Author

D. Grid

Observed names: D. GRID, Djamal Grid

Institutions: Inserm, Assistance Publique – Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Université Pierre-et-Marie-Curie

Observed institutions: Inserm, Assistance Publique – Hôpitaux de Paris, Association Francaise contre les Myopathies, Pitié-Salpêtrière Hospital, Hôpital Mustapha Pacha, Université Pierre-et-Marie-Curie, Physiopathologie des Comportements

OpenAlex ID: A5034648541

Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations

2006 · H. Azzedine, N. Ravisé, et al. · Neurology · 107

Autosomal-Recessive Forms of Demyelinating Charcot-Marie-Tooth Disease

2006 · O. Dubourg, H. Azzedine, et al. · NeuroMolecular Medicine · 95

A Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 1q21.2-q21.3

1999 · Ahmed Bouhouche, Ali Benomar, et al. · The American Journal of Human Genetics · 93

The Autosomal Recessive Form of CMT Disease Linked to 5q31‐q33

1999 · A. GUILBOT, M. KESSALI, et al. · Annals of the New York Academy of Sciences · 12

Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33

1997 · E. LeGuern, A. Guilbot, et al. · Neuromuscular Disorders · 12

The Autosomal Recessive Form of CMT Disease Linked to 5q31‐q33

1999 · A. GUILBOT, M. KESSALI, et al. · Annals of the New York Academy of Sciences · 7

Works count: 6

Citation count: 326

H-index: 6

I10-index: 5