Zapletalová J - Search Results

1

[Pendred syndrome among patients with hypothyroidism: genetic diagnosis, phenotypic variability and occurrence of phenocopies].

Banghová K, Al TE, Novotná D, Zapletalová J, Hníková O, Cáp J, Klabochová J, Kúseková M, Lebl J. Banghová K, et al. Among authors: zapletalova j. Cas Lek Cesk. 2008;147(12):616-22. Cas Lek Cesk. 2008. PMID: 19235486 Czech.

2

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: zapletalova j. 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

3

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: zapletalova j. 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

4

[Adult height of patients after long-term treatment of idiopathic growth hormone deficiency. (Czech Registry 1991-1998)].

Zapletalová J, Lebl J, Janstová V, Kalvachová B, Novotná D, Philippiová O. Zapletalová J, et al. Cas Lek Cesk. 2000 Aug 30;139(17):529-32. Cas Lek Cesk. 2000. PMID: 11109285 Czech.

5

[Analysis of specific sequences in female patients with Turner syndrome--initial study].

Vodicka R, Vrtĕl R, Adamová K, Zapletalová J, Lebl J, Santavý J, Santavá A, Kolárová J, Konvalinka D, Krejciríková E. Vodicka R, et al. Among authors: zapletalova j. Cas Lek Cesk. 2002 Jul;141(13):421-4. Cas Lek Cesk. 2002. PMID: 12238030 Slovak.

6

Prepubertal girls with Turner syndrome and children with isolated SHOX deficiency have similar bone geometry at the radius.

Soucek O, Zapletalova J, Zemkova D, Snajderova M, Novotna D, Hirschfeldova K, Plasilova I, Kolouskova S, Rocek M, Hlavka Z, Lebl J, Sumnik Z. Soucek O, et al. Among authors: zapletalova j. J Clin Endocrinol Metab. 2013 Jul;98(7):E1241-7. doi: 10.1210/jc.2013-1113. Epub 2013 May 10. J Clin Endocrinol Metab. 2013. PMID: 23666967

7

An isolated Xp deletion is linked to autoimmune diseases in Turner syndrome.

Stoklasova J, Zapletalova J, Frysak Z, Hana V, Cap J, Pavlikova M, Soucek O, Lebl J. Stoklasova J, et al. Among authors: zapletalova j. J Pediatr Endocrinol Metab. 2019 May 27;32(5):479-488. doi: 10.1515/jpem-2019-0067. J Pediatr Endocrinol Metab. 2019. PMID: 31075085

8

Bone geometry and volumetric bone density at the radius in patients with isolated SHOX deficiency.

Soucek O, Lebl J, Zapletalova J, Novotna D, Plasilova I, Kolouskova S, Zemkova D, Rocek M, Hlavka Z, Hirschfeldova K, Sumnik Z. Soucek O, et al. Among authors: zapletalova j. Exp Clin Endocrinol Diabetes. 2013 Feb;121(2):109-14. doi: 10.1055/s-0032-1333260. Epub 2013 Feb 20. Exp Clin Endocrinol Diabetes. 2013. PMID: 23426705

9

[Celiac disease as a cause of short stature in children].

Zapletalová J, Kolek A, Venhácová J. Zapletalová J, et al. Cas Lek Cesk. 1995 Mar 22;134(6):176-8. Cas Lek Cesk. 1995. PMID: 7758069 Czech.

10

Auxological and endocrine phenotype in a population-based cohort of patients with PROP1 gene defects.

Lebl J, Vosáhlo J, Pfaeffle RW, Stobbe H, Cerná J, Novotná D, Zapletalová J, Kalvachová B, Hána V, Weiss V, Blum WF. Lebl J, et al. Among authors: zapletalova j. Eur J Endocrinol. 2005 Sep;153(3):389-96. doi: 10.1530/eje.1.01989. Eur J Endocrinol. 2005. PMID: 16131601

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

311 results

Search Page

Filters