Balogh I - Search Results

1

Human epididymis protein 4 (HE4) levels inversely correlate with lung function improvement (delta FEV₁) in cystic fibrosis patients receiving ivacaftor treatment.

Nagy B Jr, Bene Z, Fejes Z, Heltshe SL, Reid D, Ronan NJ, McCarthy Y, Smith D, Nagy A, Joseloff E, Balla G, Kappelmayer J, Macek M Jr, Bell SC, Plant BJ, Amaral MD, Balogh I. Nagy B Jr, et al. Among authors: balogh i. J Cyst Fibros. 2019 Mar;18(2):271-277. doi: 10.1016/j.jcf.2018.08.013. Epub 2018 Sep 27. J Cyst Fibros. 2019. PMID: 30268371 Free article.

2

Membranous glomerulonephritis in a patient with inherited activated protein C resistance.

Regéczy N, Lakos G, Balogh I, Kappelmayer J, Kiss E. Regéczy N, et al. Among authors: balogh i. Clin Nephrol. 2000 May;53(5):390-3. Clin Nephrol. 2000. PMID: 11305813

3

A novel homozygous mutation (1619delC) in GPIIb gene associated with Glanzmann thrombasthenia, the decay of GPIIb-mRNA and the synthesis of a truncated GPIIb unable to form complex with GPIIIa.

Losonczy G, Rosenberg N, Kiss C, Kappelmayer J, Vereb G, Kerényi A, Balogh I, Muszbek L. Losonczy G, et al. Among authors: balogh i. Thromb Haemost. 2005 May;93(5):904-9. doi: 10.1160/TH04-12-0848. Thromb Haemost. 2005. PMID: 15886807

4

Investigation of Thr715Pro P-selectin gene polymorphism and soluble P-selectin levels in type 2 diabetes mellitus.

Nagy B Jr, Csongrádi E, Bhattoa HP, Balogh I, Blaskó G, Paragh G, Kappelmayer J, Káplár M. Nagy B Jr, et al. Among authors: balogh i. Thromb Haemost. 2007 Jul;98(1):186-91. Thromb Haemost. 2007. PMID: 17598012

5

Distribution of CFTR mutations in Eastern Hungarians: relevance to genetic testing and to the introduction of newborn screening for cystic fibrosis.

Ivady G, Madar L, Nagy B, Gonczi F, Ajzner E, Dzsudzsak E, Dvořáková L, Gombos E, Kappelmayer J, Macek M Jr, Balogh I. Ivady G, et al. Among authors: balogh i. J Cyst Fibros. 2011 May;10(3):217-20. doi: 10.1016/j.jcf.2010.12.009. Epub 2011 Feb 4. J Cyst Fibros. 2011. PMID: 21296036 Free article.

6

Detection of mutations by flow cytometric melting point analysis of PCR products.

Imre L, Balogh I, Kappelmayer J, Szabó M, Melegh B, Wanker E, Szabó G. Imre L, et al. Among authors: balogh i. Cytometry A. 2011 Sep;79(9):720-6. doi: 10.1002/cyto.a.21104. Epub 2011 Jul 19. Cytometry A. 2011. PMID: 21774077 Free article.

7

Human Epididymis Protein 4: A Novel Serum Inflammatory Biomarker in Cystic Fibrosis.

Nagy B Jr, Nagy B, Fila L, Clarke LA, Gönczy F, Bede O, Nagy D, Újhelyi R, Szabó Á, Anghelyi A, Major M, Bene Z, Fejes Z, Antal-Szalmás P, Bhattoa HP, Balla G, Kappelmayer J, Amaral MD, Macek M Jr, Balogh I. Nagy B Jr, et al. Among authors: balogh i. Chest. 2016 Sep;150(3):661-72. doi: 10.1016/j.chest.2016.04.006. Epub 2016 Apr 19. Chest. 2016. PMID: 27105680

8

Congenital Hyperinsulinism Caused by a De Novo Mutation in the ABCC8 Gene - A Case Report.

Molnár Z, Balogh L, Kappelmayer J, Madar L, Gombos É, Balogh I. Molnár Z, et al. Among authors: balogh l, balogh i. EJIFCC. 2017 Mar 8;28(1):85-91. eCollection 2017 Mar. EJIFCC. 2017. PMID: 28439221 Free PMC article.

9

Analytical parameters and validation of homopolymer detection in a pyrosequencing-based next generation sequencing system.

Ivády G, Madar L, Dzsudzsák E, Koczok K, Kappelmayer J, Krulisova V, Macek M Jr, Horváth A, Balogh I. Ivády G, et al. Among authors: balogh i. BMC Genomics. 2018 Feb 21;19(1):158. doi: 10.1186/s12864-018-4544-x. BMC Genomics. 2018. PMID: 29466940 Free PMC article.

10

Comprehensive genetic testing in children with a clinical diagnosis of ARPKD identifies phenocopies.

Szabó T, Orosz P, Balogh E, Jávorszky E, Máttyus I, Bereczki C, Maróti Z, Kalmár T, Szabó AJ, Reusz G, Várkonyi I, Marián E, Gombos É, Orosz O, Madar L, Balla G, Kappelmayer J, Tory K, Balogh I. Szabó T, et al. Among authors: balogh i, balogh e. Pediatr Nephrol. 2018 Oct;33(10):1713-1721. doi: 10.1007/s00467-018-3992-5. Epub 2018 Jun 28. Pediatr Nephrol. 2018. PMID: 29956005

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