Neudle.com: gene therapy

Differential
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abdominal cramps

abducens nerve paralysis

abscess, intracerebral

abscess, intracranial

abscess, perivalvular

acetylcholinesterase deficiency

achilles tendon, enlarged

achondroplasia

acid maltase deficiency

acid maltase deficiency, adult

aciduria

acoustic neurinoma

acoustic neurinoma, bilateral

ACTH

activated protein C resistance

acute disseminated encephalomyelitis

acute intermittant porphyria

acyl CoA dehydrogenase deficiency

Addison's disease

adenosine deaminase deficiency

adolescent medicine

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

affect, inappropriate

agoraphobia

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

alternative medicine

aluminum

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, diagnosis of

Alzheimer's disease, familial

Alzheimer's disease, incidence

Alzheimer's disease, pathogenesis

Alzheimer's disease, treatment of

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, Dutch type

amyloid angiopathy, hereditary cystatin C

amyloid beta protein

amyloid imaging

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

aneurysm, intracranial

aneurysm, intracranial, delayed cerebral ischemia with

aneurysm, intracranial, familial

aneurysm, intracranial, screening for

aneurysm, intracranial, treatment of

aneurysm, multiple intracranial

angiography, cerebral

anterior horn cell disease

anterior tibial muscle weakness

anterocollis

antibiotic prophylaxis

antibiotics

antibiotics, neurologic complications with

antibodies to voltage-gated calcium channels

anticholinergic drugs

anticholinesterase

anticipation

anticoagulant, treatment

anticonvulsants

anticonvulsants, discontinuation in seizure-free epileptics

anticonvulsants, effectiveness

anticonvulsants, hypersensitivity syndrome

anticonvulsants, selection of

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

antioxidant

antiviral agents

anxiety

aortic valve, bicuspid

aortic valve, lesion of

apraxia of eye movements

apraxia, constructional

arterial dissection, carotid

arterial dissection, vertebral

arteriovenous malformation

arteriovenous malformation, cerebral

arteriovenous malformation, pulmonary

arthralgia

arthritis

arthrogryposis multiplex

arylsulfatase A

ascites

Asians

aspartate aminotransferase

ataxia telangiectasia

atidarsagene autotemcel

atogepant

atrial fibrillation

atrial paralysis

atrioventricular block

attention

attention deficit disorder with hyperactivity

attention span

atypical

audiogram

auditory evoked brainstem potentials

autism

autism, screening for

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

autoimmune meningitis

autonomic dysfunction

autonomic nervous system

autonomic neuropathy

autonomic neuropathy, idiopathic

autosomal dominant nocturnal frontal lobe epilepsy

Babinski sign

bacterial endocarditis, neurologic manifestations of

bacterial infection

baldness

basal ganglia

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

behavior

behavior modification

behavior, combative

behavioral disorder

benign essential tremor

benign essential tremor, refractory

benign sexual headache

benzodiazepine

beta adrenergic agonist

beta adrenergic blocker

biotin deficiency, juvenile form

biotinidase deficiency

biotin-responsive basal ganglia disease

bitemporal visual field defect

blood dyscrasias, neurologic findings with

body odor

bone age

bone density

bone density, increased

bone marrow transplantation

botulinum toxin

botulism

brachial plexus neuropathy

brain biopsy, false negative

brain biopsy, indication

brain transplantation

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

brainstem, vascular malformation of

calcification, intracranial

calcitonin gene related peptide

calcitonin gene-related peptide receptor blocker

carcinoembryonic antigen

carcinoma

carcinoma of pancreas

cardiac arrest

cardiac surgery

cardiomyopathy

cardiovascular disease

caries

carnitine deficiency

carnitine deficiency myopathy

carotid artery

carotid artery disease

carotid artery occlusion, bilateral

carotid artery occlusion, neck

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

CAT scan, isodense lesion with acute hemorrhage

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, disease of

cerebellum, neoplasms of

cerebral arteries

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral edema, vasogenic

cerebral embolism

cerebral embolism, cardiac origin

cerebral embolism, carotid origin

cerebral vasculature, calcification

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, beta-D-glucan

cerebrospinal fluid, childhood

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure increased

cerebrospinal fluid, protein of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, multiple

