J. D. De Bleecker

Nonsense mutations in alpha-II spectrin in three families with juvenile onset hereditary motor neuropathy.

B. Asselbergh, A. Malandrini, M. Dotti, 2019, Brain : a journal of neurology.

Recommendations for the management of myasthenia gravis in Belgium.

G. Remiche, V. Van Parys, J. D. De Bleecker, 2024, Acta Neurologica Belgica.

Retrospective Study Shows That Serum Levels of Chemokine CXCL10 and Cytokine GDF15 Support a Diagnosis of Sporadic Inclusion Body Myositis and Immune-Mediated Necrotizing Myopathy

K. Bracke, B. De Paepe, J. D. De Bleecker, 2023, Brain sciences.

New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy.

G. Comi, B. Koritnik, K. Claeys, 2020, Brain : a journal of neurology.

Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis

A. Singleton, J. Lamb, F. Mastaglia, 2016, Neurobiology of Aging.