Volume 10; Issue 1

Main
Neuromuscular Disorders
Volume 10; Issue 1

Neuromuscular Disorders

Volume 10; Issue 1

1

Dermatomyositis and Whipple's disease

T.R. Helliwell, R.E. Appleton, N.C. Mapstone, J. Davidson, K.P. Walsh

Journal:

Neuromuscular Disorders

Year:

2000

Language:

english

File:

PDF, 1.19 MB

english, 2000

2

Neuromuscular disorders in childhood: a descriptive epidemiological study from western Sweden

N Darin, M Tulinius

Journal:

Neuromuscular Disorders

Year:

2000

Language:

english

File:

PDF, 277 KB

english, 2000

3

Identification of homozygous and heterozygous dy2J mice by PCR

Jean-Thomas Vilquin, Nicolas Vignier, Jacques P. Tremblay, Eva Engvall, Ketty Schwartz, Marc Fiszman

Journal:

Neuromuscular Disorders

Year:

2000

Language:

english

File:

PDF, 318 KB

english, 2000

4

Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity

M.A.M Salih, T Maisonobe, M Kabiraj, M Al Rayess, M.H.S Al-Turaiki, M Akbar, A Tahan, J.A Urtizberea, D Grid, T Hamadouche, A Guilbot, A Brice, E Leguern

Journal:

Neuromuscular Disorders

Year:

2000

Language:

english

File:

PDF, 398 KB

english, 2000

5

Two distal mutations in the gene encoding emerin have profoundly different effects on emerin protein expression

Juliet A Ellis, Charlotte A Brown, L Denise Tilley, John Kendrick-Jones, J Edward Spence, John R.W Yates

Journal:

Neuromuscular Disorders

Year:

2000

Language:

english

File:

PDF, 263 KB

english, 2000

6

Different effects of mexiletine on two mutant sodium channels causing paramyotonia congenita and hyperkalemic periodic paralysis

K. Weckbecker, A. Würz, B. Mohammadi, T. Mansuroglu, A.L. George Jr, H. Lerche, R. Dengler, F. Lehmann-Horn, N. Mitrovic

Journal:

Neuromuscular Disorders

Year:

2000

Language:

english

File:

PDF, 279 KB

english, 2000

7

An Italian family with Ala-47 transthyretin mutation associated with cardiomyopathy and polyneuropathy

C Solaro, A Schenone, A Di Sapio, L Pradotto, G.L Mancardi, A Primavera, A Mauro

Journal:

Neuromuscular Disorders

Year:

2000

Language:

english

File:

PDF, 133 KB

english, 2000

8

Muscle membrane–skeleton protein changes and histopathological characterization of muscle-eye-brain disease

M Auranen, J Rapola, H Pihko, M Haltia, I Leivo, S Soinila, I Virtanen, H Kalimo, L.V.B Anderson, P Santavuori, H Somer

Journal:

Neuromuscular Disorders

Year:

2000

Language:

english

File:

PDF, 693 KB

english, 2000

9

Effects of aerobic training on lactate and catecholaminergic exercise responses in mitochondrial myopathies

Gabriele Siciliano, Maria Laura Manca, Maria Renna, Concetta Prontera, Antonella Mercuri, Luigi Murri

Journal:

Neuromuscular Disorders

Year:

2000

Language:

english

File:

PDF, 185 KB

english, 2000

10

Amyotrophic lateral sclerosis: copper/zinc superoxide dismutase (SOD1) gene mutations

Richard W. Orrell

Journal:

Neuromuscular Disorders

Year:

2000

Language:

english

File:

PDF, 62 KB

english, 2000

11

Single large-scale mitochondrial DNA deletion in a patient with encephalopathy, cardiomyopathy, and prominent intestinal pseudo-obstruction

Yolanda Campos, Miguel A Martı́n, Cristina Caballero, Juan C Rubio, Francisco de la Cruz, Teresa Tuñón, Joaquı́n Arenas

Journal:

Neuromuscular Disorders

Year:

2000

Language:

english

File:

PDF, 45 KB

english, 2000

12

Ten years of ENMC – from a patients’ initiative to a successful European research institution: the story of the European Neuromuscular Centre

Reinhardt Rüdel, Giovanni Nigro, Ysbrand Poortman

Journal:

Neuromuscular Disorders

Year:

2000

Language:

english

File:

PDF, 635 KB

english, 2000

13

5th Workshop of the European CMT Consortium, 69th ENMC International Workshop: Therapeutic approaches in CMT neuropathies and related disorders 23–25 April 1999, Soestduinen, The Netherlands

Rudolf Martini, José Berciano, Christine Van Broeckhoven

Journal:

Neuromuscular Disorders

Year:

2000

Language:

english

File:

PDF, 71 KB

english, 2000