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Differential
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abdominal muscle paralysis

abducens nerve paralysis

abscess, intracerebral

abscess, intracranial

acetazolamide

acid maltase deficiency

acid maltase deficiency, adult

acoustic nerve, vestibular division of

acoustic neurinoma

acoustic neurinoma, bilateral

acrocyanosis

acromicria

activities of daily living

activities of daily living scale

acute intermittant porphyria

acyl CoA dehydrogenase deficiency

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

aggression

agitation

agoraphobia

Aicardi-Goutieres syndrome

alcohol

alcohol intoxication

alcohol, blood level of

alcohol, neurologic complications with

alcoholic blackout

alcoholic coma

alcoholic dementia

alcoholic polyneuropathy

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

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement, impaired

alternative medicine

aluminum

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, age of onset

Alzheimer's disease, behavioral symptoms

Alzheimer's disease, diagnosis of

Alzheimer's disease, driving with

Alzheimer's disease, early onset

Alzheimer's disease, early symptoms

Alzheimer's disease, familial

Alzheimer's disease, familial, late onset

Alzheimer's disease, incidence

Alzheimer's disease, pathogenesis

Alzheimer's disease, preclinical

Alzheimer's disease, treatment of

amyloid angiopathy, cerebral

amyloid beta protein

amyloid imaging

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, treatment of

aneurysm, asymptomatic

aneurysm, berry

aneurysm, intracranial

aneurysm, intracranial, familial

aneurysm, intracranial, natural history

aneurysm, intracranial, screening for

aneurysm, intracranial, treatment of

aneurysm, multiple intracranial

angiography, cerebral

angiography, posterior fossa

anterior horn cell disease

anterior tibial muscle weakness

anterocollis

anti MAG antibodies

antibiotic prophylaxis

antibodies to voltage-gated calcium channels

anticholinesterase

anticoagulant, treatment

anticonvulsants

anticonvulsants, effectiveness

anticonvulsants, selection of

antidepressant

antiphospholipid antibodies

antithrombin III deficiency

anxiety

aphasia

aphasia, progressive, primary

apraxia of eye movements

apraxia, constructional

arterial dissection, carotid

arterial dissection, ruptured

arterial dissection, vertebral

arteriopathy

arteriovenous malformation

arteriovenous malformation, cerebral

arteriovenous malformation, multiple

arteriovenous malformation, pulmonary

artificial nutrition and hydration

ascites

ash leaf spots

Asians

aspartate aminotransferase

ataxia telangiectasia

atlanto-axial subluxation

attention deficit disorder with hyperactivity

attention span

atypical

audiogram

auditory evoked brainstem potentials

autism

autism, screening for

autistic behavior

autoimmune disease

autonomic dysfunction

autonomic nervous system

autonomic neuropathy

autonomic neuropathy, idiopathic

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

battered child syndrome

behavior

behavior modification

behavior, combative

behavioral disorder

benign essential tremor

benign essential tremor, refractory

beta adrenergic blocker

blood dyscrasias, neurologic findings with

body odor

bone marrow transplantation

botulinum toxin

bovine spongiform encephalopathy

brachycephaly

brain atrophy

brain biopsy

brain transplantation

brainstem, atrophy

brainstem, lesion of

brainstem, neoplasms of

brainstem, vascular malformation of

calcification, intracranial

calcifications, intracranial, punctate

calcium channel dysfunction

carcinoembryonic antigen

carcinoma

carcinoma of pancreas

cardiomegaly

cardiomyopathy

cardiovascular disease

caregiver

caries

carnitine deficiency

carnitine deficiency myopathy

carotid artery occlusion, bilateral

CAT scan

CAT scan, abdomen

CAT scan, abnormal

CAT scan, angiography

CAT scan, chest

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar hemangioma

cerebellar hemorrhage

cerebellar lesion

cerebellum, neoplasms of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral edema, vasogenic

cerebral embolism

cerebral embolism, carotid origin

cerebral infarction

cerebral infarction, subcortical

cerebral ischemia

cerebral palsy

cerebral palsy, risk factors

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure increased

cerebrospinal fluid, protein of

cerebrovascular accident

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, familial occurrence

cerebrovascular accident, genetic

cerebrovascular accident, infancy and childhood

cerebrovascular accident, intrauterine

cerebrovascular accident, location of

cerebrovascular accident, multiple

cerebrovascular accident, neonatal

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, prevention of

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, surgical treatment of

ceruloplasmin, serum

channelopathy

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chilbran skin lesions

child abuse

children

chloride channel dysfunction

choline acetyltransferase

chorea

choreoathetosis

chromosomal abnormality

chronic graft versus host disease

chronic progressive external ophthalmoplegia

cirrhosis

Clinical Pathologic Conference(C.P.C.)

