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S Hadj-Rabia

Showing results (61-70 of 88) with videos related to

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The British Journal of Dermatology|May 23, 2018
Paediatric mastocytosis: long-term follow-up of 53 patients with whole sequencing of KIT. A prospective studyC Meni, S Georgin-Lavialle, L Le Saché de Peufeilhoux, et al.
The British Journal of Dermatology|June 22, 2019
Does surgery of lymphatic malformations lead to an increase in superficial lymphangiectasia? A retrospective study of 43 patientsA Schreiber, V Soupre, N Kadlub, et al.
The British Journal of Dermatology|January 3, 2013
Unexpected extradermatological findings in 31 patients with xeroderma pigmentosum type CS Hadj-Rabia, D Oriot, N Soufir, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndromeS Hadj-Rabia, R Salomon, A Pelet, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|May 27, 2021
Management of albinism: French guidelines for diagnosis and careE Moreno-Artero, F Morice-Picard, D Bremond-Gignac, et al.
Prenatal Diagnosis|August 9, 2001
Prenatal diagnosis of respiratory chain deficiency by direct mutation screeningJ Amiel, N Gigarel, A Benacki, et al.
Annales De Dermatologie Et De Venereologie|July 4, 2021
Development and co-construction of a therapeutic patient education program for albinismH Dufresne, A de Longcamp, S Compain, et al.
The British Journal of Dermatology|November 4, 2014
Psoriasis and obesity in French children: a case-control, multicentre studyE Mahé, A Beauchet, C Bodemer, et al.
Clinical Genetics|January 21, 2017
Dental and extra-oral clinical features in 41 patients with WNT10A gene mutations: A multicentric genotype-phenotype studyC Tardieu, S Jung, K Niederreither, et al.
The British Journal of Dermatology|June 2, 2020
The challenging management of a series of 43 infants with Netherton syndrome: unexpected complications and novel mutationsN Bellon, S Hadj-Rabia, F Moulin, et al.
Pageof 9

Showing results (61-70 of 88) with videos related to

Sort By:
Pageof 9
The British Journal of Dermatology|May 23, 2018
Paediatric mastocytosis: long-term follow-up of 53 patients with whole sequencing of KIT. A prospective studyC Meni, S Georgin-Lavialle, L Le Saché de Peufeilhoux, et al.
The British Journal of Dermatology|June 22, 2019
Does surgery of lymphatic malformations lead to an increase in superficial lymphangiectasia? A retrospective study of 43 patientsA Schreiber, V Soupre, N Kadlub, et al.
The British Journal of Dermatology|January 3, 2013
Unexpected extradermatological findings in 31 patients with xeroderma pigmentosum type CS Hadj-Rabia, D Oriot, N Soufir, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndromeS Hadj-Rabia, R Salomon, A Pelet, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|May 27, 2021
Management of albinism: French guidelines for diagnosis and careE Moreno-Artero, F Morice-Picard, D Bremond-Gignac, et al.
Prenatal Diagnosis|August 9, 2001
Prenatal diagnosis of respiratory chain deficiency by direct mutation screeningJ Amiel, N Gigarel, A Benacki, et al.
Annales De Dermatologie Et De Venereologie|July 4, 2021
Development and co-construction of a therapeutic patient education program for albinismH Dufresne, A de Longcamp, S Compain, et al.
The British Journal of Dermatology|November 4, 2014
Psoriasis and obesity in French children: a case-control, multicentre studyE Mahé, A Beauchet, C Bodemer, et al.
Clinical Genetics|January 21, 2017
Dental and extra-oral clinical features in 41 patients with WNT10A gene mutations: A multicentric genotype-phenotype studyC Tardieu, S Jung, K Niederreither, et al.
The British Journal of Dermatology|June 2, 2020
The challenging management of a series of 43 infants with Netherton syndrome: unexpected complications and novel mutationsN Bellon, S Hadj-Rabia, F Moulin, et al.
Pageof 9