Detalles de la búsqueda
1.
The Applied Genomics Development Strategy by the Croatian Academy of Sciences and Arts paves the way for the future development of applied genomics in Croatia.
Croat Med J;
65(3): 297-302, 2024 Jun 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-38868976
2.
GLUCAGON-LIKE PEPTIDE-1 AFFECTS TASTE PERCEPTION DIFFERENTLY IN WOMEN: A RANDOMIZED, PLACEBO-CONTROLLED CROSSOVER STUDY.
Acta Clin Croat;
58(2): 240-248, 2019 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-31819319
3.
Testicular adrenal rest tumors in congenital adrenal hyperplasia-cross-sectional study of 51 Croatian male patients.
Eur J Pediatr;
176(10): 1393-1404, 2017 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-28879515
4.
Glycoprotein YKL-40: a novel biomarker of chronic graft-vs-host disease activity and severity?
Croat Med J;
57(3): 239-46, 2016 Jun 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-27374825
5.
GUIDELINES FOR THE PREVENTION, DETECTION AND THERAPY OF VITAMIN D DEFICIENCY IN ADULTS.
Lijec Vjesn;
138(5-6): 121-132, 2016 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-29182823
6.
Primary hypothyroidism and nipple hypoplasia in a girl with Wolcott-Rallison syndrome.
Eur J Pediatr;
173(4): 529-31, 2014 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-24194294
7.
Fertility and sexual activity in patients with Triple A syndrome.
Front Endocrinol (Lausanne);
15: 1357084, 2024.
Artículo
en Inglés
| MEDLINE | ID: mdl-38544685
8.
Relative Frequency of Islet Autoimmunity in Children and Adolescents with Autoimmune Thyroid Disease
J Clin Res Pediatr Endocrinol;
15(4): 348-355, 2023 11 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-37074226
9.
The prevalence and genotype of 21-hydroxylase deficiency in the Croatian Romani population.
Front Endocrinol (Lausanne);
14: 1170449, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37324261
10.
Long-term clinical follow-up and molecular genetic findings in eight patients with triple A syndrome.
Eur J Pediatr;
171(10): 1453-9, 2012 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-22538409
11.
[Croatian Society of Endocrinology guidelines for the diagnosis and treatment of acromegaly]. / Smjernice Hrvatskoga endokrinoloskog drustva za dijagnostiku i lijecenje akromegalije.
Lijec Vjesn;
134(3-4): 65-8, 2012.
Artículo
en Croata
| MEDLINE | ID: mdl-22768678
12.
[Congenital hyperinsulinism--novel insights into etiology, diagnosis and treatment]. / Kongenitalni hiperinzulinizam- -novosti o nastanku, dijagnosticiranju i lijecenju bolesti.
Lijec Vjesn;
134(9-10): 286-92, 2012.
Artículo
en Croata
| MEDLINE | ID: mdl-23297514
13.
Two siblings with triple A syndrome and novel mutation presenting as hereditary polyneuropathy.
Eur J Pediatr;
170(3): 393-6, 2011 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-20931227
14.
AXIN-1 protein expression and localization in glioblastoma.
Coll Antropol;
35 Suppl 1: 101-6, 2011 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-21648318
15.
Diversity of bone cell activity as a histomorphometric feature of idiopathic osteoporosis in men.
Aging Male;
13(1): 18-24, 2010 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-20148745
16.
Steroid 11-beta hydroxylase deficiency caused by compound heterozygosity for a novel mutation in intron 7 (IVS 7 DS+4A to G) in one CYP11B1 allele and R448H in exon 8 in the other.
Eur J Pediatr;
169(7): 891-4, 2010 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-20024693
17.
Metals in human placenta: focus on the effects of cadmium on steroid hormones and leptin.
J Appl Toxicol;
30(3): 242-53, 2010 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-19847775
18.
The Effect of a Moderate Exercise Program on Serum Markers of Bone Metabolism in Dogs.
Animals (Basel);
10(9)2020 Aug 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-32842472
19.
Classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Croatia between 1995 and 2006.
Horm Res;
72(4): 247-51, 2009.
Artículo
en Inglés
| MEDLINE | ID: mdl-19786796
20.
Classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in croatia between 1995 and 2006.
Horm Res;
72(5): 310-4, 2009.
Artículo
en Inglés
| MEDLINE | ID: mdl-19844117