Volume 12; Issue 3

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Neuromuscular Disorders
Volume 12; Issue 3

Neuromuscular Disorders

Volume 12; Issue 3

1

Involvement of KCa2+ channels in the local abnormalities and hyperkalemia following the ischemia-reperfusion injury of rat skeletal muscle

Domenico Tricarico, Raffaele Capriulo, Diana Conte Camerino

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 213 KB

english, 2002

2

Bethlem myopathy (BETHLEM) 86th ENMC International Workshop, 10–11 November 2000, Naarden, The Netherlands

Guglielmina Pepe, Marianne de Visser, Enrico Bertini, Kate Bushby, Olga Camacho Vanegas, Mon-Li Chu, Giovanna Lattanzi, Luciano Merlini, Francesco Muntoni, Andoni Urtizberea

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 108 KB

english, 2002

3

Primary γ-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profile

C.G. Bönnemann, J. Wong, K.J. Jones, H.G.W. Lidov, C.A. Feener, F. Shapiro, B.T. Darras, L.M. Kunkel, K.N. North

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 428 KB

english, 2002

4

Charles Bell (1774–1842) and an early case of muscular dystrophy: The Third Meryon Society Lecture read at Worcester College, Oxford on 28 July, 2000

Christopher Gardner-Thorpe

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 120 KB

english, 2002

5

A quantitative study of bioenergetics in skeletal muscle lacking utrophin and dystrophin

M.A. Cole, J.A. Rafael, D.J. Taylor, R. Lodi, K.E. Davies, P. Styles

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 215 KB

english, 2002

6

Normal calcium homeostasis in dystrophin-expressing facioscapulohumeral muscular dystrophy myotubes

Clarisse Vandebrouck, Nathalie Imbert, Bruno Constantin, Gérard Duport, Guy Raymond, Christian Cognard

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 273 KB

english, 2002

7

Two amino-acid substitutions in the myelin protein zero gene of a case of Charcot–Marie–Tooth disease associated with light-near dissociation

H.M.E. Bienfait, F. Baas, A.A.W.M. Gabreëls-Festen, J.H.T.M. Koelman, C.T. Langerhorst, M. de Visser

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 174 KB

english, 2002

8

A family with autosomal dominant mutilating neuropathy not linked to either Charcot–Marie–Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci

Emilia Bellone, Carmelo Rodolico, Antonio Toscano, Emilio Di Maria, Denise Cassandrini, Antonio Pizzuti, Simona Pigullo, Anna Mazzeo, Vincenzo Macaione, Paolo Girlanda, Giuseppe Vita, Franco Ajmar, Pa

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 144 KB

english, 2002

9

Report of the 84th ENMC Workshop: PROMM (Proximal Myotonic Myopathy) and Other Myotonic Dystrophy-Like Syndromes: 2nd Workshop. 13–15th October, 2000, Loosdrecht, The Netherlands

Richard T. Moxley III, Giovanni Meola, Bjarne Udd, Kenneth Ricker

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 121 KB

english, 2002

10

Presynaptic neuromuscular transmission block in Guillain–Barré syndrome associated with anti-GQ1b antibodies

I. Wirguin, G. Ifergane, Y. Almog, D. Lieberman, M. Bersudsky, Y.O. Herishanu

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 55 KB

english, 2002

11

Vertebral compression in Duchenne muscular dystrophy following deflazacort

B. Talim, C. Malaguti, S. Gnudi, L. Politano, L. Merlini

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 57 KB

english, 2002

12

Defects of mitochondrial β-oxidation: a growing group of disorders

Jerry Vockley, David A.H. Whiteman

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 245 KB

english, 2002

13

Letter on Schneider article

Ibrahim Mahjneh

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 30 KB

english, 2002

14

Response from author

C. Schneider, D. Brechtelsbauer

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 35 KB

english, 2002

15

The gene for a novel glycosyltransferase is mutated in congenital muscular dystrophy MDC1C and limb girdle muscular dystrophy 2I

Martin Brockington, Derek J. Blake, Susan C. Brown, Francesco Muntoni

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 44 KB

english, 2002

16

Neuromuscular disorders: gene location

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 78 KB

english, 2002

17

Mitochondrial encephalomyopathies: gene mutation

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 49 KB

english, 2002

18

Instructions to authors

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 39 KB

english, 2002