Chabrol, Brigitte

A large multicenter study of pediatric myotonic dystrophy type 1 for evidence-based management

Lagrue, E., Dogan, C., De Antonio, M., Audic, F., Bach, N., Barnerias, C., Bellance, R., Cances, C., Chabrol, B., Cuisset, J.-M., et al. (2019) · Neurology

Genetic Neurodegenerative DiseasesGenetics and Neurodevelopmental Disorders

Cited by 76

Heterogeneity of follow‐up procedures in French and Belgian patients with treated hereditary tyrosinemia type 1: results of a questionnaire and proposed guidelines

Schiff, M., Broue, P., Chabrol, B., De Laet, C., Habes, D., Mention, K., Sarles, J., Spraul, A., Valayannopoulos, V., Ogier de Baulny, H., et al. (2012) · Journal of Inherited Metabolic Disease

Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism

Cited by 28