Neudle.com: polyneuropathy familial

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Differential
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abdominal distention

abducens nerve paralysis

abscess, intracerebral

abscess, intracerebral, recurrent

acid maltase deficiency

acid maltase deficiency, adult

acoustic nerve, vestibular division of

acoustic neurinoma

acral sensory symptoms

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

Aicardi-Goutieres syndrome

alcohol intolerance

alcohol intoxication

alcohol, blood level of

alcohol, neurologic complications with

alcoholic blackout

alcoholic dementia

alcoholic polyneuropathy

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

alkylating agents

alpha-fetoprotein

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alternating rapid movement, impaired

alternative medicine

Alzheimer's disease

Alzheimer's disease, diagnosis of

Alzheimer's disease, early onset

Alzheimer's disease, familial

Alzheimer's disease, incidence

Alzheimer's disease, preclinical

Alzheimer's disease, treatment of

aminoacidopathies

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, Dutch type

amyloid angiopathy, hereditary cystatin C

amyloid beta protein

amyloid plaques

amyloidosis, oculoleptomeningeal, familial

amyotrophic chorea-acanthocytosis

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, guamian type of

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

anesthesia, general

aneurysm, intracranial, screening for

Angelman syndrome

angiofibroma, facial

angiomyolipomas

animal exposure

ankle reflex, absent

anterior horn cell disease

anterior interosseous neuropathy

anterior tibial muscle weakness

anti MAG antibodies

antibiotic prophylaxis

anticholinergic drugs

anticonvulsants

anticonvulsants, selection of

aphasia, progressive, primary

apolipoprotein E

apraxia of eye movements

arrhythmia, cardiac

arteriovenous malformation

arteriovenous malformation, cerebral

arteriovenous malformation, multiple

arteriovenous malformation, pulmonary

arteritis, temporal

arthrogryposis multiplex

arthropathy, neuropathic

arylsulfatase A

Asperger's syndrome

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, sensory

ataxia, truncal

atherosclerosis, premature

attention deficit disorder with hyperactivity

auditory evoked brainstem potentials

autism, screening for

autistic behavior

autoimmune disease

automatic implantable cardioverter-defibrillator

autonomic dysfunction

autonomic nervous system

autonomic neuropathy

autonomic neuropathy, idiopathic

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal degeneration

axonal spheroid

B 12 deficiency

bacterial infection

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

behavior, combative

behavioral disorder

benign essential tremor

bicaudate index

biologic markers

biotinidase deficiency

bitemporal visual field defect

bladder dysfunction

bleeding disorder

blinking, reduced

blood dyscrasias, neurologic findings with

bone marrow transplantation

bovine spongiform encephalopathy

brachial neuritis

brachial neuritis, acute

brachial neuritis, bilateral

brachial plexus

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brainstem, atrophy

brainstem, dysfunction

brainstem, lesion of

Brown-Vialetto-Van Laere syndrome

burning paresthesia

calcification, intracranial

calf hypertrophy

caloric testing

Canavan's disease

carcinoembryonic antigen

cardiovascular disease

carotid angiogram

carpal tunnel syndrome

CAT scan, abdomen

CAT scan, abnormal

CAT scan, chest

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, metrizamide

CAT scan, myelogram with

CAT scan, ring sign

cataracts, congenital

cauda equina, enhancement

cauda equina, lesion of

caudate nucleus

caudate nucleus, atrophy

cavernous hemangioma

cavernous sinus

cavernous sinus, lesion of

central core disease

central nervous system, infection of

central pontine myelinolysis

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 lesion

cerebellum, disease 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, vasogenic

