Neudle.com: hereditary peripheral neuropathy

Differential
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abdominal distention

abducens nerve paralysis

acanthocytosis

acoustic nerve

acoustic nerve, vestibular division of

acral sensory symptoms

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alcohol

alcohol intolerance

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.

altered states of consciousness

alternating rapid movement

amyloid angiopathy, cerebral

amyloidosis

amyloidosis, oculoleptomeningeal, familial

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

anemia

ankle reflex, absent

anosmia

anterior interosseous neuropathy

anterior tibial muscle weakness

antimetabolite

aphasia

apraxia of eye movements

areflexia

arm atrophy

arm weakness

Arnold Chiari malformation

arrhythmia, cardiac

arteritis, temporal

arthralgia

arthrogryposis multiplex

arthropathy

arthropathy, neuropathic

ataxia telangiectasia

atherosclerosis, premature

atonic bladder

auditory evoked brainstem potentials

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

Bassen-Kornzweig syndrome

behavioral disorder

benign essential tremor

blood dyscrasias, neurologic findings with

brachial neuritis

brachial neuritis, acute

brachial neuritis, bilateral

brachial neuritis, prognosis of

brachial plexus

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brainstem

brainstem, atrophy

brainstem, dysfunction

brainstem, lesion of

Brown-Vialetto-Van Laere syndrome

calcification, intracranial

caloric testing

carcinoembryonic antigen

carcinoma

cardiomyopathy

carotid angiogram

carpal tunnel syndrome

CAT scan

CAT scan, abnormal

CAT scan, base of skull

CAT scan, metrizamide

CAT scan, myelogram with

cataracts

cataracts, congenital

cauda equina

cauda equina, enhancement

cauda equina, lesion of

caudate nucleus

caudate nucleus, atrophy

cavernous sinus

cavernous sinus, lesion of

central core disease

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

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 edema

cerebral infarction, subcortical

cerebral palsy

cerebritis

cerebro hepato renal syndrome

cerebrospinal fluid, abnormal

cerebrospinal fluid, culture of, viral

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, pressure low

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chromosomal abnormality

chronic progressive external ophthalmoplegia

cirrhosis

cirrhosis, infancy

claudication, intermittent of cauda equina

cleft palate

Clinical Pathologic Conference(C.P.C.)

compression neuropathy

compression neuropathy, recurrent

conduction block

congestive heart failure

corpus callosum, lesion of

corpus callosum, thinning

cough

cranial nerve enhancement

cranial nerve enlargement

cranial nerve palsies

cranial nerve palsies, familial

cranial nerve tumor

cranial nerves

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

crying

Cuba

cytochrome c oxidase

cytochrome c oxidase, deficiency

deafness

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

deep tendon reflexes

degenerative diseases of CNS

Dejerine-Sottas syndrome

dementia

dementia, childhood

dementia, rapidly progressive

demyelinating disease

denervation of muscle

dermatitis

dermatomyositis

developmental milestones, loss of

diabetes mellitus

diarrhea

differential diagnosis

diplegia, brachial

diplopia

diplopia, transient

disability, neurological

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

drug abuse, inhalation

drug induced neurologic disorders

dysarthria

dysdiadochokinesia

dyskinesia, buccal lingual facial

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electroencephalogram, inflammatory disease

electromyogram

electron microscopy

electronystagmography

electroretinograph

emergencies, neurologic

Emery-Dreifuss muscular dystrophy

encephalopathy

endarterectomy, carotid

enophthalmous

entrapment neuropathy

enzyme, defect

enzyme, muscle disease

ependymoma

epidemiology of neurology

episodic neurologic deficits

extraocular muscle lesion

eye movement, disorders of

Fabry's disease

face, numbness of

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, familial

facial nerve palsy, recurrent

facial pain

facial weakness

facial weakness, bilateral

fatty acid, elevated plasma content

Fazio-Londe's disease

fetal alcohol syndrome

fever

fibrillations

fine motor function, impaired

finger nose finger test

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

frataxin

Friedreich's ataxia

frontal lobe, pathologic signs of

fundus, abnormality of

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genu of corpus callosum

giant axonal neuropathy

globoid cells

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucose tolerance test, abnormal