collagen vascular disease

compression neuropathy

compulsivity

confidentiality

congenital heart disease

congenital heart disease, CNS complications with

congenital malformation

congenital myasthenic syndromes

congenital myopathy

congestive heart failure

controversies in neurology

contusion, cerebral

copper

copper metabolism, abnormal

corpus callosum, infarction of

corpus callosum, lesion of

corpus callosum, thinning

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cultured skin fibroblasts

cyanosis

cyst

cyst, peritumoral

cyst, epidermoid of CNS

cyst, neoplastic cerebellum

cytochrome c oxidase, deficiency

cytomegalovirus infection

degenerative diseases of CNS

Dejerine-Sottas syndrome

dementia, age at onset

dementia, childhood

dementia, differential diagnosis of

dementia, familial

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, transmissible

dementia, treatment of

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

developmental venous anomalies

diamond on quadriceps

diaphragmatic paralysis

diarrhea

diet

dieting

differential diagnosis

difficulty climbing stairs

diplopia

disability rating scale, neurological

disability, neurological

disinhibition-dementia-parkinsonism-amyotrophic complex

dislocated hip, congenital

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dropped head syndrome

drug induced neurologic disorders

dural sinus thrombosis

Durett hemorrhages

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, post traumatic

dystonia, prevalence of

dystonia, symptomatic

dystonia, treatment of

echocardiogram, contrast

echolalia

ectatic basilar artery

eczema

edema, pedal

Ehlers-Danlos syndrome

Ehlers-Danlos syndrome, classification

electrocardiogram, abnormal

electroconvulsive therapy

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, monitoring, continuous

electroencephalogram, periodic complexes

electromyogram

electromyogram, decremental response

electron microscopy

electronystagmography

electroretinograph

embolism

embolism, paradoxical

embolism, septic

embolism, systemic

embolization, therapeutic

Emery-Dreifuss muscular dystrophy

encephalopathy, anoxic

encephalopathy, neonatal

encephalopathy, progressive

endocarditis, prophylaxis

endolymphatic sac tumors

epidemiology of neurology

epidermoid

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

executive dysfunction

exercise

exercise intolerance

exercise-induced neurologic dysfunction

exhibitionism

exome sequencing

eye injury

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nevus

facial weakness

facial weakness, bilateral

Fahr disease

failed medical management

failure to thrive

falling

familial

familial hemiplegic migraine

fatty acid dehydrogenase deficiency

fatty acid, elevated plasma content

feeding disorder

fetal alcohol syndrome

fever

fibrinolytic agents, contraindications

fibroma, ungual

fibromuscular dysplasia

fine motor function, impaired

finger nose finger test

fish

fistula, arterio-venous

fistula, arterio-venous, carotid-cavernous

fistula, arterio-venous, dural

fistula, arterio-venous, pulmonary

floppy infant

fluctuate

fluency

fluorescene in situ hybridization

Fragile-X associated tremor/ataxia-syndrome

Friedreich's ataxia, late onset

frontal balding

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

fucosidosis

fundus, abnormality of

gastrointestinal bleeding

gastrointestinal motility

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genu valgum

Gerstmann-Straussler-Scheinker disease

gests antagoniste

giant axonal neuropathy

Gilles de la Tourette syndrome

glaucoma

glioblastoma multiforme(astrocytoma Gr.III)

