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Results: 4

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
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