| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Accumulating autofluorescent material as a marker for early changes in the spinal cord of the Mnd mouse
|
Messer, Anne
|
|
1993
|
3 |
2 |
p. 129-134
6 p.
|
artikel
|
| 2 |
Deficiency of dystrophin-associated proteins: A common mechanism leading to muscle cell necrosis in severe childhood muscular dystrophies
|
Matsumura, Kiichiro
|
|
1993
|
3 |
2 |
p. 109-118
10 p.
|
artikel
|
| 3 |
Duchenne muscular dystrophy, 2nd edn.
|
Dubowitz, Victor
|
|
1993
|
3 |
2 |
p. 181-
1 p.
|
artikel
|
| 4 |
Dystrophin-positive myotubes in innervated muscle cultures from Duchenne and Becker muscular dystrophy patients
|
Fanin, M.
|
|
1993
|
3 |
2 |
p. 119-127
9 p.
|
artikel
|
| 5 |
Handbook of clinical neurology
|
Emery, Alan E.H.
|
|
1993
|
3 |
2 |
p. 179-
1 p.
|
artikel
|
| 6 |
Handbook of clinical neurology
|
Munsat, Theodore L.
|
|
1993
|
3 |
2 |
p. 180-
1 p.
|
artikel
|
| 7 |
Inherited ataxias
|
Morrison, Patrick J.
|
|
1993
|
3 |
2 |
p. 180-181
2 p.
|
artikel
|
| 8 |
Manifesting carriers of Xp21 muscular dystrophy; Lack of correlation between dystrophin expression and clinical weakness
|
Sewry, C.A.
|
|
1993
|
3 |
2 |
p. 141-148
8 p.
|
artikel
|
| 9 |
Molecular basis of inherited disease, 2nd edn.
|
Emery, Alan E.H.
|
|
1993
|
3 |
2 |
p. 179-180
2 p.
|
artikel
|
| 10 |
Molecular biology and pathology of skeletal and cardiac myogenesis
|
Amati, Paolo
|
|
1993
|
3 |
2 |
p. 169-171
3 p.
|
artikel
|
| 11 |
Muscle fibre degeneration in distal myopathy (Welander)—Ultrastructure related to immunohistochemical observations on cytoskeletal proteins and Leu-19 antigen
|
Borg, Kristian
|
|
1993
|
3 |
2 |
p. 149-155
7 p.
|
artikel
|
| 12 |
Neuromuscular disorders: Gene location
|
|
|
1993
|
3 |
2 |
p. 173-177
5 p.
|
artikel
|
| 13 |
Non-dystrophic myotonias and periodic paralyses
|
Lehmann-Horn, Frank
|
|
1993
|
3 |
2 |
p. 161-168
8 p.
|
artikel
|
| 14 |
Periodic paralysis, myotonia congenita and sarcolemmal ion channels: A success of the candidate gene approach
|
Fontaine, Bertrand
|
|
1993
|
3 |
2 |
p. 101-107
7 p.
|
artikel
|
| 15 |
Sarcolemmal distribution of abnormal dystrophin in Xp21 carriers
|
Vainzof, Mariz
|
|
1993
|
3 |
2 |
p. 135-140
6 p.
|
artikel
|
| 16 |
The glycinamide ribonucleotide transformylase (GART) gene is not responsible for familial amyotrophic lateral sclerosis
|
Goto, Jun
|
|
1993
|
3 |
2 |
p. 157-160
4 p.
|
artikel
|
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