Showing results (51-60 of 81) with videos related to

Sort By:
Pageof 9
Pediatric Endocrinology Reviews : PER|July 29, 2016
LHX4 Gene Alterations: Patient Report and Review of the LiteratureZoran Gucev, Velibor Tasic, Dijana Plaseska-Karanfilska, et al.
Orphanet Journal of Rare Diseases|May 10, 2022
Consensus statement on enzyme replacement therapy for mucopolysaccharidosis IVA in Central and South-Eastern European countriesMartin Magner, Zsuzsanna Almássy, Zoran Gucev, et al.
Prilozi (Makedonska Akademija Na Naukite I Umetnostite. Oddelenie Za Medicinski Nauki)|July 17, 2022
Alström Syndrome with Early Vision and Hearing ImpairementArdiana Beqiri-Jashari, Aleksandra Janchevska, Irfan Ahmeti, et al.
Plos One|December 24, 2011
Clinical and functional characterization of URAT1 variantsVelibor Tasic, Ann Marie Hynes, Kenichiro Kitamura, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 12, 2009
Analysis of TSHZ2 and TSHZ3 genes in congenital pelvi-ureteric junction obstructionDagan Jenkins, Xavier Caubit, Aleksandar Dimovski, et al.
Open Access Macedonian Journal of Medical Sciences|December 19, 2018
<i>IGF1R</i> Gene Alterations in Children Born Small for Gestitional Age (SGA)Aleksandra Janchevska, Marina Krstevska-Konstantinova, Heike Pfäffle, et al.
European Journal of Medical Genetics|January 25, 2019
Heterotopic ossifications and Charcot joints: Congenital insensitivity to pain with anhidrosis (CIPA) and a novel NTRK1 gene mutationZoran Gucev, Velibor Tasic, Ivona Bogevska, et al.
American Journal of Medical Genetics. Part A|April 24, 2019
Severe digital malformations in a rare variant of fibrodysplasia ossificans progressivaZoran Gucev, Velibor Tasic, Dijana Plaseska-Karanfilska, et al.
Italian Journal of Pediatrics|December 16, 2014
First-line therapy in atypical hemolytic uremic syndrome: consideration on infants with a poor prognosisNóra Szarvas, Ágnes Szilágyi, Velibor Tasic, et al.
The Journal of Clinical Endocrinology and Metabolism|November 5, 2019
A Comprehensive Cohort Analysis Comparing Growth and GH Therapy Response in IGF1R Mutation Carriers and SGA ChildrenEric Göpel, Denise Rockstroh, Heike Pfäffle, et al.
Pageof 9