cerebral embolism

cerebral infarction

cerebral infarction, subcortical

cerebral peduncle

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, culture of, viral

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure low

cerebrospinal fluid, protein of

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, multiple

cerebrovascular accident, neonatal

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

ceruloplasmin, serum

Charcot-Marie-Tooth

Chediak-Higashi syndrome

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chilbran skin lesions

cholesterol, HDL

chorea, familial

choreoathetosis

chromosomal abnormality

chronic graft versus host disease

chronic progressive external ophthalmoplegia

cingulate gyrus

cirrhosis, infancy

claudication, intermittent of cauda equina

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

clubfoot as related to neurologic disease

Cockayne's syndrome

coenzyme Q10 deficiency

cognition, slowed

cold hands sign

cold temperature

collagen vascular disease

compression neuropathy

compression neuropathy, recurrent

conduction block

congenital heart disease

congestive heart failure

contractures, joint

contraindications

controversies in neurology

cornea, abnormal

cornea, opacity of

corneal dystrophy

corpus callosum

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cost effectiveness

cranial nerve enlargement

cranial nerve palsies

cranial nerve tumor

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cultured skin fibroblasts

cyst, peritumoral

cyst, neoplastic cerebellum

cyst, parenchymal

cytochrome c oxidase

cytochrome c oxidase, deficiency

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

Dejerine-Sottas syndrome

delay in diagnosis

dementia, age at onset

dementia, childhood

dementia, familial

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, screening for

dementia, subcortical

dementia, transmissible

demyelinating disease

denervation of muscle

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

dermatomyositis

developmental disability

developmental evaluation

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diagnostic criteria

diamond on quadriceps

diaphragmatic paralysis

differential diagnosis

difficulty climbing stairs

diplopia, transient

disability rating scale, neurological

disability, neurological

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

diurnal variation

dopamine agonist

down-beat nystagmus

drug abuse, inhalation

drug induced neurologic disorders

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dyskinesia, buccal lingual facial

dysostosis multiplex

dystonia, cervical

dystonia, children

dystroglycanopathies

ears of the Lynx MR sign

eating disorder

Ehlers-Danlos syndrome

Ehlers-Danlos syndrome, classification

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, inflammatory disease

electroencephalogram, monitoring, continuous

electroencephalogram, periodic complexes

electron microscopy

electronystagmography

electroretinograph

embolism, paradoxical

embolism, septic

emergencies, neurologic

Emery-Dreifuss muscular dystrophy

emotional lability

encephalitis, viral

encephalopathy, neonatal

encephalopathy, progressive

endarterectomy, carotid

endocarditis, prophylaxis

endolymphatic sac tumors

endovascular therapy

entrapment neuropathy

enzyme treatment

enzyme, muscle disease

epidemiology of neurology

epileptic encephalopathy

episodic neurologic deficits

epistaxis, recurrent

erythromelalgia

esophageal varices

ethics in neurology

evoked potentials

exercise intolerance

exome sequencing

extraocular muscle lesion

eye movement, disorders of

Fabry's disease

face, elongated

face, numbness of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, familial

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

failure to thrive

family planning

fatal familial insomnia

fatty acid, elevated plasma content

Fazio-Londe's disease

feeding disorder

fetal alcohol syndrome

fibrinolytic agents, contraindications

fibroma, ungual

fine motor function, impaired

finger nose finger test

fistula, arterio-venous, pulmonary

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

fundus, abnormality of

funduscopic exam

F-wave response

gait, festinating

gangliosidosis GM1

gangliosidosis GM2

gastrointestinal bleeding

gastrointestinal disease, neurologic complications

gastrointestinal motility

Gaucher's disease

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genu of corpus callosum

Gerstmann-Straussler-Scheinker disease

giant axonal neuropathy

Gilles de la Tourette syndrome

glioblastoma multiforme(astrocytoma Gr.III)

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucocerebrosidase

glucose tolerance test, abnormal

GLUT1 deficiency syndrome

glutaric acidemia

glycogen storage disease

Gowers maneuver

granulomatosis with polyangiitis

granulomatous disease

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, familial

Hallervorden Spatz disease

Hallgren's syndrome

headache, sudden onset of

hearing loss, sudden, unilateral

hearing problems in children

heavy metal intoxication

heel-knee-shin test

hemangioblastoma

hemiparesis, transient

hemochromatosis

hemochromatosis, primary

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hepatic encephalopathy

hepatic failure

hepatitis C virus

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

high arched feet

hockey stick sign

hormone replacement

Horner's syndrome

H-reflex testing

human immunodeficiency virus type 1

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

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's chorea, late onset

Huntington's chorea, misdiagnosis of

Huntington's chorea, presymptomatic detection of

Huntington's chorea, sporadic form

Huntington's disease, children

Hurler's syndrome

hyperinsulinism

hyperpyrexia, CNS disorder causing

hypertriglyceridemia

hypoalbuminemia

hypofibrinogenemia

hypoglossal nerve paralysis

hypoglycorrhachia

hypogonadism, hypogonadotropic

hypometric saccades

hypopigmentation of skin

hypotension, systemic

hypotonia, causes of

hypotonia, infants

hypoxic-ischemic leukoencephalopathy

iatrogenic neurologic disorders

idiopathic polyneuropathy

ileus, paralytic

imbalance, postural

immunodeficiency

immunologic disease

immunosuppression

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

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

infantile spasm

infection, recurrent

inflexibility, mental

intellectual deficit

intellectual deterioration

interferon alpha

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracerebral hemorrhage, lobar