cerebrovascular accident, neonatal

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, cardiovascular disease with

cerebrovascular disease, surgical treatment of

chemotherapy, CNS treatment and complications with

chenodeoxycholic acid

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chewing, impaired

children

chloride channel dysfunction

cholelithiasis

cholestanol

choline acetyltransferase

chorea

chorea, treatment of

choreoathetosis

choreoathetosis, paroxysmal

chromosomal abnormality

chronic graft versus host disease

chronic progressive external ophthalmoplegia

cirrhosis

cirrhosis, causes of childhood

cleft lip

cleft palate

Clinical Pathologic Conference(C.P.C.)

cobalamin C deficiency

Cockayne's syndrome

coenzyme Q10 deficiency

collagen vascular disease

colloid cyst

color vision

color vision, impaired

compression neuropathy

compulsivity

confusion

congenital deformities

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital malformation, non CNS

congenital myasthenic syndromes

congestive heart failure

controversies in neurology

copper

copper metabolism, abnormal

coprolalia

cornea, abnormal

cornea, opacity of

corpus callosum, lesion of

cortical blindness

cortical blindness, transient

cortical vein thrombosis

cost

cost effectiveness

coumarin

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

cranio-cervical junction

craniopharyngioma

creatine phosphokinase(CPK)elevated

cry, weak

crying

crying, pathologic

cryopyrin-associated periodic syndrome

cryptococcal meningitis

cryptorchidism

cultured skin fibroblasts

cyst, epidermoid of CNS

cyst, neoplastic cerebellum

degenerative diseases of CNS

delay in diagnosis

delayed muscle relaxation

dementia

dementia, autoimmune

dementia, childhood

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

developmental disability

developmental evaluation

developmental milestones, loss of

developmental retardation

developmental venous anomalies

diabetes mellitus

diagnostic criteria

diamond on quadriceps

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

dilantin

dilantin, hypersensitivity to

dilantin, toxicity

diplopia

diplopia, transient

disability, neurological

disease modifying agents

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, transesophageal, false negative

