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Reuven Bergman

Showing results (131-140 of 163) with videos related to

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The Journal of Investigative Dermatology|March 22, 2003
Epidermolytic hyperkeratosis and epidermolysis bullosa simplex caused by frameshift mutations altering the v2 tail domains of keratin 1 and keratin 5Eli Sprecher, Gil Yosipovitch, Reuven Bergman, et al.
International Journal of Dermatology|November 28, 2002
Clinicopathologic reassessment of non-mycosis fungoides primary cutaneous lymphomas during 17 yearsReuven Bergman, Bat-Sheva Marcus-Farber, Lena Manov, et al.
Archives of Dermatological Research|March 21, 2007
Identification of mutations in the human hairless gene in two new families with congenital atrichiaRegina C Betz, Margarita Indelman, Jana Pforr, et al.
Human Genetics|September 10, 2005
A novel homozygous missense mutation in FGF23 causes Familial Tumoral Calcinosis associated with disseminated visceral calcificationIlana Chefetz, Raoul Heller, Assimina Galli-Tsinopoulou, et al.
The American Journal of Dermatopathology|September 16, 2014
A deep penetrating facial congenital melanocytic tumor with bone involvement and ipsilateral eye blindnessReuven Bergman, Miriam W Ben-Arush, Rachel Bar-Shalom, et al.
Journal of the American Academy of Dermatology|August 16, 2006
Homozygosity mapping as a screening tool for the molecular diagnosis of hereditary skin diseases in consanguineous populationsMordechai Mizrachi-Koren, Saar Shemer, Michal Morgan, et al.
American Journal of Human Genetics|September 9, 2006
A deleterious mutation in SAMD9 causes normophosphatemic familial tumoral calcinosisOrit Topaz, Margarita Indelman, Ilana Chefetz, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|December 21, 2010
Large leg ulcers due to autoimmune diseasesAlexander P Rozin, Dana Egozi, Yehuda Ramon, et al.
The Journal of Allergy and Clinical Immunology|May 15, 2009
IL-22-producing "T22" T cells account for upregulated IL-22 in atopic dermatitis despite reduced IL-17-producing TH17 T cellsKristine E Nograles, Lisa C Zaba, Avner Shemer, et al.
Archives of Dermatological Research|September 30, 2008
A large duplication in LIPH underlies autosomal recessive hypotrichosis simplex in four Middle Eastern familiesSagi Nahum, Sandra M Pasternack, Jana Pforr, et al.
Pageof 17

Showing results (131-140 of 163) with videos related to

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Pageof 17
The Journal of Investigative Dermatology|March 22, 2003
Epidermolytic hyperkeratosis and epidermolysis bullosa simplex caused by frameshift mutations altering the v2 tail domains of keratin 1 and keratin 5Eli Sprecher, Gil Yosipovitch, Reuven Bergman, et al.
International Journal of Dermatology|November 28, 2002
Clinicopathologic reassessment of non-mycosis fungoides primary cutaneous lymphomas during 17 yearsReuven Bergman, Bat-Sheva Marcus-Farber, Lena Manov, et al.
Archives of Dermatological Research|March 21, 2007
Identification of mutations in the human hairless gene in two new families with congenital atrichiaRegina C Betz, Margarita Indelman, Jana Pforr, et al.
Human Genetics|September 10, 2005
A novel homozygous missense mutation in FGF23 causes Familial Tumoral Calcinosis associated with disseminated visceral calcificationIlana Chefetz, Raoul Heller, Assimina Galli-Tsinopoulou, et al.
The American Journal of Dermatopathology|September 16, 2014
A deep penetrating facial congenital melanocytic tumor with bone involvement and ipsilateral eye blindnessReuven Bergman, Miriam W Ben-Arush, Rachel Bar-Shalom, et al.
Journal of the American Academy of Dermatology|August 16, 2006
Homozygosity mapping as a screening tool for the molecular diagnosis of hereditary skin diseases in consanguineous populationsMordechai Mizrachi-Koren, Saar Shemer, Michal Morgan, et al.
American Journal of Human Genetics|September 9, 2006
A deleterious mutation in SAMD9 causes normophosphatemic familial tumoral calcinosisOrit Topaz, Margarita Indelman, Ilana Chefetz, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|December 21, 2010
Large leg ulcers due to autoimmune diseasesAlexander P Rozin, Dana Egozi, Yehuda Ramon, et al.
The Journal of Allergy and Clinical Immunology|May 15, 2009
IL-22-producing "T22" T cells account for upregulated IL-22 in atopic dermatitis despite reduced IL-17-producing TH17 T cellsKristine E Nograles, Lisa C Zaba, Avner Shemer, et al.
Archives of Dermatological Research|September 30, 2008
A large duplication in LIPH underlies autosomal recessive hypotrichosis simplex in four Middle Eastern familiesSagi Nahum, Sandra M Pasternack, Jana Pforr, et al.
Pageof 17