glycogen storage disease

granulomatosis with polyangiitis

granulomatous disease

growth retardation

Guillain Barre syndrome

hair analysis

Hallervorden Spatz disease

hearing problems in children

heart block

heavy metal intoxication

heel-knee-shin test

hemianopia

hemiparesis

hemiparesis, transient

hemiplegia

hemochromatosis

hemochromatosis, primary

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hepatic encephalopathy

hepatic failure

hepatitis C virus

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

human immunodeficiency virus type 1

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

hyperinsulinism

hyperostosis

hyperostosis cranialis interna

hypoglossal nerve paralysis

hypogonadism

hypogonadism, hypogonadotropic

hypotension, systemic

hypotonia

idiopathic polyneuropathy

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

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

incoordination

infection

intellectual deficit

intellectual deterioration

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracranial pressure, increased

intrinsic hand muscles, wasting of

Kearns-Sayre syndrome

keratitis

klippel feil syndrome

Korsakoff's psychosis

Krabbe's disease

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lacunar infarction

laminectomy, cervical

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

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

light-near dissociation, causes of

lip, biting

lipid storage disorder of CNS

lipomatosis

lipomatosis, multiple symmetrical

liver disease

liver transplantation

LMNA gene

long thoracic nerve

lumbosacral plexopathy

lumbosacral plexus

lymphadenopathy

lymphoma

lymphoma involving CNS

lymphomatoid granulomatosis

macular degeneration

magnetic stimulation

magnetic stimulation, brain

Marinesco-Sjogren syndrome

memory, defect of recent

memory, impairment of

meningioma

meningismus

meningoencephalopathy

mental retardation

MERRF syndrome

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

methotrexate

methylhydrazine derivatives

methylmalonic acid, serum

microcephaly

microhemorrhage, intracerebral

midbrain, atrophy

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine

misdiagnosis

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

MNGIE syndrome

molecular genetics

monoamine oxidase inhibitors

monoclonal gammopathy

mononeuropathy

mononeuropathy multiplex

mononeuropathy, children

mononeuropathy, recurrent

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, brachial plexus

MRI, contrast enhanced

MRI, cranial nerves

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, functional

MRI, peripheral nerve

MRI, spinal cord

MRI, spine

MRS

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle culture

muscle diseases, characteristics of

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

muscular dystrophy, congenital

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenic crisis

myelin protein zero gene

myelopathy, chronic progressive

myopathy, carcinomatous

myopathy, distal

myopathy, distal, Welander's

myopathy, mitochondrial

myopathy, thyroid disease causing

neoplasm, peripheral nerve

neoplasm, primary of CNS

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, causes of

neuroblastoma

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurofibroma

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, burden

neurologic disease, diagnoses of

neuromuscular disease, electrodiagnosis of

neuromyotonia

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronopathy

neuronopathy, sensory

neuropathology

neuropathology, brain

neuropathy

neuropathy, amyloid

neuropathy, ataxic

neuropathy, classification of

neuropathy, demyelinating

neuropathy, diabetic

neuropathy, etiologies of

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, medication induced

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

neurotoxin

neurotrophin-3

neutropenia

next-generation sequencing

nutritional deficiency

nystagmus

nystagmus, dissociated

nystagmus, gaze-evoked

nystagmus, vertical

ocular motility, disorders of

ophthalmoplegia

ophthalmoplegia, progressive external

opisthotonus

optic atrophy

optic atrophy, hereditary

optic nerve

optic nerve, enlarged

optic nerve, lesion of

optic neuropathy

optical coherence tomography

orthostatic hypotension

orthostatic hypotension, idiopathic

osteosclerosis, autosomal dominant

ovarian dysgenesis

pacemaker, cardiac-transvenous

paraparesis, familial spastic

paresthesias, lower extremity

Parkinson disease

Parkinson disease, classification

Parkinson disease, etiology of

Parkinson disease, heterogeneity of

Parkinson disease, pathogenesis of

Parkinson disease, subtypes

Parkinsonism syndrome

past pointing

pathology

patient information and support

peroneal muscle atrophy, causes of

peroneal nerve

peroneal nerve, lesion of

photosensitivity, skin

phytanic acid

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pneumonia

poison, mercury

poison, neurologic problems with

POLG1 gene

poliomyelitis

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, chronic idiopathic

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic relapsing

polyneuropathy, familial

pons, lesion of

porphyria

positional head-hanging test

positive sharp waves

post polio syndrome

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prisoners of war, neurologic complications in

