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                             14 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Ageing muscle: clonal expansions of mitochondrial DNA point mutations and deletions cause focal impairment of mitochondrial function Fayet, Guillemette
2002
12 5 p. 484-493
10 p.
artikel
2 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 Yamasoba, Tatsuya
2002
12 5 p. 506-512
7 p.
artikel
3 Brain MRI features of congenital- and adult-form myotonic dystrophy type 1: case-control study Di Costanzo, Alfonso
2002
12 5 p. 476-483
8 p.
artikel
4 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 Nédellec, Patrick
2002
12 5 p. 457-465
9 p.
artikel
5 Instructions to authors 2002
12 5 p. 530-531
2 p.
artikel
6 Intracellular pH regulation in isolated fast-twitch skeletal muscle from dystrophin-deficient mouse Decostre, V
2002
12 5 p. 447-456
10 p.
artikel
7 Mitochondrial encephalomyopathies: gene mutation 2002
12 5 p. 524-529
6 p.
artikel
8 Muscle development genes: their relevance in neuromuscular disorders Muntoni, Francesco
2002
12 5 p. 438-446
9 p.
artikel
9 Neuromuscular disorders: gene location 2002
12 5 p. 513-523
11 p.
artikel
10 Novel deletion at the M and P promoters of the human dystrophin gene associated with a Duchenne muscular dystrophy Frisso, Giulia
2002
12 5 p. 494-497
4 p.
artikel
11 Rapid scanning of myotubularin (MTM1) gene by denaturing high-performance liquid chromatography (DHPLC) Flex, Elisabetta
2002
12 5 p. 501-505
5 p.
artikel
12 Severe progressive form of congenital muscular dystrophy with calf pseudohypertrophy, macroglossia and respiratory insufficiency Quijano-Roy, Susana
2002
12 5 p. 466-475
10 p.
artikel
13 The Journal: a crisis of space and time Dubowitz, Victor
2002
12 5 p. 437-
1 p.
artikel
14 Two new mutations in the myophosphorylase gene in Italian patients with McArdle's disease Bruno, Claudio
2002
12 5 p. 498-500
3 p.
artikel
                             14 gevonden resultaten
 
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