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Reuven Bergman

Showing results (121-130 of 163) with videos related to

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The Israel Medical Association Journal : IMAJ|May 20, 2014
Human amnion membrane as a substrate for the detection of autoantibodies in pemphigus vulgaris and bullous pemphigoidTanya Sezin, Emily Avitan-Hersh, Margarita Indelman, et al.
Pediatric Rheumatology Online Journal|June 26, 2012
Prolidase deficiency associated with systemic lupus erythematosus (SLE): single site experience and literature reviewYonatan Butbul Aviel, Hana Mandel, Emily Avitan Hersh, et al.
Anti-Cancer Drugs|August 11, 2016
Acne during adolescence did not predict skin rash reaction to cetuximabGil Bar-Sela, Sharon Avgush, Orit Kaidar-Person, et al.
The Journal of Investigative Dermatology|November 26, 2002
A missense mutation in CDH3, encoding P-cadherin, causes hypotrichosis with juvenile macular dystrophyMargarita Indelman, Reuven Bergman, Raziel Lurie, et al.
Archives of Dermatology|March 19, 2008
Defective lamellar granule secretion in arthrogryposis, renal dysfunction, and cholestasis syndrome caused by a mutation in VPS33BDov Hershkovitz, Hannah Mandel, Akemi Ishida-Yamamoto, et al.
The Journal of Investigative Dermatology|January 28, 2014
Olmsted syndrome caused by a homozygous recessive mutation in TRPV3Ori Eytan, Dana Fuchs-Telem, Baruch Mevorach, et al.
Cancer|December 15, 2005
Classic Kaposi sarcoma. Which KSHV-seropositive individuals are at risk?Emma Guttman-Yassky, Jonathan Dubnov, Zippi Kra-Oz, et al.
Journal of the American Academy of Dermatology|March 12, 2005
Familial mycosis fungoides: report of 6 kindreds and a study of the HLA systemEmmilia Hodak, Tirza Klein, Boaz Gabay, et al.
The Journal of Clinical Endocrinology and Metabolism|November 19, 2013
Postzygotic HRAS mutation causing both keratinocytic epidermal nevus and thymoma and associated with bone dysplasia and hypophosphatemia due to elevated FGF23Emily Avitan-Hersh, Sameh Tatur, Margarita Indelman, et al.
Experimental Dermatology|March 27, 2013
The sound of silence: autosomal recessive congenital ichthyosis caused by a synonymous mutation in ABCA12Tomer Goldsmith, Dana Fuchs-Telem, Shirli Israeli, et al.
Pageof 17

Showing results (121-130 of 163) with videos related to

Sort By:
Pageof 17
The Israel Medical Association Journal : IMAJ|May 20, 2014
Human amnion membrane as a substrate for the detection of autoantibodies in pemphigus vulgaris and bullous pemphigoidTanya Sezin, Emily Avitan-Hersh, Margarita Indelman, et al.
Pediatric Rheumatology Online Journal|June 26, 2012
Prolidase deficiency associated with systemic lupus erythematosus (SLE): single site experience and literature reviewYonatan Butbul Aviel, Hana Mandel, Emily Avitan Hersh, et al.
Anti-Cancer Drugs|August 11, 2016
Acne during adolescence did not predict skin rash reaction to cetuximabGil Bar-Sela, Sharon Avgush, Orit Kaidar-Person, et al.
The Journal of Investigative Dermatology|November 26, 2002
A missense mutation in CDH3, encoding P-cadherin, causes hypotrichosis with juvenile macular dystrophyMargarita Indelman, Reuven Bergman, Raziel Lurie, et al.
Archives of Dermatology|March 19, 2008
Defective lamellar granule secretion in arthrogryposis, renal dysfunction, and cholestasis syndrome caused by a mutation in VPS33BDov Hershkovitz, Hannah Mandel, Akemi Ishida-Yamamoto, et al.
The Journal of Investigative Dermatology|January 28, 2014
Olmsted syndrome caused by a homozygous recessive mutation in TRPV3Ori Eytan, Dana Fuchs-Telem, Baruch Mevorach, et al.
Cancer|December 15, 2005
Classic Kaposi sarcoma. Which KSHV-seropositive individuals are at risk?Emma Guttman-Yassky, Jonathan Dubnov, Zippi Kra-Oz, et al.
Journal of the American Academy of Dermatology|March 12, 2005
Familial mycosis fungoides: report of 6 kindreds and a study of the HLA systemEmmilia Hodak, Tirza Klein, Boaz Gabay, et al.
The Journal of Clinical Endocrinology and Metabolism|November 19, 2013
Postzygotic HRAS mutation causing both keratinocytic epidermal nevus and thymoma and associated with bone dysplasia and hypophosphatemia due to elevated FGF23Emily Avitan-Hersh, Sameh Tatur, Margarita Indelman, et al.
Experimental Dermatology|March 27, 2013
The sound of silence: autosomal recessive congenital ichthyosis caused by a synonymous mutation in ABCA12Tomer Goldsmith, Dana Fuchs-Telem, Shirli Israeli, et al.
Pageof 17