Cinek O - Search Results

1

Genetic analysis of the CYP21A2 gene in neonatal dried blood spots from children with transiently elevated 17-hydroxyprogesterone.

Malikova J, Votava F, Vrzalova Z, Lebl J, Cinek O. Malikova J, et al. Among authors: cinek o. Clin Endocrinol (Oxf). 2012 Aug;77(2):187-94. doi: 10.1111/j.1365-2265.2012.04358.x. Clin Endocrinol (Oxf). 2012. PMID: 22313422

2

High prevalence of coeliac disease in siblings of children with type 1 diabetes.

Sumnik Z, Kolouskova S, Malcova H, Vavrinec J, Venhacova J, Lebl J, Cinek O. Sumnik Z, et al. Among authors: cinek o. Eur J Pediatr. 2005 Jan;164(1):9-12. doi: 10.1007/s00431-004-1547-1. Epub 2004 Oct 7. Eur J Pediatr. 2005. PMID: 15480779

3

Absence of breast-feeding is associated with the risk of type 1 diabetes: a case-control study in a population with rapidly increasing incidence.

Malcova H, Sumnik Z, Drevinek P, Venhacova J, Lebl J, Cinek O. Malcova H, et al. Among authors: cinek o. Eur J Pediatr. 2006 Feb;165(2):114-9. doi: 10.1007/s00431-005-0008-9. Epub 2005 Oct 7. Eur J Pediatr. 2006. PMID: 16211397

4

Risk of celiac disease in children with type 1 diabetes is modified by positivity for HLA-DQB1*02-DQA1*05 and TNF -308A.

Sumnik Z, Cinek O, Bratanic N, Kordonouri O, Kulich M, Roszai B, Arato A, Lebl J, Soltesz G, Danne T, Battelino T, Schober E. Sumnik Z, et al. Among authors: cinek o. Diabetes Care. 2006 Apr;29(4):858-63. doi: 10.2337/diacare.29.04.06.dc05-1923. Diabetes Care. 2006. PMID: 16567828

5

Thyroid autoimmunity in children with coexisting type 1 diabetes mellitus and celiac disease: a multicenter study.

Sumnik Z, Cinek O, Bratanic N, Lebl J, Rozsai B, Limbert C, Paskova M, Schober E. Sumnik Z, et al. Among authors: cinek o. J Pediatr Endocrinol Metab. 2006 Apr;19(4):517-22. J Pediatr Endocrinol Metab. 2006. PMID: 16759037

6

Pendred syndrome among patients with congenital hypothyroidism detected by neonatal screening: identification of two novel PDS/SLC26A4 mutations.

Banghova K, Al Taji E, Cinek O, Novotna D, Pourova R, Zapletalova J, Hnikova O, Lebl J. Banghova K, et al. Among authors: cinek o. Eur J Pediatr. 2008 Jul;167(7):777-83. doi: 10.1007/s00431-007-0588-7. Epub 2007 Sep 18. Eur J Pediatr. 2008. PMID: 17876604

7

Autosomal inheritance of diabetes in two families characterized by obesity and a novel H241Q mutation in NEUROD1.

Gonsorcíková L, Průhová S, Cinek O, Ek J, Pelikánová T, Jørgensen T, Eiberg H, Pedersen O, Hansen T, Lebl J. Gonsorcíková L, et al. Among authors: cinek o. Pediatr Diabetes. 2008 Aug;9(4 Pt 2):367-72. doi: 10.1111/j.1399-5448.2008.00379.x. Epub 2008 Mar 5. Pediatr Diabetes. 2008. PMID: 18331410

8

Unusually severe phenotype of neonatal primary hyperparathyroidism due to a heterozygous inactivating mutation in the CASR gene.

Obermannova B, Banghova K, Sumník Z, Dvorakova HM, Betka J, Fencl F, Kolouskova S, Cinek O, Lebl J. Obermannova B, et al. Among authors: cinek o. Eur J Pediatr. 2009 May;168(5):569-73. doi: 10.1007/s00431-008-0794-y. Epub 2008 Aug 27. Eur J Pediatr. 2009. PMID: 18751724

9

Thyroidectomy in a patient with multinodular dyshormonogenetic goitre--a case of Pendred syndrome confirmed by mutations in the PDS/SLC26A4 gene.

Banghova K, Cinek O, Al Taji E, Zapletalova J, Vidura R, Lebl J. Banghova K, et al. Among authors: cinek o. J Pediatr Endocrinol Metab. 2008 Dec;21(12):1179-84. doi: 10.1515/jpem.2008.21.12.1179. J Pediatr Endocrinol Metab. 2008. PMID: 19189692

10

Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY).

Boesgaard TW, Pruhova S, Andersson EA, Cinek O, Obermannova B, Lauenborg J, Damm P, Bergholdt R, Pociot F, Pisinger C, Barbetti F, Lebl J, Pedersen O, Hansen T. Boesgaard TW, et al. Among authors: cinek o. BMC Med Genet. 2010 Mar 12;11:42. doi: 10.1186/1471-2350-11-42. BMC Med Genet. 2010. PMID: 20226046 Free PMC article.

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