Neudle.com: primary familial brain calcification

Differential
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abdominal distention

abducens nerve paralysis

abscess, intracerebral

abulia

acanthocytosis

acid maltase deficiency

acid maltase deficiency, adult

acoustic nerve

acoustic nerve, vestibular division of

acoustic neurinoma

acoustic neurinoma, bilateral

acral sensory symptoms

acrocyanosis

acute disseminated encephalomyelitis

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

affect, inappropriate

agenesis of corpus callosum

aggression

agnosia

Aicardi-Goutieres syndrome

alcohol, blood level of

alcohol, neurologic complications with

alcoholic blackout

alcoholic coma

alcoholic dementia

alcoholic polyneuropathy

alcoholic withdrawal states, DT's, convulsions, etc.

alcoholism

Alexanders disease

Alexanders disease, adult onset

algorithm

alkylating agents

alpha galactosidase A deficiency

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alternating rapid movement, impaired

Alzheimer's disease

Alzheimer's disease, familial

Alzheimer's disease, pathogenesis

Alzheimer's disease, treatment of

amyloid angiopathy, cerebral

amyloidosis, oculoleptomeningeal, familial

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

aneurysm, intracranial

aneurysm, intracranial, familial

Angelman syndrome

angiitis

angiitis, granulomatous of CNS

angiitis, isolated of CNS

anticoagulant, contraindications

anticonvulsants

antimetabolite

antiphospholipid antibodies

antithrombin III deficiency

anxiety

aphasia

aphasia, progressive

aphasia, progressive, primary

apnea

apnea, primary central

apraxia

apraxia, constructional

arachnodactyly

areflexia

arrhythmia, cardiac

arteriovenous malformation

arteriovenous malformation, cerebral

asterixis, unilateral

astrocytoma

asymptomatic

ataxia

ataxia telangiectasia

atherosclerosis, premature

atonic bladder

ATP1A3 gene

atrial appendage closure

atrial fibrillation

atrial fibrillation, surgical treatment

atrial fibrillation, treatment

atrial myxoma

attention deficit disorder with hyperactivity

attention span

atypical

audiogram

auditory evoked brainstem potentials

autism

autistic behavior

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

behavior modification

behavior, combative

behavioral disorder

Behcet's syndrome

benign essential tremor

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

bladder dysfunction

blepharospasm

blindness

blood dyscrasias, neurologic findings with

body odor

bone marrow biopsy

bone marrow transplantation

brainstem, dysfunction

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

calcification, intracranial

calcification, muscle

calcium oxalate crystals

carbon monoxide poisoning

carbonic anhydrase II deficiency

carcinoma

carcinoma of pancreas

CAT scan, abscess, cerebral

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, isodense lesion with acute hemorrhage

