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Journal of Cellular Biochemistry|May 1, 1992
Sharing of antigenic epitopes between synaptophysin and granulophysinA Shalev, J M Gerrard, C Robertson, et al.Biochemical Medicine and Metabolic Biology|October 1, 1986
The salivary flow rate and composition of whole and parotid resting and stimulated saliva in young and old healthy subjectsH Ben-Aryeh, A Shalev, R Szargel, 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.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.American Journal of Medical Genetics. Part A|September 15, 2015
A PIGN mutation responsible for multiple congenital anomalies-hypotonia-seizures syndrome 1 (MCAHS1) in an Israeli-Arab familyMorad Khayat, Joseph Mark Tilghman, Ilana Chervinsky, et al.Pageof 25