Willem De Ridder - University of Antwerp

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论文共 27 篇作者统计合作学者相似作者

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Heterozygous Loss-of-function Variants in SPTAN1 Cause a Novel Early Childhood Onset Distal Myopathy with Chronic Neurogenic Features

medRxiv the preprint server for health sciences (2024)

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Congenital Myasthenic Syndromes in Belgium: Genetic and Clinical Characterization of Pediatric and Adult Patients

PEDIATRIC NEUROLOGY (2024): 57-65

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Dominant NARS1 Mutations Causing Axonal Charcot-Marie-Tooth Disease Expand NARS1-associated Diseases

Danique Beijer,Sheila Marte, Jiaxin C. Li,Willem De Ridder, Jessie Z. Chen,Abigail L. D. Tadenev,Kathy E. Miers,Tine Deconinck,Richard Macdonell,Wilson Marques Jr,Peter De Jonghe, Samia L. Pratt,Rebecca Meyer-Schuman,Stephan Zuchner,Anthony Antonellis,Robert W. Burgess,Jonathan Baets

BRAIN COMMUNICATIONS（2024）

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Pembrolizumab-associated Myositis with Striking Extraocular Muscle Contrast Enhancement

Lisa Van Doeselaer,Simon Nicolay,Willem De Ridder

Acta Neurologica Belgicapp.1-3, (2024)

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Contracturing Granulomatous Myositis in a Patient with Rheumatoid Arthritis: a Case Report

Willem De Ridder, Laurens Van Herck,Gert Cypers, Isabelle Ravelingien,Jonathan Baets

NEUROMUSCULAR DISORDERS（2024）

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A Homozygous Loss of Function Variant in POPDC3: from Invalidating Exercise Intolerance to a Limb-Girdle Muscular Dystrophy Phenotype

Willem De Ridder, Geert de Vries,Kristof Van Schil,Tine Deconinck,Vincent Mouly,Volker Straub,Jonathan Baets

Neuromuscular disorders NMD（2023）

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Distinct Features in Adult Polyglucosan Body Disease: a Case Series

Jonathan De Winter,Gert Cypers,Edwin Jacobs,Stephanie Vanden Bossche,Tine Deconinck,Willem De Ridder,Sven Dekeyzer,Jonathan Baets

Neuromuscular disordersno. 2 (2023): 148-152

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Analysis of Muscle Magnetic Resonance Imaging of a Large Cohort of Patient with VCP-mediated Disease Reveals Characteristic Features Useful for Diagnosis

Diana Esteller,Marianela Schiava,José Verdú-Díaz,Rocío-Nur Villar-Quiles,Boris Dibowski,Nadia Venturelli,Pascal Laforet,Jorge Alonso-Pérez,Montse Olive,Cristina Domínguez-González,Carmen Paradas,Beatriz Vélez,Anna Kostera-Pruszczyk,Biruta Kierdaszuk,Carmelo Rodolico,Kristl Claeys,Endre Pál,Edoardo Malfatti,Sarah Souvannanorath,Alicia Alonso-Jiménez,Willem de Ridder,Eline De Smet,George Papadimas,Constantinos Papadopoulos,Sofia Xirou,Sushan Luo,Nuria Muelas,Juan J. Vilchez,Alba Ramos-Fransi,Mauro Monforte,Giorgio Tasca,Bjarne Udd,Johanna Palmio,Srtuhi Sri,Sabine Krause,Benedikt Schoser,Roberto Fernández-Torrón,Adolfo López de Munain,Elena Pegoraro,Maria Elena Farrugia, Mathias Vorgerd,Georgious Manousakis,Jean Baptiste Chanson,Aleksandra Nadaj-Pakleza,Hakan Cetin,Umesh Badrising,Jodi Warman-Chardon, Jorge Bevilacqua,Nicholas Earle,Mario Campero,Jorge Díaz,Chiseko Ikenaga,Thomas E. Lloyd,Ichizo Nishino,Yukako Nishimori,Yoshihiko Saito,Yasushi Oya,Yoshiaki Takahashi,Atsuko Nishikawa,Ryo Sasaki,Chiara Marini-Bettolo,Michela Guglieri,Volker Straub,Tanya Stojkovic,Robert Y. Carlier,Jordi Díaz-Manera

Journal of neurology（2023）

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Neurological Features of Noonan Syndrome and Related RASopathies: Pain and Nerve Enlargement Characterized by Nerve Ultrasound

Willem De Ridder,Baziel van Engelen,Nens van Alfen

AMERICAN JOURNAL OF MEDICAL GENETICS PART A（2022）

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High prevalence of sporadic late-onset nemaline myopathy in a cohort of whole-exome sequencing negative myopathy patients

Willem De Ridder,Peter De Jonghe,Volker Straub,Jonathan Baets

Neuromuscular disorders : NMD（2021）

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