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Results: 1-8 |
Results: 8
Distal infantile neuroaxonal dystrophy - a new familial variant with perineuronal argyrophilic bodies
Authors: Kyllerman, M Mansson, JE Lichtenstein, M Percy, AK Nordborg, C
Citation: M. Kyllerman et al., Distal infantile neuroaxonal dystrophy - a new familial variant with perineuronal argyrophilic bodies, ACT NEUROP, 102(1), 2001, pp. 83-88
Superoxide dismutase and glutathione peroxidase function in progressive myoclonus epilepsies
Authors: Ben-Menachem, E Kyllerman, M Marklund, S
Citation: E. Ben-menachem et al., Superoxide dismutase and glutathione peroxidase function in progressive myoclonus epilepsies, EPILEPSY R, 40(1), 2000, pp. 33-39
Evaluation of the role of the D2 dopamine receptor in myoclonus dystonia
Authors: Klein, C Gurvich, N Sena-Esteves, M Bressman, S Brin, MF Ebersole, BJ Fink, S Forsgren, L Friedman, J Grimes, D Holmgren, G Kyllerman, M Lang, AE de Leon, D Leung, J Prioleau, C Raymond, D Sanner, G Saunders-Pullman, R Vieregge, P Wahlstrom, J Breakefield, XO Kramer, PL Ozelius, LJ Sealfon, SC
Citation: C. Klein et al., Evaluation of the role of the D2 dopamine receptor in myoclonus dystonia, ANN NEUROL, 47(3), 2000, pp. 369-373
Children with septo-optic dysplasia - How to improve and sharpen the diagnosis
Authors: Hellstrom, A Aronsson, M Axelson, C Kyllerman, M Kopp, S Steffenburg, S Stromland, K Westphal, O Wiklund, LM Wikland, KA
Citation: A. Hellstrom et al., Children with septo-optic dysplasia - How to improve and sharpen the diagnosis, HORMONE RES, 53, 2000, pp. 19-25
Autosomal dominant myopathy: Missense mutation (Glu-706 -> Lys) in the myosin heavy chain IIa gene
Authors: Martinsson, T Oldfors, A Darin, N Berg, K Tajsharghi, H Kyllerman, M Wahlstrom, J
Citation: T. Martinsson et al., Autosomal dominant myopathy: Missense mutation (Glu-706 -> Lys) in the myosin heavy chain IIa gene, P NAS US, 97(26), 2000, pp. 14614-14619
A major locus for myoclonus-dystonia maps to chromosome 7q in eight families
Authors: Klein, C Schilling, K Saunders-Pullman, RJ Garrels, J Breakefield, XO Brin, MF deLeon, D Doheny, D Fahn, S Fink, JS Forsgren, L Friedman, J Frucht, S Harris, J Holmgren, G Kis, B Kurlan, R Kyllerman, M Lang, AE Leung, J Raymond, D Robishaw, JD Sanner, G Schwinger, E Tabamo, RE Tagliati, M Vieregge, P Wahlstrom, J Wendt, KJ Kramer, PL Bressman, SB Ozelius, LJ
Citation: C. Klein et al., A major locus for myoclonus-dystonia maps to chromosome 7q in eight families, AM J HU GEN, 67(5), 2000, pp. 1314-1319
Multiple mitochondrial DNA deletions in hereditary inclusion body myopathy
Authors: Jansson, M Darin, N Kyllerman, M Martinsson, T Wahlstrom, J Oldfors, A
Citation: M. Jansson et al., Multiple mitochondrial DNA deletions in hereditary inclusion body myopathy, ACT NEUROP, 100(1), 2000, pp. 23-28
Dominant hereditary inclusion-body myopathy gene (IBM3) maps to chromosomeregion 17p13.1
Authors: Martinsson, T Darin, N Kyllerman, M Oldfors, A Hallberg, B Wahlstrom, J
Citation: T. Martinsson et al., Dominant hereditary inclusion-body myopathy gene (IBM3) maps to chromosomeregion 17p13.1, AM J HU GEN, 64(5), 1999, pp. 1420-1426
Risultati: 1-8 |