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, young adult

intracranial pressure, increased

intraventricular hemorrhage

intrinsic hand muscles, wasting of

Isaacs syndrome

ischemic exercise test

islet cell tumor

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

jaw jerk, abnormal

joint hypermobility

juvenile myoclonus epilepsy

Kayser-Fleischer ring

Kearns-Sayre syndrome

kinesia paradoxica

klippel feil syndrome

Korsakoff's psychosis

Krabbe's disease

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

lacunar infarction

Lafora's disease

laminectomy, cervical

laminectomy, lumbar

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

learning disability

learning disability, in children

Leber's congenital amaurosis

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukoencephalopathy

leukoencephalopathy, hereditary diffuse

Lhermitte's sign

life expectancy

light-near dissociation, causes of

limb-girdle weakness

lipid storage disorder of CNS

lipomatosis, multiple symmetrical

liver function enzymes

liver transplantation

lumbar puncture

lumbosacral plexopathy

lumbosacral plexus

lymphadenopathy

lymphangiomyomatosis

lymphoma involving CNS

lymphoma, primary of CNS

lymphomatoid granulomatosis

lysosomal storage disease

macular degeneration

magnetic stimulation

magnetic stimulation, brain

magnetic susceptibility

magnetoencephalography

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, familial

malformation, vascular, screening for

maple syrup urine disease

marche a petits pas

McArdle's disease

McLeod syndrome

median neuropathy

medical-legal aspects of neurology

medulla oblongata, neoplasm of

memory, defect of recent

memory, impairment of

meningitis, carcinomatous

meningoencephalopathy

mental retardation

mental retardation, familial

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

methylhydrazine derivatives

microangiopathy, brain

microhemorrhage, intracerebral

midbrain, atrophy

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine with aura

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

molecular genetics

monoamine oxidase inhibitors

mononeuropathy multiplex

mononeuropathy, children

mononeuropathy, recurrent

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, angiography

MRI, complications with

MRI, contrast enhanced

MRI, cranial nerves

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, functional

MRI, gradient-echo

MRI, indications for

MRI, paramagnetic effect

MRI, peripheral nerve

MRI, punctate pattern

MRI, spinal cord

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle diseases, characteristics of

muscle hypertrophy

muscle phosphorylase deficiency

muscle stiffness

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle, metabolic disorders 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, 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, misdiagnosis of

myasthenia gravis, seronegative

myasthenia gravis, treatment of

myasthenic crisis

myelin protein zero gene

myelitis, transverse

myelogram, cervical

myeloneuropathy

myelopathy, chronic progressive

myeloradiculopathy

myoclonic jerks

myopathy, alcoholic

myopathy, carcinomatous

myopathy, distal

myopathy, distal, Welander's

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, metabolic

myopathy, mitochondrial

myopathy, quadriceps

myopathy, thyroid disease causing

myopathy, vacuolar

myotonia dystrophica

nausea and vomiting

neonatal epilepsy syndromes

neonatal epileptic encephalopathy

neonatal intensive care unit

neonatal screening, genetic neurologic disorders

neoplasm, peripheral nerve

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplasm, primary of CNS-aged

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-treatment of

nerve biopsy, indication

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve growth factor

nerve growth stimulating activity

nerve hypertrophy

nerve root enhancement

nerve root hypertrophy

neuraminidase deficiency

neuritis, causes of

neurocutaneous disease

neurodegeneration with brain iron accumulation

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurofibromatosis 2

neurofibromatosis 2, presymptomatic

neurogenic bladder

neurogenic vs.myopathic atrophy

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic history

neurologic signs

neurologic symptoms

neurologic testing

neuromuscular disease, electrodiagnosis of

neuromyelitis optica (Devic's disease)

neuromyelitis optica spectrum disorder

neuromyelitis optica, IgG

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal intranuclear inclusion disease

