Neudle.com: polyneuropathy familial

Differential
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abdominal distention

abducens nerve paralysis

abscess, intracerebral

abscess, intracerebral, recurrent

absence

acanthocytosis

acid maltase deficiency

acid maltase deficiency, adult

acoustic nerve

acoustic nerve, vestibular division of

acoustic neurinoma

acral sensory symptoms

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

agoraphobia

Aicardi-Goutieres syndrome

alcohol, blood level of

alcohol, neurologic complications with

alcoholic blackout

alcoholic coma

alcoholic dementia

alcoholic polyneuropathy

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

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

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, Dutch type

amyloid angiopathy, hereditary cystatin C

amyloid beta protein

amyloid plaques

amyloidosis

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

anemia

anesthesia, general

aneurysm

aneurysm, intracranial, screening for

anterior horn cell disease

anterior interosseous neuropathy

anterior tibial muscle weakness

anti MAG antibodies

antibiotic prophylaxis

anticholinergic drugs

anticonvulsants

anticonvulsants, selection of

antimetabolite

anxiety

aphasia

aphasia, progressive, primary

apolipoprotein E

apraxia of eye movements

arteriovenous malformation

arteriovenous malformation, cerebral

arteriovenous malformation, multiple

arteriovenous malformation, pulmonary

arteritis, temporal

arthralgia

arthrogryposis multiplex

arthropathy

arthropathy, neuropathic

ataxia telangiectasia

atherosclerosis, premature

atonic bladder

ATP1A3 gene

attention deficit disorder with hyperactivity

atypical

auditory evoked brainstem potentials

autism

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

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

behavior

behavior, combative

behavioral disorder

benign essential tremor

bicaudate index

biologic markers

biotinidase deficiency

bitemporal visual field defect

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, dysfunction

brainstem, lesion of

Brown-Vialetto-Van Laere syndrome

calcification, intracranial

carcinoembryonic antigen

carcinoma

cardiomegaly

cardiomyopathy

cardiovascular disease

carotid angiogram

carpal tunnel syndrome

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, metrizamide

CAT scan, myelogram with

CAT scan, ring sign

cataracts

cataracts, congenital

cauda equina

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

cerebral edema, vasogenic

cerebral embolism

cerebral infarction

cerebral infarction, subcortical

cerebral palsy

cerebral peduncle

cerebritis

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

chromosomal abnormality

chronic graft versus host disease

chronic progressive external ophthalmoplegia

cingulate gyrus

cirrhosis

cirrhosis, infancy

claudication, intermittent of cauda equina

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

collagen vascular disease

coloboma

coma

complications

compression neuropathy

compression neuropathy, recurrent

compulsivity

conduction block

confusion

congenital heart disease

congestive heart failure

consanguinity

contractures, joint

contraindications

controversies in neurology

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cost effectiveness

cough

cranial nerve enlargement

cranial nerve palsies

cranial nerve tumor

cranial nerves

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cultured skin fibroblasts

cyanosis

cyst

cyst, peritumoral

cyst, neoplastic cerebellum

cyst, parenchymal

cytochrome c oxidase

cytochrome c oxidase, deficiency

deafmute

deafness

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

Dejerine-Sottas syndrome

delay in diagnosis

delusion

dementia

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

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

dermatitis

dermatomyositis

developmental disability

developmental evaluation

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diagnostic criteria

diamond on quadriceps

diaphragmatic paralysis

diarrhea

diet

differential diagnosis

difficulty climbing stairs

diplopia

diplopia, transient

disability rating scale, neurological

disability, neurological

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

drug abuse, inhalation

drug induced neurologic disorders

dwarfism

dying

dysarthria

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dyskinesia, buccal lingual facial

