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B Mevorah

Showing results (21-30 of 36) with videos related to

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The British Journal of Dermatology|May 13, 2005
Novel mutation of connexin 31 causing erythrokeratoderma variabilisL Feldmeyer, L Plantard, B Mevorah, et al.
The British Journal of Dermatology|December 1, 1981
X-linked recessive ichthyosis in three sisters: evidence for homozygosityB Mevorah, E Frenk, C R Müller, et al.
Human Genetics|January 1, 1983
Linkage studies in a family with X-linked recessive ichthyosis employing a cloned DNA sequence from the distal short arm of the X chromosomeP Wieacker, K E Davies, B Mevorah, et al.
Acta Dermato-Venereologica|January 1, 1991
Autosomal dominant ichthyosis and X-linked ichthyosis. Comparison of their clinical and histological phenotypesB Mevorah, A Krayenbuhl, E H Bovey, et al.
Journal of the American Academy of Dermatology|June 1, 1993
Natural history of the Naegeli-Franceschetti-Jadassohn syndrome and further delineation of its clinical manifestationsP H Itin, S Lautenschlager, R Meyer, et al.
Clinical Genetics|July 1, 1980
Autosomal dominant and X-linked ichthyosis in the same family. Biochemical analysis of steroid sulfatase activityB Migl, B Mevorah, C R Müller, et al.
The British Journal of Dermatology|May 22, 2001
Adolescent-onset ichthyosiform-like erythroderma with lichenoid tissue reaction: a new entity?B Mevorah, M Landau, A Gat, et al.
Dermatology (Basel, Switzerland)|September 6, 2000
High body mass index, dry scaly leg skin and atopic conditions are highly associated with keratosis pilarisG Yosipovitch, B Mevorah, J Mashiach, et al.
The British Journal of Dermatology|March 16, 2006
Clinical variation in X-linked dominant chondrodysplasia punctata (X-linked dominant ichthyosis)L Feldmeyer, B Mevorah, K H Grzeschik, et al.
Clinical and Experimental Dermatology|May 14, 2011
Erythrokeratoderma variabilis caused by a recessive mutation in GJB3D Fuchs-Telem, Y Pessach, B Mevorah, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
The British Journal of Dermatology|May 13, 2005
Novel mutation of connexin 31 causing erythrokeratoderma variabilisL Feldmeyer, L Plantard, B Mevorah, et al.
The British Journal of Dermatology|December 1, 1981
X-linked recessive ichthyosis in three sisters: evidence for homozygosityB Mevorah, E Frenk, C R Müller, et al.
Human Genetics|January 1, 1983
Linkage studies in a family with X-linked recessive ichthyosis employing a cloned DNA sequence from the distal short arm of the X chromosomeP Wieacker, K E Davies, B Mevorah, et al.
Acta Dermato-Venereologica|January 1, 1991
Autosomal dominant ichthyosis and X-linked ichthyosis. Comparison of their clinical and histological phenotypesB Mevorah, A Krayenbuhl, E H Bovey, et al.
Journal of the American Academy of Dermatology|June 1, 1993
Natural history of the Naegeli-Franceschetti-Jadassohn syndrome and further delineation of its clinical manifestationsP H Itin, S Lautenschlager, R Meyer, et al.
Clinical Genetics|July 1, 1980
Autosomal dominant and X-linked ichthyosis in the same family. Biochemical analysis of steroid sulfatase activityB Migl, B Mevorah, C R Müller, et al.
The British Journal of Dermatology|May 22, 2001
Adolescent-onset ichthyosiform-like erythroderma with lichenoid tissue reaction: a new entity?B Mevorah, M Landau, A Gat, et al.
Dermatology (Basel, Switzerland)|September 6, 2000
High body mass index, dry scaly leg skin and atopic conditions are highly associated with keratosis pilarisG Yosipovitch, B Mevorah, J Mashiach, et al.
The British Journal of Dermatology|March 16, 2006
Clinical variation in X-linked dominant chondrodysplasia punctata (X-linked dominant ichthyosis)L Feldmeyer, B Mevorah, K H Grzeschik, et al.
Clinical and Experimental Dermatology|May 14, 2011
Erythrokeratoderma variabilis caused by a recessive mutation in GJB3D Fuchs-Telem, Y Pessach, B Mevorah, et al.
Pageof 4