Gauthier Remiche
Route De Lennik 808
Anderlecht, BRU 1070, Belgium
Anderlecht, BRU 1070, Belgium
Last Updated: 09/26/2026
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Found 33 publications
Tracing neuropathological signatures: TARDBP and C9orf72 double mutations in a Sicilian family.
Journal: Human molecular genetics
Published: July 28, 2025
Loss of function of retinol dehydrogenase 11 causes a recessive syndrome characterized by myopathy, retinal dystrophy, juvenile cataracts, and microcephaly.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: July 04, 2025
Phenotype variability and therapeutic response to Patisiran in patients with hereditary transthyretin amyloidosis: a Belgian real-world experience.
Journal: Acta clinica Belgica
Published: February 19, 2025
Early-Onset Autosomal Dominant Myopathy with Vacuolated Fibers and Tubular Aggregates but No Periodic Paralysis, in a Patient with the c.1583G>A (p.R528H) mutation in the CACNA1S Gene.
Journal: Journal of neuromuscular diseases
Published: May 24, 2024
Recommendations for the management of myasthenia gravis in Belgium.
Journal: Acta neurologica Belgica
Published: February 07, 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.
Journal: European journal of neurology
Published: December 07, 2023
A First Case of Acute Flaccid Myelitis Related to Enterovirus D68 in Belgium: Case Report.
Journal: Case reports in neurology
Published: July 03, 2023
Telemedicine in Neuromuscular Diseases During Covid-19 Pandemic: ERN-NMD European Survey.
Journal: Journal of neuromuscular diseases
Published: November 14, 2022
A pathogenic CTBP1 variant featuring HADDTS with dystrophic myopathology.
Journal: Neuromuscular disorders : NMD
Published: September 08, 2022
Rituximab Responsive Relapsing-Remitting IgG4 Anticontactin 1 Chronic Inflammatory Demyelinating Polyradiculoneuropathy Associated With Membranous Nephropathy: A Case Description and Brief Review.
Journal: Journal of clinical neuromuscular disease
Published: May 24, 2022
A retrospective survey of patients with hereditary transthyretin-mediated (hATTR) amyloidosis treated with patisiran in real-world clinical practice in Belgium.
Journal: Acta neurologica Belgica
Published: March 15, 2022
Last Updated: 09/26/2026