Peter Y K Van den Bergh

11PUBLICATIONS
52CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesMedical genetics (excl. cancer genetics)Pacific Peoples and disability
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Publications (11)

|Jul 05, 2024
Electrodiagnostic subtyping in Guillain-Barré syndrome patients in the International Guillain-Barré Outcome Study.

Samuel Arends, Judith Drenthen, Laura de Koning

|Mar 20, 2024
Lessons for future clinical trials in adults with Becker muscular dystrophy: Disease progression detected by muscle magnetic resonance imaging, clinical and patient-reported outcome measures.

Bram De Wel, Louise Iterbeke, Lotte Huysmans

|Oct 10, 2023
European Academy of Neurology/Peripheral Nerve Society Guideline on diagnosis and treatment of Guillain-Barré syndrome.

Pieter A van Doorn, Peter Y K Van den Bergh, Robert D M Hadden

|Oct 10, 2023
European Academy of Neurology/Peripheral Nerve Society Guideline on diagnosis and treatment of Guillain-Barré syndrome.

Pieter A van Doorn, Peter Y K Van den Bergh, Robert D M Hadden

|Jun 14, 2022
Electrodiagnostic subtyping in Guillain-Barré syndrome: Use of criteria in practice based on a survey study in IGOS.

Samuel Arends, Judith Drenthen, Peter Y K Van den Bergh

|Mar 23, 2022
European Academy of Neurology guidance for developing and reporting clinical practice guidelines on rare neurological diseases.

Katina Aleksovska, Teia Kobulashvili, Joao Costa

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Frequent Collaborators

8 joint publications

Robert D M Hadden

6 joint publications

Pieter A van Doorn

5 joint publications

Yusuf A Rajabally

4 joint publications

Patrik Vankrunkelsven