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Reuven Bergman

Showing results (91-100 of 163) with videos related to

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Journal of the American Academy of Dermatology|September 12, 2016
Remarkable differences in the epidemiology of pemphigus among two ethnic populations in the same geographic regionKhalaf Kridin, Shira Zelber-Sagi, Mogher Khamaisi, et al.
Archives of Dermatology|March 23, 2005
The alopecias associated with vitamin D-dependent rickets type IIA and with hairless gene mutations: a comparative clinical, histologic, and immunohistochemical studyReuven Bergman, Rinat Schein-Goldshmid, Zeev Hochberg, et al.
The American Journal of Dermatopathology|July 21, 2012
Acrokeratosis verruciformis of Hopf showing P602L mutation in ATP2A2 and overlapping histopathological features with Darier diseaseReuven Bergman, Tanya Sezin, Margarita Indelman, et al.
Journal of the American Academy of Dermatology|January 20, 2010
Disadhesion of epidermal keratinocytes: a histologic clue to palmoplantar keratodermas caused by DSG1 mutationsReuven Bergman, Dov Hershkovitz, Dana Fuchs, et al.
Archives of Dermatological Research|November 24, 2007
Rapid detection of homozygous mutations in congenital recessive ichthyosisJennie Lugassy, Hans Christian Hennies, Margarita Indelman, et al.
Journal of Cutaneous Pathology|July 24, 2002
Human telomerase RNA component expression in Spitz nevi, common melanocytic nevi, and malignant melanomasEmma Guttman-Yassky, Reuven Bergman, Lena Manov, et al.
Frontiers in Cellular and Infection Microbiology|July 26, 2021
Global CpG DNA Methylation Footprint in Kaposi's SarcomaGuy Journo, Anuj Ahuja, David Dias-Polak, et al.
The Journal of Investigative Dermatology|April 17, 2004
Homozygous splice site mutations in PKP1 result in loss of epidermal plakophilin 1 expression and underlie ectodermal dysplasia/skin fragility syndrome in two consanguineous familiesEli Sprecher, Vered Molho-Pessach, Arieh Ingber, et al.
The American Journal of Dermatopathology|July 24, 2019
A Case of Oral Florid Papillomatosis (Verrucous Carcinoma) With Lack of Evidence for Human Papillomavirus InvolvementDavid Dias-Polak, Zipi Kra-Oz, Moran Szwarcwort-Cohen, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|January 9, 2007
The autologous serum skin test in a cohort of chronic idiopathic urticaria patients compared to respiratory allergy patients and healthy individualsEmma Guttman-Yassky, Reuven Bergman, Carcom Maor, et al.
Pageof 17

Showing results (91-100 of 163) with videos related to

Sort By:
Pageof 17
Journal of the American Academy of Dermatology|September 12, 2016
Remarkable differences in the epidemiology of pemphigus among two ethnic populations in the same geographic regionKhalaf Kridin, Shira Zelber-Sagi, Mogher Khamaisi, et al.
Archives of Dermatology|March 23, 2005
The alopecias associated with vitamin D-dependent rickets type IIA and with hairless gene mutations: a comparative clinical, histologic, and immunohistochemical studyReuven Bergman, Rinat Schein-Goldshmid, Zeev Hochberg, et al.
The American Journal of Dermatopathology|July 21, 2012
Acrokeratosis verruciformis of Hopf showing P602L mutation in ATP2A2 and overlapping histopathological features with Darier diseaseReuven Bergman, Tanya Sezin, Margarita Indelman, et al.
Journal of the American Academy of Dermatology|January 20, 2010
Disadhesion of epidermal keratinocytes: a histologic clue to palmoplantar keratodermas caused by DSG1 mutationsReuven Bergman, Dov Hershkovitz, Dana Fuchs, et al.
Archives of Dermatological Research|November 24, 2007
Rapid detection of homozygous mutations in congenital recessive ichthyosisJennie Lugassy, Hans Christian Hennies, Margarita Indelman, et al.
Journal of Cutaneous Pathology|July 24, 2002
Human telomerase RNA component expression in Spitz nevi, common melanocytic nevi, and malignant melanomasEmma Guttman-Yassky, Reuven Bergman, Lena Manov, et al.
Frontiers in Cellular and Infection Microbiology|July 26, 2021
Global CpG DNA Methylation Footprint in Kaposi's SarcomaGuy Journo, Anuj Ahuja, David Dias-Polak, et al.
The Journal of Investigative Dermatology|April 17, 2004
Homozygous splice site mutations in PKP1 result in loss of epidermal plakophilin 1 expression and underlie ectodermal dysplasia/skin fragility syndrome in two consanguineous familiesEli Sprecher, Vered Molho-Pessach, Arieh Ingber, et al.
The American Journal of Dermatopathology|July 24, 2019
A Case of Oral Florid Papillomatosis (Verrucous Carcinoma) With Lack of Evidence for Human Papillomavirus InvolvementDavid Dias-Polak, Zipi Kra-Oz, Moran Szwarcwort-Cohen, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|January 9, 2007
The autologous serum skin test in a cohort of chronic idiopathic urticaria patients compared to respiratory allergy patients and healthy individualsEmma Guttman-Yassky, Reuven Bergman, Carcom Maor, et al.
Pageof 17