Authors:
Jaksch, M
Horvath, R
Horn, N
Auer, DP
Macmillan, C
Peters, J
Gerbitz, KD
Kraegeloh-Mann, I
Muntau, A
Karcagi, V
Kalmanchey, R
Lochmuller, H
Shoubridge, EA
Freisinger, P
Citation: M. Jaksch et al., Homozygosity (E140K) in SCO2 causes delayed infantile onset of cardiomyopathy and neuropathy, NEUROLOGY, 57(8), 2001, pp. 1440-1446
Authors:
Horvath, R
Abicht, A
Shoubridge, EA
Karcagi, V
Rozsa, C
Komoly, S
Lochmuller, H
Citation: R. Horvath et al., Leber's hereditary optic neuropathy presenting as multiple sclerosis-like disease of the CNS, J NEUROL, 247(1), 2000, pp. 65-67
Authors:
Lahermo, P
Laitinen, V
Sistonen, P
Beres, J
Karcagi, V
Savontaus, ML
Citation: P. Lahermo et al., MtDNA polymorphism in the Hungarians: comparison to three other Finno-Ugric-speaking populations, HEREDITAS, 132(1), 2000, pp. 35-42
Authors:
Abicht, A
Stucka, R
Karcagi, V
Herczegfalvi, A
Horvath, R
Mortier, W
Schara, U
Ramaekers, V
Jost, W
Brunner, J
Janssen, G
Seidel, U
Schlotter, B
Muller-Felber, W
Pongratz, D
Rudel, R
Lochmuller, H
Citation: A. Abicht et al., A common mutation (epsilon 1267delG) in congenital myasthenic patients of Gypsy ethnic origin, NEUROLOGY, 53(7), 1999, pp. 1564-1569