Kytnarová J - Search Results

1

Two novel mutations in seven Czech and Slovak kindreds with familial neurohypophyseal diabetes insipidus-benefit of genetic testing.

Hrčková G, Jankó V, Kytnarová J, Čižmárová M, Tesařová M, Košťálová Ľ, Virgová D, Dallos T, Hána V, Lebl J, Zeman J, Kovács L. Hrčková G, et al. Among authors: kytnarova j. 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

2

High Incidence of Heterozygous ABCC8 and HNF1A Mutations in Czech Patients With Congenital Hyperinsulinism.

Rozenkova K, Malikova J, Nessa A, Dusatkova L, Bjørkhaug L, Obermannova B, Dusatkova P, Kytnarova J, Aukrust I, Najmi LA, Rypackova B, Sumnik Z, Lebl J, Njølstad PR, Hussain K, Pruhova S. Rozenkova K, et al. Among authors: kytnarova j. J Clin Endocrinol Metab. 2015 Dec;100(12):E1540-9. doi: 10.1210/jc.2015-2763. Epub 2015 Oct 2. J Clin Endocrinol Metab. 2015. PMID: 26431509

3

Clinical Heterogeneity, Tissue Distribution, and Intergenerational Segregation of mtDNA Mutation A3243G.

Tesarova M, Hansikova H, Kytnarova J, Houstkova H, Bohm M, Cerna L, Zeman J, Houstek J. Tesarova M, et al. Among authors: kytnarova j. Toxicol Mech Methods. 2004;14(1-2):79-84. doi: 10.1080/15376520490257527. Toxicol Mech Methods. 2004. PMID: 20021128

4

Cytosine-Adenosine (CA)n repeats polymorphism in IGF-I gene and early growth in infants born appropriate and small for gestational age.

Kytnarova J, Vesela K, Zlatohlavkova B, Dohnalova A, Fedorova M, Krsek M, Zeman J. Kytnarova J, et al. Neuro Endocrinol Lett. 2009;30(4):501-5. Neuro Endocrinol Lett. 2009. PMID: 20010501

5

Isoelectric Focusing of Serum Apolipoprotein C-III as a Sensitive Screening Method for the Detection of O-glycosylation Disturbances.

Ondrušková N, Honzík T, Kytnarová J, Matoulek M, Zeman J, Hansíková H. Ondrušková N, et al. Among authors: kytnarova j. Prague Med Rep. 2015;116(2):73-86. doi: 10.14712/23362936.2015.48. Prague Med Rep. 2015. PMID: 26093664 Free article.

6

Post-natal growth of 157 children born as extremely premature neonates.

Kytnarova J, Zlatohlavková B, Kubena A, Markova D, Dokoupilova M, Plavka R, Zeman J. Kytnarova J, et al. J Paediatr Child Health. 2011 Mar;47(3):111-6. doi: 10.1111/j.1440-1754.2010.01897.x. Epub 2010 Nov 21. J Paediatr Child Health. 2011. PMID: 21091582

7

[Metabolic studies in 28 families of patients with cystinuria].

Kytnarová J, Zeman J, Hyánek J, Rubín A, Nĕmcová D. Kytnarová J, et al. Cesk Pediatr. 1988 Jun;43(6):338-40. Cesk Pediatr. 1988. PMID: 3401967 Czech. No abstract available.

8

Five-year survival without major disability of extremely preterm infants born at 22-27 weeks' gestation admitted to a NICU.

Zlatohlávková B, Kytnarová J, Kuběna A, Fleischnerová A, Dokoupilová M, Plavka R. Zlatohlávková B, et al. Among authors: kytnarova j. Acta Paediatr. 2010 Nov;99(11):1618-23. doi: 10.1111/j.1651-2227.2010.01895.x. Epub 2010 Jun 17. Acta Paediatr. 2010. PMID: 20528794

9

Diseases caused by defects of energy level and loss of coherence in living cells.

Jandová A, Pokorný J, Pokorný J, Kobilková J, Nedbalová M, Čoček A, Jelínek F, Vrba J, Vrba J Jr, Dohnalová A, Kytnarová J, Tuszyński JA, Foletti A. Jandová A, et al. Among authors: kytnarova j. Electromagn Biol Med. 2015;34(2):151-5. doi: 10.3109/15368378.2015.1036076. Electromagn Biol Med. 2015. PMID: 26098528

10

[Enzyme therapy in children with severe forms of Gaucher's disease].

Zeman J, Hrebícek M, Vepreková L, Kytnarová J, Houstková H, Malinová V, Hodanová K, Poupĕtová H, Ledvinová J, Hoza J. Zeman J, et al. Among authors: kytnarova j. Cas Lek Cesk. 1997 Feb 5;136(3):95-7. Cas Lek Cesk. 1997. PMID: 9221177 Czech.

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