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European Journal of Medical Genetics|July 24, 2020
Based on a cohort of 52,879 microarrays, recurrent intragenic FBN2 deletion encompassing exons 1-8 does not cause Beals syndromeIdit Maya, Sarit Kahana, Ifaat Agmon-Fishman, et al.
ERJ Open Research|January 28, 2025
Treatment effects of CFTR modulators on people with cystic fibrosis carrying the Q359K/T360K variantKarin Yaacoby-Bianu, Moshe Heching, Mordechai R Kramer, et al.
The Israel Medical Association Journal : IMAJ|November 29, 2020
The Impact of the COVID-19 Pandemic on General Surgery Acute Admissions and Urgent Operations: A Comparative Prospective StudyEyal Aviran, Shachar Laks, Haggai Benvenisti, et al.
Prenatal Diagnosis|December 17, 2021
High rate of abnormal findings in Prenatal Exome Trio in low risk pregnancies and apparently normal fetusesNoam Vaknin, Noy Azoulay, Erez Tsur, et al.
American Journal of Human Genetics|September 9, 2006
A deleterious mutation in SAMD9 causes normophosphatemic familial tumoral calcinosisOrit Topaz, Margarita Indelman, Ilana Chefetz, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|July 6, 2018
Abdominal computed tomography (CT) scan in the evaluation of refractory puerperal fever: impact on managementMichal Fishel Bartal, Baha M Sibai, Tali Ben-Mayor Bashi, et al.
BMC Medical Education|September 17, 2014
The effect of medical students' gender, ethnicity and attitude towards poetry-reading on the evaluation of a required, clinically-integrated poetry-based educational interventionMordechai Muszkat, Orly Barak, Gadi Lalazar, et al.
Journal of Reproductive Immunology|November 5, 2018
Progesterone treatment enhances the expansion of placental immature myeloid cells in a mouse model of premature laborOla Gutzeit, Linoy Segal, Rivka Hertz, et al.
Prenatal Diagnosis|December 7, 2025
Fetal Macrocephaly: Prenatal Findings and Follow-Up in Cases With High Risk for Abnormal OutcomeHadas Miremberg, Gustavo Malinger, Deborah Kidron, et al.
Journal of Clinical Medicine|August 16, 2020
Should We Report 15q11.2 BP1-BP2 Deletions and Duplications in the Prenatal Setting?Idit Maya, Sharon Perlman, Mordechai Shohat, et al.
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