Florence Riant
Inserm(FR)Université Paris Cité(FR)Saint Louis University Hospital(US)Assistance Publique – Hôpitaux de Paris(FR)Hôpital Saint-Louis(FR)
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Vascular Malformations Diagnosis and Treatment, Intracranial Aneurysms: Treatment and Complications, Neurological disorders and treatments, Intracerebral and Subarachnoid Hemorrhage Research
Most-Cited Works
- → Genotype–phenotype correlations in cerebral cavernous malformations patients(2006)264 cited
- → Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis(2001)250 cited
- → Recent insights into cerebral cavernous malformations: the molecular genetics of CCM(2010)179 cited
- → Pathogenic Mutations Associated with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Differently Affect Jagged1 Binding and Notch3 Activity via the RBP/JK Signaling Pathway(2004)160 cited
- → Defective membrane expression of the Na + -HCO 3 − cotransporter NBCe1 is associated with familial migraine(2010)148 cited
- → De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine(2010)132 cited