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Prilozi|January 31, 2012
A giant osteochondroma in a boy with multiple exostosesI Kirovski, Z S Gucev, V Tasic, et al.Prilozi|January 21, 2010
Growth hormone deficiency (GHD) and small for gestational age (SGA): genetic alterationsA Jancevska, Z S Gucev, V Tasic, et al.Prilozi|September 9, 2009
Type I Gaucher disease (GDI) in three siblings: enzyme replacement treatment (ERT) requiredZ S Gucev, V Tasic, N Pop-Jordanova, 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.Prilozi|August 9, 2011
Early-onset ocular ochronosis in a girl with alkaptonuria (AKU) and a novel mutation in homogentisate 1,2-dioxygenase (HGD)Z S Gucev, N Slaveska, N Laban, et al.Prilozi|August 9, 2011
Rare diseases with renal involvement in the Republic of MacedoniaV Tasic, V J Lozanovski, D Danilovski, et al.Prilozi|January 31, 2012
Hunter syndrome (Muccopolysaccharridosis Type II) in Macedonia and BulgariaZ S Gucev, V Tasic, I Sinigerska, et al.Prilozi|January 31, 2012
Acute Gallbladder Hydrops and Arthritis: unusual initial manifestations of Wilson's Disease (WD): Case ReportZ S Gucev, N Pop-Jordanova, V Calovska, et al.Indian Pediatrics|May 9, 2012
Aldosterone synthase deficiency type II with hypospadiasZ Gucev, V Tasic, N Pop-Jordanova, et al.Prilozi|August 9, 2011
On rare and "super-rare" diseases: an insight from the Republic of MacedoniaZ S Gucev, V Tasic, M PolenakovicPageof 5