Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Reuven Bergman

Showing results (101-110 of 163) with videos related to

Pageof 17
Sort By:
International Archives of Allergy and Immunology|February 8, 2007
A novel missense mutation in CIAS1 encoding the pyrin-like protein, cryopyrin, causes familial cold autoinflammatory syndrome in a family of Ethiopian originStavit A Shalev, Eli Sprecher, Margarita Indelman, et al.
JAMA Dermatology|April 18, 2014
Atrophic skin patches with abnormal elastic fibers as a presenting sign of the MASS phenotype associated with mutation in the fibrillin 1 geneReuven Bergman, Mariela Judith Nevet, Hadas Gescheidt-Shoshany, et al.
The American Journal of Dermatopathology|December 24, 2010
A case of H syndrome showing immunophenotye similarities to Rosai-Dorfman diseaseEmily Avitan-Hersh, Hanna Mandel, Margarita Indelman, et al.
The American Journal of Dermatopathology|July 18, 2019
Primary Cutaneous Clonal CD8+ T-Cell Lymphoproliferative Disorder Associated With Immunodeficiency due to RAG1 MutationEmily Avitan-Hersh, Polina Stepensky, Irina Zaidman, et al.
The American Journal of Dermatopathology|May 19, 2005
Absence of intraepidermal glycosyltransferase ppGalNac-T3 expression in familial tumoral calcinosisOrit Topaz, Reuven Bergman, Ulla Mandel, et al.
The Journal of Investigative Dermatology|August 25, 2005
Identification of a novel locus associated with congenital recessive ichthyosis on 12p11.2-q13Mordechai Mizrachi-Koren, Dan Geiger, Margarita Indelman, et al.
International Journal of Dermatology|June 30, 2005
A comparison of anti-desmoglein antibodies and indirect immunofluorescence in the serodiagnosis of pemphigus vulgarisIrena Zagorodniuk, Sara Weltfriend, Lily Shtruminger, et al.
Journal of Cutaneous Pathology|October 10, 2019
Follicular eruption with folliculotropic lymphocytic infiltrates associated with anti-tumor necrosis factor alpha therapy: Report and study of 3 casesEmily Avitan-Hersh, David Dias-Polak, Michal Ramon, et al.
NMR in Biomedicine|April 23, 2015
In vivo assessment of aged human skin with a unilateral NMR scannerElad Bergman, Yifat Sarda, Noa Ritz, et al.
Dermatology (Basel, Switzerland)|March 1, 2014
Molecular analysis of a series of Israeli families with Comèl-Netherton syndromeShirli Israeli, Ofer Sarig, Ben Zion Garty, et al.
Pageof 17

Showing results (101-110 of 163) with videos related to

Sort By:
Pageof 17
International Archives of Allergy and Immunology|February 8, 2007
A novel missense mutation in CIAS1 encoding the pyrin-like protein, cryopyrin, causes familial cold autoinflammatory syndrome in a family of Ethiopian originStavit A Shalev, Eli Sprecher, Margarita Indelman, et al.
JAMA Dermatology|April 18, 2014
Atrophic skin patches with abnormal elastic fibers as a presenting sign of the MASS phenotype associated with mutation in the fibrillin 1 geneReuven Bergman, Mariela Judith Nevet, Hadas Gescheidt-Shoshany, et al.
The American Journal of Dermatopathology|December 24, 2010
A case of H syndrome showing immunophenotye similarities to Rosai-Dorfman diseaseEmily Avitan-Hersh, Hanna Mandel, Margarita Indelman, et al.
The American Journal of Dermatopathology|July 18, 2019
Primary Cutaneous Clonal CD8+ T-Cell Lymphoproliferative Disorder Associated With Immunodeficiency due to RAG1 MutationEmily Avitan-Hersh, Polina Stepensky, Irina Zaidman, et al.
The American Journal of Dermatopathology|May 19, 2005
Absence of intraepidermal glycosyltransferase ppGalNac-T3 expression in familial tumoral calcinosisOrit Topaz, Reuven Bergman, Ulla Mandel, et al.
The Journal of Investigative Dermatology|August 25, 2005
Identification of a novel locus associated with congenital recessive ichthyosis on 12p11.2-q13Mordechai Mizrachi-Koren, Dan Geiger, Margarita Indelman, et al.
International Journal of Dermatology|June 30, 2005
A comparison of anti-desmoglein antibodies and indirect immunofluorescence in the serodiagnosis of pemphigus vulgarisIrena Zagorodniuk, Sara Weltfriend, Lily Shtruminger, et al.
Journal of Cutaneous Pathology|October 10, 2019
Follicular eruption with folliculotropic lymphocytic infiltrates associated with anti-tumor necrosis factor alpha therapy: Report and study of 3 casesEmily Avitan-Hersh, David Dias-Polak, Michal Ramon, et al.
NMR in Biomedicine|April 23, 2015
In vivo assessment of aged human skin with a unilateral NMR scannerElad Bergman, Yifat Sarda, Noa Ritz, et al.
Dermatology (Basel, Switzerland)|March 1, 2014
Molecular analysis of a series of Israeli families with Comèl-Netherton syndromeShirli Israeli, Ofer Sarig, Ben Zion Garty, et al.
Pageof 17