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 |