echocardiogram, transthoracic

echocardiogram, transthoracic, false negative

Ehlers-Danlos syndrome

Ehlers-Danlos syndrome, classification

electrocardiogram, abnormal

electroconvulsive therapy

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, monitoring, continuous

electroencephalogram, video monitoring with

electromyogram

electron microscopy

electronystagmography

electroretinograph

eletriptan

embolism

embolism, paradoxical

embolism, septic

embolism, systemic

embolization, therapeutic

Embryonal tumors

emergencies, neurologic

emergencies, ocular

Emery-Dreifuss muscular dystrophy

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, diagnosis of

encephalitis, etiology

encephalitis, Japanese

encephalitis, viral

encephalitis, viral-causes of

encephalopathy

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

endocarditis

endocarditis, acute bacterial

endocarditis, prophylaxis

endolymphatic sac tumors

endovascular therapy

enterovirus

enterovirus infection of CNS

entrapment neuropathy

enzyme treatment

enzyme, defect

enzyme, muscle disease

enzyme, serum

ependymoma

epidemiology of neurology

epidermoid

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

epistaxis

epistaxis, recurrent

epsilon sarcoglycan gene

executive dysfunction

exercise

exercise intolerance

exercise-induced neurologic dysfunction

exome sequencing

eye movement, disorders of

eye, pain in

eyes, sunken

Fabry's disease

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nevus

facial weakness

facial weakness, bilateral

Factor V Leiden

Fahr disease

failed medical management

familial hemiplegic migraine

familial periodic ataxia

familial rectal pain

fasciculation

fatal familial insomnia

fatigue

fatty acid, elevated plasma content

feeding disorder

ferric chloride test

fetal alcohol syndrome

fibrinolytic agents, contraindications

fibroma, ungual

fibromuscular dysplasia

fine motor function, impaired

fistula, arterio-venous, pulmonary

flail arm syndrome

flow study, carotid artery

fluctuate

flunarizine

fluorescein angiography

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

fundus, abnormality of

gastrointestinal bleeding

Gaucher's disease

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genu of corpus callosum

geographic location

gests antagoniste

Gilles de la Tourette syndrome

glabellar sign

glaucoma

glioblastoma multiforme(astrocytoma Gr.III)

glioma

glioma, low-grade

globoid cells

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

globus pallidus, stimulation

glucose tolerance test, abnormal

GLUT1

GLUT1 deficiency syndrome

glutamic acid decarboxylase

glutaric acidemia

glycogen storage disease

granular osmiphilic material

Hallervorden Spatz disease

head retraction reflex

headache, preventive treatment

headache, recurrent

headache, severe

headache, treatment of

headache, vascular

health insurance

hearing loss

hearing loss, bilateral

hearing loss, sudden, unilateral

hemangioma, brainstem

hemangioma, facial

hemangioma, leptomeningeal

hemangioma, skin

hematuria, gross

hemianopia

hemianopia, transient

hemiparesis

hemiparesis, transient

hemiplegia

hemochromatosis

hemochromatosis, primary

hemophagocytic lymphohistiocytosis

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hemoptysis

hemorrhagic diathesis

hepatic encephalopathy

hepatic failure

hepatitis

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)

herniated disc, thoracic

herpes simplex encephalitis

human immunodeficiency virus type 1

Huntington's chorea

Huntington's chorea, genetic counselling

Hurler's syndrome

hydrocephalus

hydrocephalus, viral induced

hyperkalemic periodic paralysis

hyperpigmentation of skin

hyperreflexia

hypersensitivity reaction

hypertrophic cardiomyopathy

hypokalemic periodic paralysis

hypometric saccades

hypoparathyroidism

hypophosphatemia

hypopigmentation of skin

hyporeflexia

hypotension, systemic

hypoxic-ischemic leukoencephalopathy

hypsarrhythmia

iatrogenic neurologic disorders

immunology and the nervous system

immunomodulation

immunosuppression

immunosuppressive agents

immunotherapy

implantable cardioverter defibrillator

impulsivity

in situ hybridization

inappropriate behavior

inattention

inborn errors of metabolism

inborn errors of metabolism, screening

incidental finding

inclusion bodies

inclusion bodies, intranuclear

inclusion body myositis

incoordination

infantile bilateral striatal necrosis

intellectual deterioration

intelligence quotient

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracerebral hemorrhage, lobar

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, young adult

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

iron, brain

irritability

ischemic exercise test

islet cell tumor

JAK2 V617F mutation

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

juvenile myoclonus epilepsy

karyotyping

Kayser-Fleischer ring

Kearns-Sayre syndrome

ketogenic diet

kinesia paradoxica

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactate

lactic acidemia

lactic dehydrogenase(LDH)

