Detalhe da pesquisa
1.
Thyroid function and dysfunction in preterm infants-Challenges in evaluation, diagnosis and therapy.
Clin Endocrinol (Oxf)
; 95(4): 556-570, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33864279
2.
First insights into the genetics of 21-hydroxylase deficiency in the Roma population.
Clin Endocrinol (Oxf)
; 95(1): 41-46, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33605469
3.
Trends and cyclical variation in the incidence of childhood type 1 diabetes in 26 European centres in the 25 year period 1989-2013: a multicentre prospective registration study.
Diabetologia
; 62(3): 408-417, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30483858
4.
Efficacy and safety of a fixed combination of insulin degludec/insulin aspart in children and adolescents with type 1 diabetes: A randomized trial.
Pediatr Diabetes
; 19(7): 1263-1270, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30014589
5.
Targets and teamwork: Understanding differences in pediatric diabetes centers treatment outcomes.
Pediatr Diabetes
; 19(3): 559-565, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29159931
6.
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.
BMC Endocr Disord
; 15: 82, 2015 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26666878
7.
Clinical practice: experience with newborn screening for congenital hypothyroidism in the Republic of Macedonia - a multiethnic country.
Eur J Pediatr
; 174(4): 443-8, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25192932
8.
Metabolic outcomes in young children with type 1 diabetes differ between treatment centers: the Hvidoere Study in Young Children 2009.
Pediatr Diabetes
; 14(6): 422-8, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22957743
9.
Prevalence of congenital hypothyroidism in North Macedonia: data from a newborn screening program conducted for twenty years.
Turk J Pediatr
; 65(2): 227-234, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37114688
10.
Mutational Spectrum and Genotype-phenotype Correlations in Neurofibromatosis Type 1 Patients from North Macedonia: Identification of Ten Novel NF1 Pathogenic Variants
Balkan Med J
; 40(4): 252-261, 2023 07 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37073110
11.
Unique concurrent appearance of two rare conditions in a young girl: central precocious puberty due to hypothalamic hamartoma and uncommon type of diabetes.
J Pediatr Endocrinol Metab
; 24(9-10): 815-8, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-22145483
12.
Characteristics of In2G Variant in Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.
Front Endocrinol (Lausanne)
; 12: 788812, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-35140681
13.
A novel 9 bp deletion (c.1271_1279delGTGCCCGCG) in exon 10 of CYP21A2 gene causing severe congenital adrenal hyperplasia.
Endocrine
; 73(1): 196-202, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33715135
14.
Current Status of Newborn Screening in Southeastern Europe.
Front Pediatr
; 9: 648939, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34026686
15.
Neonatal Screening in Europe Revisited: An ISNS Perspective on the Current State and Developments Since 2010.
Int J Neonatal Screen
; 7(1)2021 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33808002
16.
Disease progression and search for monogenic diabetes among children with new onset type 1 diabetes negative for ICA, GAD- and IA-2 Antibodies.
BMC Endocr Disord
; 10: 16, 2010 Sep 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-20863361
17.
Genotype-phenotype correlation in CAH patients with severe CYP21A2 point mutations in the Republic of Macedonia.
J Pediatr Endocrinol Metab
; 23(9): 921-6, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21175091
18.
Clinical outcomes and characteristics of P30L mutations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Endocrine
; 69(2): 262-277, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32367336
19.
Genetics of Gland-in-situ or Hypoplastic Congenital Hypothyroidism in Macedonia.
Front Endocrinol (Lausanne)
; 11: 413, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32765423
20.
The impact of CYP21A2 (P30L/I172N) genotype on female fertility in one family.
Eur J Med Res
; 24(1): 21, 2019 Jun 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-31217034