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Results: 1-15 |
Results: 15

Authors: Gasser, T Dichgans, M Finsterer, J Hausmanowa-Petrusewicz, I Jurkat-Rott, K Klopstock, T Leguern, E Lehesjoki, AE Lehmann-Horn, F Lynch, T Morris, H Rossor, M Steinlein, OK Wood, N Zaremba, J Zeviani, M Zoharn, A
Citation: T. Gasser et al., EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - Second of two parts, EUR J NEUR, 8(5), 2001, pp. 407-424

Authors: Gasser, T Dichgans, M Finsterer, J Hausmanowa-Petrusewicz, I Jurkat-Rott, K Klopstock, T LeGuern, E Lehesjoki, AE Lehmann-Horn, F Lynch, T Morris, H Rossor, M Steinlein, OK Wood, N Zaremba, J Zeviani, M Zoharn, A
Citation: T. Gasser et al., EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - First of two parts, EUR J NEUR, 8(4), 2001, pp. 299-314

Authors: Rudnik-Schoneborn, S Hausmanowa-Petrusewicz, I Borkowska, J Zerres, K
Citation: S. Rudnik-schoneborn et al., The predictive value of achieved motor milestones assessed in 441 patientswith infantile spinal muscular atrophy types II and III, EUR NEUROL, 45(3), 2001, pp. 174-181

Authors: Zalewska, E Hausmanowa-Petrusewicz, I
Citation: E. Zalewska et I. Hausmanowa-petrusewicz, Effectiveness of motor unit potentials classification using various parameters and indexes, CLIN NEU, 111(8), 2000, pp. 1380-1387

Authors: Bolino, A Muglia, M Conforti, FL LeGuern, E Salih, MAM Georgiou, DM Christodoulou, K Hausmanowa-Petrusewicz, I Mandich, P Schenone, A Gambardella, A Bono, F Quattrone, A Devoto, M Monaco, AP
Citation: A. Bolino et al., Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2, NAT GENET, 25(1), 2000, pp. 17-19

Authors: Bolino, A Levy, ER Muglia, M Conforti, FL LeGuern, E Salih, MAM Georgiou, DM Hausmanowa-Petrusewicz, I Mandich, P Gambardella, A Quattrone, A Devoto, M Monaco, AP
Citation: A. Bolino et al., Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22, GENOMICS, 63(2), 2000, pp. 271-278

Authors: Piotrkiewicz, M Hausmanowa-Petrusewicz, I Mierzejewska, J
Citation: M. Piotrkiewicz et al., Are motoneurons involved in muscular dystrophy?, CLIN NEU, 110(6), 1999, pp. 1111-1122

Authors: Zalewska, E Hausmanowa-Petrusewicz, I
Citation: E. Zalewska et I. Hausmanowa-petrusewicz, Global and detailed features of motor unit potential in myogenic and neurogenic disorders, MED ENG PHY, 21(6-7), 1999, pp. 421-429

Authors: Piotrkiewicz, M Hausmanowa-Petrusewicz, I Mierzejewska, J
Citation: M. Piotrkiewicz et al., Motoneurons are altered in muscular dystrophy, J PHYSL-PAR, 93(1-2), 1999, pp. 167-173

Authors: Rowinska-Marcinska, K Zalewska, E Hausmanowa-Petrusewicz, I
Citation: K. Rowinska-marcinska et al., Double discharges of motor units in neuromuscular disorders, J PHYSL-PAR, 93(1-2), 1999, pp. 175-182

Authors: Zakrzewska-Pniewska, B Jablonska, S Kowalska-Oledzka, E Blaszczyk, M Hausmanowa-Petrusewicz, I
Citation: B. Zakrzewska-pniewska et al., Sympathetic skin response in scleroderma, scleroderma overlap syndromes and inflammatory myopathies, CLIN RHEUMA, 18(6), 1999, pp. 473-480

Authors: Zalewska, E Hausmanowa-Petrusewicz, I
Citation: E. Zalewska et I. Hausmanowa-petrusewicz, On the classification of nonsimple motor unit potentials, MUSCLE NERV, 22(6), 1999, pp. 780-781

Authors: Chou, FL Angelini, C Daentl, D Garcia, C Greco, C Hausmanowa-Petrusewicz, I Fidzianska, A Wessel, H Hoffman, EP
Citation: Fl. Chou et al., Calpain III mutation analysis of a heterogeneous limb-girdle muscular dystrophy population, NEUROLOGY, 52(5), 1999, pp. 1015-1020

Authors: Niebroj-Dobosz, I Jamrozik, Z Janik, P Hausmanowa-Petrusewicz, I Kwiecinski, H
Citation: I. Niebroj-dobosz et al., Anti-neural antibodies in serum and cerebrospinal fluid of amyotrophic lateral sclerosis (ALS) patients, ACT NEUR SC, 100(4), 1999, pp. 238-243

Authors: Goldberg, LR Hausmanowa-Petrusewicz, I Fidzianska, A Duggan, DJ Steinberg, LS Hoffman, EP
Citation: Lr. Goldberg et al., A dystrophin missense mutation showing persistence of dystrophin and dystrophin-associated proteins yet a severe phenotype, ANN NEUROL, 44(6), 1998, pp. 971-976
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