DIAGNOSES |
REFERENCES/NOTES |
Amyotrophic lateral sclerosis (ALS) |
(Brownell, Oppenheimer et al. 1970) |
Alzheimer disease (AD) |
(Mirra, Heyman et al. 1991) |
Alzheimer disease Lewy body variant (ADLBV) |
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Binswanger disease |
|
CADASIL |
|
Cerebral amyloid angiopathy (CAA) |
|
Cerebral metastasis (carcinoma) |
|
Corticobasal degeneration (CBD) |
(Rebeiz, Kolodny et al. 1968) |
Creutzfeldt-Jakob disease (CJD) |
|
Dementia lacking distinctive histology features (DLDH) |
|
Dementia pugilistica |
|
Dementia with argyrophilic grains (DAG) |
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Dementia with Lewy body, brainstem predominant |
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Dementia with Lewy body, limbic or transitional |
|
Dementia with Lewy body, neocortical |
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Dentato-rubro-pallido-luysian atrophy (DRPLA) |
|
Depression |
Clinical diagnosis of depression; no |
Frontal lobe dementia |
(Cairns, Bigio et al. 2001) |
Huntington disease, grade 1 |
|
Huntington disease, grade 2 |
|
Huntington disease, grade 3 |
|
Huntington disease, grade 4 |
|
Infarct, old |
|
Infarct, recent |
|
Leptomeningeal carcinomatosis |
|
Lewy body dementia |
See Dementia with Lewy body… |
Motor neuron disease |
See ALS |
Multi-infarct dementia (MID) |
(del Ser, Bermejo et al. 1990) |
Multiple sclerosis |
|
Multiple system atrophy (MSA) |
(Wenning, Ben Shlomo et al. 1994) |
Olivo-ponto-cerebellar atrophy |
See MSA |
Parkinson disease |
(Forno 1996) |
Pick disease |
|
Pick disease, type A |
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Pick disease, type B |
|
Pick disease, type C |
|
Progressive supranuclear palsy, combined |
|
Progressive supranuclear palsy, typical |
|
Schizophrenia |
Clinical diagnosis of schizophrenia; no |
Spino-cerbellar ataxia |
|
Spongiform Encephalopathies |
See CJD |
Striato-nigral degeneration |
See MSA |
Vascular dementia |
See multi-infarct dementia (MID) |