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Pick Disease of the Brain
Pick disease of the brain
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Cognitive disorders
(18)
Aids dementia complex
Alzheimer's disease
Corticobasal degeneration
Frontotemporal dementia
Frontotemporal lobar degeneration
Frontotemporal lobar degeneration
Lewy body disease
Multi-infarct dementia
Primary progressive aphasia
Progressive supranuclear palsy
Semantic dementia
Binswanger's disease
Clinical Dementia Rating
Delirium
Dementia
Frontotemporal dementia and parkinsonism linked to chromosome 17
Logopenic progressive aphasia
Prevention of dementia
Progressive nonfluent aphasia
more...
Neurological disorders
(18)
Alpers disease
Acute disseminated encephalomyelitis
CAMFAK syndrome
Fazio-Londe
Machado-joseph disease
Machado-joseph disease
Wolman disease
Marchiafava Bignami disease
Hereditary sensory and autonomic neuropathies
Cerebral amyloid angiopathy
Neuronal ceroid lipofuscinosis
Abulia
Batten disease
Hemiparesis
Semantic dementia
Multi-infarct dementia
Lewy body disease
Corticobasal degeneration
Alzheimer's disease
more...
Diseases and disorders
(48)
Niemann Pick disease
Advanced sleep phase syndrome
Demyelinating disease
Amaurosis fugax
Lipidosis
Lipidosis
Herpesviral encephalitis
Spinal muscular atrophies of childhood
Lysosomal storage diseases
Gaucher disease
Canavan disease
Tay Sachs disease
Organic brain syndrome
Metachromatic leukodystrophy
Normal pressure hydrocephalus
Anterior cerebral artery syndrome
Krabbe disease
Postpoliomyelitis syndrome
Histiocytosis non-langerhans-cell
Cataplexy
Multiple system atrophy
Alexander disease
Lupus erythematosus, cutaneous
Purpura, schoenlein-henoch
Pompe disease
Lateral pontine syndrome
Medial pontine syndrome
Physiologic nystagmus
Alpers disease
Acute disseminated encephalomyelitis
Frontotemporal dementia
Multi-infarct dementia
Lewy body disease
CAMFAK syndrome
Fazio-Londe
Aids dementia complex
Progressive supranuclear palsy
Primary progressive aphasia
Corticobasal degeneration
Frontotemporal lobar degeneration
Machado-joseph disease
Wolman disease
Marchiafava Bignami disease
Alzheimer's disease
Hereditary sensory and autonomic neuropathies
Cerebral amyloid angiopathy
Neuronal ceroid lipofuscinosis
Batten disease
Hemiparesis
more...
Lipid storage disorders
(14)
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Gangliosidosis
Gangliosidosis
Gaucher disease
Krabbe disease
Multiple sulfatase deficiency
Niemann Pick disease
Niemann-Pick disease, type C
Sandhoff disease
Schindler disease
Tay Sachs disease
Wolman disease
more...
Metabolic disorders
(60)
Activated protein C resistance
Adenosine deaminase deficiency
Albinism
Alcohol flush reaction
Antithrombin III deficiency
Antithrombin III deficiency
Baker IDI Heart and Diabetes Institute
Blue diaper syndrome
Childhood obesity
Congenital disorder of glycosylation
Congenital hyperinsulinism
Crigler-Najjar syndrome
Diagnostic fast
Disaccharidase
Disorders of calcium metabolism
Ectopic calcification
Farber disease
Fructose malabsorption
GM1 gangliosidoses
GM2 gangliosidoses
Galactosemia
Galactosemic cataract
Gangliosidosis
Gaucher disease
Glycogen storage disease type 0
Hereditary fructose intolerance
Homocystinuria
Hyperglycemia
Hyperinsulinemic hypoglycemia
Hyperinsulinism
Hypoglycemia
Inborn errors of metabolism
Ketotic hypoglycemia
Krabbe disease
Lactose intolerance
Lipid storage disorders
List of causes of hypoglycemia
Metab-L
Methemoglobinemia
Neuronal ceroid lipofuscinosis
Niemann Pick disease
Niemann-Pick disease, type C
Obesity
Obesogen
Pickardt syndrome
Pycnodysostosis
Refeeding syndrome
Richner Hanhart syndrome
Rotor syndrome
Salicylate sensitivity
Schindler disease
Selfish Brain Theory
Sitosterolemia
Stress hyperglycemia
Sucrose intolerance
Tay Sachs disease
Triosephosphate isomerase deficiency
Urbach–Wiethe disease
Urea cycle disorder
Winchester syndrome
Wolman disease
more...
Autosomal recessive disorders
(13)
Niemann Pick disease
Lipidosis
CAMFAK syndrome
Spinal muscular atrophies of childhood
Gaucher disease
Gaucher disease
Canavan disease
Tay Sachs disease
Wolman disease
Metachromatic leukodystrophy
Krabbe disease
Neuronal ceroid lipofuscinosis
Pompe disease
Batten disease
more...
Neurology
(12)
Neurofibrillary tangles
The nervous system
Gliosis
Niemann Pick disease
Acute disseminated encephalomyelitis
Acute disseminated encephalomyelitis
Demyelinating disease
Amaurosis fugax
Frontotemporal dementia
Tay Sachs disease
Frontotemporal lobar degeneration
Normal pressure hydrocephalus
Adrenoleuk- odystrophy
more...
Extrapyramidal and movement disorders
(19)
Pantothenate kinase-associated neurodegeneration
Postencephalitic parkinsonism
Akathisia
Blepharospasm
Choreia (disease)
Choreia (disease)
Dystonia
Essential tremor
Meige's syndrome
Movement disorder
Multiple system atrophy
Myoclonus
Neuroleptic malignant syndrome
Parkinson's disease
Parkinsonism
Progressive supranuclear palsy
Restless legs syndrome
Spasmodic torticollis
Stiff person syndrome
Tardive dyskinesia
more...
Abnormal psychology
Acute stress reaction
Brain disorder
Adjustment disorder
Alzheimer's disease
Medicine
Arnold Pick
Pierre Robin (surgeon)
Vascular myelopathy
Diseases and disorders
Primary progressive aphasia
Symptoms
(12)
Difficulty finding a word
Movement/c- oordination difficulties
Decreased ability to read or write
Weak uncoordinated speech sounds
Shrinking vocabulary
Shrinking vocabulary
Problems with personal hygiene
Abrupt mood changes
Memory loss that gets worse
Decreased interest in daily living
Amaurosis fugax
Cataplexy
Abulia
more...
Lysosomal storage diseases
(40)
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Cholesteryl ester storage disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidosis
Gaucher disease
Glycoproteinosis
Hunter syndrome
Hurler syndrome
I-cell disease
Krabbe disease
Lipidosis
Lysosomal storage disease
Metachromatic leukodystrophy
Morquio syndrome
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidosis
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann Pick disease
Niemann-Pick disease, type C
Pompe disease
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Schindler disease
Sialidosis
Sly syndrome
Tay Sachs disease
Wolman disease
more...
See also
(20)
Sphingomyelinase
Sphingomyelin
NPC1
Tau proteins
Congenital malformations
Congenital malformations
Pick bodies
Systemic atrophies
Creutzfeldt-Jacob disease
NPC2
Enzyme replacement therapy
Lysosomal storage disease
The Brain
Acute alcohol intoxication
NP-C
Temporal lobes
Primary motor cortex
Glycolipid
DYT1
Hepatosplenomegaly
Adrenoleuk- odystrophy
more...
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