Leïla Lazaro

Congenital Titinopathy: Comprehensive characterization and pathogenic insights

Emily C. Oates, Kristi Jones, Sandra Donkervoort et al. · Annals of Neurology · 2018 · 164 citations · Full text

Medicine, Molecular Genetics, Pathology +13

Genotype-Phenotype Correlations in Charcot-Marie-Tooth Disease Type 2 Caused by Mitofusin 2 Mutations

Judith Calvo, Benoît Funalot, Robert Ouvrier et al. · Archives of Neurology · 2009 · 121 citations · Full text

Medicine, Genetics, Neurology +17

Enteroviral Meningoencephalitis after Anti‐CD20 (Rituximab) Treatment

Pierre Quartier, Olivier Tournilhac, Christine Archimbaud et al. · Clinical Infectious Diseases · 2003 · 112 citations · Full text

Life Sciences, Hematology, Immunology +17

Age-Dependent Mendelian Predisposition to Herpes Simplex Virus Type 1 Encephalitis in Childhood

Laurent Abel, Sabine Plancoulaine, Emmanuelle Jouanguy et al. · The Journal of Pediatrics · 2010 · 107 citations

Medicine, Neurology, Pediatrics +13

Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores

Nicole Monnier, Isabelle Marty, Julien Fauré et al. · Human Mutation · 2008 · 106 citations

Life Sciences, Genetics, Molecular Genetics +17