| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Actin myopathy with nemaline bodies, intranuclear rods, and a heterozygous mutation in ACTA1 (Asp154Asn)
|
Schröder, J. M.
|
|
2004
|
108 |
3 |
p. 250-256
|
artikel
|
| 2 |
Biphasic NF-κB activation in the excitotoxic hippocampus
|
Caba, Ebru
|
|
2004
|
108 |
3 |
p. 173-182
|
artikel
|
| 3 |
Cortical ubiquitin-positive inclusions in frontotemporal dementia without motor neuron disease: a quantitative immunocytochemical study
|
Kövari, Enikö
|
|
2004
|
108 |
3 |
p. 207-212
|
artikel
|
| 4 |
Expression of tyrosine kinases FAK and Pyk2 in 331 human astrocytomas
|
Gutenberg, A.
|
|
2004
|
108 |
3 |
p. 224-230
|
artikel
|
| 5 |
Extracellular protein deposition correlates with glial activation and oxidative stress in Creutzfeldt-Jakob and Alzheimer’s disease
|
Everbroeck, Bart Van
|
|
2004
|
108 |
3 |
p. 194-200
|
artikel
|
| 6 |
Glyceraldehyde-derived advanced glycation end products in Alzheimer’s disease
|
Choei, Hiroshi
|
|
2004
|
108 |
3 |
p. 189-193
|
artikel
|
| 7 |
Induction of nerve growth factor mRNA in a rat dorsal root ganglion after application of a tourniquet
|
Abe, Sumiko
|
|
2004
|
108 |
3 |
p. 183-188
|
artikel
|
| 8 |
α-Internexin aggregates are abundant in neuronal intermediate filament inclusion disease (NIFID) but rare in other neurodegenerative diseases
|
Cairns, Nigel J.
|
|
2004
|
108 |
3 |
p. 213-223
|
artikel
|
| 9 |
Marked reduction of focal adhesion kinase, serum response factor and myocyte enhancer factor 2C, but increase in RhoA and myostatin in the hindlimb dy mouse muscles
|
Sakuma, Kunihiro
|
|
2004
|
108 |
3 |
p. 241-249
|
artikel
|
| 10 |
Oligodendrocytes within astrocytes (“emperipolesis”) in the white matter in Creutzfeldt-Jakob disease
|
Shintaku, Masayuki
|
|
2004
|
108 |
3 |
p. 201-206
|
artikel
|
| 11 |
Rimmed vacuoles in facioscapulohumeral muscular dystrophy: a unique ultrastructural feature
|
Neudecker, Stephan
|
|
2004
|
108 |
3 |
p. 257-259
|
artikel
|
| 12 |
Subcortical angiopathic encephalopathy in a German kindred suggests an autosomal dominant disorder distinct from CADASIL
|
Hagel, C.
|
|
2004
|
108 |
3 |
p. 231-240
|
artikel
|
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