Showing results (11-20 of 105) with videos related to
Sort By:
Pageof 11
International Journal of Dermatology|August 12, 2023
Bath psoralen plus ultraviolet-A photochemotherapy for chronic graft-versus-host disease: a retrospective cohort studyRiad Kassem, Aviv Barzilai, Elon Pras, et al.The Israel Medical Association Journal : IMAJ|July 5, 2003
Clinical manifestations in Israeli cystinuria patients and molecular assessment of carrier rates in Libyan Jewish controlsRoy Sidi, Etgar Levy-Nissenbaum, Y Kreiss, et al.Journal of Assisted Reproduction and Genetics|November 7, 2025
Chromosomal abnormalities in primary and secondary recurrent miscarriages: significance for PGT-AJacques Cohen, Michal Kirshenbaum, Anat Grossman-Jonish, et al.Health Expectations : an International Journal of Public Participation in Health Care and Health Policy|May 13, 2014
Factors that affect the decision to undergo amniocentesis in women with normal Down syndrome screening results: it is all about the ageJulia Grinshpun-Cohen, Talya Miron-Shatz, Liat Ries-Levavi, et al.The Israel Medical Association Journal : IMAJ|August 23, 2007
A combined approach to the molecular analysis of cystinuria: from urinalysis to sequencing via genotypingDanny Lotan, Guy Yoskovitz, Luigi Bisceglia, et al.The Israel Medical Association Journal : IMAJ|October 18, 2020
Chromosomal Microarray Evaluation of Fetal VentriculomegalyArik Toren, Sharon Alpern, Michal Berkenstadt, et al.Journal of Applied Physiology (Bethesda, Md. : 1985)|March 3, 2004
Human ACE I/D polymorphism is associated with individual differences in exercise heat toleranceYuval Heled, Daniel S Moran, Liran Mendel, et al.The Journal of Rheumatology|March 3, 2010
Familial Mediterranean fever in children presenting with attacks of fever aloneShai Padeh, Avi Livneh, Elon Pras, et al.The Journal of Pediatrics|March 16, 2010
Familial Mediterranean Fever in the first two years of life: a unique phenotype of disease in evolutionShai Padeh, Avi Livneh, Elon Pras, et al.Journal of Medical Screening|December 14, 2011
The D1152H cystic fibrosis mutation in prenatal carrier screening, patients and prenatal diagnosisLeah Peleg, Mazal Karpati, Silvia Bronstein, et al.Pageof 11