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Journal of the Pediatric Infectious Diseases Society|March 14, 2019
A Pilot Study to Reduce Central Line-Associated Bloodstream Infections in Children From Extremely Low-Income Settings With Intestinal Failure-Meeting the ChallengeInbal Fuchs, Dov Rosenbaum, Ilana Klein, et al.
The Israel Medical Association Journal : IMAJ|March 26, 2025
The Effect of Consanguineous Marriage on the Epidemiology of Wilson Disease among Children: A Report from Southern IsraelRaouf Nassar, Nour Ealiwa, Lior Hassan, et al.
Frontiers in Pediatrics|October 29, 2020
Bedouin Children With Celiac Disease: Less Symptoms but More Severe Histological Features at PresentationBaruch Yerushalmi, Sergei Vosko, Galina Ling, et al.
Journal of Pediatric Hematology/Oncology|November 23, 2006
Imerslund-Grasbeck syndrome associated with recurrent aphthous stomatitis and defective neutrophil functionArnon Broides, Baruch Yerushalmi, Rachel Levy, et al.
Acta Paediatrica (Oslo, Norway : 1992)|April 20, 2026
Ethnic Differences in Foreign Body Ingestion: Insights Into Social and Epidemiological AspectsNadine Abboud, Nitzan Abelson, Leon Qarawani, et al.
Journal of Pediatric Gastroenterology and Nutrition|April 9, 2020
Automated Analyzers Are Suited for Diagnosing Celiac Disease Without a BiopsyOrit Rozenberg, Firas Rinawi, Yifat Haritan, et al.
Inflammatory Bowel Diseases|February 21, 2009
Comparison of two dosing methods for induction of response and remission with oral budesonide in active pediatric Crohn's disease: a randomized placebo-controlled trialArie Levine, Michal Kori, Gabriel Dinari, et al.
Journal of Clinical Immunology|March 17, 2017
Incidence of typically Severe Primary Immunodeficiency Diseases in Consanguineous and Non-consanguineous PopulationsArnon Broides, Amit Nahum, Amarilla B Mandola, et al.
Antibiotics (Basel, Switzerland)|September 28, 2024
The Effectiveness of Taurolidine Antimicrobial Locks in Preventing Catheter-Related Bloodstream Infections (CRBSIs) in Children Receiving Parenteral Nutrition: A Case SeriesGalina Ling, Shalom Ben-Shimol, Siham Elamour, et al.
American Journal of Human Genetics|November 2, 2010
Hyperchlorhidrosis caused by homozygous mutation in CA12, encoding carbonic anhydrase XIIMaya Feldshtein, Suliman Elkrinawi, Baruch Yerushalmi, et al.
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