Ricardo Reisin

Mutation Update and Genotype-Phenotype Correlations of Novel and Previously Described Mutations in<i>TPM2</i>and<i>TPM3</i>Causing Congenital Myopathies

M. Marttila, Vilma‐Lotta Lehtokari, Steven B. Marston et al. · Human Mutation · 2014 · 108 citations · Full text

Calcium channel blockers and transmitter release at the normal human neurornuscular junction

Darío A. Protti, Ricardo Reisin, Tomas Angelillo Mackinley et al. · Neurology · 1996 · 101 citations

Misdiagnosis in Fabry Disease

Cintia Marchesoni, Norma Roa, A.M. Pardal et al. · The Journal of Pediatrics · 2010 · 90 citations

Fabry Disease, Mendelian Disorder, Genetic Disorder +5

Time delays in the diagnosis and treatment of Fabry disease

Ricardo Reisin, Amandine Perrin, Pablo García‐Pavía · International Journal of Clinical Practice · 2017 · 87 citations

Current treatment practice of Guillain-Barré syndrome

Christine Verboon, Alex Y. Doets, Giuliana Galassi et al. · Neurology · 2019 · 87 citations · Full text