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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 28, 2014
Impaired renal growth hormone JAK/STAT5 signaling in chronic kidney diseaseDebbie Wiezel, Mohammed Hani Assadi, Daniel Landau, et al.
The Pediatric Infectious Disease Journal|July 10, 2024
Differential Serum Phosphate Levels in Pediatric Febrile Syndromes and Their Clinical SignificanceYonatan Milman, Daniel Landau, Asaf Lebel, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|August 25, 2011
A marked deficiency in circulating and renal IGF-I peptide does not inhibit compensatory renal enlargement in uninephrectomized miceDaniel Landau, Jaclyn Biada, Yu Chen, et al.
The Pediatric Infectious Disease Journal|November 19, 2019
Q Fever and Kingella kingae Endocarditis in a Toddler: A Rare Coinfection CaseShelly Kagan, Itzhak Levy, Liat Ashkenazi-Hoffnung, et al.
Kidney International Reports|January 1, 2020
Eculizumab Safety: Five-Year Experience From the Global Atypical Hemolytic Uremic Syndrome RegistryEric Rondeau, Spero R Cataland, Imad Al-Dakkak, et al.
Plos One|September 12, 2019
The enemy's gaze: Immersive virtual environments enhance peace promoting attitudes and emotions in violent intergroup conflictsYossi Hasson, Noa Schori-Eyal, Daniel Landau, et al.
The Journal of Pediatrics|March 18, 2003
Transient neonatal hyperkalemia in the antenatal (ROMK defective) Bartter syndromeGal Finer, Hanna Shalev, Ohad S Birk, et al.
Pediatric Transplantation|November 24, 2021
EBV, CMV, and BK viral infections in pediatric kidney transplantation: Frequency, risk factors, treatment, and outcomesShelly Levi, Miriam Davidovits, Hadas Alfandari, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 15, 2003
The effect of growth hormone on the development of diabetic kidney disease in ratsDaniel Landau, Eytan Israel, Inessa Rivkis, et al.
Molecular Genetics and Metabolism|March 21, 2007
Identification and characterization of the first mutation (Arg776Cys) in the C-terminal domain of the Human Molybdenum Cofactor Sulfurase (HMCS) associated with type II classical xanthinuriaHava Peretz, Meirav Shtauber Naamati, David Levartovsky, et al.
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