Items where Author is "Karcagi, Veronika"

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Bladen, C. L. and Rafferty, K. and Straub, V. and Monges, S. and Moresco, A. and Karcagi, Veronika and Herczegfalvi, Ágnes (2013) The TREAT-NMD Duchenne Muscular Dystrophy Registries: Conception, Design, and Utilization by Industry and Academia. Human Mutation, 34 (11). pp. 1449-1457. ISSN 1059-7794 (print), 1098-1004 (online)

Lehtokari, V. L. and Pelin, K. and Herczegfalvi, Ágnes and Karcagi, Veronika and Pouget, J. (2011) Nemaline myopathy caused by mutations in the nebulin gene may present as a distal myopathy. NEUROMUSCULAR DISORDERS, 21 (8). pp. 556-562. ISSN 0960-8966

Muller, J. S. and Herczegfalvi, Ágnes and Vilchez, J. J. and Colomer, J. and Bachinski, L. L. and Karcagi, Veronika (2007) Phenotypical spectrum of DOK7 mutations in congenital myasthenic syndromes. BRAIN, 130 (Pt 6). pp. 1497-1506. ISSN 0006-8950

Morar, B. and Gresham, D. and Angelicheva, D. and Tournev, I. and Gooding, R. and Tordai, Attila and Nagy, Melinda and Karcagi, Veronika and Herczegfalvi, Ágnes (2004) Mutation History of the Roma/Gypsies. AMERICAN JOURNAL OF HUMAN GENETICS, 75 (4). pp. 596-609. ISSN 0002-9297


Karcagi, Veronika and Balog, Judit and Hajdu, Krisztina and Herczegfalvi, Ágnes and Kékesdyné dr. Siska, Éva and Pikó, Henriett and Tímár, László and Tóth, András (2007) Izomdystrophiák differenciál-diagnosztikai vizsgálata molekuláris genetikai, valamint immunhisztokémiai és immunoblot analízisek segítségével = Differential diagnostic study of muscle dystrophies by molecular genetic, immunohystochemical and Western-blot analyses. Project Report. OTKA.

László, Aranka and Béres, Judit and Karcagi, Veronika and Szabó, János and Varga, Tibor (2006) Genetikai kórképek hazai roma populatióban = Genetic disorders in Romani population. Project Report. OTKA.

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