procarbazine

progeria

prognosis

progressive neurologic disorder

proptosis

proximal muscle atrophy

pseudobulbar palsy

pseudoxanthoma elasticum

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

pulmonary function tests

pulmonary infection

pulmonary infiltrates

pupil

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, scalloped

pyramidal

pyramidal tract

pyramidal tract dysfunction

pyridoxine deficiency

quadriparesis

quadriplegia

quadriplegia, transient

quality of life

radial nerve, palsy of

radiation hypersensitivity

radiculopathy

ragged-red fibers

rash

reading disorder, acquired

recurrent laryngeal nerve paralysis

refractive errors

Refsum's disease

remote effect of cancer on the nervous system

renal tubular acidosis

respiratory depression

respiratory failure

restless leg syndrome

reversible neurologic disorder

review article

RFC1 gene

RFLPs

riboflavin transporter deficiency

saccadic eye movements, abnormal

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory loss

sensory loss, leg

sensory loss, truncal

sensory nerve action potentials

sensory polyneuropathy

serratus anterior muscle, weakness

single photon emission computed tomography

skin, biopsy

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep

small vessel disease

small vessel disease, cerebral

somatosensory evoked potentials

speech disorder, childhood

speech disorder, non aphasic

spinal cord

spinal cord, compression of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, intramedullary

spinal cord, pathologic exam of

spinal muscular atrophy

spinal stenosis

spinal stenosis, familial

spinocerebellar ataxia

spinocerebellar ataxia type 2

spinocerebellar ataxia type 7

spinocerebellar degeneration

splenium of corpus callosum

splenomegaly

spontaneous muscle activity

spontaneous remission

steppage gait

steroid therapy, CNS treatment and complications with

stiff man syndrome

striatum, lesion of

strokelike episodes

subarachnoid hemorrhage

subdural hematoma

substantia nigra

sudden death

suprascapular neuropathy

sural nerve

symmetric brain lesions

tapetoretinal degeneration

tauopathy

telangiectases

thalamus, lesion of

thalamus, lesion of-bilateral

tomaculous neuropathy

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

trigeminal nerve, hypertrophy

trigeminal neuralgia

trinucleotide repeats

tyrosine

tyrosinemia

ulnar neuropathy

ultrasonography, nerve

vestibular function, tests of

vestibulopathy

vibratory sensation, abnormal

vinblastine

vincristine neurotoxicity

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, congenital

voice, abnormality of

Von Hippel Lindau

walking frame

walking, difficulty with

walking, difficulty with in dark

war

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 matter disease

white matter disease, subcortical

Showing articles 2950 to 3000 of 5264 << Previous Next >>

Complete Genomic Screen in Late-Onset Familial Alzheimer Disease, Evidence for a New Locus on Chromosome 12
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Idiopathic Granulomatous Angiitis of the CNS Manifesting as Diffuse White Matter Disease
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Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
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Magnetic Resonance Imaging of the Brachial Plexus in Patients with Multifocal Motor Neuropathy
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Cordarone (Amiodarone)
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Preliminary Results of Linear Accelerator Radiosurgery for Acoustic Schwannomas
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Epidural Corticosteroid Injections for Sciatica Due to Herniated Nucleus Pulposus
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The X-Linked Infantile Spasms Syndrome (MIM 308350) Maps to Xp11. 4-Xpter in Two Pedigrees
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Predictors of Recurrent Febrile Seizures
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The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
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Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
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Gradenigo Syndrome in a Human Immunodeficiency Virus-Positive Patient
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Multiple-System Atrophy is Genet Distinct from Ident Inherited Causes of Spinocerebellar Degen
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Olfactory Dysfunction in Familial Parkinsonism
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Clinicopath Conf
Large B-Cell Lymphoma with Subarachnoid & Periph Nr Invol (Neurolymphomatosis) Case 39-1997, NEJM 33, :1829,1997., 1997

Chronic Inflammatory Demyelinating Polyradiculoneuropathy in Children
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Mutations in the Sarcoglycan Genes in Patients with Myopathy
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Brachial Plexus Neuropathy After Botulinum Toxin Injection
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Ocular Findings in Ramsay Hunt Syndrome
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A News Locus for Hemiplegic Migraine Maps to Chromosome 1q31
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An Acute Neurologic Syndrome Temporally Associated with Postexposure Trtm of Rabies
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Guillain-Barre Syndrome Following Allogeneic Bone Marrow Transplantation
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Treatment of Gustatory Sweating with Botulinum Toxin
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The 5-Year Risk of MS After Optic Neuritis
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Diagnosis of Chronic Manganese Intoxication by Magnetic Resonance Imaging
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CT and MR Findings of Neuroacanthocytosis
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Clinicopath Conf
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Clinicopath Conf
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Showing articles 2950 to 3000 of 5264 << Previous Next >>