Herczegfalvi A - Search Results

1

[Role of associated alleles and hypomethylation status in the clinical expression of facioscapulohumeral muscular dystrophy].

Pikó H, Molnár MJ, Herczegfalvi A, Mayer P, Karcagi V. Pikó H, et al. Among authors: herczegfalvi a. Orv Hetil. 2011 Sep 25;152(39):1576-85. doi: 10.1556/OH.2011.29179. Orv Hetil. 2011. PMID: 21920844 Hungarian.

2

[Carnitine-deficient cardiomyopathy].

Kádár K, Melegh B, Szendrei E, Herczegfalvi A. Kádár K, et al. Among authors: herczegfalvi a. Orv Hetil. 1994 Feb 27;135(9):473-4. Orv Hetil. 1994. PMID: 8139852 Hungarian.

3

[Phenotypic variants of A3243G mitochondrial DNA mutation in a Hungarian family].

Komlósi K, Bene J, Havasi V, Tihanyi M, Herczegfalvi A, Móser J, Melegh B. Komlósi K, et al. Among authors: herczegfalvi a. Orv Hetil. 2004 Aug 29;145(35):1805-9. Orv Hetil. 2004. PMID: 15493224 Hungarian.

4

[Carrier detection in families affected by Duchenne/Becker muscular dystrophy].

Pikó H, Nagy B, Balog J, Bán Z, Herczegfalvi A, Karcagi V. Pikó H, et al. Among authors: herczegfalvi a. Orv Hetil. 2007 Dec 23;148(51):2403-9. doi: 10.1556/OH.2007.28190. Orv Hetil. 2007. PMID: 18055393 Hungarian.

5

Muscular dystrophies: diagnostic approaches in Hungary.

Pikó H, Vancsó V, Nagy B, Balog J, Nagymihály M, Herczegfalvi A, Tímár L, Bán Z, Karcagi V. Pikó H, et al. Among authors: herczegfalvi a. Acta Physiol Hung. 2008 Dec;95(4):405-18. doi: 10.1556/APhysiol.95.2008.4.7. Acta Physiol Hung. 2008. PMID: 19009915 Clinical Trial.

6

[Clinical and genetic diagnosis of Dravet syndrome: report of 20 cases].

Siegler Z, Neuwirth M, Hegyi M, Paraicz E, Pálmafy B, Tegzes A, Barsi P, Karcagi V, Claes L, De Jonghe P, Herczegfalvi A, Fogarasi A. Siegler Z, et al. Among authors: herczegfalvi a. Ideggyogy Sz. 2008 Nov 30;61(11-12):402-8. Ideggyogy Sz. 2008. PMID: 19070316 Hungarian.

7

[Screening for hereditary neuromuscular disorders with molecular genetic methods in the Roma population of Hungary].

Herczegfalvi A, Pikó H, Karcagi V. Herczegfalvi A, et al. Ideggyogy Sz. 2008 Nov 30;61(11-12):426-30. Ideggyogy Sz. 2008. PMID: 19070320 Hungarian.

8

Dystrophin gene analysis in Hungarian Duchenne/Becker muscular dystrophy families - detection of carrier status in symptomatic and asymptomatic female relatives.

Pikó H, Vancsó V, Nagy B, Bán Z, Herczegfalvi A, Karcagi V. Pikó H, et al. Among authors: herczegfalvi a. Neuromuscul Disord. 2009 Feb;19(2):108-12. doi: 10.1016/j.nmd.2008.10.011. Epub 2008 Dec 11. Neuromuscul Disord. 2009. PMID: 19084397

9

[Quantitative analysis of the genes determining spinal muscular atrophy].

Nagymihály M, Herczegfalvi A, Tímár L, Karcagi V. Nagymihály M, et al. Among authors: herczegfalvi a. Ideggyogy Sz. 2009 Nov 30;62(11-12):390-7. Ideggyogy Sz. 2009. PMID: 20025129 Hungarian.

10

Nemaline myopathy caused by mutations in the nebulin gene may present as a distal myopathy.

Lehtokari VL, Pelin K, Herczegfalvi A, Karcagi V, Pouget J, Franques J, Pellissier JF, Figarella-Branger D, von der Hagen M, Huebner A, Schoser B, Lochmüller H, Wallgren-Pettersson C. Lehtokari VL, et al. Among authors: herczegfalvi a. Neuromuscul Disord. 2011 Aug;21(8):556-62. doi: 10.1016/j.nmd.2011.05.012. Epub 2011 Jul 2. Neuromuscul Disord. 2011. PMID: 21724397

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

33 results

Search Page

Filters