| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Absence of mutations in the Mn superoxide dismutase or catalase genes in familial amyotrophic lateral sclerosis
|
Parboosingh, Jillian S.
|
|
1995
|
5 |
1 |
p. 7-10
4 p.
|
artikel
|
| 2 |
Chaos in the classification of SMA: A possible resolution
|
Dubowitz, Victor
|
|
1995
|
5 |
1 |
p. 3-5
3 p.
|
artikel
|
| 3 |
Commentary from the editor
|
Dubowitz, Victor
|
|
1995
|
5 |
1 |
p. 1-2
2 p.
|
artikel
|
| 4 |
Congenital symmetrical weakness of the upper limbs resembling brachial plexus palsy: A possible sequel of drug toxicity in first trimester of pregnancy?
|
Philpot, Joanne
|
|
1995
|
5 |
1 |
p. 67-69
3 p.
|
artikel
|
| 5 |
Diabetic muscle infarction: A new perspective on pathogenesis and management
|
Bjornskov, Elizabeth K.
|
|
1995
|
5 |
1 |
p. 39-45
7 p.
|
artikel
|
| 6 |
Diagnostic criteria for the limb-girdle muscular dystrophies: Report of the ENMC consortium on limbgirdle dystrophies
|
Bushby, K.M.D.
|
|
1995
|
5 |
1 |
p. 71-74
4 p.
|
artikel
|
| 7 |
Editorial Board
|
|
|
1995
|
5 |
1 |
p. IFC-
1 p.
|
artikel
|
| 8 |
Erratum
|
|
|
1995
|
5 |
1 |
p. 79-
1 p.
|
artikel
|
| 9 |
Exclusion of the candidate locus FSP1 in six families with late-onset autosomal dominant spastic paraplegia
|
Fontaine, Bertrand
|
|
1995
|
5 |
1 |
p. 11-17
7 p.
|
artikel
|
| 10 |
Exclusion of the gene locus for spinal muscular atrophy on chromosome 5q in a family with infantile olivopontocerebellar atrophy (OPCA) and anterior horn cell degeneration
|
Rudnik-Schöneborn, Sabine
|
|
1995
|
5 |
1 |
p. 19-23
5 p.
|
artikel
|
| 11 |
Experimental Thyrotoxic myopathy: Radioautography of protien synthesis in skeletal muscle and motor neurons of spinal cord
|
Kazakov, V.M.
|
|
1995
|
5 |
1 |
p. 47-52
6 p.
|
artikel
|
| 12 |
Malignant hyperthermia in a patient with Becker muscular dystrophy: Dystrophin analysis and caffeine contracture study
|
Ohkoshi, Norio
|
|
1995
|
5 |
1 |
p. 53-58
6 p.
|
artikel
|
| 13 |
Mitochondrial encephalomyopathies: Gene mutation
|
|
|
1995
|
5 |
1 |
p. IX-XII
nvt p.
|
artikel
|
| 14 |
Neuromuscular disorders: Gene location
|
|
|
1995
|
5 |
1 |
p. I-VII
nvt p.
|
artikel
|
| 15 |
Olivopontocerebellar hypoplasia with anterior horn cell involvement (SMA) does not localize to chromosome 5q
|
Dubowitz, V.
|
|
1995
|
5 |
1 |
p. 25-29
5 p.
|
artikel
|
| 16 |
Recurrent congenital arthrogryposis leading to a diagnosis of myasthenia gravis in an initially asymptomatic mother
|
Barnes, Phillip R.J.
|
|
1995
|
5 |
1 |
p. 59-65
7 p.
|
artikel
|
| 17 |
Rimmed basophilic vacuoles and filamentous inclusions in neuromuscular disorders
|
Jongen, Peter J.H.
|
|
1995
|
5 |
1 |
p. 31-38
8 p.
|
artikel
|
| 18 |
11th meeting of the peripheral nerve study group (PNSG)
|
Schroder, J.Michael
|
|
1995
|
5 |
1 |
p. 75-77
3 p.
|
artikel
|
Tijdschrift beschrijving