Nektaria Alexandri

Identification of an Agrin Mutation that Causes Congenital Myasthenia and Affects Synapse Function

Caroline Huzé, Stéphanie Bauché, Pascale Richard et al. · The American Journal of Human Genetics · 2009 · 166 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +8

Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7

Asma Ammar, François Petit, Nektaria Alexandri et al. · Journal of Neurology · 2009 · 78 citations

Mendelian Disorder, Genetic Disorder, Genetics +7

Analysis of frequency and severity of relapses in multiple sclerosis patients treated with cladribine tablets or placebo: The CLARITY and CLARITY Extension studies

Nicola De Stefano, Maria Pia Sormani, Gavin Giovannoni et al. · Multiple Sclerosis Journal · 2021 · 28 citations · Full text

Patient Power Revolution in Multiple Sclerosis: Navigating the New Frontier

David Yeandle, Peter Rieckmann, Gavin Giovannoni et al. · Neurology and Therapy · 2018 · 27 citations · Full text

Joint Healthcare Professional and Patient Development of Communication Tools to Improve the Standard of MS Care

Celia Oreja‐Guevara, Stanca Potra, Birgit Bauer et al. · Advances in Therapy · 2019 · 20 citations · Full text