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The British Journal of Dermatology
|
January 4, 2021
Genotypic and phenotypic analysis of 34 cases of inherited junctional epidermolysis bullosa caused by COL17A1 mutations
A L Hérissé, A Charlesworth, N Bellon, et al.
Cell Death and Differentiation
|
July 7, 2007
Human lipodystrophies linked to mutations in A-type lamins and to HIV protease inhibitor therapy are both associated with prelamin A accumulation, oxidative stress and premature cellular senescence
M Caron, M Auclair, B Donadille, et al.
The British Journal of Dermatology
|
September 10, 2020
Genotypic and Phenotypic Analysis of 34 Cases of Inherited Junctional Epidermolysis Bullosa caused by COL17A1 Mutations
A Charlesworth, A L Hérissé, N Bellon, et al.
The British Journal of Dermatology
|
September 18, 2008
Cutaneous manifestations of immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome
M Halabi-Tawil, F M Ruemmele, S Fraitag, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
September 21, 2021
Practical management of epidermolysis bullosa: consensus clinical position statement from the European Reference Network for Rare Skin Diseases
C Has, M El Hachem, H Bučková, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
June 15, 2013
Absence of circulating mast cell precursors in paediatric mastocytosis: could it reflect a different pathophysiology between adults and children with mastocytosis?
S Georgin-Lavialle, L Le Saché-de Peufeilhoux, L Martin, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
February 1, 2019
Long-term evolving profile of childhood autoimmune blistering diseases: Retrospective study on 38 children
A Welfringer-Morin, L Bekel, N Bellon, et al.
Human Mutation
|
March 14, 2007
Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus
E Bal, L Baala, C Cluzeau, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 28, 2003
[Childhood-onset systemic lupus erythematosus]
B Bader-Meunier, P Quartier, G Deschênes, et al.
The British Journal of Dermatology
|
February 10, 2015
Paediatric mastocytosis: a systematic review of 1747 cases
C Méni, J Bruneau, S Georgin-Lavialle, et al.
Page
of 22
Search research articles
Search
Showing results (141-150 of 214) with videos related to
Sort By:
Page
of 22
The British Journal of Dermatology
|
January 4, 2021
Genotypic and phenotypic analysis of 34 cases of inherited junctional epidermolysis bullosa caused by COL17A1 mutations
A L Hérissé, A Charlesworth, N Bellon, et al.
Cell Death and Differentiation
|
July 7, 2007
Human lipodystrophies linked to mutations in A-type lamins and to HIV protease inhibitor therapy are both associated with prelamin A accumulation, oxidative stress and premature cellular senescence
M Caron, M Auclair, B Donadille, et al.
The British Journal of Dermatology
|
September 10, 2020
Genotypic and Phenotypic Analysis of 34 Cases of Inherited Junctional Epidermolysis Bullosa caused by COL17A1 Mutations
A Charlesworth, A L Hérissé, N Bellon, et al.
The British Journal of Dermatology
|
September 18, 2008
Cutaneous manifestations of immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome
M Halabi-Tawil, F M Ruemmele, S Fraitag, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
September 21, 2021
Practical management of epidermolysis bullosa: consensus clinical position statement from the European Reference Network for Rare Skin Diseases
C Has, M El Hachem, H Bučková, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
June 15, 2013
Absence of circulating mast cell precursors in paediatric mastocytosis: could it reflect a different pathophysiology between adults and children with mastocytosis?
S Georgin-Lavialle, L Le Saché-de Peufeilhoux, L Martin, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
February 1, 2019
Long-term evolving profile of childhood autoimmune blistering diseases: Retrospective study on 38 children
A Welfringer-Morin, L Bekel, N Bellon, et al.
Human Mutation
|
March 14, 2007
Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus
E Bal, L Baala, C Cluzeau, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 28, 2003
[Childhood-onset systemic lupus erythematosus]
B Bader-Meunier, P Quartier, G Deschênes, et al.
The British Journal of Dermatology
|
February 10, 2015
Paediatric mastocytosis: a systematic review of 1747 cases
C Méni, J Bruneau, S Georgin-Lavialle, et al.
Page
of 22