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                             26 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Atlas of Clinical Neurology. Roger N. Rosenberg, editor. Butterworth Heinemann, Feb 1998, 600 pages, hardback, ISBN: 0 7506 9922 1, £105, CD ROM Jan 1998, ISBN: 0 7506 9923 x, £120 exc VAT Nixon, John
2001
11 1 p. 96-
1 p.
artikel
2 Autosomal dominant distal myopathy: further evidence of a chromosome 14 locus Voit, T
2001
11 1 p. 11-19
9 p.
artikel
3 Cationic channels in normal and dystrophic human myotubes Vandebrouck, C
2001
11 1 p. 72-79
8 p.
artikel
4 Center for the Study of the Human Genome, University of São Paulo, São Paulo, Brazil 2001
11 1 p. 101-
1 p.
artikel
5 Commentary from the Editor 2001
11 1 p. 1-2
2 p.
artikel
6 Corrigendum to “Rhabdomyosarcoma ρ0 cells: isolation and characterization of mitochondrial DNA depleted cell line with ‘muscle-like’ properties” [Neuromuscular Disorders 10 (2000) 454–459] Vergani, Lodovica
2001
11 1 p. 99-
1 p.
artikel
7 Dysferlinopathy (LGMD2B): a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutations Mahjneh, Ibrahim
2001
11 1 p. 20-26
7 p.
artikel
8 Ethical Dilemmas in Neurology. Adam Zeman and Linda Emanuel, editors. Saunders/Harcourt Brace, 2000, 224 pages, hardback, ISBN 0-7020-2227-6, £55.00 Cardy, Peter
2001
11 1 p. 96-97
2 p.
artikel
9 Evaluation of the dystrophin–glycoprotein complex, α-actinin, dysferlin and calpain 3 in an autosomal recessive muscular dystrophy in Labrador retrievers Olby, Natasha J.
2001
11 1 p. 41-49
9 p.
artikel
10 Gene Mutation 2001
11 1 p. 104-120
17 p.
artikel
11 Gene Mutation 2001
11 1 p. 121-130
10 p.
artikel
12 Instructions to authors 2001
11 1 p. 131-132
2 p.
artikel
13 Linkage of a new locus for autosomal recessive axonal form of Charcot–Marie–Tooth disease to chromosome 8q21.3 Barhoumi, C
2001
11 1 p. 27-34
8 p.
artikel
14 Mast cell proliferation and alterations in bFGF amount and localization are involved in the response of muscle to dystrophin deficiency in hypertrophic feline dystrophy Seiler, Gabriela
2001
11 1 p. 56-71
16 p.
artikel
15 Mediterranean Society of Myology: Capri, September 2000 2001
11 1 p. 103-
1 p.
artikel
16 Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle α-actin (ACTA1) gene Jungbluth, H
2001
11 1 p. 35-40
6 p.
artikel
17 MNGIE: from nuclear DNA to mitochondrial DNA Nishino, Ichizo
2001
11 1 p. 7-10
4 p.
artikel
18 Muscle news from around the world 2001
11 1 p. 100-
1 p.
artikel
19 MYO-CLUSTER 2001
11 1 p. 102-
1 p.
artikel
20 Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies Pogue, Robert
2001
11 1 p. 80-87
8 p.
artikel
21 Surface Anatomy for Clinical Needle Electromyography. Hang J. Lee and Joel A. DeLisa, Demos Publishing, 1999, 240 pages, ISBN: 1 888799 41 2, $51.50; Manual of Nerve Conduction Studies. Ralph M. Buschbacher, Demos Publishing, 1999, 450 pages, soft back, ISBN:1 888799 36 6, $60.00 Kennett, Robin
2001
11 1 p. 97-98
2 p.
artikel
22 Surplus protein myopathies Goebel, Hans H.
2001
11 1 p. 3-6
4 p.
artikel
23 Textbook of Neurology. Julien Ogousslavsky and Mark Fisher, Butterworth Heinemann, 1998, hardback, £70, ISBN: 0 7506 9918 3 Hill, Marguerite
2001
11 1 p. 98-
1 p.
artikel
24 64th ENMC International Workshop: Therapeutic approaches to dermatomyositis, polymyositis, and inclusion body myositis29–31 January 1999, Naarden, The Netherlands Müller-Felber, Wolfgang
2001
11 1 p. 88-92
5 p.
artikel
25 Use of magnetic resonance imaging for noninvasive characterization and follow-up of an experimental injury to normal mouse muscles Wishnia, Arnold
2001
11 1 p. 50-55
6 p.
artikel
26 Workshop on inflammatory myopathy Bethesda, 5–6 April 2000 Plotz, Paul H.
2001
11 1 p. 93-95
3 p.
artikel
                             26 gevonden resultaten
 
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