| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel mutation, Thr65Ala, in the MPZ gene in a patient with Charcot-Marie-Tooth type 1B disease with focally folded myelin
|
Kochanski, A.
|
|
2004
|
14 |
3 |
p. 229-232
4 p.
|
artikel
|
| 2 |
Clinical Neurology
|
Pinto, Ashwin
|
|
2004
|
14 |
3 |
p. 233-
1 p.
|
artikel
|
| 3 |
Different tissue distribution of a mitochondrial DNA duplication and the corresponding deletion in a patient with a mild mitochondrial encephalomyopathy: deletion in muscle, duplication in blood
|
Houshmand, Massoud
|
|
2004
|
14 |
3 |
p. 195-201
7 p.
|
artikel
|
| 4 |
Editorial Board
|
|
|
2004
|
14 |
3 |
p. IFC-
1 p.
|
artikel
|
| 5 |
Human Molecular Biology: An Introduction to the Molecular Basis of Health and Disease
|
Emery, Alan
|
|
2004
|
14 |
3 |
p. 233-
1 p.
|
artikel
|
| 6 |
Instruction to Authors
|
|
|
2004
|
14 |
3 |
p. 235-236
2 p.
|
artikel
|
| 7 |
Linkage to two separate loci in a family with a novel distal myopathy phenotype (MPD3)
|
Haravuori, Henna
|
|
2004
|
14 |
3 |
p. 183-187
5 p.
|
artikel
|
| 8 |
Molecular phenotyping of the mouse ky mutant reveals UCP1 upregulation at the neuromuscular junctions of dystrophic soleus muscle
|
Blanco, G
|
|
2004
|
14 |
3 |
p. 217-228
12 p.
|
artikel
|
| 9 |
Novel truncating RAPSN mutations causing congenital myasthenic syndrome responsive to 3,4-diaminopyridine
|
Banwell, Brenda L
|
|
2004
|
14 |
3 |
p. 202-207
6 p.
|
artikel
|
| 10 |
Principles of Treatment in Multiple Sclerosis
|
Scolding, N.J.
|
|
2004
|
14 |
3 |
p. 234-
1 p.
|
artikel
|
| 11 |
Subclinical cardiac involvement in myotonic dystrophy manifesting as decreased myocardial Doppler velocities
|
Vinereanu, Dragos
|
|
2004
|
14 |
3 |
p. 188-194
7 p.
|
artikel
|
| 12 |
Tubular aggregates are from whole sarcoplasmic reticulum origin: alterations in calcium binding protein expression in mouse skeletal muscle during aging
|
Chevessier, F
|
|
2004
|
14 |
3 |
p. 208-216
9 p.
|
artikel
|
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