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Two novel mutations in seven Czech and Slovak kindreds with familial neurohypophyseal diabetes insipidus-benefit of genetic testing.
Eur J Pediatr. 2016 Sep;175(9):1199-1207. doi: 10.1007/s00431-016-2759-x. Epub 2016 Aug 18.
Eur J Pediatr. 2016.
PMID: 27539621
Late onset of familial neurogenic diabetes insipidus in monozygotic twins.
Cizmarova M, Nagyova G, Janko V, Pribilincova Z, Virgova D, Ilencikova D, Kovacs L.
Cizmarova M, et al. Among authors: virgova d.
Endocr Regul. 2013 Oct;47(4):211-6. doi: 10.4149/endo_2013_04_211.
Endocr Regul. 2013.
PMID: 24156710
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Melanocortin-4 receptor gene mutations in obese Slovak children.
Stanikova D, Surova M, Ticha L, Petrasova M, Virgova D, Huckova M, Skopkova M, Lobotkova D, Valentinova L, Mokan M, Stanik J, Klimes I, Gasperikova D.
Stanikova D, et al. Among authors: virgova d.
Physiol Res. 2015;64(6):883-90. doi: 10.33549/physiolres.932968. Epub 2015 Jun 5.
Physiol Res. 2015.
PMID: 26047380
Free article.
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