cataracts, congenital

catecholamine

caudate nucleus, atrophy

caudate nucleus, lesion of

cavernous hemangioma

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemangioma

cerebellar hypoplasia

cerebellar infarction

cerebellar lesion

cerebellar vermis

cerebellum

cerebellum, disease of

cerebellum, neoplasms of

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral embolism

cerebral embolism, cardiac origin

cerebral infarction

cerebral infarction, hemorrhagic

cerebral ischemia

cerebral vasculature, calcification

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebritis

cerebroretinal vasculopathy

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, amonia

cerebrospinal fluid, cell culture of

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, glutamine

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure low

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, cryptogenic

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, neonatal

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, prevention of

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease, risk factors in

ceruloplasmin, serum

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

cherry red spot

chilbran skin lesions

chromosomal abnormality

chronic progressive external ophthalmoplegia

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

cobalamin C deficiency

coin lesion on chest X-ray

compression neuropathy

conus medullaris, lesion of

conversion reaction

copper metabolism, abnormal

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical blindness, transient

cough

Cowden syndrome

cranial nerve palsies

cranial nerve tumor

cranial neuropathy

cranial neuropathy, multiple

cranio-cervical junction

craniopharyngioma

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

crossed adductor reflex

crying, pathologic

Cuba

cultured skin fibroblasts

cyst, epidermoid of CNS

cyst, neoplastic cerebellum

deafness, bilateral progressive vs.unilateral acute

degenerative diseases of CNS

dementia, age at onset

dementia, childhood

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, thalamic

dementia, transmissible

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

diaphragmatic paralysis

diarrhea

diet

differential diagnosis

difficulty climbing stairs

dilantin

diplopia

disinhibition-dementia-parkinsonism-amyotrophic complex

dizziness

donepezil

dopa responsive dystonia

dopamine

drooling

dropped head syndrome

drug induced neurologic disorders

dwarfism

dying

dysarthria

dysarthria-clumsy hand syndrome

dystonia musculorum deformens

dystonia, cervical

dystonia, children

dystonia, classification

dystonia, etiology of

dystonia, evaluation of

dystonia, face

dystonia, focal

dystonia, painful

dystonia, treatment of

dystonic reaction, acute

Ehlers-Danlos syndrome

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, monitoring, continuous

electromyogram

electron microscopy

electronystagmography

encephalitis, Japanese

encephalitis, viral

encephalopathy

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

entrapment neuropathy

enzyme, defect

ependymoma

epidemiology of neurology

epidermoid

epileptic encephalopathy

episodic neurologic deficits

executive dysfunction

exercise intolerance

exome sequencing

extraocular muscle lesion

eye movement, disorders of

Fabry's disease

facial anomalies

facial appearance, abnormal

facial expression abnormality

facial hypoplasia

facial nerve palsy

facial nerve palsy, bilateral

facial pain

Factor V Leiden

factor V, deficiency

factor VII, deficiency

familial periodic ataxia

fasciculation

fatigue

fatty acid dehydrogenase deficiency

feeding disorder

fetal alcohol syndrome

fever

fibroma, ungual

fibromuscular dysplasia

finger nose finger test

fingerprint bodies

fingers, abnormal

fish

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, pulmonary

flavivirus

flow study, carotid artery

fluctuate

fluency

fluorescene in situ hybridization

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal bossing

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

fundus, abnormality of

gamma amino butyric acid

gangliosidosis, generalized

gargoylism

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastroparesis

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

gests antagoniste

Gilles de la Tourette syndrome

Gillespie syndrome

glaucoma

glioblastoma multiforme(astrocytoma Gr.III)

glioma

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

granular osmiphilic material

granulomatosis with polyangiitis

granulomatous disease

growth retardation

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

headache, thunderclap

health insurance

hearing loss

hearing loss, bilateral

hearing problems in children

hematoma, epidural-cranial

hematopoietic tissue, extramedullary

hematuria, gross

hematuria, microscopic

hemianopia

hemianopia, homonymous

hemidystonia

hemiparesis

hemiplegia

hemoglobin abnormality, neurologic complications of

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hemoptysis

hemorrhagic diathesis

hemorrhoids

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic encephalopathy, treatment of

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration, non-Wilsonian

hepatomegaly

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

human T-lymphotropic virus type I(HTLV-I)

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's disease, children

Hurler's syndrome

hydrocephalus

hydrocephalus, communicating

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypogammaglobulinemia

hypopigmentation of skin

hyporeflexia

hyposmia

hypothermia

hypothermia, causes of

hypotonia

hypotonia, infants

hypoxic encephalopathy

hypoxic-ischemic leukoencephalopathy

iatrogenic neurologic disorders

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inappropriate behavior

inattention

inborn errors of metabolism

inborn errors of metabolism, screening

incidental finding

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

incoordination

infantile bilateral striatal necrosis

infantile spasm

inflexibility, mental

insulin resistance

intellectual deficit

intellectual deterioration

intelligence quotient

interferon alpha

internet

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracerebral hemorrhage, work up