glioma

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutaric acidemia

glycine

glycogen storage disease

growth hormone deficiency

growth retardation

Guillain Barre syndrome

gynecomastia

gyrus, abnormal

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

head injury, pediatric

hearing loss, sudden, unilateral

hemangioma, leptomeningeal

hemangioma, skin

hematuria, gross

hemihypertrophy, congenital

hemiparesis

hemoglobin abnormality, neurologic complications of

hemoptysis

hemorrhagic diathesis

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatomegaly

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

human immunodeficiency virus type 1

huntingtin

Huntington's chorea

Huntington's chorea, genetic counselling

hydrocephalus

hydrocephalus, complications with

hydrocephalus, etiology

hydrocephalus, fetal

hydrocephalus, treatment of

hyperactivity

hypercapnia

hyperglycinemia

hyperglycinemia, nonketotic

hyperphagia

hyperpyrexia, CNS disorder causing

hypertrophic cardiomyopathy

hypokalemic periodic paralysis

hypomelanosis of Ito

hyponatremia

hypophosphatemia

hypopigmentation of skin

hypoxic encephalopathy

hypoxic-ischemic leukoencephalopathy

iatrogenic neurologic disorders

inappropriate behavior

inattention

inborn errors of metabolism

inborn errors of metabolism, screening

incidental finding

inclusion bodies

inclusion bodies, intranuclear

inclusion body myositis

inflexibility, mental

informed consent

intellectual deficit

intellectual deterioration

intelligence quotient

interobserver agreement

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracerebral hemorrhage, lobar

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, young adult

intracranial hemorrhage

intracranial hypertension, benign

intracranial hypertension, benign, differential diagnosis

intracranial hypertension, benign, pathogenesis of

intracranial pressure, increased

intrathecal chemotherapy

intrauterine

intraventricular hemorrhage

intrinsic hand muscles, wasting of

ischemic exercise test

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

jaundice

joint hypermobility

Kayser-Fleischer ring

Kearns-Sayre syndrome

Kleine-Levin syndrome

Krabbe's disease

kuru

kyphoscoliosis, neurologic causes of

language disorders in children

laterocollis

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

L-dopa, drug interactions with and side effects of

learning disability

learning disability, in children

Leber's hereditary optic neuropathy

leg atrophy

leg spasms

leg spasms, painful

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leukoencephalopathy, adult onset, sporadic

