Tasic V - Search Results

1

Type I Gaucher disease (GDI) in three siblings: enzyme replacement treatment (ERT) required.

Gucev ZS, Tasic V, Pop-Jordanova N, Kirovski I, Stomnaroska O, Martinova M, Jancevska A, Kremensky I, Sinigerska I. Gucev ZS, et al. Among authors: tasic v. Prilozi. 2009 Jul;30(1):233-40. Prilozi. 2009. PMID: 19736544

2

Stress tolerance test and SDS-PAGE for the analysis of urinary proteins in children and youths.

Tasic V, Korneti P, Gucev Z, Korneti B. Tasic V, et al. Clin Chem Lab Med. 2001 Jun;39(6):478-83. doi: 10.1515/CCLM.2001.078. Clin Chem Lab Med. 2001. PMID: 11506456

3

Aseptic necrosis of both tali in a child with steroid-dependent nephrotic syndrome.

Tasic V, Trajkovski Z, Zafirovski G, Gucev Z, Trompeter RS. Tasic V, et al. Nephrol Dial Transplant. 2006 Jun;21(6):1702-4. doi: 10.1093/ndt/gfi131. Epub 2006 Jan 6. Nephrol Dial Transplant. 2006. PMID: 16399767 No abstract available.

4

Atypical presentation of distal renal tubular acidosis in two siblings.

Tasic V, Korneti P, Gucev Z, Hoppe B, Blau N, Cheong HI. Tasic V, et al. Pediatr Nephrol. 2008 Jul;23(7):1177-81. doi: 10.1007/s00467-008-0796-z. Epub 2008 Apr 2. Pediatr Nephrol. 2008. PMID: 18386070

5

Autoimmune thyroiditis in a child with steroid-dependent nephrotic syndrome.

Tasic V, Angjeleska M, Ristoska-Bojkovska N, Petrusevska G, Gucev Z. Tasic V, et al. Eur J Pediatr. 2009 Feb;168(2):229-31. doi: 10.1007/s00431-008-0734-x. Epub 2008 May 7. Eur J Pediatr. 2009. PMID: 18461358

6

Novel beta-galactosidase gene mutation p.W273R in a woman with mucopolysaccharidosis type IVB (Morquio B) and lack of response to in vitro chaperone treatment of her skin fibroblasts.

Gucev ZS, Tasic V, Jancevska A, Zafirovski G, Kremensky I, Sinigerska I, Nanba E, Higaki K, Gucev F, Suzuki Y. Gucev ZS, et al. Among authors: tasic v. Am J Med Genet A. 2008 Jul 1;146A(13):1736-40. doi: 10.1002/ajmg.a.32318. Am J Med Genet A. 2008. PMID: 18546276

7

Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE) syndrome: CNS malformations and seizures may be a component of this disorder.

Gucev ZS, Tasic V, Jancevska A, Konstantinova MK, Pop-Jordanova N, Trajkovski Z, Biesecker LG. Gucev ZS, et al. Among authors: tasic v. Am J Med Genet A. 2008 Oct 15;146A(20):2688-90. doi: 10.1002/ajmg.a.32515. Am J Med Genet A. 2008. PMID: 18816642 Free PMC article.

8

Friedreich ataxia (FA) associated with diabetes mellitus type 1 and hyperthrophic cardiomyopathy.

Gucev Z, Tasic V, Jancevska A, Popjordanova N, Koceva S, Kuturec M, Sabolic V. Gucev Z, et al. Among authors: tasic v. Bosn J Basic Med Sci. 2009 May;9(2):107-10. doi: 10.17305/bjbms.2009.2828. Bosn J Basic Med Sci. 2009. PMID: 19485941 Free PMC article.

9

Friedreich's ataxia (FA) associated with diabetes mellitus type 1 and hypertrophic cardiomyopathy: analysis of a FA family.

Gucev Z, Tasic V, Jancevska A, Jordanova NP, Koceva S, Kuturec M, Sabolic V. Gucev Z, et al. Among authors: tasic v. Med Arh. 2009;63(2):110-1. Med Arh. 2009. PMID: 19537671

10

A case of Silver-Russell syndrome (SRS): multiple pituitary hormone deficiency, lack of H19 hypomethylation and favourable growth hormone (GH) treatment response.

Gucev ZS, Tasic V, Jancevska A, Kirovski I. Gucev ZS, et al. Among authors: tasic v. J Genet. 2009 Aug;88(2):239-43. doi: 10.1007/s12041-009-0033-y. J Genet. 2009. PMID: 19700863

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