ears of the Lynx MR sign

eating disorder

echocardiogram

edema, pedal

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

electromyogram

electron microscopy

electronystagmography

electroretinograph

ELISA

embolism, paradoxical

embolism, septic

emergencies, neurologic

Emery-Dreifuss muscular dystrophy

encephalopathy, neonatal

encephalopathy, progressive

endarterectomy, carotid

endocarditis, prophylaxis

endolymphatic sac tumors

endovascular therapy

enophthalmous

entrapment neuropathy

enzyme treatment

enzyme, defect

enzyme, muscle disease

ependymoma

epidemiology of neurology

epileptic encephalopathy

episodic neurologic deficits

extraocular muscle lesion

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, familial

facial nerve palsy, recurrent

facial pain

facial weakness

facial weakness, bilateral

fatal familial insomnia

fatigue

fatty acid, elevated plasma content

Fazio-Londe's disease

feeding disorder

fetal alcohol syndrome

fever

fibrinolytic agents, contraindications

fibroma, ungual

fine motor function, impaired

finger nose finger test

finger tapping

fistula, arterio-venous, pulmonary

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

frataxin

Friedreich's ataxia

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

fucosidosis

fundus, abnormality of

gastrointestinal bleeding

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastroparesis

Gaucher's disease

gaze palsy

gaze palsy, supranuclear

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

glabellar sign

glaucoma

glioblastoma multiforme(astrocytoma Gr.III)

glioma

globoid cells

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucocerebrosidase

glucose tolerance test, abnormal

GLUT1

GLUT1 deficiency syndrome

glutaric acidemia

glycogen storage disease

glycoprotein

Gowers maneuver

granulomatosis with polyangiitis

granulomatous disease

grimacing

growth hormone

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, familial

gynecomastia

hair analysis

Hallervorden Spatz disease

headache, sudden onset of

hearing loss

hearing loss, sudden, unilateral

hearing problems in children

heart block

heavy metal intoxication

hemiparesis, transient

hemiplegia

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

hepatomegaly

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

human immunodeficiency virus type 1

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

huntingtin

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

hyperpyrexia, CNS disorder causing

hypoglossal nerve paralysis

hypoglycorrhachia

hypogonadism

hypogonadism, hypogonadotropic

hypometric saccades

hyponatremia

hypopigmentation of skin

hyporeflexia

hyposmia

hypotelorism

hypotension, systemic

hypoxic-ischemic leukoencephalopathy

iatrogenic neurologic disorders

idiopathic polyneuropathy

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

inattention

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

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

intrauterine

intraventricular hemorrhage

intrinsic hand muscles, wasting of

ischemic exercise test

islet cell tumor

isoniazid

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

juvenile myoclonus epilepsy

Kayser-Fleischer ring

Kearns-Sayre syndrome

klippel feil syndrome

Korsakoff's psychosis

Krabbe's disease

Kugelberg-Welander syndrome

kuru

kyphoscoliosis, neurologic causes of

lactic acidemia

lacunar infarction

Lafora's disease

laminectomy, cervical

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

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

leprosy

leukemia

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukocytes

leukodystrophy

leukoencephalopathy

leukoencephalopathy, hereditary diffuse

light-near dissociation, causes of

limb-girdle weakness

lip, biting

lipid storage disorder of CNS

lipomatosis

lipomatosis, multiple symmetrical

Lisch nodules

liver disease

liver function enzymes

liver transplantation

lumbosacral plexopathy

lymphoma involving CNS

lymphoma, primary of CNS

lymphomatoid granulomatosis

lysosomal storage disease

macrocephaly

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

mania

maple syrup urine disease

medical-legal aspects of neurology

medulla oblongata, neoplasm of

MELAS syndrome

memory, defect of recent

memory, impairment of

meningioma

meningismus

meningitis, carcinomatous

meningoencephalopathy

mental retardation

mental retardation, familial

MERRF syndrome

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

methotrexate

methylhydrazine derivatives

metronidazole

microangiopathy, brain

microcephaly

micrographia

microhemorrhage, intracerebral

midbrain, atrophy

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

MNGIE syndrome

molecular genetics

monoamine oxidase inhibitors

mononeuropathy

mononeuropathy multiplex

mononeuropathy, children

mononeuropathy, recurrent

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI

MRI, abnormal

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, paramagnetic effect

MRI, peripheral nerve

MRI, punctate pattern

MRI, spinal cord

MRI, spine

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRS

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle culture

muscle diseases, characteristics of

muscle hypertrophy

muscle pain

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

myelopathy, chronic progressive

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

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

nerve biopsy, indication

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve culture

nerve growth factor

nerve growth stimulating activity

nerve hypertrophy

nerve root enhancement

nerve root hypertrophy

neuraminidase deficiency

neuritis

neuritis, causes of

neuroblastoma

neurocutaneous disease

neurodegeneration with brain iron accumulation

neuroendocrinology

neurofibrillary degeneration

neurofibroma

neurofibromatosis 1

neurofibromatosis 2

neurofibromatosis 2, presymptomatic

neurogenic bladder

neurogenic vs.myopathic atrophy

neuroleptic

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neuromuscular disease, electrodiagnosis of

