Mathias Woidy

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论文共 26 篇作者统计合作学者相似作者

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Repurposing SGLT2 Inhibitors: Treatment of Renal Proximal Tubulopathy in Fanconi-Bickel Syndrome with Empagliflozin

Ruben J. Overduin,Sarah C. Gruenert,Martine T. P. Besouw,Mathieu S. Bolhuis, Joost Groen,Andrea B. Schreuder,Mathias Woidy,Simona Murko,Rene Santer,Terry G. J. Derks

Journal of inherited metabolic diseaseno. 5 (2024): 1018-1027

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Accumulation of Α-Synuclein Mediates Podocyte Injury in Fabry Nephropathy

Journal of Clinical Investigationno. 11 (2023)

引用3浏览0WOS引用

Disorders of Carbohydrate Absorption, Transmembrane Transport and Metabolism

Terry G. J. Derks,Charlotte M. A. Lubout,Mathias Woidy,René Santer

Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseasespp.649-700, (2022)

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Long-Term Antibody Response to SARS-CoV-2 in Children

Gabor A. Dunay,Madalena Barroso,Mathias Woidy,Marta K. Danecka,Geraldine Engels,Katharina Hermann, Friederike S. Neumann,Kevin Paul,Jan Beime,Gabriele Escherich, Kristin Fehse,Lev Grinstein, Franziska Haniel, Luka J. Haupt,Laura Hecher,Torben Kehl, Christoph Kemen,Markus J. Kemper,Robin Kobbe,Aloisa Kohl, Thomas Klokow,Dominik Nörz,Jakob Olfe,Friderike Schlenker,Jessica Schmiesing,Johanna Schrum,Freya Sibbertsen,Philippe Stock,Stephan Tiede,Eik Vettorazzi,Dimitra E. Zazara,Antonia Zapf,Marc Lütgehetmann,Jun Oh,Thomas S. Mir,Ania C. Muntau,Søren W. Gersting,Stefanie Etzold

Journal of Clinical Immunologyno. 1 (2022): 46-56

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Evaluation of the CD4+ T cell response to SARS-CoV-2 infection and cross reactivity to beta variant in children of all ages

K. Paul, F. Sibbertsen,D. Weiskopf,M. Luetgehetmann, M. Barroso,M. K. Danecka,L. Glau, L. Hecher, K. Hermann, A. Kohl, J. Oh,J. Schulze zur Wiesch,A. Sette,E. Tolosa,E. Vettorazzi,M. Woidy,A. Zapf, D. E. Zazara,T. S. Mir,A. C. Muntau,S. W. Gersting,G. A. Dunay

medRxiv (2022)

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Edgetic Perturbations Contribute to Phenotypic Variability in PEX26 Deficiency

Amelie S. Lotz-Havla,Mathias Woidy,Philipp Guder,Jessica Schmiesing,Ralf Erdmann,Hans R. Waterham,Ania C. Muntau,Soren W. Gersting

FRONTIERS IN GENETICS（2021）

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Dominant KPNA3 Mutations Cause Infantile-Onset Hereditary Spastic Paraplegia

Claudia Schob,Maja Hempel,Dana Safka Brozkova,Huafang Jiang,Soo Yeon Kim,Nurit Assia Batzir,Naama Orenstein,Tatjana Bierhals,Jessika Johannsen,Anna Uhrova Meszarosova,Jong-Hee Chae,Pavel Seeman,Mathias Woidy, Fang,Christian Kubisch,Stefan Kindler,Jonas Denecke

Annals of neurology（2021）

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Synuclein Alpha Accumulation Drives Lysosomal Dysfunction in Fabry Podocytopathy

Fabian Braun,Ahmed Abed,Mathias Woidy,Oystein Eikrem,Nicola Wanner,Katharina M. von Cossel,Soeren W. Gersting,Ania C. Muntau,Behzad Najafian,Camilla Tøndel,Michael Mauer,Florian Grahammer,Thorsten Eierhoff,Hans-Peter Marti,Victor G. Puelles,Christoph Schell,Tobias B. Huber

Journal of the American Society of Nephrologyno. 10S (2021): 428-428

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Ibret Screen of the ABCD1 Peroxisomal Network and Mutation-Induced Network Perturbations

Amelie S. Lotz-Havla,Mathias Woidy,Philipp Guder,Caroline C. Friedel, Julian M. Klingbeil, Ana-Maria Bulau, Anja Schultze, Ilona Dahmen, Heidi Noll-Puchta,Stephan Kemp,Ralf Erdmann,Ralf Zimmer,Ania C. Muntau,Soren W. Gersting

Journal of Proteome Research（2021）

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论文共 26 篇作者统计合作学者相似作者