Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Michal Stern Zimmer"'
Autor:
Odelia Chorin, Yoel Hirsch, Rachel Rock, Liat Salzer Sheelo, Yael Goldberg, Hanna Mandel, Tova Hershkovitz, Nicole Fleischer, Lior Greenbaum, Uriel Katz, Ortal Barel, Nasrin Hamed, Bruria Ben-Zeev, Shoshana Greenberger, Nadra Nasser Samra, Michal Stern Zimmer, Annick Raas-Rothschild, Ben Pode-Shakked
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Introduction: Vici Syndrome is a rare, severe, neurodevelopmental/neurodegenerative disorder with multi-systemic manifestations presenting in infancy. It is mainly characterized by global developmental delay, seizures, agenesis of the corpus callosum
Externí odkaz:
https://doaj.org/article/8e8a48b5d2af47e29c4d8e95ea739427
Autor:
Lilach C. Regev-Epstein, Yaacov Frishberg, Miriam Davidovits, Daniel Landau, Daniella Magen, Irit Weismann, Michal Stern-Zimmer, Pazit Beckerman, Lital Keinan-Boker, Ronit Calderon-Margalit, Asaf Vivante
Publikováno v:
Clinical Journal of the American Society of Nephrology. 18:363-373
Autor:
Maayan Kagan, Rotem Semo-Oz, Yishay Ben Moshe, Danit Atias-Varon, Irit Tirosh, Michal Stern-Zimmer, Aviva Eliyahu, Annick Raas-Rothschild, Maayan Bivas, Omer Shlomovitz, Odelia Chorin, Rachel Rock, Michal Tzadok, Bruria Ben-Zeev, Gali Heimer, Yoav Bolkier, Noah Gruber, Adi Dagan, Bat El Bar Aluma, Itai M. Pessach, Gideon Rechavi, Ortal Barel, Ben Pode-Shakked, Yair Anikster, Asaf Vivante
Publikováno v:
Frontiers in Genetics. 13
Background: Genetic conditions contribute a significant portion of disease etiologies in children admitted to general pediatric wards worldwide. While exome sequencing (ES) has improved clinical diagnosis and management over a variety of pediatric su
Autor:
Gilad Twig, Tomer Erlich, Estela Derazne, Gil Efron, Michal Stern-Zimmer, Asaf Vivante, Dorit Tzur, Oren Pleniceanu, Arnon Afek, Jeremy D. Kark, Lital Keinan-Boker, Ronit Calderon-Margalit
Publikováno v:
Kidney International Reports, Vol 6, Iss 4, Pp 946-952 (2021)
Kidney International Reports
Kidney International Reports
Introduction Congenital anomalies of the kidney and urinary tract (CAKUT) are the most common kidney diseases in childhood. Alterations in genes governing nephrogenesis may cause CAKUT, and in some cases may contribute to development of urinary tract
Autor:
Tomer Erlich, Arnon Afek, Karl Skorecki, Asaf Vivante, Guy Verhovsky, Gilad Twig, Ronit Calderon-Margalit, Dorit Tzur, Michal Stern-Zimmer, Oren Pleniceanu, Lital Keinan-Boker
Publikováno v:
J Am Soc Nephrol
Background Increasing cancer incidence among children alongside improved treatments has resulted in a growing number of pediatric cancer survivors. Despite childhood cancer survivors' exposure to various factors that compromise kidney function, few s
Autor:
Dorit Tzur, Noah Gruber, Asaf Vivante, Gilad Twig, Michal Stern-Zimmer, Tomer Erlich, Karl Skorecki, Arnon Afek, Oren Pleniceanu, Ronit Calderon-Margalit, Lital Keinan-Boker
Publikováno v:
Pediatric Nephrology. 36:333-340
Diabetic kidney disease (DKD) is becoming increasingly common among children. We aimed to estimate the risk of end-stage renal disease (ESKD) and mortality among adolescents with type 1 diabetes mellitus (T1DM) or type 2 diabetes mellitus (T2DM) and
Publikováno v:
Pediatric Nephrology. 36:1387-1396
Chronic kidney disease (CKD) is a major public health challenge, affecting as much as 8 to 18% of the world population. Identifying childhood risk factors for future CKD may help clinicians make early diagnoses and initiation of preventive interventi
Autor:
Oren, Pleniceanu, Gilad, Twig, Dorit, Tzur, Noah, Gruber, Michal, Stern-Zimmer, Arnon, Afek, Tomer, Erlich, Lital, Keinan-Boker, Karl, Skorecki, Ronit, Calderon-Margalit, Asaf, Vivante
Publikováno v:
Pediatric nephrology (Berlin, Germany). 36(2)
Diabetic kidney disease (DKD) is becoming increasingly common among children. We aimed to estimate the risk of end-stage renal disease (ESKD) and mortality among adolescents with type 1 diabetes mellitus (T1DM) or type 2 diabetes mellitus (T2DM) and
Publikováno v:
Pediatric Nephrology. 36:1661-1661
The authors regret that the name of the author Michal Stern-Zimmer was incorrectly rendered as “Michal Stern Zimmer.”
Autor:
Ronit Calderon-Margalit, Gil Efron, Oren Pleniceanu, Dorit Tzur, Michal Stern-Zimmer, Arnon Afek, Tomer Erlich, Estela Derazne, Jeremy D. Kark, Lital Keinan-Boker, Gilad Twig, Asaf Vivante
Publikováno v:
Kidney International Reports, Vol 6, Iss 4, Pp 946-952 (2021)
Introduction: Congenital anomalies of the kidney and urinary tract (CAKUT) are the most common kidney diseases in childhood. Alterations in genes governing nephrogenesis may cause CAKUT, and in some cases may contribute to development of urinary trac
Externí odkaz:
https://doaj.org/article/ad3fa5fb64264c1db97537f8881490fc