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The British Journal of Dermatology
|
June 16, 2015
Keratotic follicular plugs with calcifications in Conradi-Hünermann-Happle syndrome: histological, biochemical and genetic testing correlation
S Leclerc-Mercier, F Dufernez, S Fraitag, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
March 16, 2022
Perceived clinical severity of atopic dermatitis in children: comparison between patients' and parents' evaluation
E Mahe, J Shourick, S Mallet, et al.
Clinical Genetics
|
March 19, 2010
X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findings
F Clauss, N Chassaing, A Smahi, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
October 3, 2020
Immunological and virological profile of children with chilblain-like lesions and SARS-CoV-2
L Fertitta, A Welfringer-Morin, A Ouedrani, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
May 26, 2025
Drug management of lichen planus in a paediatric series of 25 patients
E Benassaia, A Welfringer-Morin, N Bellon, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
March 15, 2019
Cutaneous granulomas with primary immunodeficiency in children: a report of 17 new patients and a review of the literature
S Leclerc-Mercier, D Moshous, B Neven, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
September 29, 2021
Feelings of guilt in parents of children with atopic dermatitis
A C Bursztejn, J Shourick, C Bodemer, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
July 17, 2021
Characteristics of children and adolescents with atopic dermatitis who attended therapeutic patient education
S Barbarot, F Boralevi, J Shourick, et al.
European Journal of Human Genetics : EJHG
|
July 1, 1997
Three novel point mutations in the keratinocyte transglutaminase (TGK) gene in lamellar ichthyosis: significance for mutant transcript level, TGK immunodetection and activity
E Petit, M Huber, A Rochat, et al.
American Journal of Human Genetics
|
October 27, 1997
Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibril formation
A Hovnanian, A Rochat, C Bodemer, et al.
Page
of 22
Search research articles
Search
Showing results (161-170 of 214) with videos related to
Sort By:
Page
of 22
The British Journal of Dermatology
|
June 16, 2015
Keratotic follicular plugs with calcifications in Conradi-Hünermann-Happle syndrome: histological, biochemical and genetic testing correlation
S Leclerc-Mercier, F Dufernez, S Fraitag, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
March 16, 2022
Perceived clinical severity of atopic dermatitis in children: comparison between patients' and parents' evaluation
E Mahe, J Shourick, S Mallet, et al.
Clinical Genetics
|
March 19, 2010
X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findings
F Clauss, N Chassaing, A Smahi, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
October 3, 2020
Immunological and virological profile of children with chilblain-like lesions and SARS-CoV-2
L Fertitta, A Welfringer-Morin, A Ouedrani, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
May 26, 2025
Drug management of lichen planus in a paediatric series of 25 patients
E Benassaia, A Welfringer-Morin, N Bellon, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
March 15, 2019
Cutaneous granulomas with primary immunodeficiency in children: a report of 17 new patients and a review of the literature
S Leclerc-Mercier, D Moshous, B Neven, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
September 29, 2021
Feelings of guilt in parents of children with atopic dermatitis
A C Bursztejn, J Shourick, C Bodemer, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
July 17, 2021
Characteristics of children and adolescents with atopic dermatitis who attended therapeutic patient education
S Barbarot, F Boralevi, J Shourick, et al.
European Journal of Human Genetics : EJHG
|
July 1, 1997
Three novel point mutations in the keratinocyte transglutaminase (TGK) gene in lamellar ichthyosis: significance for mutant transcript level, TGK immunodetection and activity
E Petit, M Huber, A Rochat, et al.
American Journal of Human Genetics
|
October 27, 1997
Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibril formation
A Hovnanian, A Rochat, C Bodemer, et al.
Page
of 22