Neuromuscular Disorders

The Journal: a crisis of space and time
pp. 437-437(1)
Author: Dubowitz V.

Muscle development genes: their relevance in neuromuscular disorders
pp. 438-446(9)
Authors: Muntoni F.; Brown S.; Sewry C.; Patel K.

Intracellular pH regulation in isolated fast-twitch skeletal muscle from dystrophin-deficient mouse
pp. 447-456(10)
Authors: Decostre V.; Gailly P.; Debaix H.; Colson-Van Schoor M.; Cao M.L.; Gillis J.M.

Glucocorticoid treatment induces expression of small heat shock proteins in human satellite cell populations: consequences for a desmin-related myopathy involving the R120G alpha B-crystallin mutation
pp. 457-465(9)
Authors: Nedellec P.; Edling Y.; Perret E.; Fardeau M.; Vicart P.

Severe progressive form of congenital muscular dystrophy with calf pseudohypertrophy, macroglossia and respiratory insufficiency
pp. 466-475(10)
Authors: Quijano-Roy S.; Galan L.; Ferreiro A.; Cheliout-Heraut F.; Gray F.; Fardeau M.; Barois A.; Guicheney P.; Romero N.B.; Estournet B.

Brain MRI features of congenital- and adult-form myotonic dystrophy type 1: case-control study
pp. 476-483(8)
Authors: Di Costanzo A.; Di Salle F.; Santoro L.; Bonavita V.; Tedeschi G.

Ageing muscle: clonal expansions of mitochondrial DNA point mutations and deletions cause focal impairment of mitochondrial function
pp. 484-493(10)
Authors: Fayet G.; Jansson M.; Sternberg D.; Moslemi A.-R.; Blondy P.; Lombes A.; Fardeau M.; Oldfors A.

Novel deletion at the M and P promoters of the human dystrophin gene associated with a Duchenne muscular dystrophy
pp. 494-497(4)
Authors: Frisso G.; Sampaolo S.; Pastore L.; Carlomagno A.; Calise R.M.; Di Iorio G.; Salvatore F.

Two new mutations in the myophosphorylase gene in Italian patients with McArdle's disease
pp. 498-500(3)
Authors: Bruno C.; Lanzillo R.; Biedi C.; Iadicicco L.; Minetti C.; Santoro L.

Rapid scanning of myotubularin (MTM1) gene by denaturing high-performance liquid chromatography (DHPLC)
pp. 501-505(5)
Authors: Flex E.; De Luca A.; D'Apice M.R.; Buccino A.; Dallapiccola B.; Novelli G.

Atypical muscle pathology and a survey of cis-mutations in deaf patients harboring a 1555 A-to-G point mutation in the mitochondrial ribosomal RNA gene
pp. 506-512(7)
Authors: Yamasoba T.; Goto Y.-i.; Oka Y.; Nishino I.; Tsukuda K.; Nonaka I.

Neuromuscular disorders: gene location
pp. 513-523(11)

Mitochondrial encephalomyopathies: gene mutation
pp. 524-529(6)

Instructions to authors
pp. 530-531(2)