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Neurodegenerative Disorder
Neurodegenerative disorder
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Neurological disorders
(18)
Spinocerebellar ataxia
Batten disease
Neuronal ceroid lipofuscinosis
Huntington disease
Corticobasal degeneration
Corticobasal degeneration
Familial dysautonomia
Semantic dementia
Polyglutamine disease
Cerebellar ataxia
Machado-joseph disease
HSAN-IV
Friedreich ataxia
Neurological disorder
Hereditary sensory neuropathies
Transmissible spongiform encephalopathies
Dementia with Lewy bodies
Olivoponto- cerebellar atrophy
Motor neuron disease
more...
Neurology
(12)
Niemann Pick disease
Bradykinesia
Dyskinesias
Frontotemporal dementia
Tay Sachs disease
Tay Sachs disease
Movement disorders
Fatal familial insomnia
Adrenoleuk- odystrophy
J. Neurol.
Dystonia
Neuroprotection
Neurological disorders
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Disability
Brain disorder
Neurological disorders
Spinocerebellar ataxia
Genetic disorders
(17)
Boder-Sedgwick syndrome
Spinal muscular atrophy
Canavan disease
Globoid cell leukodystrophy
Gaucher disease
Gaucher disease
Morquio syndrome
Metachromatic leukodystrophy
Spinocerebellar ataxia
Batten disease
Huntington disease
Niemann Pick disease
Polyglutamine disease
Machado-joseph disease
Tay Sachs disease
Friedreich ataxia
Hereditary sensory neuropathies
Adrenoleuk- odystrophy
more...
Lysosomal storage diseases
(40)
Lysosomal storage disease
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Canavan disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidosis
Gaucher disease
Globoid cell leukodystrophy
Glycogen storage disease type II
Glycoproteinosis
Hunter syndrome
Hurler syndrome
I-cell disease
Lipid storage disorder
Metachromatic leukodystrophy
Morquio syndrome
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidosis
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann Pick disease
Niemann-Pick disease, type C
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Schindler disease
Sialidosis
Sly syndrome
Tay Sachs disease
Wolman disease
more...
Autosomal recessive disorders
(12)
Batten disease
Neuronal ceroid lipofuscinosis
Niemann Pick disease
Familial dysautonomia
HSAN-IV
HSAN-IV
Tay Sachs disease
Friedreich ataxia
Canavan disease
Globoid cell leukodystrophy
Gaucher disease
Morquio syndrome
Metachromatic leukodystrophy
more...
Rare diseases
(10)
Multiple system atrophy
Amyotrophic lateral sclerosis
Neuronal ceroid lipofuscinosis
Niemann Pick disease
HSAN-IV
HSAN-IV
Tay Sachs disease
Globoid cell leukodystrophy
Gaucher disease
Morquio syndrome
Metachromatic leukodystrophy
more...
Genes
Gene
Huntingtin
MeCP2
Extrapyramidal and movement disorders
(19)
Pantothenate kinase-associated neurodegeneration
Parkinson disease
Parkinsonism
Progressive supranuclear palsy
Akathisia
Akathisia
Blepharospasm
Choreia (disease)
Dystonia
Essential tremor
Meige's syndrome
Movement disorders
Multiple system atrophy
Myoclonus
Neuroleptic malignant syndrome
Postencephalitic parkinsonism
Restless legs syndrome
Spasmodic torticollis
Stiff person syndrome
Tardive dyskinesia
more...
Cognitive disorders
(19)
AIDS dementia complex
Alzheimer's disease
Binswanger's disease
Clinical Dementia Rating
Corticobasal degeneration
Corticobasal degeneration
Delirium
Dementia
Dementia with Lewy bodies
Frontotemporal dementia
Frontotemporal dementia and parkinsonism linked to chromosome 17
Frontotemporal lobar degeneration
Logopenic progressive aphasia
Multi-infarct dementia
Pick's disease
Prevention of dementia
Primary progressive aphasia
Progressive nonfluent aphasia
Progressive supranuclear palsy
Semantic dementia
more...
Transmissible spongiform encephalopathies
(12)
Creutzfeldt-Jakob disease
Prion disease
Bovine spongiform encephalopathy
Chronic wasting disease
Deaths from Creutzfeldt-Jakob disease
Deaths from Creutzfeldt-Jakob disease
Fatal familial insomnia
Feline spongiform encephalopathy
Gerstmannâ- €“Sträussler–Scheinker syndrome
Kuru (disease)
Prion
Scrapie
Transmissible mink encephalopathy
more...
Leukodystrophies
Adrenoleuk- odystrophy
Alexander disease
Canavan disease
Globoid cell leukodystrophy
Metachromatic leukodystrophy
Pelizaeus-- Merzbacher disease
Zellweger syndrome
Gene
SOD1
CLN3
TDP43
NPC1
DCTN1
Tripeptidyl peptidase I
Ataxin 1
Proteins
Ubiquitinated
Ataxin 7
Ataxin-3
Huntingtin
Ataxin 1
Diseases and disorders
(37)
Amyloid plaques
Spinocerebellar ataxia 1
Spastic paraparesis
Optic atrophy
Neurological disorders
Neurological disorders
Batten disease
Neuronal ceroid lipofuscinosis
Huntington disease
Corticobasal degeneration
Parkinson disease
Multiple system atrophy
Progressive supranuclear palsy
Niemann Pick disease
Bradykinesia
Familial dysautonomia
Dyskinesias
Frontotemporal dementia
Machado-joseph disease
HSAN-IV
Tay Sachs disease
Prion disease
Friedreich ataxia
Movement disorders
Boder-Sedgwick syndrome
Spinal muscular atrophy
Canavan disease
Globoid cell leukodystrophy
Hereditary sensory neuropathies
Gaucher disease
Transmissible spongiform encephalopathies
Amyotrophic lateral sclerosis
Fatal familial insomnia
Dementia with Lewy bodies
Olivoponto- cerebellar atrophy
Dystonia
Morquio syndrome
Metachromatic leukodystrophy
more...
See also
(20)
Diseases and disorders
Rem sleep behavior disorder
Allopregnanolone
Friedreich
Neurodegeneration
Neurodegeneration
Polyglutamine tract
Max Bielschowsky
Substantia nigra
NCLS
Mitochondrial permeability transition
Sistema Nacional de Creadores de Arte
Prion protein
Motor neurons
Neurons
Central nervous system
Central nervous system disease
Proteopathy
Autosomal recessive
Fals
Putamen
more...
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