leukoencephalopathy, differential diagnosis

leukopenia

Lewy body

Lhermitte-Duclos disease

libido, increased

life expectancy

life support, withdrawal of

life support, withholding of

life sustaining treatment

limb-girdle weakness

lipid storage disorder of CNS

lipid storage myopathy

Lisch nodules

liver disease

liver function enzymes

liver transplantation

lobar atrophy

locus ceruleus, lesion of

lymphoma, primary of CNS

lysosomal storage disease

magnetic susceptibility

magnetoencephalography

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, familial

malformation, vascular, screening for

malignant hyperpyrexia

managed care

manic-depressive

maple syrup urine disease

Marfan syndrome

masked facies

McArdle's disease

medical-legal aspects of neurology

medulla oblongata, neoplasm of

memory, defect of recent

memory, impairment of

meningeal enhancement

meningioma

meningitis, carcinomatous

menses

mental retardation

mental retardation, familial

MERRF syndrome

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metronidazole

Mexican

microcephaly

microhemorrhage, intracerebral

microsurgery

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine

migraine, hemiplegic

mild cognitive impairment

mimics

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, treatment of

MRI, complications with

MRI, contrast enhanced

MRI, diffusion tensor

MRI, diffusion weighted

MRI, eye of tiger sign

MRI, incidental finding

MRI, negative

MRI, paramagnetic effect

MRI, punctate pattern

MRI, repeat

MRI, spinal cord

MRI, spine

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRI, target sign

MRI, volumetry

MRS

mucopolysaccharidoses

multiple endocrine neoplasia

multiple sclerosis

multiple sclerosis, clinical patterns

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

multiple sclerosis, misdiagnosis

multiple sclerosis, pathogenesis

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, progressive

muscle atrophy, static

muscle phosphorylase deficiency

muscle stiffness

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

muscular dystrophy, pattern of muscle involvement

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, differential diagnosis

myasthenia gravis, etiology of

myasthenia gravis, familial incidence of

myasthenia gravis, misdiagnosis of

myasthenia gravis, seronegative

myelitis, longitudinal

myopathy, distal Laing

myopathy, distal, vacuolar

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, metabolic

myopathy, mitochondrial

myotonia dystrophica, classification

neonatal epilepsy syndromes

neonatal epileptic encephalopathy

neoplasm, intracranial

neoplasm, intracranial-incidence and epidemiology of

neoplasm, metastatic to CNS

neoplasm, metastatic to CNS-treatment of

neoplasm, peripheral nerve

neoplasm, posterior fossa

neoplasm, primary intracerebral

neoplasm, primary intracerebral, reoperation

neoplasm, primary intracranial

neoplasm, primary intracranial-treatment of

neoplasm, primary of CNS

neoplasm, primary of CNS-aged

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-familial occurrence

neoplasm, primary of CNS-incidence of

neoplasm, primary of CNS-surgical treatment of

neoplasm, primary of CNS-treatment of

nerve biopsy

nerve conduction studies

nerve growth factor

nerve hypertrophy

neuroaxonal leukodystrophy

neurochemistry

neurocutaneous disease

neurodegeneration with brain iron accumulation

neuroendocrinology

neurofibrillary degeneration

neurofibroma

neurofibromatosis 1

neurofibromatosis 2

neurofibromatosis 2, presymptomatic

neuroichthyosis

neuroleptic

neuroleptic, atypical

neurologic complications of, chronic pulmonary disease

neurologic complications of, systemic disease

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic education

neurologic evaluation

neurologic examination, focal

neuromuscular disease, electrodiagnosis of

neuromyelitis optica (Devic's disease)

