Vincent El Ghouzzi
0000-0001-5894-8978
Publication & Citation Trends
Publications
0 total
Autosomal recessive primary microcephaly due to ASPM mutations: An update OA
Cited by 2
Semantic Scholar
ZIKA virus elicits P53 activation and genotoxic stress in human neural progenitors similar to mutations involved in severe forms of genetic microcephaly and p53 OA
Cited by 105
Semantic Scholar
Dymeclin de fi ciency causes postnatal microcephaly , hypomyelination and reticulum-to-Golgi traf fi cking defects in mice and humans
Cited by 1
Semantic Scholar
Implanted Neurosphere-Derived Precursors Promote Recovery After Neonatal Excitotoxic Brain Injury
Cited by 29
Semantic Scholar
Dyggve–Melchior–Clausen syndrome and Smith–McCort dysplasia: Clinical and molecular findings in three families supporting genetic heterogeneity in Smith–McCort dysplasia
Cited by 34
Semantic Scholar
Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndrome OA
Cited by 127
Semantic Scholar
Exclusion of the dymeclin and PAPSS2 genes in a novel form of spondyloepimetaphyseal dysplasia and mental retardation OA
Cited by 10
Semantic Scholar
Succinate dehydrogenase deficiency in human
Cited by 88
Semantic Scholar
Homozygosity mapping of a Dyggve-Melchior-Clausen syndrome gene to chromosome 18q21.1 OA
Cited by 28
Semantic Scholar
Craniosynostosis and fetal exposure to sodium valproate.
Cited by 103
Semantic Scholar
Research Topics
Craniofacial Disorders and Treatments
(15)
Cleft Lip and Palate Research
(13)
Cellular transport and secretion
(10)
Microtubule and mitosis dynamics
(8)
Genetics and Neurodevelopmental Disorders
(7)
Affiliations
Hôpital Necker-Enfants Malades
Schneider Electric (France)
Inserm
Délégation Paris 7
Université Paris Cité