Wittmann I - Search Results

1

Dramatic decrease of carnitine esters after interruption of exogenous carnitine supply in hemodialysis patients.

Bene J, Csiky B, Wittmann I, Sulyok E, Melegh B. Bene J, et al. Among authors: wittmann i. Ren Fail. 2012;34(5):555-8. doi: 10.3109/0886022X.2012.664509. Epub 2012 Mar 15. Ren Fail. 2012. PMID: 22417076

2

[Hypertension and 24-hours blood pressure monitoring in kidney diseases].

Csiky B, Wittmann I, Nagy J. Csiky B, et al. Among authors: wittmann i. Orv Hetil. 2004 Feb 15;145(7):323-6. Orv Hetil. 2004. PMID: 15049046 Review. Hungarian.

3

[Effect of ACE gene polymorphism on carbohydrate metabolism, on oxidative stress and on end-organ damage in type-2 diabetes mellitus].

Molnár GA, Wagner Z, Wagner L, Melegh B, Kószegi T, Degrell P, Bene J, Tamaskó M, Laczy B, Nagy J, Wittmann I. Molnár GA, et al. Among authors: wittmann i. Orv Hetil. 2004 Apr 18;145(16):855-9. Orv Hetil. 2004. PMID: 15156690 Hungarian.

4

Detection of the Leu40Arg variant of the platelet glycoprotein IIb/IIIa receptor in subjects with thrombotic diseases.

Nádasi E, Bene J, Havasi V, Komlósi K, Talián G, Melegh G, Papp E, Gasztonyi B, Szolnoki Z, Sándor J, Mózsik G, Tóth K, Melegh B, Wittmann I. Nádasi E, et al. Among authors: wittmann i. Thromb Res. 2005;116(6):479-82. doi: 10.1016/j.thromres.2005.01.008. Epub 2005 Feb 16. Thromb Res. 2005. PMID: 16181983 No abstract available.

5

Serum carboxymethyllysine predicts mortality in hemodialysis patients.

Wagner Z, Molnár M, Molnár GA, Tamaskó M, Laczy B, Wagner L, Csiky B, Heidland A, Nagy J, Wittmann I. Wagner Z, et al. Among authors: wittmann i. Am J Kidney Dis. 2006 Feb;47(2):294-300. doi: 10.1053/j.ajkd.2005.10.010. Am J Kidney Dis. 2006. PMID: 16431258

6

[Search for mitochondrial DNA T4291C mutation in Hungarian patients with metabolic syndrome].

Maász A, Horvatovich K, Magyari L, Talián Csaba G, Bokor S, Laczy B, Tamaskó M, Molnár D, Wittmann I, Melegh B. Maász A, et al. Among authors: wittmann i. Orv Hetil. 2006 Apr 16;147(15):693-6. Orv Hetil. 2006. PMID: 16734181 Hungarian.

7

[Importance of hereditary haemochromatosis in the care of diabetes mellitus].

Wittmann I, Wagner L, Markó L, Tamaskó M, Laczy B, Márton M, Cseh J, Melegh B. Wittmann I, et al. Orv Hetil. 2007 Jan 21;148(3):111-5. doi: 10.1556/OH.2007.27901. Orv Hetil. 2007. PMID: 17289614 Review. Hungarian.

8

Apolipoprotein A5 T-1131C variant confers risk for metabolic syndrome.

Maász A, Kisfali P, Horvatovich K, Mohás M, Markó L, Csöngei V, Faragó B, Járomi L, Magyari L, Sáfrány E, Sipeky C, Wittmann I, Melegh B. Maász A, et al. Among authors: wittmann i. Pathol Oncol Res. 2007;13(3):243-7. doi: 10.1007/BF02893505. Epub 2007 Oct 7. Pathol Oncol Res. 2007. PMID: 17922054 Free article.

9

Apolipoprotein A5 IVS3+476A allelic variant associates with increased trigliceride levels and confers risk for development of metabolic syndrome in Hungarians.

Kisfali P, Mohás M, Maasz A, Hadarits F, Markó L, Horvatovich K, Oroszlán T, Bagosi Z, Bujtor Z, Gasztonyi B, Wittmann I, Melegh B. Kisfali P, et al. Among authors: wittmann i. Circ J. 2008 Jan;72(1):40-3. doi: 10.1253/circj.72.40. Circ J. 2008. PMID: 18159097 Free article.

10

Serum total LDH activity and LDH-2 isozyme in nephrotic syndrome.

Mohás M, Szigeti N, Markó L, Molnár GA, Cseh J, Laczy B, Tamaskó M, Balla J, Kappelmayer J, Wagner L, Wagner Z, Csiky B, Nagy J, Wittmann I. Mohás M, et al. Among authors: wittmann i. Kidney Blood Press Res. 2008;31(1):47-54. doi: 10.1159/000112960. Epub 2008 Jan 10. Kidney Blood Press Res. 2008. PMID: 18185017

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