Gucev Z - Search Results

1

Cystinuria AA (B): digenic inheritance with three mutations in two cystinuria genes.

Gucev Z, Ristoska-Bojkovska N, Popovska-Jankovic K, Sukarova-Stefanovska E, Tasic V, Plaseska-Karanfilska D, Efremov GD. Gucev Z, et al. J Genet. 2011 Apr;90(1):157-9. doi: 10.1007/s12041-011-0045-2. J Genet. 2011. PMID: 21677404 No abstract available.

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. Among authors: gucev z. 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. Among authors: gucev z. 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. Among authors: gucev z. 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. Among authors: gucev z. 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. 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. 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. 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. 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. J Genet. 2009 Aug;88(2):239-43. doi: 10.1007/s12041-009-0033-y. J Genet. 2009. PMID: 19700863

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