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

lens, dislocation of

lens, ectopic

lenticular nucleus, lesion of, bilateral

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

lipid storage disorder of CNS

lipid storage myopathy

liver biopsy

liver disease

liver function enzymes

liver transplantation

locus ceruleus, lesion of

lymphoma, primary of CNS

lysosomal storage disease

lysosomes, abnoral

macular degeneration

magnetic susceptibility

magnetoencephalography

malabsorption

malaise

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, screening for

malignancy screen

malignant hyperpyrexia

maple syrup urine disease

marche a petits pas

Marcus Gunn pupil

marfanoid skeletal abnormalities

masked facies

McArdle's disease

medulla oblongata, neoplasm of

medulloblastoma

MELAS syndrome

memory, impairment of

meningeal enhancement

meningitis, bacterial

meningitis, carcinomatous

meningitis, chronic

meningitis, fungal

meningitis, helminthic

meningitis, noninfectious

meningitis, parameningeal

meningitis, parasitic

meningitis, TB

meningitis, treatment of

meningitis, treatment of, empirical

meningitis, viral etiology in

meningitis-encephalitis PCR panel

menses

mental retardation

mental status, abnormal

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

metachromatic leukodystrophy, late-infantile

methylmalonic acidemia

methylmalonic aciduria

microhemorrhage, intracerebral

microsurgery

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, intractable

migraine, pathogenesis

migraine, prophylaxis

migraine, treatment of

mild cognitive impairment

Mills syndrome

mimics

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

monoclonal antibodies

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, paroxysmal

movement disorder, treatment of

MRI, complications with

MRI, contrast enhanced

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, incidental finding

MRI, muscle

MRI, negative

MRI, optic nerve

MRI, paramagnetic effect

MRI, repeat

MRI, serial

MRI, spinal cord

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRI, venography

MRI, volumetry

MRS

mucopolysaccharidoses

multiple endocrine neoplasia

multiple sclerosis

multiple sclerosis, clinical patterns

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, pathogenesis

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle pain

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, differential diagnosis of

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, distal weakness

myasthenia gravis, familial incidence of

myasthenia gravis, infantile and juvenile

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, neonatal

myasthenia gravis, neuromuscular junction in

myasthenia gravis, receptor site in

myasthenia gravis, seronegative

myasthenia gravis, treatment of

myasthenic syndrome

myelination of nervous system

myelitis, longitudinal

myelodysplasia

myelomalacia

myelopathy

myelopathy, chronic progressive

myeloproliferative disorder

myoblast transfer

myocardial abscess

myocardial infarction

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, metabolic

myopathy, mitochondrial

neonatal epilepsy syndromes

neonatal epileptic encephalopathy

neonatal screening, genetic neurologic disorders

neoplasm, intracranial

neoplasm, intracranial-incidence and epidemiology of

neoplasm, metastatic to CNS

neoplasm, metastatic to CNS-treatment of

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-children

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-familial occurrence

neoplasm, primary of CNS-incidence of

neoplasm, primary of CNS-recurrent

neoplasm, primary of CNS-surgical treatment of

neoplasm, primary of CNS-survival

neoplasm, primary of CNS-treatment of

nerve biopsy

nerve conduction studies

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neuroleptic, atypical

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromyotonia

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuropathy, ataxia, retinitis pigmentosa

