Showing results (1-10 of 124) with videos related to

Sort By:
Pageof 13
Hippokratia|November 24, 2011
Ceftriaxone associated urolithiasis in a child with hypercalciuriaV J Lozanovski, Z Gucev, V J Avramoski, et al.
Prilozi|January 25, 2011
Four generations in a family with neurofibromatosis 1: precocious puberty and optic nerve tumor (OPT)Z Gucev, M Krstevska-Konstantinova, V Tasic, et al.
Pediatric Endocrinology Reviews : PER|April 11, 2014
The many faces of rare diseases (RD): meeting report on Rare Disease in South-Eastern Europe, 15-16 November 2013, Skopje, Republic of MacedoniaZ Gucev, V Tasic, M Polenakovic
Clinical Chemistry and Laboratory Medicine|August 17, 2001
Stress tolerance test and SDS-PAGE for the analysis of urinary proteins in children and youthsV Tasic, P Korneti, Z Gucev, et al.
Indian Pediatrics|May 9, 2012
Aldosterone synthase deficiency type II with hypospadiasZ Gucev, V Tasic, N Pop-Jordanova, et al.
Prilozi|January 31, 2012
A giant osteochondroma in a boy with multiple exostosesI Kirovski, Z S Gucev, V Tasic, et al.
World Journal of Pediatrics : WJP|August 9, 2011
OCRL1 mutation in a boy with Dent disease, mild mental retardation, but without cataractsVladimir J Lozanovski, N Ristoska-Bojkovska, P Korneti, et al.
Balkan Journal of Medical Genetics : BJMG|May 5, 2015
X-Linked Recessive form of Nephrogenic Diabetes Insipidus in a 7-Year-Old BoyA Janchevska, V Tasic, Z Gucev, et al.
Prilozi|February 22, 2013
Children born small for gestational age (SGA)A Jancevska, V Tasic, N Damcevski, et al.
Nucleosides, Nucleotides & Nucleic Acids|December 3, 2011
HPRT deficiency: identification of twenty-four novel variants including an unusual deep intronic mutationA Corrigan, M Arenas, E Escuredo, et al.
Pageof 13