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Items: 9

1.

A Genome-Wide Association Study Using a Custom Genotyping Array Identifies Variants in GPR158 Associated With Reduced Energy Expenditure in American Indians.

Piaggi P, Masindova I, Muller YL, Mercader J, Wiessner GB, Chen P; SIGMA Type 2 Diabetes Consortium, Kobes S, Hsueh WC, Mongalo M, Knowler WC, Krakoff J, Hanson RL, Bogardus C, Baier LJ.

Diabetes. 2017 Aug;66(8):2284-2295. doi: 10.2337/db16-1565. Epub 2017 May 5.

2.

Admixture Mapping Identifies an Amerindian Ancestry Locus Associated with Albuminuria in Hispanics in the United States.

Brown LA, Sofer T, Stilp AM, Baier LJ, Kramer HJ, Masindova I, Levy D, Hanson RL, Moncrieft AE, Redline S, Rosas SE, Lash JP, Cai J, Laurie CC, Browning S, Thornton T, Franceschini N.

J Am Soc Nephrol. 2017 Jul;28(7):2211-2220. doi: 10.1681/ASN.2016091010. Epub 2017 Jan 30.

3.

MARVELD2 (DFNB49) mutations in the hearing impaired Central European Roma population--prevalence, clinical impact and the common origin.

Mašindová I, Šoltýsová A, Varga L, Mátyás P, Ficek A, Hučková M, Sůrová M, Šafka-Brožková D, Anwar S, Bene J, Straka S, Janicsek I, Ahmed ZM, Seeman P, Melegh B, Profant M, Klimeš I, Riazuddin S, Kádasi Ľ, Gašperíková D.

PLoS One. 2015 Apr 17;10(4):e0124232. doi: 10.1371/journal.pone.0124232. eCollection 2015.

4.

Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss.

Nayak G, Varga L, Trincot C, Shahzad M, Friedman PL, Klimes I, Greinwald JH Jr, Riazuddin SA, Masindova I, Profant M, Khan SN, Friedman TB, Ahmed ZM, Gasperikova D, Riazuddin S, Riazuddin S.

Hum Genet. 2015 Apr;134(4):423-37. doi: 10.1007/s00439-015-1532-y. Epub 2015 Feb 10.

5.

Is deafness etiology important for prediction of functional outcomes in pediatric cochlear implantation?

Varga L, Kabátová Z, Mašindová I, Nechojdomová D, Gašperíková D, Klimeš I, Profant M.

Acta Otolaryngol. 2014 Jun;134(6):571-8. doi: 10.3109/00016489.2014.894253. Epub 2014 Apr 11.

PMID:
24720341
6.

Prevalence of DFNB1 mutations among cochlear implant users in Slovakia and its clinical implications.

Varga L, Mašindová I, Hučková M, Kabátová Z, Gašperíková D, Klimeš I, Profant M.

Eur Arch Otorhinolaryngol. 2014 Jun;271(6):1401-7. doi: 10.1007/s00405-013-2559-0. Epub 2013 May 23.

PMID:
23700267
7.

Molecular and hereditary mechanisms of sensorineural hearing loss with focus on selected endocrinopathies.

Masindova I, Varga L, Stanik J, Valentinova L, Profant M, Klimes I, Gasperikova D.

Endocr Regul. 2012 Jul;46(3):167-86. Review.

PMID:
22808909
8.

Impact of Type 2 diabetes on Glucokinase diabetes (GCK-MODY) phenotype in a Roma (Gypsy) family - case report.

Stanik J, Kusekova M, Huckova M, Valentinova L, Masindova I, Stanikova D, Ferenczova J, Gasperikova D, Klimes I.

Endocr Regul. 2012 Apr;46(2):99-105.

PMID:
22540858
9.

[Genetics of monogenic forms of diabetes].

Staník J, Hucková M, Staníková D, Masindová I, Valentínová L, Gasperíková D, Klimes I.

Vnitr Lek. 2011 Nov;57(11):937-45. Review. Slovak.

PMID:
22165700

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