neuromyelitis optica spectrum disorder

neuromyelitis optica, IgG

neuromyotonia

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal migration disorder

neuronopathy

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, amyloid

neuropathy, classification of

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, peripheral, treatment

neuropathy, work up for

neurotransmitter

newborn, evaluation of

next-generation sequencing

Niemann-Pick disease

night blindness

nigrostriatal pathway

obsessive-compulsive disorder

ocular motility, disorders of

olanzapine

oligodendroglioma

ophthalmoplegia

ophthalmoplegia, progressive external

opiate

optic atrophy

optic atrophy, hereditary

optic glioma

optic nerve

optic nerve sheath fenestration

optic nerve, decompression of

optic nerve, hypoplasia of

optic nerve, neoplasm of

optic neuritis

optic neuritis, bilateral

optic neuropathy

orbit, tomograms of

orthopnea

osteogenesis imperfecta

osteoporosis

overlap syndrome

owl's eye sign of spinal cord

pain, increased response

palilalia

palliative care

pallido-ponto-nigral degeneration

paralysis, acute areflexic

paramyotonia congenita

paranoia

paraparesis

paraparesis, acute

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraparesis, transient

paraplegia

paraplegia, recurrent

paraplegin

paraspinal muscle

paraspinal muscle weakness

paresthesias

Parkinson disease

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, dystonia with

Parkinson disease, etiology of

Parkinson disease, familial

Parkinson disease, nonmotor problems of

Parkinson disease, pathogenesis of

Parkinson disease, presymptomatic detection

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, young onset

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal kinesigenic dyskinesia

paroxysmal neurologic deficits

PAS positive

pathologic reflex

pathology

patient information and support

pectus excavatum

Pelizaeus Merzbacher

penicillamine

percussion induced muscle contraction

periodic paralysis

periodic paralysis, thyrotoxic

periventricular leukomalacia

peroxisomal disease

persistent vegetative state

phosphorylase b kinase deficiency

photic sneeze reflex

photophobia

photosensitivity, skin

Pick's disease

pigmentary retinopathy

pimozide

Pittsburgh Compound B

pituitary, adenoma

pituitary, hormones of

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

pneumonia

polycystic kidneys

polycythemia, primary

polyhydramnios

polymerase chain reaction

polyneuropathy, familial

polyps, gastrointestinal tract

Pompe's disease of glycogen storage

porphyria

port wine nevus

portal caval shunt

posterior leukoencephalopathy syndrome

postural abnormality

potassium

potassium channel antibodies

potassium channel dysfunction

practice guidelines

Prader-Labhart-Willi syndrome

pramipexole

precipitating factors

preclinical

precocious puberty

pregnancy, neurologic complications in

premature infant

prenatal

prenatal diagnosis by amniocentesis

presenilin-1 gene

presenilin-2 gene

prevention of neurologic disorders

primary episodic ataxia

progressive myoclonic epilepsy

progressive neurologic disorder

progressive subcortical gliosis

propranolol

proprioception, abnormal

protein 14-3-3, cerebrospinal fluid

protein C deficiency

protein S deficiency

proximal muscle atrophy

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

psychosis

psychosocial aspects

PTEN hamartoma tumor syndrome

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

quadriparesis

quadriparesis, acute

quadriplegia

quadriplegia, transient

quality of life

quetiapine

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

radiculopathy

ragged-red fibers

raphe nuclei

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

reading problem, causes of

real-time quaking-induced conversion

repetitive nerve stimulation

repetitive questioning

research

respirator

respiratory depression

respiratory failure

restless leg syndrome

reversible neurologic disorder

rhabdomyosarcoma of heart

right to die

rigidity

riluzole

rippling muscle disease

risk factors

risk factors, modification

saccadic eye movements, abnormal

scoliosis, neurologic association with

second wind phenomena

seizure

seizure, children

seizure, classification of

seizure, complications following

seizure, diagnosis of

seizure, differential diagnosis of

seizure, incidence of

seizure, injury following

seizure, intractable

seizure, neonatal

seizure, paradoxical

seizure, photosensitive

seizure, prevalence of

seizure, prognosis in adults

seizure, prognosis in childhood

seizure, psychomotor-temporal lobe

seizure, tonic-clonic

seizure, treatment of

seizure, workup of

selective serotonin reuptake inhibitors

self-mutilation

senile plaques

sensorineural hearing loss

sensory loss

sensory tricks

seronegative

sexual behavior, disorder of

shadowing

shagreen patch

shaken infant syndrome

shaking

short neck

short stature

shunt procedure, lumboperitoneal

shunt procedure, ventricular

shunt procedure, ventricular-complications of

sickle cell disease

sinemet

single photon emission computed tomography

Sjogren-Larsson syndrome

skin, biopsy

skin, darkening of

skin, hyperextensible

skin, lesions in neurologic disorders

skin, thin

skin, translucent

skull x-ray, abnormal

skull x-ray, bony defect on

sleep

sleep paralysis

sleep pathology and physiology

slit lamp examination

small vessel disease

small vessel disease, cerebral

sodium channel dysfunction

speech disorder, childhood

speech, delayed development of

spinal cord

spinal cord degeneration

spinal cord, compression of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, intramedullary

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spine, metastasis to

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 2

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 6

spinocerebellar ataxia type 7

spinocerebellar ataxia type 8

spinocerebellar degeneration

splenomegaly

spongy degeneration of brain

stem cell transplantation

stereotyped behavior, drug induced

stereotypy

steroid

steroid therapy, CNS treatment and complications with

stimulant drugs

stimulation, deep brain

Sturge-Weber syndrome

subarachnoid hemorrhage

subarachnoid hemorrhage, familial

subdural hematoma

subdural hematoma, neonates and infants

subependymal nodules

substantia nigra

subthalamic nucleus

subthalamic nucleus deep brain stimulation

succinate dehydrogenase deficiency

survival motor neuron gene

sweating

symmetric brain lesions

systemic illness

tachycardia

tandem gait, ataxic

tapetoretinal degeneration

telangiectases, retinal

temper tantrums

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

tensilon test, false negative

term infant

testicular atrophy

thalamotomy

thalamus, focused ultrasound ablation

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine

thrombocytopenia

thyroid function tests

thyrotoxicosis

tic

tic, chronic multiple

tinnitus

toe walking

tongue, enlarged

tongue, fasciculations of

tongue, protrusion of

tongue, weakness

topiramate

torticollis

torticollis, post traumatic

transient ischemic attack

transient ischemic attack, recurrent

trauma

treatment of neurologic disorder

treatment, non-pharmacologic

tremor, surgical treatment of

tremor, thalamic stimulation for suppression of

trientine dihydrochloride

trinucleotide repeats

tuberous sclerosis, screening for

tumor suppressor gene

twins

ubiquilin 1

undiagnosed

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

urinary catecholamines

urinary incontinence

urine test for metabolic disorders

ventriculostomy, endoscopic

vertebral-basilar insufficiency

vertigo

very long chain fatty acids

vibratory sensation, abnormal

viral infection

vision loss, sequential

vision, failure of in childhood

visual acuity

visual acuity, decreased

visual evoked response

visual loss, progressive

visual loss, slow

visual loss, sudden

visuospatial disturbance

Von Hippel Lindau, carrier

Von Hippel Lindau, screening protocol for

von Hippel-Lindau, screening

walking frame

walking, difficulty with

wandering

water channel antibodies

weakness

weakness, acute

weakness, episodic

weakness, fluctuating

weakness, generalized

weakness, progressive

weakness, proximal

web sites

weight loss

Wernicke's encephalopathy

wheelchair

white freckles

white matter disease

white matter disease, location

white matter disease, pattern

white matter disease, subcortical

word-finding difficulty

X-linked bulbospinal neuronopathy

x-linked hydrocephalus

x-linked intellectual deficit

zinc

Showing articles 150 to 200 of 5458 << Previous Next >>

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Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,et al, 1998

The Human Genome Project,Application in the Diagnosis and Treatment of Neurologic Diseases
Arch Neurol 55:1287-1290, Evans,G.A., 1998

Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
NEJM 339:1994-2004, Johnson,R.T. & Gibbs,Jr.,C.J., 1998