neuropathy, demyelinating

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, peripheral, treatment

neuropathy, work up for

neurotomy

neurotransmitter

neutropenia

next-generation sequencing

Niemann-Pick disease

night blindness

nigrostriatal pathway

nonsteroidal anti-inflammatory drug

normal

Notch3 gene

nusinersen

nutritional deficiency

obsessive-compulsive disorder

occipital lobe, infarction

occipital lobe, lesion of

ocrelizumab

ocular motility, disorders of

oculopharyngeal muscular dystrophy

oligodendroglioma

opened mouth

ophthalmoplegia

ophthalmoplegia, progressive external

opisthotonus

opportunistic infection

opportunistic infection, CNS

optic atrophy

optic atrophy, bilateral

optic atrophy, hereditary

optic disc edema

optic nerve

optic nerve sheath fenestration

optic nerve, compression of

optic nerve, decompression of

optic nerve, enhancement

optic nerve, enlarged

optic nerve, lesion of

optic neuritis

optic neuritis, bilateral

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

oral contraceptives

oral contraceptives, cerbrovascular disease and

oral contraceptives, neurologic complications with

organomegaly

orgasm

ornithine transcarbamylase deficiency

osteoporosis

ovarian insufficiency

oxazepam

pacemaker, cardiac-transvenous

paralysis, acute areflexic

paralysis, recurrent

paramyotonia congenita

paranoia

paraparesis

paraparesis, acute

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraparesis, transient

paraplegia, recurrent

paraspinal muscle

paresthesias

Parkinson disease

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, etiology of

Parkinson disease, familial

Parkinson disease, freezing phenomena in

Parkinson disease, juvenile

Parkinson disease, nonmotor problems of

Parkinson disease, on-off phenomena in

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinsonism syndrome

paroxysmal dystonic choreoathetosis

paroxysmal exercise-induced dyskinesia

paroxysmal exertion-induced dyskinesia

paroxysmal extreme pain disorder

paroxysmal kinesigenic dyskinesia

paroxysmal neurologic deficits

paroxysmal neurologic disorder

PAS positive

pathology

patient information and support

pectus excavatum

penicillamine

percussion induced muscle contraction

periodic paralysis

periodic paralysis, thyrotoxic

phenylketonuria, adult onset

pheochromocytoma

phlebotomy

phosphorylase b kinase deficiency

photophobia

photosensitivity, skin

PICU

pigmentary retinopathy

pimozide

Pittsburgh Compound B

pituitary, adenoma

placebo effect

platelet aggregation

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

pneumonia

poison, neurologic problems with

polycystic kidneys

polycythemia, primary

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, familial

pomalidomide

Pompe's disease of glycogen storage

Pompe's disease, infantile

porphyria

port wine nevus

portal caval shunt

posterior cerebral artery territory infarction

posterior column disease

postural abnormality

potassium

potassium channel dysfunction

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

preclinical

precocious puberty

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

primary episodic ataxia

primary familial brain calcification

primary lateral sclerosis

primary thrombocythemia

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

prolactin, elevated

propranolol

proprioception, abnormal

ProSavin

protein S deficiency

proteinuria

proximal muscle atrophy

pseudarthrosis

pseudobulbar palsy

pseudohypoparathyroidism

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

quadriparesis

quadriparesis, acute

quadriplegia

quadriplegia, transient

quality of life

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

reading problem, causes of

respirations in CNS disease

respirator

respiratory depression

respiratory failure

respiratory tract infection

restless leg syndrome

retinal vasculopathy with cerebral leukodystrophy

reversible neurologic disorder

rhabdomyosarcoma of heart

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

rippling muscle disease

risk factors

risk factors, modification

saccadic eye movements, abnormal

safety

salivation, excessive

scoliosis, neurologic association with

second wind phenomena

sedimentation rate, elevated

seizure

seizure, cardiac arrhythmia causing

seizure, children

seizure, complications following

seizure, crying as manifestation of

seizure, diagnosis of

seizure, differential diagnosis of

seizure, drug resistance

seizure, drug-induced

seizure, laughing as manifestation

seizure, photosensitive

seizure, prognosis in adults

seizure, psychomotor-temporal lobe

seizure, psychosocial aspects of

seizure, stimulus sensitive

seizure, treatment of

seizure, workup of

senile plaques

sensorineural hearing loss

shunt procedure, lumboperitoneal

sick sinus syndrome

sinemet

single photon emission computed tomography

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 apnea

sleep apnea, obstructive

sleep pathology and physiology

slit lamp examination

slurred speech

SMN1 gene

socialisation

sodium channel dysfunction

sodium valproate

somatosensory evoked potentials

speech disorder, childhood

speech, delayed development of

speech, soft

spinal cord

spinal cord degeneration

spinal cord, compression of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinal stenosis

