Nadine Le Forestier

<i>SOD1</i>, <i>ANG</i>, <i>VAPB</i>, <i>TARDBP</i>, and <i>FUS</i> mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations

Stéphanie Millecamps, François Salachas, C. Cazeneuve et al. · Journal of Medical Genetics · 2010 · 296 citations · Full text

Life Sciences, Genetics, Neurology +17

Glutamate levels in cerebrospinal fluid in amyotrophic lateral sclerosis: a reappraisal using a new HPLC method with coulometric detection in a large cohort of patients

Odile Spreux‐Varoquaux, Gilbert Bensimon, Lucette Lacomblez et al. · Journal of the Neurological Sciences · 2002 · 279 citations

Life Sciences, Neurology, Neuroscience +12

Impaired glucose tolerance in patients with amyotrophic lateral sclerosis

Pierre‐François Pradat, Gaëlle Bruneteau, Luc Dupuis et al. · Amyotrophic Lateral Sclerosis · 2010 · 173 citations

Life Sciences, Neurology, Neuroscience +12

Phenotype difference between ALS patients with expanded repeats in <i>C9ORF72</i> and patients with mutations in other ALS-related genes

Stéphanie Millecamps, Séverine Boillée, Isabelle Le Ber et al. · Journal of Medical Genetics · 2012 · 173 citations · Full text

Life Sciences, Genetics, Neurology +16

The cerebral network of COVID-19-related encephalopathy: a longitudinal voxel-based 18F-FDG-PET study

Aurélie Kas, M. Soret, Nadya Pyatigoskaya et al. · European Journal of Nuclear Medicine and Molecular Imaging · 2021 · 171 citations · Full text

Medicine, Neurology, Neuroscience +14