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The British Journal of Dermatology
|
May 13, 2005
Novel mutation of connexin 31 causing erythrokeratoderma variabilis
L Feldmeyer, L Plantard, B Mevorah, et al.
The British Journal of Dermatology
|
December 1, 1981
X-linked recessive ichthyosis in three sisters: evidence for homozygosity
B 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 chromosome
P 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 phenotypes
B 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 manifestations
P 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 activity
B 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 pilaris
G 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 GJB3
D Fuchs-Telem, Y Pessach, B Mevorah, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 36) with videos related to
Sort By:
Page
of 4
The British Journal of Dermatology
|
May 13, 2005
Novel mutation of connexin 31 causing erythrokeratoderma variabilis
L Feldmeyer, L Plantard, B Mevorah, et al.
The British Journal of Dermatology
|
December 1, 1981
X-linked recessive ichthyosis in three sisters: evidence for homozygosity
B 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 chromosome
P 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 phenotypes
B 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 manifestations
P 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 activity
B 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 pilaris
G 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 GJB3
D Fuchs-Telem, Y Pessach, B Mevorah, et al.
Page
of 4