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A 4-Year-Old Boy with Beckwith Wiedemann Syndrome (BWS).
Janchevska A, Tasic V, Laban N, Polenakovic M, Gucev Z, Bachmann N, Bergmann C. Janchevska A, et al. Among authors: laban n. Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2018 Dec 1;39(2-3):131-135. doi: 10.2478/prilozi-2018-0052. Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2018. PMID: 30864369 Free article.
Emanuel Syndrome (ES): new case-report and review of the literature.
Jancevska S, Kitanovski M, Laban N, Danilovski D, Tasic V, Gucev ZS. Jancevska S, et al. Among authors: laban n. Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2015;36(1):205-8. Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2015. PMID: 26076791 Review.
Duplication of The SOX3 Gene in an Sry-negative 46,XX Male with Associated Congenital Anomalies of Kidneys and the Urinary Tract: Case Report and Review of the Literature.
Tasic V, Mitrotti A, Riepe FG, Kulle AE, Laban N, Polenakovic M, Plaseska-Karanfilska D, Sanna-Cherchi S, Kostovski M, Gucev Z. Tasic V, et al. Among authors: laban n. Balkan J Med Genet. 2019 Aug 28;22(1):81-88. doi: 10.2478/bjmg-2019-0006. eCollection 2019 Jun. Balkan J Med Genet. 2019. PMID: 31523625 Free PMC article.
Billateral polycystic kidneys in a girl with WAGR syndrome.
Gucev Z, Muratovska O, Laban N, Misevska L, Jancevska A, Crolla J, Tasic V. Gucev Z, et al. Among authors: laban n. Indian J Pediatr. 2011 Oct;78(10):1290-2. doi: 10.1007/s12098-011-0457-2. Epub 2011 Jun 10. Indian J Pediatr. 2011. PMID: 21660403
IGF1R Gene Alterations in Children Born Small for Gestitional Age (SGA).
Janchevska A, Krstevska-Konstantinova M, Pfäffle H, Schlicke M, Laban N, Tasic V, Gucev Z, Mironska K, Dimovski A, Kratzsch J, Klammt J, Pfäffle R. Janchevska A, et al. Among authors: laban n. Open Access Maced J Med Sci. 2018 Nov 10;6(11):2040-2044. doi: 10.3889/oamjms.2018.416. eCollection 2018 Nov 25. Open Access Maced J Med Sci. 2018. PMID: 30559857 Free PMC article.
52 results