Sukarova-Angelovska E - Search Results

1

Optic glioma and precocious puberty in a girl with neurofibromatosis type 1 carrying an R681X mutation of NF1: case report and review of the literature.

Kocova M, Kochova E, Sukarova-Angelovska E. Kocova M, et al. BMC Endocr Disord. 2015 Dec 15;15:82. doi: 10.1186/s12902-015-0076-4. BMC Endocr Disord. 2015. PMID: 26666878 Free PMC article. Review.

2

Skewed X-chromosome inactivation in unsolved neurodevelopmental disease cases can guide re-evaluation For X-linked genes.

Giovenino C, Trajkova S, Pavinato L, Cardaropoli S, Pullano V, Ferrero E, Sukarova-Angelovska E, Carestiato S, Salmin P, Rinninella A, Battaglia A, Bertoli L, Fadda A, Palermo F, Carli D, Mussa A, Dimartino P, Bruselles A, Froukh T, Mandrile G, Pasini B, De Rubeis S, Buxbaum JD, Pippucci T, Tartaglia M, Rossato M, Delledonne M, Ferrero GB, Brusco A. Giovenino C, et al. Among authors: sukarova angelovska e. Eur J Hum Genet. 2023 Nov;31(11):1228-1236. doi: 10.1038/s41431-023-01324-w. Epub 2023 Mar 6. Eur J Hum Genet. 2023. PMID: 36879111 Free article.

3

Pituitary pseudotumor with unusual presentation reversed shortly after the introduction of thyroxine replacement therapy.

Kocova M, Netkov S, Sukarova-Angelovska E. Kocova M, et al. J Pediatr Endocrinol Metab. 2001 Nov-Dec;14(9):1665-9. doi: 10.1515/jpem.2001.14.9.1665. J Pediatr Endocrinol Metab. 2001. PMID: 11795659 Review.

4

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

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

5

Implementation of Fluorescent in situ hybridization (FISH) as a method for detecting microdeletion syndromes - our first experiences.

Sukarova-Angelovska E, Piperkova K, Sredovska A, Ilieva G, Kocova M. Sukarova-Angelovska E, et al. Prilozi. 2007 Dec;28(2):87-98. Prilozi. 2007. PMID: 18356781

6

Methodological and organizational aspects of newborn screening for congenital hypothyroidism in Macedonia.

Gjurkova B, Anastasovska V, Sukarova Angelovska E, Kocova M. Gjurkova B, et al. Prilozi. 2008 Jul;29(1):93-106. Prilozi. 2008. PMID: 18709003

7

HLA-DR-DQ haplotypes and type 1 diabetes in Macedonia.

Ilonen J, Kocova M, Lipponen K, Sukarova-Angelovska E, Jovanovska A, Knip M. Ilonen J, et al. Hum Immunol. 2009 Jun;70(6):461-3. doi: 10.1016/j.humimm.2009.03.014. Epub 2009 Mar 27. Hum Immunol. 2009. PMID: 19332095

8

The unique combination of dermatological and ocular phenotypes in Alström syndrome: severe presentation, early onset and two novel ALMS1 mutations.

Kocova M, Sukarova-Angelovska E, Kacarska R, Maffei P, Milan G, Marshall JD. Kocova M, et al. Br J Dermatol. 2011 Apr;164(4):878-80. doi: 10.1111/j.1365-2133.2010.10157.x. Epub 2011 Mar 16. Br J Dermatol. 2011. PMID: 21128906 Free PMC article. No abstract available.

9

Unique concurrent appearance of two rare conditions in a young girl: central precocious puberty due to hypothalamic hamartoma and uncommon type of diabetes.

Kocova M, Zdraveska N, Sukarova-Angelovska E. Kocova M, et al. J Pediatr Endocrinol Metab. 2011;24(9-10):815-8. doi: 10.1515/jpem.2011.192. J Pediatr Endocrinol Metab. 2011. PMID: 22145483

10

The many faces of oral-facial-digital syndrome.

Sukarova-Angelovska E, Angelkova N, Palcevska-Kocevska S, Kocova M. Sukarova-Angelovska E, et al. Balkan J Med Genet. 2012 Jun;15(1):37-44. doi: 10.2478/v10034-012-0006-y. Balkan J Med Genet. 2012. PMID: 24052721 Free PMC article.

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