This index provides a clean navigation layer for the diseases section of NeuroWiki. It currently lists 491 published diseases pages organized into logical categories for easier navigation.
Total: 491 pages
| Category | Description |
|---|---|
| Alzheimer's & Tauopathies | AD, tauopathies, amyloid disorders |
| Parkinson's & Synucleinopathies | PD, DLB, MSA, PSP, CBS |
| FTD & Related | FTD, bvFTD, PPA, CBD |
| ALS & Motor Neuron | ALS, PLS, PMA, Kennedy's |
| Prion Diseases | CJD, vCJD, FFI, GSS |
| Huntington's & Movement | HD, chorea, dystonia |
| Cerebellar Ataxias | SCAs, Friedreich, DRPLA |
| Mitochondrial & Metabolic | MELAS, Leigh, LHON |
| Lysosomal Storage | Gaucher, Batten, Niemann-Pick |
| Vascular & Small Vessel | CADASIL, Binswanger, CAA |
| Rare Genetic | NBIA, leukodystrophies |
| Psychiatric & Neurological | Depression, epilepsy, TBI |
| Investment Landscapes | Therapeutic investment by disease |
Mitochondrial Diseases and Neurodegeneration Comparison Matrix
Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia (ALSP)
Ataxia with Oculomotor Apraxia Type 2 (AOA2) Genetic Variants
CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy)
Frontotemporal Dementia with Parkinsonism linked to Chromosome 17 (FTDP-17)
FTD-17 (Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17)
FTLD-ALS: Frontotemporal Lobar Degeneration with Motor Neuron Disease
HTLV-1 Associated Myelopathy (HAM) / Tropical Spastic Paraparesis (TSP)
Japanese and German Case Series in Corticobasal Degeneration
MELAS Syndrome (Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes)
Mitochondrial Membrane Protein-Associated Neurodegeneration (MPAN)
Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD)
Quality of Life and Caregiver Burden in Progressive Supranuclear Palsy
Semantic Dementia (Semantic Variant Primary Progressive Aphasia)