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Journal of Pediatric Orthopedics|September 25, 2008
Correction of lower limb deformities in children with renal osteodystrophy by the Ilizarov methodElhanan Bar-On, Zvi Horesh, Kalman Katz, et al.
European Journal of Pediatrics|July 15, 2020
Pediatrician, watch out for corona-phobiaChen Rosenberg Danziger, Irit Krause, Oded Scheuerman, et al.
Pediatric Transplantation|November 27, 2023
Clinical profile of re-hospitalizations in pediatric kidney and liver transplant recipientsAdi Shohet, Noa Ziv, Rachel Gavish, et al.
European Journal of Human Genetics : EJHG|September 28, 2018
Variant in SCYL1 gene causes aberrant splicing in a family with cerebellar ataxia, recurrent episodes of liver failure, and growth retardationAdi Shohet, Lior Cohen, Danielle Haguel, et al.
JIMD Reports|February 20, 2020
An ancestral variant causing type I xanthinuria in Turkmen and Arab families is predicted to prevail in the Afro-Asian stone-forming beltHava Peretz, Michael Korostishevsky, David M Steinberg, et al.
Gene|May 17, 2023
A novel SLC25A13 gene splice site variant causes Citrin deficiency in an infantNimrod Sachs, Oded Wechsberg, Yuval E Landau, et al.
The Israel Medical Association Journal : IMAJ|March 22, 2023
The Effect of the COVID-19 Pandemic on Pediatric Respiratory HospitalizationsNimrod Sachs, Lotem Goldberg, Yoel Levinsky, et al.
Clinical Transplantation|August 5, 2016
Focal segmental glomerulosclerosis in pediatric kidney transplantation: 30 years' experienceRoxana Cleper, Irit Krause, Nathan Bar Nathan, et al.
Pediatric Nephrology (Berlin, Germany)|July 22, 2018
Response to erythropoietin in pediatric patients with chronic kidney disease: insights from an in vitro bioassayRachel Gavish, Salmas Watad, Nathalie Ben-Califa, et al.
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