Dumic M - Search Results

1

Long-term clinical follow-up and molecular genetic findings in eight patients with triple A syndrome.

Dumic M, Barišic N, Kusec V, Stingl K, Skegro M, Stanimirovic A, Koehler K, Huebner A. Dumic M, et al. Eur J Pediatr. 2012 Oct;171(10):1453-9. doi: 10.1007/s00431-012-1745-1. Epub 2012 Apr 28. Eur J Pediatr. 2012. PMID: 22538409

2

Two siblings with triple A syndrome and novel mutation presenting as hereditary polyneuropathy.

Dumić M, Barišić N, Rojnić-Putarek N, Kušec V, Stanimirović A, Koehler K, Huebner A. Dumić M, et al. Eur J Pediatr. 2011 Mar;170(3):393-6. doi: 10.1007/s00431-010-1314-4. Epub 2010 Oct 8. Eur J Pediatr. 2011. PMID: 20931227

3

Low bone mineral density for age/osteoporosis in triple A syndrome-an overlooked symptom of unexplained etiology.

Dumic M, Putarek NR, Kusec V, Barisic N, Koehler K, Huebner A. Dumic M, et al. Osteoporos Int. 2016 Feb;27(2):521-6. doi: 10.1007/s00198-015-3265-0. Epub 2015 Aug 5. Osteoporos Int. 2016. PMID: 26243364

4

Primary hypothyroidism and nipple hypoplasia in a girl with Wolcott-Rallison syndrome.

Spehar Uroić A, Mulliqi Kotori V, Rojnić Putarek N, Kušec V, Dumić M. Spehar Uroić A, et al. Among authors: dumic m. Eur J Pediatr. 2014 Apr;173(4):529-31. doi: 10.1007/s00431-013-2189-y. Epub 2013 Nov 6. Eur J Pediatr. 2014. PMID: 24194294

5

Molecular genetic analysis in 93 patients and 193 family members with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Croatia.

Dumic KK, Grubic Z, Yuen T, Wilson RC, Kusec V, Barisic I, Stingl K, Sansovic I, Skrabic V, Dumic M, New MI. Dumic KK, et al. Among authors: dumic m. J Steroid Biochem Mol Biol. 2017 Jan;165(Pt A):51-56. doi: 10.1016/j.jsbmb.2016.03.035. Epub 2016 Mar 31. J Steroid Biochem Mol Biol. 2017. PMID: 27041116

6

Testicular adrenal rest tumors in congenital adrenal hyperplasia-cross-sectional study of 51 Croatian male patients.

Dumic M, Duspara V, Grubic Z, Oguic SK, Skrabic V, Kusec V. Dumic M, et al. Eur J Pediatr. 2017 Oct;176(10):1393-1404. doi: 10.1007/s00431-017-3008-7. Epub 2017 Sep 6. Eur J Pediatr. 2017. PMID: 28879515

7

Five patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency (one with associated neuroblastoma) discovered in three generations of one family.

Janjanin N, Dumic M, Skrabic V, Kusec V, Grubic Z, Spehar Uroic A. Janjanin N, et al. Among authors: dumic m. Horm Res. 2007;67(3):111-6. doi: 10.1159/000096420. Epub 2006 Oct 19. Horm Res. 2007. PMID: 17057407

8

Xerostomia in patients with triple A syndrome--a newly recognised finding.

Dumić M, Mravak-Stipetić M, Kaić Z, Ille J, Plavsić V, Batinica S, Cvitanović M. Dumić M, et al. Eur J Pediatr. 2000 Dec;159(12):885-8. doi: 10.1007/pl00008361. Eur J Pediatr. 2000. PMID: 11131343

9

The effect of 17 years of increased salt iodization on the prevalence and nature of goiter in Croatian schoolchildren.

Vučinić M, Kušec V, Dundović S, Ille J, Dumić M. Vučinić M, et al. Among authors: dumic m. J Pediatr Endocrinol Metab. 2018 Sep 25;31(9):995-1000. doi: 10.1515/jpem-2018-0129. J Pediatr Endocrinol Metab. 2018. PMID: 30055100 Free article.

10

[Primary pigmented nodular adrenocortical disease as cause of Cushing's syndrome associated with Carney complex].

Dumić M, Janjanin N, Uroić AS, Ille J, Skegro M, Kusec V, Marjanac I, Matić T, Jelasić D. Dumić M, et al. Lijec Vjesn. 2006 Sep-Oct;128(9-10):268-73. Lijec Vjesn. 2006. PMID: 17128664 Croatian.

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