neuronal migration disorder

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, amyloid

neuropathy, ataxia, retinitis pigmentosa

neuropathy, ataxic

neuropathy, classification of

neuropathy, demyelinating

neuropathy, diabetic

neuropathy, etiologies of

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, motor

neuropathy, onion bulb

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, recurrent

neuropathy, sensory

neuropathy, sensory, hereditary

neuropathy, vasculitic, systemic

neuropathy, work up for

neurotransmitter

newborn, evaluation of

next-generation sequencing

Niemann-Pick disease

night blindness

nitrogen mustard

numbness, extremity

nutritional deficiency

nystagmus, dissociated

nystagmus, monocular

nystagmus, vertical

obsessive-compulsive disorder

ocular motility, disorders of

ocular myopathy

old age, neurology of

oligodendroglioma

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy, hereditary

optic nerve, enlarged

optic nerve, lesion of

optic neuritis, bilateral

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

optical coherence tomography

orthostatic hypotension

orthostatic hypotension, idiopathic

ovarian dysgenesis

pacemaker, cardiac-transvenous

pain, abdominal

pain, increased response

palliative care

pancreatic cyst

paralysis, recurrent

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraparesis, spastic, tropical

paresthesias, feet

paresthesias, lower extremity

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, classification

Parkinson disease, diagnosis

Parkinson disease, dystonia with

Parkinson disease, etiology of

Parkinson disease, freezing phenomena in

Parkinson disease, heterogeneity of

Parkinson disease, misdiagnosis

Parkinson disease, pathogenesis of

Parkinson disease, presymptomatic detection

Parkinson disease, subtypes

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

patient information and support

peripheral blood smear

peroneal muscle atrophy, causes of

peroneal nerve, lesion of

peroxisomal disease

Perrault syndrome

personality change

pheochromocytoma

phosphorylase b kinase deficiency

photosensitivity, skin

pigmentary retinopathy

pituitary, hormones of

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

poison, mercury

poison, neurologic problems with

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy, chronic idiopathic

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic relapsing

polyneuropathy, familial

pons, lesion of

portal caval shunt

positional head-hanging test

post polio syndrome

posterior leukoencephalopathy syndrome

postural abnormality

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

presenilin-2 gene

prevention of neurologic disorders

prion protein gene

prisoners of war, neurologic complications in

progressive myoclonic epilepsy

progressive neurologic disorder

protein 14-3-3, cerebrospinal fluid

proximal muscle atrophy

pseudobulbar palsy

pseudoretinitis pigmentosa

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

psychosocial aspects

ptosis, bilateral

pulmonary function tests

pulmonary hypertension

pulmonary infection

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, scalloped

pyramidal tract

pyramidal tract dysfunction

quadriplegia, transient

quality of life

radial nerve, palsy of

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reading disorder, acquired

real-time quaking-induced conversion

recombinant DNA

recurrent laryngeal nerve paralysis

refractive errors

Refsum's disease

release phenomena

renal cell carcinoma

renal tubular acidosis

respiratory depression

respiratory failure

restless leg syndrome

retina, abnormal

retinal degeneration

retinal hamartoma

retinal hemangioma

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

rhabdomyoma, cardiac

rhabdomyosarcoma of heart

riboflavin transporter deficiency

Riley-Day syndrome

rippling muscle disease

root lesion, nerve

Roussy Levy syndrome

saccadic eye movements, abnormal

sarcoglycanopathy

scoliosis, neurologic association with

second wind phenomena

seizure, children

seizure, complications following

seizure, diagnosis of

seizure, differential diagnosis of

seizure, etiology of

seizure, familial

seizure, neonatal

seizure, paradoxical

seizure, psychomotor-temporal lobe

seizure, stimulus sensitive

seizure, treatment of

seizure, workup of

self-mutilation

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory loss, leg

sensory loss, truncal

sensory nerve action potentials

sensory polyneuropathy

serologic testing

shoulder, numbness

Shy-Drager syndrome

single photon emission computed tomography

skin, darkening of

skin, hyperextensible

skin, lesions in neurologic disorders

skin, translucent

sleep pathology and physiology

slit lamp examination

small vessel disease

small vessel disease, cerebral

sodium valproate

somatosensory evoked potentials

Southern immunoblot test

spastic diplegia

spastic paraplegia, type 11

spastic paraplegia, type 15

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

Spielmeyer Vogt syndrome

spinal cord degeneration

spinal cord, compression of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, intramedullary

