Balogh I - Search Results

1

[The absence of the common LRRK2 G2019S mutation in 120 young onset Hungarian Parkinon's disease patients].

Balicza P, Bereznai B, Takáts A, Klivényi P, Dibó G, Hidasi E, Balogh I, Molnár MJ. Balicza P, et al. Among authors: balogh i. Ideggyogy Sz. 2012 Jul 30;65(7-8):239-42. Ideggyogy Sz. 2012. PMID: 23074843 Hungarian.

2

[Laboratory diagnosis of a rare congenital neurodegenerative disease: cerebrotendinous xanthomatosis].

Varga VE, Katkó M, Harangi J, Balogh I, Kapás I, Madar L, Seres I, Molnár MJ, Paragh G, Kovács GG, Harangi M. Varga VE, et al. Among authors: balogh i. Orv Hetil. 2014 May 25;155(21):811-6. doi: 10.1556/OH.2014.29887. Orv Hetil. 2014. PMID: 24836315 Review. Hungarian.

3

[Transthyretin familial amyloid polyneuropathy - three Hungarian cases with rare mutations (His88Arg and Phe33Leu)].

Csillik A , Pozsonyi Z , Soós K , Balogh I , Bodó I , Arányi Z . Csillik A , et al. Among authors: balogh i. Ideggyogy Sz. 2016 Jul 30;69(7-8):245-253. doi: 10.18071/isz.69.0245. Ideggyogy Sz. 2016. PMID: 29465889 Free article. Hungarian.

4

Cerebrotendinous xanthomatosis with the c.379C>T (p.R127W) mutation in the CYP27A1 gene associated with premature age-associated limbic tauopathy.

Kapás I, Katkó M, Harangi M, Paragh G, Balogh I, Kóczi Z, Regelsberger G, Molnár MJ, Kovacs GG. Kapás I, et al. Among authors: balogh i. Neuropathol Appl Neurobiol. 2014 Apr;40(3):345-50. doi: 10.1111/nan.12058. Neuropathol Appl Neurobiol. 2014. PMID: 23659550 No abstract available.

5

Utilization of acute vascular imaging and neurointervention for acute ischaemic stroke patients in 20 Hungarian stroke centers.

Pozsegovits K , Szabó G , Szupera Z , Nagy P , Németh L , Kondákor I , Tusa C , Berente L , Salacz P , Vécsei L , Sas K , Semjén J , Nikl J , Szapáry L , Kakuk A , Rózsa C , Horváth M , Imre P , Köves Á , Balogh I , Molnár S , Folyovich A , Al-Muhanna N , Béres-Molnár AK , Hahn K , Kristóf P , Szász AS , Szűcs A , Bereczki D . Pozsegovits K , et al. Among authors: balogh i. Ideggyogy Sz. 2019 Nov 30;72(11-12):407-412. doi: 10.18071/isz.72.0407. Ideggyogy Sz. 2019. PMID: 31834684 Free article. English.

6

Different phenotypes in identical twins with cerebrotendinous xanthomatosis: case series.

Zádori D, Szpisjak L, Madar L, Varga VE, Csányi B, Bencsik K, Balogh I, Harangi M, Kereszty É, Vécsei L, Klivényi P. Zádori D, et al. Among authors: balogh i. Neurol Sci. 2017 Mar;38(3):481-483. doi: 10.1007/s10072-016-2776-6. Epub 2016 Nov 25. Neurol Sci. 2017. PMID: 27888347

7

Frequencies of two common mutations (c.35delG and c.167delT) of the connexin 26 gene in different populations of Hungary.

Bors A, Andrikovics H, Kalmár L, Erdei N, Galambos S, Losonczi A, Füredi S, Balogh I, Szalai C, Tordai A. Bors A, et al. Among authors: balogh i. Int J Mol Med. 2004 Dec;14(6):1105-8. Int J Mol Med. 2004. PMID: 15547683

8

Hereditary and non-hereditary etiologies associated with extensive brain calcification: case series.

Salamon A, Zádori D, Ujfalusi A, Szpisjak L, Lukács M, Bihari B, Szépfalusi N, Németh VL, Maróti Z, Horváth E, Balogh I, Bereczki C, Klivényi P, Kalmár T. Salamon A, et al. Among authors: balogh i. Metab Brain Dis. 2021 Oct;36(7):2131-2139. doi: 10.1007/s11011-021-00790-9. Epub 2021 Jul 21. Metab Brain Dis. 2021. PMID: 34287746

9

Establishing the Mutational Spectrum of Hungarian Patients with Familial Hypercholesterolemia.

Madar L, Juhász L, Szűcs Z, Kerkovits L, Harangi M, Balogh I. Madar L, et al. Among authors: balogh i. Genes (Basel). 2022 Jan 15;13(1):153. doi: 10.3390/genes13010153. Genes (Basel). 2022. PMID: 35052492 Free PMC article.

10

The Leiden mutation of coagulation factor V in Hungarian SLE patients.

Regéczy N, Lakos G, Balogh I, Ajzner E, Kiss E, Szegedi G. Regéczy N, et al. Among authors: balogh i. Clin Appl Thromb Hemost. 2000 Jan;6(1):41-5. doi: 10.1177/107602960000600107. Clin Appl Thromb Hemost. 2000. PMID: 10726048 Free article.

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