intracerebral hemorrhage, young adult

intracranial pressure, increased

intrathecal chemotherapy

intrauterine

intraventricular hemorrhage

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Kayser-Fleischer ring

Kearns-Sayre syndrome

keratoconus

Kluver-Bucy syndrome

Korsakoff's psychosis

Krabbe's disease

kyphoscoliosis, neurologic causes of

kyphosis

lactic acidemia

lacunar infarction

laminar necrosis, cortical

language disorder in adults

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

learning disability, in children

Leber's congenital amaurosis

left atrial appendage, percutaneous closure

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lens, dislocation of

lens, ectopic

lenticular nucleus, lesion of, bilateral

leukemia

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

leukopenia

level of consciousness, decreased

Lhermitte-Duclos disease

life expectancy

linear lesion

lipid storage disorder of CNS

liver function enzymes

lymphoma involving CNS

lymphoma, primary of CNS

lymphomatoid granulomatosis

lysosomal storage disease

lysosomes, abnoral

macrocephaly

macrognathia

magnetic susceptibility

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, familial

malformation, Vein of Galen

manganese intoxication

maple syrup urine disease

marihuana

Marinesco-Sjogren syndrome

medulloblastoma

megalencephaly

melanoma, malignant

melanomatosis, primary malignant

MELAS syndrome

memory, impairment of

meningeal enhancement

meningitis, carcinomatous

meningoencephalopathy

mental retardation

mental retardation, familial

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methemoglobin

methotrexate

methylhydrazine derivatives

methylmalonic acidemia

metronidazole

microcephaly

microhemorrhage, intracerebral

microspherophakia

microsurgery

midbrain, atrophy

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine

migraine, hemiplegic

mild cognitive impairment

mineralization

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

MNGIE syndrome

molecular genetics

molybdenum cofactor deficiency

mongolism

monoamine oxidase inhibitors

monoamines

mononeuropathy

mononeuropathy multiplex

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, treatment of

MRI, CAT scan compared to

MRI, complications with

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, FLAIR

MRI, gradient-echo

MRI, hypointense signal foci on

MRI, incidental finding

MRI, negative

MRI, paramagnetic effect

MRI, punctate pattern

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRI, volumetry

MRS

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, chronic progressive

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, prognosis

multiple system atrophy

muscle weakness, proximal

muscular dystrophy

mutism

myasthenia gravis

myelinolysis, extrapontine

myeloproliferative disorder

myopathy, mitochondrial

neonatal epilepsy syndromes

neonatal epileptic encephalopathy

neoplasm, intracranial

neoplasm, intracranial, multiple

neoplasm, intracranial-incidence and epidemiology of

neoplasm, metastatic to CNS

neoplasm, metastatic to CNS-treatment of

neoplasm, peripheral nerve

neoplasm, primary intracerebral

neoplasm, primary intracerebral, reoperation

neoplasm, primary intracranial

neoplasm, primary intracranial-treatment of

neoplasm, primary of CNS

neoplasm, primary of CNS assoc.with primary malig.other sites

neoplasm, primary of CNS-aged

neoplasm, primary of CNS-children

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-familial occurrence

neoplasm, primary of CNS-incidence of

neoplasm, primary of CNS-multiple

neoplasm, primary of CNS-recurrent

neoplasm, primary of CNS-surgical treatment of

neoplasm, primary of CNS-treatment of

nephrocalcinosis

nerve biopsy

nerve conduction studies

nerve growth factor

neuritis

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neuroaxonal leukodystrophy

neurochemistry

neurocutaneous disease

neurodegeneration with brain iron accumulation

neuroendocrinology

neurofibrillary degeneration

neurofibroma

neurofibromatosis 1

neurofibromatosis 2

neurofibromatosis 2, presymptomatic

neuroichthyosis

neuroleptic

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic examination, focal

neurologic signs

neurologic testing

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronal migration disorder

neuronopathy

neuronopathy, sensory

neuropathology

neuropathology, brain

neuropathy

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, sensory

neuropathy, vasculitic, systemic

neurotoxin

neurotransmitter

neutropenia

nevoid basal cell carcinoma syndrome

nevus

next-generation sequencing

nystagmus, dissociated

nystagmus, gaze-evoked

nystagmus, gaze-paretic

nystagmus, monocular

nystagmus, pendular

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating-in primary position of gaze

nystagmus, vertical

obesity

obsessive-compulsive disorder

occipital lobe, lesion of

ocular myopathy

old age, neurology of

oligodendroglioma

ophthalmoplegia

ophthalmoplegia, progressive external

optic nerve, lesion of

optical coherence tomography

orbit, tomograms of

ornithine transcarbamylase deficiency

orthopnea

orthostatic hypotension

oscillopsia

osmotic demyelination syndrome

pain, increased response

palatal myoclonus

palilalia

pallido-ponto-nigral degeneration

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraparesis, spastic, tropical