spinal cord, pathologic exam of

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 stenosis, familial

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 degeneration

splenium of corpus callosum

spongy degeneration of brain

spontaneous muscle activity

spontaneous remission

startle myoclonus

startle reaction

status epilepticus

stem cell transplantation

stereotyped behavior

stereotyped behavior, drug induced

steroid therapy, CNS treatment and complications with

stiff man syndrome

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

subarachnoid hemorrhage

subcortical U fibers

subdural hematoma

subependymal nodules

substantia nigra

superoxide dismutase

suprascapular neuropathy

survival motor neuron gene

symmetric brain lesions

systemic illness

tandem gait, ataxic

Tangier's disease

tapetoretinal degeneration

temper tantrums

temporal lobe, lesion

temporal lobe, lesion, bilateral

testicular atrophy

testicular enlargement

thalamus, lesion of-bilateral

thrombocytopenia

tic, chronic multiple

tissue plasminogen activator, intravenous

tomaculous neuropathy

tongue, enlarged

tongue, fasciculations of

tongue, protrusion of

tongue, red papules

tongue, weakness

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, classification

tremor, differential diagnosis of

tremor, intention

tremor, orthostatic

tremor, physiologic

tremor, post traumatic

tremor, postural

tremor, psychogenic

tremor, resting

tremor, treatment of

tremor, writing

trichopoliodystrophy

tricresylphosphate

trientine dihydrochloride

trigeminal nerve

trigeminal nerve, hypertrophy

trigeminal neuralgia

trinucleotide repeats

tuber, cortical

tuberous sclerosis

tuberous sclerosis, screening for

tumor suppressor gene

ulnar neuropathy

ultrasonography, nerve

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

urinary incontinence

urine test for metabolic disorders

Usher's syndrome

very long chain fatty acids

vestibular areflexia

vestibular function, tests of

vibratory sensation, abnormal

vincristine neurotoxicity

viral infection

viral infection, CNS

viral isolation

visceral neuropathy

vision loss, sequential

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss, congenital

visual loss, progressive

visual loss, sudden

vitamin deficiency

vitamin E deficiency

vitreous opacities

vocal cord paralysis

voice, abnormality of

Von Hippel Lindau

Von Hippel Lindau, screening protocol for

von Hippel-Lindau, screening

walking, difficulty with

walking, difficulty with in dark

water channel antibodies

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

Werdnig-Hoffman disease

Werner's syndrome

Wernicke's encephalopathy

white matter disease

white matter disease, subcortical

wide based gait

winging of scapula

word-finding difficulty

wound healing, poor

xeroderma pigmentosa

X-linked bulbospinal neuronopathy

x-linked intellectual deficit

x-linked mental retardation

X-linked neuropathy

Showing articles 50 to 100 of 4304 << Previous Next >>

Parkinson Disease Subtypes
JAMA 71:499-504, Thenganatt, M. & Jankovic, J., 2014

Red Papules on the Tongue of a Patient with Hemiparesis
JAMA 312:741-742, Chiu, H.Y. & Lin, S.J., 2014

Inherited Metabolic Diseases of the Nervous System, Globoid Cell Leukodystrophy (Krabbe Disease, Galactocerebrosidase)
Adams & Victors Principles of Neurology, Chp 37, pg 959, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Fabry Disease
Adams & Victors Principles of Neurology, Chp 37, pg 991, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Parkinson Disease
Adams & Victors Principles of Neurology, Chp 39, pg 1082, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1109, Ropper, A.H.,et al, 2014

The Limbic-Girdle Muscular Dystrophies
Neuro Clin 32:729-749, Wicklund, M.P. and Kissel, J.T., 2014

Chediak-Higashi Syndrome: Pathognomonic Feature
Lancet 382:1514, Antunes, H.,et al, 2013

Brain Arteriovenous Malformation Multiplicity Predicts the Diagnosis of Hereditary Hemorrhagic Telangiectasia Quantitive Assessment
Stroke 43:72-78, Bharatha, A.,et al, 2012

Cerebral Amyloid Angiopathy
eMedicine, Jan, Menon, R.S., 2012

Clinical Reasoning: A Young Man with Reversible Paralysis, Cerebral White Matter Lesions, and Peripheral Neuropathy
Neurol 79: e70-e72, Zhong, L.,et al, 2012

Range of Genetic Mutations Associated with Severe Non-Syndromic Sporadic Intellectual Disability: An Exome Sequencing Study
Lancet 380:1674-1682, Rauch, A.,et al, 2012