neuromyelitis optica (Devic's disease)

neuromyelitis optica spectrum disorder

neuromyelitis optica, IgG

neuromyotonia

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal intranuclear inclusion disease

neuronal migration disorder

neuronopathy

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

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

newborn, evaluation of

next-generation sequencing

nutritional deficiency

nystagmus

nystagmus, dissociated

nystagmus, monocular

nystagmus, vertical

obesity

obsessive-compulsive disorder

ocular motility, disorders of

ocular myopathy

old age, neurology of

oligodendroglioma

ophthalmoplegia

ophthalmoplegia, progressive external

opiate

opisthotonus

optic atrophy

optic atrophy, hereditary

optic nerve

optic nerve, enlarged

optic nerve, lesion of

optic neuritis

optic neuritis, bilateral

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

optical coherence tomography

orthopnea

orthostatic hypotension

orthostatic hypotension, idiopathic

ovarian dysgenesis

pacemaker, cardiac-transvenous

pain, increased response

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraparesis, spastic, tropical

paraplegia

paresthesias

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

penicillamine

peripheral blood smear

peroneal muscle atrophy, causes of

peroneal nerve

peroneal nerve, lesion of

phosphorylase b kinase deficiency

photophobia

photosensitivity, skin

phytanic acid

PICU

pigmentary retinopathy

pimozide

pituitary, hormones of

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

pneumonia

poison, mercury

poison, neurologic problems with

polyglucosan body disease

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, chronic idiopathic

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic relapsing

polyneuropathy, familial

pons, lesion of

porphyria

portal caval shunt

positional head-hanging test

post polio syndrome

posterior leukoencephalopathy syndrome

postural abnormality

practice guidelines

Prader-Labhart-Willi syndrome

pramipexole

precipitating factors

preclinical

pregnancy, neurologic complications in

premature infant

prenatal

prenatal diagnosis by amniocentesis

presenilin-2 gene

prevention of neurologic disorders

prion disease

prion protein gene

prisoners of war, neurologic complications in

procarbazine

progeria

prognosis

progressive myoclonic epilepsy

progressive neurologic disorder

proptosis

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

pulmonary function tests

pulmonary hypertension

pulmonary infection

pulmonary infiltrates

pulvinar sign

pupil

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, scalloped

pyramidal

pyramidal tract

pyramidal tract dysfunction

quadriparesis

quadriplegia

quadriplegia, transient

quality of life

radial nerve, palsy of

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

radiculopathy

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

reading disorder, acquired

real-time quaking-induced conversion

recombinant DNA

recurrent

recurrent laryngeal nerve paralysis

renal tubular acidosis

research

respirator

respiratory depression

respiratory failure

restless leg syndrome

reversible neurologic disorder

rhabdomyosarcoma of heart

riboflavin transporter deficiency

rigidity

Riley-Day syndrome

riluzole

rippling muscle disease

saccadic eye movements, abnormal

scoliosis, neurologic association with

screening

second wind phenomena

seizure

seizure, children

seizure, complications following

seizure, diagnosis of

seizure, differential diagnosis of

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

sensory loss, leg

sensory loss, truncal

sensory nerve action potentials

sensory polyneuropathy

single photon emission computed tomography

skin, biopsy

skin, darkening of

skin, hyperextensible

skin, lesions in neurologic disorders

skin, thin

skin, translucent

sleep

sleep pathology and physiology

slit lamp examination

small vessel disease

small vessel disease, cerebral

SMN1 gene

socialisation

sodium valproate

somatosensory evoked potentials

Southern immunoblot test

spastic ataxia