paraplegia

paraspinal muscle

paraspinal muscle weakness

paresthesias

Parkinson disease

Parkinson disease, dystonia with

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

past pointing

patient information and support

photosensitivity, skin

pigmentary retinopathy

pimozide

Pittsburgh Compound B

pituitary, adenoma

platelet aggregation

pleocytosis of cerebrospinal fluid

poison, neurologic problems with

POLG1 gene

POLR3B

polycystic kidneys

polycythemia, primary

polycythemia, secondary

polydactyly

polymerase chain reaction

polyneuropathy

polyps, gastrointestinal tract

pons, atrophy

pons, lesion of

pontocerebellar atrophy

positional head-hanging test

postural abnormality

practice guidelines

precipitating factors

pregnancy, neurologic complications in

premature infant

prenatal

prenatal diagnosis by amniocentesis

pretectal syndrome

prevention of neurologic disorders

primary familial brain calcification

primary thrombocythemia

progressive infantile poliodystrophy

progressive neurologic disorder

progressive subcortical gliosis

prolactin, elevated

proprioception, abnormal

protein 14-3-3, cerebrospinal fluid

pseudohypoparathyroidism

pseudoretinitis pigmentosa

pseudotumor

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

psychosis

PTEN hamartoma tumor syndrome

ptosis

ptosis, bilateral

pulmonary embolism

pulmonary infiltrates

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal

pyramidal tract

pyramidal tract dysfunction

pyridoxine

pyridoxine deficiency

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriparesis

quadriplegia

radiation encephalopathy, delayed

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

reading disorder, acquired

reading problem, causes of

real-time quaking-induced conversion

remote effect of cancer on the nervous system

renal tubular acidosis

respiratory depression

respiratory failure

respiratory tract infection

reticulum cell sarcoma

rhabdomyosarcoma of heart

rigidity

Riley-Day syndrome

risk factors

risk factors, modification

ritalin

root lesion, nerve

Rosenthal fibers

saccadic eye movements, abnormal

scoliosis, neurologic association with

seizure, complications following

seizure, diagnosis of

seizure, pyridoxine dependent

seizure, treatment of

seizure, workup of

self-mutilation

semialdehyde dehydrogenase deficiency

senile plaques

sensorineural hearing loss

single photon emission computed tomography

Sjogren-Larsson syndrome

Sjogren's syndrome

skin, biopsy

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep

sleep pathology and physiology

slit lamp examination

smiling

somatosensory evoked potentials

spastic ataxia

spastic diplegia

spastic paraplegia, type 7

spasticity

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

Spielmeyer Vogt syndrome

spinal cord

spinal cord, compression of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, extramedullary intradural

