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A Shalev

Showing results (101-110 of 193) with videos related to

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Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|September 15, 2018
Safety of penicillin allergy skin testing in patients with low lung volumes before lung transplantDivya Padmanabhan Menon, Keith Sacco, Jefree A Shalev, et al.
American Journal of Medical Genetics. Part A|November 26, 2009
A new autosomal recessive syndrome characterized by ocular hypertelorism, distinctive face, mental retardation, brachydactyly, and genital abnormalitiesRonen Spiegel, Yoseph Horovitz, Hartmut Peters, et al.
Current Problems in Cardiology|June 17, 1998
Peripheral vascular disease, Part 1T K Bajwa, Y A Shalev, A Gupta, et al.
Genetic Testing|March 21, 2006
High incidence of deafness from three frequent connexin 26 mutations in an isolated communityJoël Zlotogora, Minerva Carasquillo, Saleh Barges, et al.
Pediatric Neurology|December 2, 2006
Hereditary hypotonia, muscle weakness, failure to thrive, and cognitive delay in a large moslem kindredMiriam Kutai, Stavit A Shalev, Ilana Chervinski, et al.
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.
The Journal of Clinical Investigation|April 1, 1993
The protein CD63 is in platelet dense granules, is deficient in a patient with Hermansky-Pudlak syndrome, and appears identical to granulophysinM Nishibori, B Cham, A McNicol, et al.
Journal of Medical Genetics|May 29, 2010
Identification of a prevalent founder mutation in an Israeli Muslim Arab village confirms the role of PRCD in the aetiology of retinitis pigmentosa in humansM J Nevet, S A Shalev, J Zlotogora, et al.
American Journal of Medical Genetics. Part A|October 4, 2011
Clinical characterization of a newly described neonatal diabetes syndrome caused by RFX6 mutationsRonen Spiegel, Angus Dobbie, Corina Hartman, et al.
Journal of Child Neurology|August 1, 1997
Deletion (4)(q33 --> qter): a case report and review of the literatureZ Borochowitz, S A Shalev, I Yehudai, et al.
Pageof 20

Showing results (101-110 of 193) with videos related to

Sort By:
Pageof 20
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|September 15, 2018
Safety of penicillin allergy skin testing in patients with low lung volumes before lung transplantDivya Padmanabhan Menon, Keith Sacco, Jefree A Shalev, et al.
American Journal of Medical Genetics. Part A|November 26, 2009
A new autosomal recessive syndrome characterized by ocular hypertelorism, distinctive face, mental retardation, brachydactyly, and genital abnormalitiesRonen Spiegel, Yoseph Horovitz, Hartmut Peters, et al.
Current Problems in Cardiology|June 17, 1998
Peripheral vascular disease, Part 1T K Bajwa, Y A Shalev, A Gupta, et al.
Genetic Testing|March 21, 2006
High incidence of deafness from three frequent connexin 26 mutations in an isolated communityJoël Zlotogora, Minerva Carasquillo, Saleh Barges, et al.
Pediatric Neurology|December 2, 2006
Hereditary hypotonia, muscle weakness, failure to thrive, and cognitive delay in a large moslem kindredMiriam Kutai, Stavit A Shalev, Ilana Chervinski, et al.
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.
The Journal of Clinical Investigation|April 1, 1993
The protein CD63 is in platelet dense granules, is deficient in a patient with Hermansky-Pudlak syndrome, and appears identical to granulophysinM Nishibori, B Cham, A McNicol, et al.
Journal of Medical Genetics|May 29, 2010
Identification of a prevalent founder mutation in an Israeli Muslim Arab village confirms the role of PRCD in the aetiology of retinitis pigmentosa in humansM J Nevet, S A Shalev, J Zlotogora, et al.
American Journal of Medical Genetics. Part A|October 4, 2011
Clinical characterization of a newly described neonatal diabetes syndrome caused by RFX6 mutationsRonen Spiegel, Angus Dobbie, Corina Hartman, et al.
Journal of Child Neurology|August 1, 1997
Deletion (4)(q33 --> qter): a case report and review of the literatureZ Borochowitz, S A Shalev, I Yehudai, et al.
Pageof 20