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S Hadj-Rabia

Showing results (31-40 of 88) with videos related to

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The British Journal of Dermatology|September 16, 2011
The EDAR370A allele attenuates the severity of hypohidrotic ectodermal dysplasia caused by EDA gene mutationC Cluzeau, S Hadj-Rabia, E Bal, et al.
Annales De Dermatologie Et De Venereologie|December 3, 2014
[Acanthosis nigricans in children and Crouzon syndrome]M Lagaude, M Barreau, M Jokic, et al.
American Journal of Human Genetics|February 11, 1999
Both recessive and dominant forms of anhidrotic/hypohidrotic ectodermal dysplasia map to chromosome 2q11-q13L Baala, S Hadj Rabia, J Zlotogora, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|January 16, 2022
Skin biopsy is helpful in the diagnosis of hereditary fibrosing POIKiloderma with tendon contractures, myopathy and pulmonary fibrosis, due to FAM111B mutationS Leclerc-Mercier, S Mercier, N Bellon, et al.
Clinical Genetics|April 24, 2010
Germline mosaicism in keratitis-ichthyosis-deafness syndrome: pre-natal diagnosis in a familial lethal formE Sbidian, D Feldmann, J Bengoa, et al.
The British Journal of Dermatology|September 8, 2011
Nutritional outcome in children with severe generalized recessive dystrophic epidermolysis bullosa: a short- and long-term evaluation of gastrostomy and enteral feedingV Colomb, E Bourdon-Lannoy, C Lambe, et al.
Annales De Dermatologie Et De Venereologie|April 8, 2015
[Wells Syndrome in children and atopy: Retrospective study of 11 cases and review of the literature]J Brun, C Chiaverini, D Bessis, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|June 12, 2020
Risk factors for corticophobia in atopic dermatitisH Dufresne, P Bataille, N Bellon, et al.
Neurology|March 27, 2002
Progressive bulbospinal amyotrophy in triple A syndrome with AAAS gene mutationC Goizet, B Catargi, F Tison, et al.
The British Journal of Dermatology|February 6, 2019
Late ulceration of residual abortive infantile haemangioma: a rare complicationA Welfringer-Morin, S Fraitag, X Balguerie, et al.
Pageof 9

Showing results (31-40 of 88) with videos related to

Sort By:
Pageof 9
The British Journal of Dermatology|September 16, 2011
The EDAR370A allele attenuates the severity of hypohidrotic ectodermal dysplasia caused by EDA gene mutationC Cluzeau, S Hadj-Rabia, E Bal, et al.
Annales De Dermatologie Et De Venereologie|December 3, 2014
[Acanthosis nigricans in children and Crouzon syndrome]M Lagaude, M Barreau, M Jokic, et al.
American Journal of Human Genetics|February 11, 1999
Both recessive and dominant forms of anhidrotic/hypohidrotic ectodermal dysplasia map to chromosome 2q11-q13L Baala, S Hadj Rabia, J Zlotogora, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|January 16, 2022
Skin biopsy is helpful in the diagnosis of hereditary fibrosing POIKiloderma with tendon contractures, myopathy and pulmonary fibrosis, due to FAM111B mutationS Leclerc-Mercier, S Mercier, N Bellon, et al.
Clinical Genetics|April 24, 2010
Germline mosaicism in keratitis-ichthyosis-deafness syndrome: pre-natal diagnosis in a familial lethal formE Sbidian, D Feldmann, J Bengoa, et al.
The British Journal of Dermatology|September 8, 2011
Nutritional outcome in children with severe generalized recessive dystrophic epidermolysis bullosa: a short- and long-term evaluation of gastrostomy and enteral feedingV Colomb, E Bourdon-Lannoy, C Lambe, et al.
Annales De Dermatologie Et De Venereologie|April 8, 2015
[Wells Syndrome in children and atopy: Retrospective study of 11 cases and review of the literature]J Brun, C Chiaverini, D Bessis, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|June 12, 2020
Risk factors for corticophobia in atopic dermatitisH Dufresne, P Bataille, N Bellon, et al.
Neurology|March 27, 2002
Progressive bulbospinal amyotrophy in triple A syndrome with AAAS gene mutationC Goizet, B Catargi, F Tison, et al.
The British Journal of Dermatology|February 6, 2019
Late ulceration of residual abortive infantile haemangioma: a rare complicationA Welfringer-Morin, S Fraitag, X Balguerie, et al.
Pageof 9