spinal cord, neoplasm, intramedullary

spinal cord, neoplasm, meningioma

spinal cord, neoplasm, neurofibroma

spinal cord, pathologic exam of

spinal cord, vascular malformation of

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 12

spinocerebellar ataxia type 2

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 5

spinocerebellar ataxia type 6

spinocerebellar ataxia type 7

spinocerebellar ataxia type 8

spinocerebellar degeneration

splenomegaly

spongy degeneration of brain

stem cell transplantation

stereotaxic surgery

stereotyped behavior

steroid therapy, CNS treatment and complications with

stimulant drugs

stimulation, deep brain

stimulation, thalamic

stooped posture

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

striopallidodentate calcifications, familial idiopathic

strokelike episodes

stuttering

subarachnoid hemorrhage

subarachnoid hemorrhage, recurrent

sulfite oxidase deficiency

superior sagittal sinus thrombosis

sural nerve

sweating, abnormality of

symmetric brain lesions

systemic illness

tandem gait, ataxic

tapetoretinal degeneration

teeth, number of in infants

teeth, wide-spaced

telangiectases

temporal lobe, atrophy

temporal lobe, lesion

term infant

thalamic tumors

thalamic tumors, bilateral

thalamus

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

tic, chronic multiple

tinnitus

titubation

tone, muscle, increased

tongue, enlarged

tongue, fasciculations of

tongue, protrusion of

tongue, weakness

tonic foot response

top of the basilar syndrome

torticollis

transient ischemic attack

transient neurologic deficit

transposition of the great vessels

trauma

treatment of neurologic disorder

trientine dihydrochloride

trinucleotide repeats

tuberin

tuberous sclerosis

tuberous sclerosis, screening for

Turcot syndrome

twins

tyrosine hydroxylase deficiency

umbilical-cord blood transplantation

upgaze, paralysis of

urea-cycle enzymopathies

urine test for metabolic disorders

venous thrombosis, non-cerebral

vertebral-basilar insufficiency

vertigo

very long chain fatty acids

vestibulopathy

vibratory sensation, abnormal

vinblastine

vincristine neurotoxicity

violent behavior

viral infection, CNS

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual loss

visual loss, sudden

visuospatial disturbance

voice, abnormality of

Von Hippel Lindau

Von Hippel Lindau, screening protocol for

walking frame

walking, difficulty with

Watchman device

weakness

weakness, generalized

weakness, progressive

weaning from respirator, failure to

web sites

weight loss

Wernicke's aphasia

Wernicke's encephalopathy

word-finding difficulty

workup

wrist drop

xerophthalmia

X-linked bulbospinal neuronopathy

zinc

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Clinical, Neuroimaging, and Pathologic Features of Progressive Nonfluent Aphasia
Ann Neurol 39:166-173, Turner,R.S.,et al, 1996

Canavan Disease:From Spongy Degeneration to Molecular Analysis
J Pediatr 127:511-517, Matalon,R.,et al, 1995

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995

Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
Lancet 1458-1463, Barrett,T.G.,et al, 1995

A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
Ann Neurol 37:289-293, 2851995., Vahedi,K.,et al, 1995

Tourette's Syndrome:A Model Neuropsychiatric Disorder
JAMA 273:498-501, Hyde,T.M.&Weinberger,D.R., 1995

A Positron Emission Tomography Study of Cerebral Activation Associated with Essential and Writing Tremor
Arch Neurol 52:299-305, Wills,A.J.,et al, 1995

The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
Neurol 45:311-317, Barth,P.G.,et al, 1995

Congential Deficienty of Factor VII in Subarachnoid Hemorrhage
Stroke 25:508-510, Papa,M.L.,et al, 1994

Turcot's Syndrome:Evidence for Linkage to the Adenomatous Polyposis Coli (APC) Locus
neurol 44:1083-1086, Lasser,D.M.,et al, 1994

Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
Neurol 43:318-325, Wullner,U.,et al, 1993

Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
Neurol 33:4-9, Nishino,H.,et al, 1993

Ornithine Transcarbamylase Deficiency Presenting with Strokelike Episodes
J Pediatrics 122:423-425, Christodoulou,J.,et al, 1993

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

Cerebromeningeal Haemophagocytic Lymphohistiocytosis
Lancet 239:104-107, Henter,J.&Elinder,G., 1992

Familial Intracranial Haemorrhage Due to Factor V Deficiency
JNNP 55:227-228, Wadia,R.S.,et al, 1992

Wilson Disease
Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

New Research in Tuberous Sclerosis, Probably More Common with More Adult Complications
BMJ 304:1647-1648, Mitchell,S.&Bradbeer,C., 1992

Progressive Language Disorder Due to Lobar Atrophy
Ann Neurol 31:174-183, Snowden,J.S.,et al, 1992

Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
Neurol 42:85-91, Aubourg,P.,et al, 1992

MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
AJR 158:413-416, Snyder,R.D.,et al, 1992

Angelman Syndrome: Clinical Profile
J Child Neurol 7:270-280, Zori,R.T.,et al, 1992

Erythromelalgia:Review of Clinical Characteristics and Pathophysiology
Am J Med 91:416-422, Jurzrock,R.&Cohen,P.R., 1991

Brain Tumors
NEJM 324:1471-1476, 1555-15641991., Black,P.McL., 1991

Nystagmus of Pelizaeus-Merzbacher Disease
Arch Neurol 48:87-91, Trobe,J.D.,et al, 1991

Diagnostic Tests for Choreoacanthocytosis
Neurol 41:1000-1006, Feinberg,T.E.,et al, 1991

Central Nervous System Involvement in Von Hippel-Lindau Disease
Neurol 41:41-46, Filling-Katz,M.R.,et al, 1991

Tourette Syndrome and Other Tic Disorders, Diagnosis, Pathophysiology, and Treatment
Medicine 70:15-32, Singer,H.S.&Walkup,J.T., 1991

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Familial Spinal Neurofibromatosis:Clinical and DNA Linkage Analysis
Neurol 41:1923-1927, Pulst,S.M.,et al, 1991

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