Showing results (161-170 of 242) with videos related to
Sort By:
Pageof 25
Infection|April 3, 2007
Conservative management of implantable cardioverter defibrillator-related endocarditis due to Bacillus sppA Shalev, J Gilad, K Riesenberg, et al.BJOG : an International Journal of Obstetrics and Gynaecology|July 24, 2004
Thrombophilia and stillbirth: possible connection by intrauterine growth restrictionZeev Weiner, Ronit Beck-Fruchter, Amir Weiss, et al.Developmental and Comparative Immunology|January 1, 1984
Specific activity of carp antisera against beta 2-microglobulin (beta 2m) and evidence for a beta 2m homologue in carp (Cyprinus carpio)A Shalev, R R Caspi, L Lögdberg, et al.European Journal of Human Genetics : EJHG|October 3, 2003
Limb-girdle muscular dystrophy 2I: phenotypic variability within a large consanguineous Bedouin family associated with a novel FKRP mutationTamar Harel, Yael Goldberg, Stavit A Shalev, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|November 27, 2004
DRD4 receptor gene exon III polymorphism in inpatient suicidal adolescentsG Zalsman, A Frisch, R Lewis, et al.NPJ Genomic Medicine|September 24, 2021
MCM9 is associated with germline predisposition to early-onset cancer-clinical evidenceYael Goldberg, Ola Aleme, Lilach Peled-Perets, et al.The Journal of Clinical Endocrinology and Metabolism|November 4, 2000
Mutations in the steroidogenic acute regulatory protein (StAR) in six patients with congenital lipoid adrenal hyperplasiaH S Bose, S Sato, J Aisenberg, et al.American Journal of Medical Genetics. Part A|December 15, 2005
Clinical variation of Aarskog syndrome in a large family with 2189delA in the FGD1 geneStavit A Shalev, Elana Chervinski, Ehud Weiner, et al.American Journal of Human Genetics|July 27, 2010
Autosomal-recessive early-onset retinitis pigmentosa caused by a mutation in PDE6G, the gene encoding the gamma subunit of rod cGMP phosphodiesteraseLiron Dvir, Gassoub Srour, Rasmi Abu-Ras, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 8, 2007
Infantile onset progressive cerebellar atrophy and anterior horn cell degeneration--a late onset variant of PCH-1?Dorit Lev, Marina Michelson-Kerman, Chana Vinkler, et al.Pageof 25