Gucev Z - Search Results

1

Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3.

Macedo DB, Abreu AP, Reis AC, Montenegro LR, Dauber A, Beneduzzi D, Cukier P, Silveira LF, Teles MG, Carroll RS, Junior GG, Filho GG, Gucev Z, Arnhold IJ, de Castro M, Moreira AC, Martinelli CE Jr, Hirschhorn JN, Mendonca BB, Brito VN, Antonini SR, Kaiser UB, Latronico AC. Macedo DB, et al. Among authors: gucev z. J Clin Endocrinol Metab. 2014 Jun;99(6):E1097-103. doi: 10.1210/jc.2013-3126. Epub 2014 Mar 14. J Clin Endocrinol Metab. 2014. PMID: 24628548 Free PMC article.

2

Autoimmune thyroiditis and diabetes mellitus type 1 after long-term gonadotropin-releasing hormone agonist treatment for central precocious puberty: evolution or coincidence?

Krstevska-Konstantinova M, Jancevska A, Gucev Z. Krstevska-Konstantinova M, et al. Among authors: gucev z. J Pediatr Endocrinol Metab. 2010 Apr;23(4):403-6. doi: 10.1515/jpem.2010.063. J Pediatr Endocrinol Metab. 2010. PMID: 20583547

3

Mutational analysis of KISS1 and KISS1R in idiopathic central precocious puberty.

Krstevska-Konstantinova M, Jovanovska J, Tasic VB, Montenegro LR, Beneduzzi D, Silveira LF, Gucev ZS. Krstevska-Konstantinova M, et al. J Pediatr Endocrinol Metab. 2014 Jan;27(1-2):199-201. doi: 10.1515/jpem-2013-0080. J Pediatr Endocrinol Metab. 2014. PMID: 23950571

4

Mutational analysis of TAC and TACR3 in idiopathic central precocious puberty.

Krstevska-Konstantinova M, Tasic VB, Montenegro LR, Dervisov D, Beneduzzi D, Gontijo Silveira LF, Gucev ZS. Krstevska-Konstantinova M, et al. Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2014;35(1):129-32. Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2014. PMID: 24802197

5

McCune-Albright syndrome (MAS): early and extensive bone fibrous dysplasia involvement and "mistaken identity" oophorectomy.

Gucev Z, Tasic V, Jancevska A, Krstevska-Konstantinova M, Pop-Jordanova N. Gucev Z, et al. J Pediatr Endocrinol Metab. 2010 Aug;23(8):837-42. doi: 10.1515/jpem.2010.135. J Pediatr Endocrinol Metab. 2010. PMID: 21073128

6

Four generations in a family with neurofibromatosis 1: precocious puberty and optic nerve tumor (OPT).

Gucev Z, Krstevska-Konstantinova M, Tasic V, Jancevska A, Kirovski I, Pop-Jordanova N. Gucev Z, et al. Prilozi. 2010;31(2):253-9. Prilozi. 2010. PMID: 21258292

7

Identical monochorionic twins with down syndrome and paternal origin of the extra chromosome 21.

Urumova A, Tasic V, Bojadjieva E, Pomponi MG, Neri G, Gucev Z. Urumova A, et al. Among authors: gucev z. Prilozi. 2012;33(2):41-6. Prilozi. 2012. PMID: 23425868

8

Premature thelarche in Macedonia: a three-year follow-up.

Krstevska-Konstantinova M, Kocova M, Gucev Z, Sukarova-Angelovska E. Krstevska-Konstantinova M, et al. Among authors: gucev z. Bratisl Lek Listy. 2007;108(8):340-3. Bratisl Lek Listy. 2007. PMID: 18203537

9

Autosomal dominant spondylocostal dysostosis in three generations of a Macedonian family: Negative mutation analysis of DLL3, MESP2, HES7, and LFNG.

Gucev ZS, Tasic V, Pop-Jordanova N, Sparrow DB, Dunwoodie SL, Ellard S, Young E, Turnpenny PD. Gucev ZS, et al. Am J Med Genet A. 2010 Jun;152A(6):1378-82. doi: 10.1002/ajmg.a.33471. Am J Med Genet A. 2010. PMID: 20503311

10

Fourteen monogenic genes account for 15% of nephrolithiasis/nephrocalcinosis.

Halbritter J, Baum M, Hynes AM, Rice SJ, Thwaites DT, Gucev ZS, Fisher B, Spaneas L, Porath JD, Braun DA, Wassner AJ, Nelson CP, Tasic V, Sayer JA, Hildebrandt F. Halbritter J, et al. J Am Soc Nephrol. 2015 Mar;26(3):543-51. doi: 10.1681/ASN.2014040388. Epub 2014 Oct 8. J Am Soc Nephrol. 2015. PMID: 25296721 Free PMC article.

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