spastic diplegia

spastic paraplegia, type 11

spastic paraplegia, type 15

spasticity

spastin

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, soft

Spielmeyer Vogt syndrome

spinal cord

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

splenomegaly

spondylolysis

spongy degeneration of brain

spontaneous muscle activity

spontaneous remission

stem cell transplantation

steppage gait

stereotyped behavior

stereotyped behavior, drug induced

steroid

steroid therapy, CNS treatment and complications with

stiff man syndrome

strabismus

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

subarachnoid hemorrhage

suprascapular neuropathy

sural nerve

survival motor neuron gene

symmetric brain lesions

tapetoretinal degeneration

temporal lobe, lesion

temporal lobe, lesion, bilateral

term infant

testicular atrophy

testicular enlargement

thalamus, lesion of-bilateral

tic, chronic multiple

tinnitus

tissue plasminogen activator, intravenous

titubation

toe walking

tomaculous neuropathy

tongue, biting

tongue, enlarged

tongue, fasciculations of

tongue, protrusion of

transient ischemic attack

transient neurologic deficit

trauma

treatment of neurologic disorder

tremor

tremor, cerebellar

tremor, classification

tremor, differential diagnosis of

tremor, intention

tremor, orthostatic

tremor, physiologic

tremor, post traumatic

trientine dihydrochloride

trigeminal nerve

trigeminal nerve, hypertrophy

trigeminal neuralgia

trinucleotide repeats

tuberous sclerosis, screening for

tumor suppressor gene

ultrasonography, nerve

undiagnosed

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

urinary incontinence

urine test for metabolic disorders

very long chain fatty acids

vestibular areflexia

vestibular function, tests of

vestibulopathy

vibratory sensation, abnormal

vinblastine

vincristine neurotoxicity

vision loss, sequential

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, congenital

visual loss, progressive

voice, abnormality of

Von Hippel Lindau

Von Hippel Lindau, screening protocol for

von Hippel-Lindau, screening

walking frame

walking, difficulty with

walking, difficulty with in dark

war

water channel antibodies

weakness

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

web sites

weight loss

Werdnig-Hoffman disease

Werner's syndrome

Wernicke's encephalopathy

wheelchair

white freckles

white matter disease

white matter disease, subcortical

wide based gait

winging of scapula

Wood's light

word-finding difficulty

X-linked bulbospinal neuronopathy

x-linked intellectual deficit

x-linked mental retardation

X-linked neuropathy

x-ray, spine

zinc

Showing articles 200 to 250 of 4304 << Previous Next >>

Molecular Genetic Advances in Fragile X Syndrome
J Pediatr 122:169-185, Tarleton,J.C.&Saul,R.A., 1993

Late-Onset Friedreich's Ataxia, Molecular Genetics, Clinical Neurophysiology, and Magnetic Resonance Imaging
Arch Neurol 50:803-806, Klockgether,T.,et al, 1993

The DNA Laboratory and Neurolgoical Practice
JNNP 56:229-233, Harding,A., 1993

Werner's Syndrome Associated with Spastic Paraparesis and Peripheral Neuropathy
Neurol 43:1252-1254, Umehara,F.,et al, 1993

Clinical Consequences of Isolating the Gene for Huntington's Disease
BMJ 307:397-398, Harper,P.S., 1993

Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease)
NEJM 329:241-245, Tsujino,S.,et al, 1993

Hereditary Motor-Sensory Neuropathy (Charcot-Marie-Tooth Disease) with Nerve Deafness:A New Variant
J Pediatr 123:431-434, Hamiel,O.P.,et al, 1993

Charcot-Marie-Tooth Disease Type 1A:Association with a Spontaneous Point Mutation in the PMP22 Gene
NEJM 329:96-101, Roa,B.B.,et al, 1993

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

Giant Axonal Neuropathy:Progressive Clinical and Radiologic CNS Involvement
Neurol 42:2220-2221, Richen,P.&Tandan,R., 1992

Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1)
Ann Neurol 31:570-572, Hallam,P.J.,et al, 1992

De-Novo Mutation in Hereditary Motor and Sensory Neuropathy Type I
Lancet 339:1081-1082, Hoogendijk,J.E.,et al, 1992

Genetic Diagnosis of Gaucher's Disease
Lancet 339:889-892, Mistry,P.K.,et al, 1992

