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Prilozi (Makedonska Akademija Na Naukite I Umetnostite. Oddelenie Za Medicinski Nauki)|March 14, 2019
A 4-Year-Old Boy with Beckwith Wiedemann Syndrome (BWS)Aleksandra Janchevska, Velibor Tasic, Nevenka Laban, et al.
Prilozi (Makedonska Akademija Na Naukite I Umetnostite. Oddelenie Za Medicinski Nauki)|December 18, 2023
Compound Heterozygosity in Cerebellar Ataxia, Mental Retardation, and Disequilibrium Syndrome Type 4Bojan Teov, Aleksandra Janchevska, Ardiana Beqiri-Jasari, et al.
Bosnian Journal of Basic Medical Sciences|June 3, 2009
Friedreich ataxia (FA) associated with diabetes mellitus type 1 and hyperthrophic cardiomyopathyZoran Gucev, Velibor Tasic, Aleksandra Jancevska, et al.
Balkan Medical Journal|February 6, 2018
Novel Founder Mutation in <i>FANCA</i> Gene (c.3446_3449dupCCCT) Among Romani Patients from the Balkan RegionMarija Dimishkovska, Vjosa Mulliqi Kotori, Zoran Gucev, et al.
Indian Journal of Pediatrics|June 11, 2011
Billateral polycystic kidneys in a girl with WAGR syndromeZoran Gucev, Olivera Muratovska, Nevenka Laban, et al.
Indian Journal of Pediatrics|February 28, 2012
Two siblings with Niemann-Pick disease (NPD) type B: clinical findings and novel mutations of the acid sphingomyelinase geneZoran Gucev, Velibor Tasic, Nada Pop-Jordanova, et al.
Medicinski Arhiv|June 23, 2009
Friedreich's ataxia (FA) associated with diabetes mellitus type 1 and hypertrophic cardiomyopathy: analysis of a FA familyZoran Gucev, Velibor Tasic, Aleksandra Jancevska, et al.
Clinical Endocrinology|June 29, 2017
Somapacitan, a once-weekly reversible albumin-binding GH derivative, in children with GH deficiency: A randomized dose-escalation trialTadej Battelino, Michael Højby Rasmussen, Jean De Schepper, et al.
Indian Journal of Human Genetics|November 18, 2011
Congenital erythropoietic porphyria with two mutations of the uroporphyrinogen III synthase gene (Cys73Arg, Thr228Met)Zoran Gucev, Nevenka Slavevska, Velibor Tasic, et al.
Pediatric Nephrology (Berlin, Germany)|January 21, 2011
Clinical and laboratory features of Macedonian children with OCRL mutationsVelibor Tasic, Vladimir J Lozanovski, Petar Korneti, et al.
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