Sandrine Tardieu

Mutations of the <i>presenilin I</i> gene in families with early-onset Alzheimer's disease

Dominique Campion, Jean‐Michel Flaman, Alexis Brice et al. · Human Molecular Genetics · 1995 · 281 citations

Life Sciences, Genetics, Molecular Genetics +17

Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion

Philippe Mouton, Sandrine Tardieu, Riadh Gouider et al. · Neurology · 1999 · 185 citations

Medicine, Neurology, Neuroscience +15

A Comprehensive Endocrine Description of Kennedy’s Disease Revealing Androgen Insensitivity Linked to CAG Repeat Length

S. Dejager, Hélène Bry‐Gauillard, Éric Bruckert et al. · The Journal of Clinical Endocrinology & Metabolism · 2002 · 173 citations · Full text

Medicine, Endocrinology, Andrology +14

X-linked Charcot-Marie-Tooth disease with connexin 32 mutations

Nazha Birouk, Éric Leguern, Thierry Maisonobe et al. · Neurology · 1998 · 170 citations

Life Sciences, Genetics, Neurology +16

Late-onset metachromatic leukodystrophy

Helmut Rauschka, Benoît Colsch, Nicole Baumann et al. · Neurology · 2006 · 114 citations

Life Sciences, Genetics, Neurology +16