adrenoleukodystrophy.
Quentin Raas, Malu-Clair van de Beek, Sonja Forss-Petter, Inge Me Dijkstra, Abigail Deschiffart, Ronald Ja Wanders

J Clin Invest· April 2021

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Mutations in TIMM50 cause severe mitochondrial dysfunction by targeting key aspects of mitochondrial physiology.
Frederic Tort, Olatz Ugarteburu, Laura Texidó, Sabrina Gea-Sorlí, Judit García-Villoria, Ronald Ja Wanders

Hum Mutat· October 2019

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Cardiac-specific succinate dehydrogenase deficiency in Barth syndrome.
Jan Dudek, I-Fen Cheng, Arpita Chowdhury, Katharina Wozny, Martina Balleininger, Ronald Ja Wanders

EMBO Mol Med· February 2016

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Genetic basis of hyperlysinemia.
Sander M Houten, Heleen Te Brinke, Simone Denis, Jos Pn Ruiter, Alida C Knegt, Ronald Ja Wanders

Orphanet J Rare Dis· April 2013

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