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Ruth Gershoni-Baruch

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American Journal of Medical Genetics. Part A|September 10, 2005
Autosomal recessive Oliver-McFarlane syndrome: retinitis pigmentosa, short stature (GH deficiency), trichomegaly, and hair anomalies or CPD syndrome (chorioretinopathy-pituitary dysfunction)Motti Haimi, Ruth Gershoni-Baruch
The Journal of Pediatrics|November 15, 2003
Prevalence and significance of mutations in the familial Mediterranean fever gene in Henoch-Schönlein purpuraRuth Gershoni-Baruch, Yiftah Broza, Riva Brik
Tumori|May 6, 2003
Cisplatin treatment triggers familial Mediterranean fever attacksElias Toubi, Ruth Gershoni-Baruch, Abraham Kuten
Preventive Medicine|February 8, 2008
Socio-demographic and clinical profile of BRCA1/2 mutation carriers opting for prophylactic oophorectomyEfrat Dagan, Sharon Gil, Ruth Gershoni-Baruch
The Israel Medical Association Journal : IMAJ|January 15, 2004
Infantile familial Mediterranean feverRiva Brik, Marwan Shinawi, Ruth Gershoni-Baruch
The Israel Medical Association Journal : IMAJ|May 21, 2004
Permanent neonatal diabetesDoua Bakri, Ruth Gershoni-Baruch, Naim Shehadeh
The New England Journal of Medicine|November 5, 2004
Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi JewsJudith Aharon-Peretz, Hanna Rosenbaum, Ruth Gershoni-Baruch
Cancer Genetics and Cytogenetics|March 14, 2007
Aberration of 3q and monosomy 7 in a child with acute myelogenous leukemiaMotti Haimi, Ronit Elhasid, Nivin Moustafa, et al.
European Journal of Human Genetics : EJHG|April 9, 2002
The differential contribution of MEFV mutant alleles to the clinical profile of familial Mediterranean feverRuth Gershoni-Baruch, Riva Brik, Marwan Shinawi, et al.
Pediatric Nephrology (Berlin, Germany)|June 23, 2006
Henoch-Schonlein purpura: polymorphisms in thrombophilia genesEfrat Dagan, Riva Brik, Yiphtah Broza, et al.
Pageof 8

Showing results (1-10 of 78) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics. Part A|September 10, 2005
Autosomal recessive Oliver-McFarlane syndrome: retinitis pigmentosa, short stature (GH deficiency), trichomegaly, and hair anomalies or CPD syndrome (chorioretinopathy-pituitary dysfunction)Motti Haimi, Ruth Gershoni-Baruch
The Journal of Pediatrics|November 15, 2003
Prevalence and significance of mutations in the familial Mediterranean fever gene in Henoch-Schönlein purpuraRuth Gershoni-Baruch, Yiftah Broza, Riva Brik
Tumori|May 6, 2003
Cisplatin treatment triggers familial Mediterranean fever attacksElias Toubi, Ruth Gershoni-Baruch, Abraham Kuten
Preventive Medicine|February 8, 2008
Socio-demographic and clinical profile of BRCA1/2 mutation carriers opting for prophylactic oophorectomyEfrat Dagan, Sharon Gil, Ruth Gershoni-Baruch
The Israel Medical Association Journal : IMAJ|January 15, 2004
Infantile familial Mediterranean feverRiva Brik, Marwan Shinawi, Ruth Gershoni-Baruch
The Israel Medical Association Journal : IMAJ|May 21, 2004
Permanent neonatal diabetesDoua Bakri, Ruth Gershoni-Baruch, Naim Shehadeh
The New England Journal of Medicine|November 5, 2004
Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi JewsJudith Aharon-Peretz, Hanna Rosenbaum, Ruth Gershoni-Baruch
Cancer Genetics and Cytogenetics|March 14, 2007
Aberration of 3q and monosomy 7 in a child with acute myelogenous leukemiaMotti Haimi, Ronit Elhasid, Nivin Moustafa, et al.
European Journal of Human Genetics : EJHG|April 9, 2002
The differential contribution of MEFV mutant alleles to the clinical profile of familial Mediterranean feverRuth Gershoni-Baruch, Riva Brik, Marwan Shinawi, et al.
Pediatric Nephrology (Berlin, Germany)|June 23, 2006
Henoch-Schonlein purpura: polymorphisms in thrombophilia genesEfrat Dagan, Riva Brik, Yiphtah Broza, et al.
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