Diagnosis and Treatment of Alzheimer Disease and Related Disorders
JAMA 278:1363-1371, Small,G.W.,et al, 1997

Genetic Testing for Alzheimer Disease, Practical and Ethical Issues
Arch Neurol 54:1226-1229, Roses,A.D., 1997

Acute Intermittent Porphyria:Clinicopathologic Correlation
Neurol 48:1678-1683, Suarez,J.I.,et al, 1997

X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

The Family Caregiver's Role in Alzheimer's Disease
Neurol 48 (Suppl 6) :S25-S29997., Haley,W.E., 1997

Familial Intracranial Aneurysms
Lancet 349:380-384, Ronkainen,A.,et al, 1997

The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
JAMA 277:832-836, Post,S.G.,et al, 1997

Frontotemporal Dementia is on the MAP
Ann Neurol 41:139-140, Wilhelmsen,K.C., 1997

Withdrawing Intensive Life-Sustaining Treatment-Recommendations for Compassionate Clin Mgmt
NEJM 336:652-657, Brody,H.,et al, 1997

Restless Legs Syndrome:Clinicoetiologic Correlates
Neurol 47:1435-1441, Ondo,W.&Jankovic,J., 1996

Practice Parameter:Genetic Testing Alert
Pract Comm Genet Testing Task Force AAN, Neurol 47:1343-13441996., , 1996

Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
Medicine 75:233-250, Murakami,T.,et al, 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Genetic Factors in Alzheimer's Disease:A Review of Recent Advances
Ann Neurol 40:829-840, Levy-Lahad,E.&Bird,T.D., 1996

The Inherited Ataxias and the New Genetics
JNNP 61:327-332, Hammans,S.R., 1996

Cerebrovascular Complications of Fabry's Disease
Ann Neurol 40:8-17, Mitsias,P.&Levine,S.R., 1996

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

From Enigmatic to Problematic:The New Molecular Genetics of Childhood Spinal Muscular Atrophy
Neurol 46:335-340, Crawford,T.O., 1996

The Challenge of the Dementias
Lancet 347:1301-1307, Eastwood,R.,et al, 1996

Familial Cerebral Cavernous Angiomas:Clinical and Radiologic Studies
Neurol 45:492-497, Kattapong,V.J.,et al, 1995

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

Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
Muscle & Nerve 18:267-275995., Ionasecu,V.V., 1995

The Prevention of Neurogenetic Disease
Arch Neurol 52:356-362, 3451995., Rosenberg,R.N.&Iannaccone,S.T., 1995

Panic Attacks and Panic Disorder:The Great Neurologic Imposters
Semin Neurol 15:126-132, Stahl,S.M.&Soefje,S., 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995

Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
Neurol 45:1739-1743, Shulman,L.M.,et al, 1995

Hereditary Hemorrhagic Telangiectasia
NEJM 333:918-924, Guttmacher,A.E.,et al, 1995

Inclusion Body Myositis and Myopathies
Ann Neurol 38:705-713, Griggs,R.C.,et al, 1995

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

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

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

Monomelic Amyotrophy
Muscle & Nerve 17:1129-1134994., Donofrio,P.D., 1994

On the Inheritance of Intracranial Aneurysms
Stroke 25:2028-2037, Schievnink,W.I.,et al, 1994

Congenital Myasthenic Syndromes
In:Neurologic Clinics, 12:401-4371994., Engel,A.G., 1994

The Relationship of Essential Tremor to Other Movement Disorders:Report on 678 Patients
Ann Neurol 35, 717-7231994., Koller,W.C.,et al, 1994

Clinical Genetics in Neurological Disease
JNNP 57:7-15, MacMillan,J.C.&Harper,P.S., 1994

Neurovascular Manifestations of Heritable Connective Tissue Disorders:A Review
Stroke 25:889-903, Schievink,W.I.,et al, 1994

Familial Alzheimer's Disease
Ann Neurol 36:335-336, Bird,T.D., 1994

Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
Neurol 44:721-727, Hirano,M.,et al, 1994

Myotonic Dystrophy
In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994

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

A Neurological Gene Map
Arch Neurol 50:1269-1271, Rosenberg,R.N., 1993

Sleep Paralysis
Lancet 341:406-407, Dahlitz,M.&Parkes,J.D., 1993

Infectious Prions or Cytotoxic Metabolites?
Lancet 341:159-161, Pablos-Mendez,A.,et al, 1993

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