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

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

Familial Neurofibromatosis Type 1:Clinical Experience with DNA Testing
J Pediatr 120:394-398, Hofman,K.J.&Boehm,C.D., 1992

Detection of Full Fragile X Mutation
Lancet 339:271-272, Pergolizzi,R.G.,et al, 1992

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

Myelopathy Associated with Human T Cell Lymphotropic Virus Type 1 in a White European Native to England
BMJ 305:453, Ali,A.&Rudge,P., 1992

Unstable DNA Sequence in Myotonic Dystrophy
Lancet 339:1125-1128, Harley,H.G.,et al, 1992

Use of CT, MRI, & Localized 1H MR Spectroscopy in Canavan's Disease:A Case Report
Ann Neurol 30:106-110, Marks,H.G.,et al, 1991

Globoid Cell Leukodystrophy:A Family with Both Late-Infantile and Adult Type
Neurol 41:1382-1384, Verdru,P.,et al, 1991

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

Lisch Nodules in Neurofibromatosis Type I
NEJM 324:1264-1266, 1283-12851991., Lubs,M-L.E.,et al, 1991

Corticosteroid-Responsive Dominantly Inherited Neuropathy in Childhood
Neurol 41:437-439, Bird,S.J.&Sladky,J.T., 1991

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

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Welander's Distal Myopathy:Clinical Neurophysiol & Muscle Biopsy Obser in Young & Middle Aged Adults with Early Symptoms
JNNP 54:494-498, Borg,K., 1991

Preclinical Detection of Parkinson's Disease
Neurology Suppl 2, 41:5-921991., Koller,W.C.&Langston,J.W., 1991

Classification and Treatment of Tremor
JAMA 266:1115-1117, Hallett,M., 1991

Fucosidosis Revisited:A Review of 77 Patients
Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991

Improved Molecular-Genetic Diagnosis of Leber's Hereditary Optic Neuropathy
NEJM 323:1488-1489, Johns,D.R., 1990

Polyneuropathy, Ophthalmoplegia, Leukoencephalopathy, and Intestinal Pseudo-Obstruction:POLIP Syndrome
Ann Neurol 28:349-360, Simon,L.T.,et al, 1990

Genetic Linkage of Hereditary Motor & SensoryNeuro Type I (Charcot-Marie-Tooth Disease) to Chrom 1 & 17
Neurol 40:1450-1453, Defesche,J.C.,et al, 1990

Tangier Disease in a Black Patient:An Unusual Clinical Presentation
Am J Med 89:105-108, Lo,W.D.,et al, 1990

Hereditary Motor and Sensory Neuropathies and Hereditary Spastic Paraplegia:A Magnetic Stimulation Study
Ann Neurol 28:43-49, Claus,D.,et al, 1990

Familial Multiple Symmetric Lipomatosis with Peripheral Neuropathy
Neurol 40:1246-1250, Chalk,C.H.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Neurologic Crises in Hereditary Tyrosinemia
NEJM 322:432-437, Mitchell,G.,et al, 1990

Peripheral Neuropathy in Amyotrophic Chorea-Acanthocytosis
Ann Neurol 26:583-587, Vista,G.,et al, 1989

Hereditary Sensory Neuropathy with Deafness:A Familial Multisystem Atrophy
Neurol 39:244-248, Horoupian,D.S., 1989

Molecular Genetics of Amyloid Neuropathy in Europe
Lancet 1:524-526, Holt,I.J.,et al, 1989

Ethanol and the Nervous System
NEJM 321:442-454, Charness,M.E.,et al, 1989

Respiratory Muscle Weakness in Charcot-Marie-Tooth Disease, A Field Study
Arch Int med 149:1389-1391, Nathanson,B.N.,et al, 1989

Hereditary Motor & Sensory Neuropathy with Optic Atrophy, Ultrastructural and Morphometic Observations
Arch Neurol 46:973-977, Sommer,C.&Schroder,J.M., 1989

Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I
Neurol 39:1173-1177, Rosen,S.A.,et al, 1989

Refsum Disease
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989

REcurrent Familial Brachial Plexus Palsies as the ONly Clinical Expression of'Tomaculous'Neuropathy
Eur Neurol 29:61-66, Martinelli,P.,et al, 1989

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