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Digestive Diseases and Sciences|March 21, 2007
The beneficial effect of aspirin and enoxaparin on fibrosis progression and regenerative activity in a rat model of cirrhosisNimer Assy, Osamah Hussein, Abdallah Khalil, et al.Israel Journal of Health Policy Research|April 12, 2022
Keeping our children safe: piloting a hospital-based home-visitation program in IsraelLigat Shalev, Anthony Luder, Sivan Spitzer, et al.Pediatric Rheumatology Online Journal|June 26, 2012
Prolidase deficiency associated with systemic lupus erythematosus (SLE): single site experience and literature reviewYonatan Butbul Aviel, Hana Mandel, Emily Avitan Hersh, et al.The Pediatric Infectious Disease Journal|September 29, 2006
Acute human parvovirus B-19 infection in hospitalized children: A serologic and molecular surveyDan Miron, Anthony Luder, Yoseph Horovitz, et al.European Journal of Pediatrics|July 15, 2020
Pediatrician, watch out for corona-phobiaChen Rosenberg Danziger, Irit Krause, Oded Scheuerman, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 25, 2009
A broad spectrum of developmental delay in a large cohort of prolidase deficiency patients demonstrates marked interfamilial and intrafamilial phenotypic variabilityTzipora C Falik-Zaccai, Morad Khayat, Anthony Luder, et al.Archives of Dermatology|March 19, 2008
Defective lamellar granule secretion in arthrogryposis, renal dysfunction, and cholestasis syndrome caused by a mutation in VPS33BDov Hershkovitz, Hannah Mandel, Akemi Ishida-Yamamoto, et al.Journal of Inherited Metabolic Disease|November 15, 2015
Primary and maternal 3-methylcrotonyl-CoA carboxylase deficiency: insights from the Israel newborn screening programJonathan Rips, Shlomo Almashanu, Hanna Mandel, et al.The Pediatric Infectious Disease Journal|October 14, 2015
Severe Acute Mastoiditis Admission is Not Related to Delayed Antibiotic Treatment for Antecedent Acute Otitis MediaZachi Grossman, Yoav Zehavi, Eugene Leibovitz, et al.American Journal of Human Genetics|June 24, 2008
Mitochondrial hsp60 chaperonopathy causes an autosomal-recessive neurodegenerative disorder linked to brain hypomyelination and leukodystrophyDaniella Magen, Costa Georgopoulos, Peter Bross, et al.Pageof 3