spinal xanthomatosis

spinocerebellar ataxia

spinocerebellar degeneration

splenium of corpus callosum

splenomegaly

spongy degeneration of brain

spontaneous remission

staggering

staphylococcus aureus

stem cell transplantation

stereotyped behavior, drug induced

stereotypy

steroid

steroid therapy, CNS treatment and complications with

stimulant drugs

stimulation, deep brain

stooped posture

storage disease of CNS

streptococcal infection

streptococcus viridans

stress, emotional

striatal encephalitis

striatonigral degeneration

striatum, lesion of

striatum, lesion of, bilateral

striopallidodentate calcifications, familial idiopathic

strokelike episodes

Sturge-Weber syndrome

subarachnoid hemorrhage

subarachnoid hemorrhage, familial

subarachnoid hemorrhage, treatment of

subependymal nodules

substantia nigra

subthalamic nucleus

subthalamic nucleus deep brain stimulation

suprascapular neuropathy

survival motor neuron gene

sweating

symmetric brain lesions

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tachycardia

tandem gait, ataxic

tantrum

tapetoretinal degeneration

tardive dystonia

tau protein

telangiectases

telangiectases, retinal

telcagepant

temozolomide

temporal lobe, lesion

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

testicular enlargement

tetrahydrobiopterin

thalamotomy

thalamus, focused ultrasound ablation

thalamus, infarction of

thalamus, lesion of-bilateral

thyroid function tests

thyrotoxicosis

tic

tic, chronic multiple

tinnitus

tinnitus, pulsatile

tissue plasminogen activator, intravenous

tocainide

toe walking

tomaculous neuropathy

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

torticollis, post traumatic

transient ischemic attack

transient neurologic deficit

trauma

treatment of neurologic disorder

tremor, surgical treatment of

tremor, thalamic stimulation for suppression of

trientine dihydrochloride

trigeminal nerve, lesion of

trigeminal neuropathy

trigeminovascular system

trinucleotide repeats

tuberous sclerosis, screening for

tumor suppressor gene

twins

tyrosine hydroxylase deficiency

ubrogepant

umbilical-cord blood transplantation

undiagnosed

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

uric acid, low

urinary catecholamines

urinary sulfatidase excretion

urinary urgency

urine test for metabolic disorders

venous thrombosis, non-cerebral

ventricular tachycardia

verapamil

vertigo

vertigo, episodic

vertigo, migraine causing

vertigo, treatment of

very long chain fatty acids

violent behavior

viral infection

viral infection, CNS

vision loss, sequential

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual acuity, decreased, monocular

visual field defect

visual field testing

visual loss

visual loss, progressive

visual loss, slow

visual loss, sudden

visual loss, transient

visuospatial disturbance

vitamin supplementation

Von Hippel Lindau, screening protocol for

von Hippel-Lindau, screening

walking

walking frame

walking, delayed

walking, difficulty with

weakness, fluctuating

weakness, generalized

weakness, progressive

weakness, proximal

web sites

weight loss

Werdnig-Hoffman disease

Wernicke's encephalopathy

Western immunoblot test

wheelchair

white freckles

white matter disease

whole genome sequencing

wide based gait

winging of scapula

Wiskott-Aldrich syndrome

x-linked intellectual deficit

x-linked mental retardation

zinc

Showing articles 200 to 250 of 11987 << Previous Next >>

The Muscular Dystrophies
BMJ 317:991-995, Emery,A.E.H., 1998

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Familial Idiopathic Intracranial Hypertension with Spinal and Radicular Pain
Arch Neurol 55:854-856, Santinelli,R.,et al, 1998

Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
Neurol 50:853-855, Nygaard,T.G.&Wooten,G.F., 1998

Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
NEJM 338:1119-1126, Krivit,W.,et al, 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Tourette Syndrome:Update and Review of the Literature
The Neurologist 4:188-195, Feigin,A.&Clarke,H., 1998

The Diagnostic Evaluation & Multidisciplinary Management of Neurofibromatosis 1 and Neurofibromatosis 2
JAMA 278:51-57, Gutmann,D.H.,et al, 1997

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

Cerebral Venous Thrombosis:Role of Activated Protein C Resistance and Factor V Gene Mutation
Stroke 27:1719-1720, Brey,R.L.&Coull,B.M., 1996

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

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

Familial Migraine with Vertigo and Essential Tremor
Neurol 46:458-460, Baloh,R.W.,et al, 1996

Cerebral Venous Sinus Thrombosis Associated with Factor V Gene Mutation
JNNP 61:204-205, Kimber,T.,et al, 1996

