| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Absence of IDH mutation identifies a novel radiologic and molecular subtype of WHO grade II gliomas with dismal prognosis
|
Metellus, Philippe
|
|
2010
|
120 |
6 |
p. 719-729
|
artikel
|
| 2 |
A cortical form of CADASIL with cerebral Aβ amyloidosis
|
Paquet, Claire
|
|
2010
|
120 |
6 |
p. 813-820
|
artikel
|
| 3 |
Benedikt Volk (1940–2010): in search of new horizons—voyages of a curious mind
|
Pagenstecher, Axel
|
|
2010
|
120 |
6 |
p. 833-834
|
artikel
|
| 4 |
Benedikt Volk (1940–2010): in search of new horizons—voyages of a curious mind
|
Pagenstecher, Axel
|
|
|
120 |
6 |
p. 833-834
|
artikel
|
| 5 |
Changes in key hypothalamic neuropeptide populations in Huntington disease revealed by neuropathological analyses
|
Gabery, Sanaz
|
|
2010
|
120 |
6 |
p. 777-788
|
artikel
|
| 6 |
Effect of topographical distribution of α-synuclein pathology on TDP-43 accumulation in Lewy body disease
|
Yokota, Osamu
|
|
2010
|
120 |
6 |
p. 789-801
|
artikel
|
| 7 |
Heterogeneous neuropathological findings in Parkinson’s disease with mild cognitive impairment
|
Adler, Charles H.
|
|
2010
|
120 |
6 |
p. 827-828
|
artikel
|
| 8 |
IgG4-related meningeal disease: clinico-pathological features and proposal for diagnostic criteria
|
Lindstrom, Katherine M.
|
|
2010
|
120 |
6 |
p. 765-776
|
artikel
|
| 9 |
Improved discrimination of melanotic schwannoma from melanocytic lesions by combined morphological and GNAQ mutational analysis
|
Küsters-Vandevelde, Heidi V. N.
|
|
2010
|
120 |
6 |
p. 755-764
|
artikel
|
| 10 |
Loss of SMARCB1/INI1 expression in poorly differentiated chordomas
|
Mobley, Bret C.
|
|
2010
|
120 |
6 |
p. 745-753
|
artikel
|
| 11 |
MYB upregulation and genetic aberrations in a subset of pediatric low-grade gliomas
|
Tatevossian, Ruth G.
|
|
2010
|
120 |
6 |
p. 731-743
|
artikel
|
| 12 |
Neuropathology in Parkinson’s disease with mild cognitive impairment
|
Jellinger, Kurt A.
|
|
2010
|
120 |
6 |
p. 829-830
|
artikel
|
| 13 |
Neuropathology of the recessive A673V APP mutation: Alzheimer disease with distinctive features
|
Giaccone, Giorgio
|
|
2010
|
120 |
6 |
p. 803-812
|
artikel
|
| 14 |
Patients with IDH1 wild type anaplastic astrocytomas exhibit worse prognosis than IDH1-mutated glioblastomas, and IDH1 mutation status accounts for the unfavorable prognostic effect of higher age: implications for classification of gliomas
|
Hartmann, Christian
|
|
2010
|
120 |
6 |
p. 707-718
|
artikel
|
| 15 |
Sensory circumventricular organs in health and disease
|
Sisó, Sílvia
|
|
2010
|
120 |
6 |
p. 689-705
|
artikel
|
| 16 |
TDP-43 plasma levels do not differentiate sporadic inclusion body myositis from other inflammatory myopathies
|
Kuiperij, H. Bea
|
|
2010
|
120 |
6 |
p. 825-826
|
artikel
|
| 17 |
Variability of diffuse plaques and amyloid angiopathy in Parkinson’s disease with mild cognitive impairment
|
Adler, Charles H.
|
|
2010
|
120 |
6 |
p. 831
|
artikel
|
| 18 |
Variably protease-sensitive prionopathy in a PRNP codon 129 heterozygous UK patient with co-existing tau, α synuclein and Aβ pathology
|
Head, Mark W.
|
|
2010
|
120 |
6 |
p. 821-823
|
artikel
|
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