Diagnostic Exome, Sequencing in Persons with Severe Intellectual Disability
NEJM 367:1921-1929, Ligt, J.,et al, 2012

Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
NEJM 367:1921-1929, Ligt, J.,et al, 2012

The Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale
Stroke 43:2871-2876, Pescini, F.,et al, 2012

LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine
Disease Models & Mechanisms 4:562-568, Lu,J.T., et al, 2011

Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
UpToDate, Feb, Shovlin, C., 2011

An unusual cause of stroke and hypoxia
BMJ 342:c7200, Bell, S.L. & Eveson, D.J., 2011

Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011

Clinical Reasoning: A 34-Year-Old Woman with Recurrent Bouts of Acral Paresthesias
Neurol 74:775-778, Karam,C. &Scelsa,S., 2010

Comparison of Clinical, Familial, and MRI Features of CADASIL and NOTCH3-Negative Patients
Neurol 74:57-63, Pantoni,L.,et al, 2010

Whole-Genome Sequencing in a Patient with Charcot-Marie-Tooth Neuropathy
NEJM 362:1181-1191, Lupski,J.R., et al, 2010

Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
Brain 133:655-670, Leen,W.G., et al, 2010

Aicardi-Gouti�res Syndrome: Neuroradiologic Findings and Follow-up
AJNR 30:1971-1976, Uggetti,C.,et al, 2009

Leukodystrophies: Classification, Diagnosis, and Treatment
Neurologist 15:319-328, Costello,D.,et al, 2009

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

Neurofibromatosis Type 2
Lancet 373:1974-1986, Astagiri,A.R.,et al, 2009

Diagnosis and New Treatments in Muscular Dystrophies
JNNP 80:706-714, Manzur,A.Y. &Muntoni,F., 2009

Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009

Autism
Lancet 374:1627-1638, Levy,S.,et al, 2009

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

MR Imaging of Familial Creutzfeldt-Jakob Disease: A Blinded and Controlled Study
AJNR 29:1638-1643, Fulbright,R.K.,et al, 2008

Neurofibromatosis
JAMA 300:352, Torpy,J.M.,et al., 2008

Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
Arch Neurol 65:19-25, Amiri,K.,et al, 2008

Spinal Muscular Atrophy
Lancet 371:2120-2133, Lunn,M.R. &Wang,C.H., 2008

Tuberous Sclerosis
Lancet 372:657-658, Curatolo,P.,et al., 2008

Neurologic Manifestations of von Hippel-Lindau Disease
JAMA 300:1334-1342, Butman,J.A.,et al, 2008

Insights into the Dynamics of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids
Neurol 71:925-929, Van Gerpen,J.A.,et al, 2008

Neuroimaging Findings in Human Prion Disease
JNNP 78:664-670, Macfarlane,R.G.,et al, 2007

Amyotrophic Lateral Sclerosis
Lancet 369:2031-2041, Mitchell,J.D. & Borasio,G.D., 2007

The Tuberous Sclerosis Complex
NEJM 355:1345-1356, Crino,P.B.,et al, 2006

Common Misdiagnosis of a Common Neurological Disorder: How Are We Misdiagnosing Essential Tremor?
Arch Neurol 63:1100-1104, Jain,S.,et al, 2006

CNS Involvement in Hereditary Neuropathy With Pressure Palsies (HNPP)
Neurol 67:2250-2252, Tackenberg,B.,et al, 2006

Mitochondrial DNA Polymerase-y and Human Disease
Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006

Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
NEJM 354:2584-2592, Case 18-2006, 2006

Finding the Causes of Inherited Neuropathies
Arch Neurol 63:812-816, Scherer,S.S., 2006

Restless Legs Syndrome: Is Treatable But Under-Recognised
BMJ 333:457-458, Medcalf,P. &Bhatia,K.P., 2006

Hereditary Motor and Sensory Neuropathies
Peripheral Neuropathy, Dyck,P.J. & Thomas,P.K. (Ed). Elsevier Publ, Vol 2, Ch 69: 1623-1635, Shy,M.E., et al, 2005

Central Nervous System Involvement in Hereditary Neuropathy With Liability to Pressure Palsies
Arch Neurol 62:1911-1914, Sanahuja,J.,et al, 2005

Adrenoleukodystrophy
JAMA 294:3131-3134, Moser,H.W.,et al, 2005

Showing articles 50 to 100 of 4304 << Previous Next >>