Gene Therapy for Cerebral Vascular Disease
Stroke 27:1688-1693, Heistad,D.D.&Faraci,F.M., 1996

Diagnosis and Management of Migraine
BMJ 312:1279-1283, Goadsby,P.J.&Olesen,J., 1996

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

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

A Greek-American Kindred with Autosomal Dominant, Levodopa-Responsive Parkinsonism and Anticipation
Ann Neurol 38:373-378, 3551995., Markopoulou,K.,et al, 1995

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

Myoblast Transfer in the Tratment of Duchenne's Muscular Dystrophy
NEJM 333:832-838, 8711995., Mendell,J.R.,et al, 1995

Spinocerebellar Ataxias and Ataxins
NEJM 333:1351-1353, Rosenberg,R.N., 1995

Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
NEJM 333:1313-1318, 13511995., Gotoda,T.,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

Anticonvulsant Hypersensitivity Syndrome
Arch Int Med 155:2285-2290, Vittorio,C.C.&Muglia,J.J., 1995

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

Progressive Multifocal Leukoencephalopathy Complicating Wiskott-Aldrich Syndrome
Arch Neurol 51:422-426, Katz,D.A.,et al, 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

Liver Transplantation as a Treatment for Familial Amyloidotic Polyneuropathy
Ann Int Med 120:133-134, Skinner,M.,et al, 1994

Cerebrotendinous Xanthomatosis:Molecular Diagnosis Enables Presymptomatic Detection of a Treatable Disease
Neurol 44:288-290, Meiner,V.,et al, 1994

Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
Neurol 44:461-466, Wilkinson,D.A.,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

The Nondystrophic Myotonias
In Myology, McGraw-Hill, 2nd Ed, Ch49, p1291-13024., Rudel,R.,et al, 1994

Gene Therapy for Neurologic Disease
Arch Neurol 50:1252-1268, Suhr,S.T.&Gage,F.H., 1993

Copper-Histidine Therapy for Menkes Disease
J Pediatr 123:828-830, Sarkar,B.,et al, 1993

Gene Therapy for Duchenne Dystrophy
Ann Neurol 34:3-4, Engel,A.G., 1993

Myoblast Transfer in Duchenne Muscular Dystrophy
Ann Neurol 34:8-18, Karpati,G.,et al, 1993

Leber's Hereditary Optic Neuropathy as a Cause of Severe Visual Loss in Childhood
Pediatrics 91:988-989, Moorman,C.M.&Elston,J.S., 1993

Atypical Leber's Hereditary Optic Neuropathy with Molecular Confiramtion
Arch Neurol 50:470-473, Weiner,N.C.,et al, 1993

Leber's Hereditary Optic Neuropathy, New Genetic Considerations
Arch Neurol 50:540-548, Newman,N.J., 1993

A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig
Neurol 42:2251-2257, Mikati,M.A.,et al, 1992

Delayed Diagnosis of Juvenile Myoclonic Epilepsy
JNNP 55:497-499, Grunewald,R.A.,et al, 1992

Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome
Pediatrics 89:395-400, Hagerman,R.J.,et al, 1992

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

Effect of Calcitonin-Gene-Related Peptide in Pts with Delayed Postop Cerebral Ischaemia after Aneurysmal SAH
Europ CGRP Study Group, Lancet 339:831-8341992., , 1992

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

Wilson's Disease:Current Status
Am J Med 92:643-654, Yarze,J.C.,et al, 1992

Startle Disease, or Hyperrekplexia:Clonazepam and Assign of Gene (STHE) to Chromosoma 5q by Linkage Analysis
Ann Neurol 31:663-668, Ryan,S.G.,et al, 1992

The First Decade of Molecular Genetics in Neurology:Changing Clinical Thought and Practice
Ann Neurol 32:207-214, Rowland,L.P., 1992

Showing articles 200 to 250 of 11987 << Previous Next >>