Kocova M - 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

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.

3

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: kocova m. Bratisl Lek Listy. 2007;108(8):340-3. Bratisl Lek Listy. 2007. PMID: 18203537

4

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. Among authors: kocova m. Prilozi. 2007 Dec;28(2):87-98. Prilozi. 2007. PMID: 18356781

5

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. Among authors: kocova m. Prilozi. 2008 Jul;29(1):93-106. Prilozi. 2008. PMID: 18709003

6

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. Among authors: kocova m. 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

7

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.

8

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

9

The many faces of oral-facial-digital syndrome.

Sukarova-Angelovska E, Angelkova N, Palcevska-Kocevska S, Kocova M. Sukarova-Angelovska E, et al. Among authors: kocova m. 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.

10

Clinical practice: experience with newborn screening for congenital hypothyroidism in the Republic of Macedonia - a multiethnic country.

Kocova M, Anastasovska V, Sukarova-Angelovska E, Tanaskoska M, Taseva E. Kocova M, et al. Eur J Pediatr. 2015 Apr;174(4):443-8. doi: 10.1007/s00431-014-2413-4. Epub 2014 Sep 7. Eur J Pediatr. 2015. PMID: 25192932

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

128 results

Search Page