nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Autopsy study of cerebellar degeneration in siblings with ataxia-telangiectasia-like disorder
|
Oba, Daiju |
|
2010 |
119 |
4 |
p. 513-520 |
artikel |
2 |
Brain damage in a large cohort of solvent abusers
|
Al-Hajri, Zahra |
|
2010 |
119 |
4 |
p. 435-445 |
artikel |
3 |
Congenital myotonic dystrophy can show congenital fiber type disproportion pathology
|
Tominaga, Kayo |
|
2010 |
119 |
4 |
p. 481-486 |
artikel |
4 |
Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2
|
Vihola, Anna |
|
2010 |
119 |
4 |
p. 465-479 |
artikel |
5 |
Kurt Jellinger Prize 2010 for Outstanding Scientific Writing in Neuropathology
|
|
|
2010 |
119 |
4 |
p. 521 |
artikel |
6 |
Loss of murine TDP-43 disrupts motor function and plays an essential role in embryogenesis
|
Kraemer, Brian C. |
|
2010 |
119 |
4 |
p. 409-419 |
artikel |
7 |
Mutant IDH1-specific immunohistochemistry distinguishes diffuse astrocytoma from astrocytosis
|
Camelo-Piragua, Sandra |
|
2009 |
119 |
4 |
p. 509-511 |
artikel |
8 |
Novel myosin heavy chain immunohistochemical double staining developed for the routine diagnostic separation of I, IIA and IIX fibers
|
Raheem, Olayinka |
|
2010 |
119 |
4 |
p. 495-500 |
artikel |
9 |
Prevalence of dementia disorders in the oldest-old: an autopsy study
|
Jellinger, Kurt A. |
|
2010 |
119 |
4 |
p. 421-433 |
artikel |
10 |
Protein coding of neurodegenerative dementias: the neuropathological basis of biomarker diagnostics
|
Kovacs, Gabor G. |
|
2010 |
119 |
4 |
p. 389-408 |
artikel |
11 |
Rapid and sensitive assessment of the IDH1 and IDH2 mutation status in cerebral gliomas based on DNA pyrosequencing
|
Felsberg, Jörg |
|
2010 |
119 |
4 |
p. 501-507 |
artikel |
12 |
The carboxy-terminal fragment of α1A calcium channel preferentially aggregates in the cytoplasm of human spinocerebellar ataxia type 6 Purkinje cells
|
Ishiguro, Taro |
|
2009 |
119 |
4 |
p. 447-464 |
artikel |
13 |
The prognostic IDH1R132 mutation is associated with reduced NADP+-dependent IDH activity in glioblastoma
|
Bleeker, Fonnet E. |
|
2010 |
119 |
4 |
p. 487-494 |
artikel |