Neudle.com: hereditary peripheral neuropathy

Differential
(Click to cross reference)

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, 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.)

clonus

clubfoot as related to neurologic disease

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

DNA probes

dopamine agonist

drooling

drug abuse, inhalation

drug induced neurologic disorders

dysarthria

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

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

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

laminectomy, lumbar

laminopathies

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, impairment of

meningioma

meningismus

meningoencephalopathy

mental retardation

MERRF syndrome

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

methotrexate

methylhydrazine derivatives

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

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, 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, 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

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 infiltrates

pupil

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, scalloped

pyramidal

pyramidal tract dysfunction

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

RFLPs

riboflavin transporter deficiency

saccadic eye movements, abnormal

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory loss

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

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

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 50 to 100 of 5139 << Previous Next >>

Indications and Usefulness of Nerve Biopsy
Arch Neurol 59:1532-1535, Said,G., 2002

Recessive Ataxia With Ocular Apraxia
Arch Neurol 58:201-205,173, Barbot,C.,et al, 2001

Clinical Spectrum of Chronic Acquired Demyelinating Polyneuropathies
Muscle & Nerve 24:311-324, Saperstein,D.S.,et al, 2001

Disability and Quality of Life in Charcot-Marie-Tooth Disease Type 1
JNNP 70:548-550, Pfeiffer,G.,et al, 2001

Acute Vocal Cord Paralysis in Hereditary Neuropathy With Liability to Pressure Palsies
Neurol 56:1415, Okhoshi,N.,et al, 2001

Craniofacial and Cutaneous Findings Expand the Phenotype of Hereditary Neuralgic Amyotrophy
Neurol 57:1963-1968, Jeannet,P.,et al, 2001

MR Imaging of the Cauda Equina in Hereditary Motor Sensory Neuropathies: Correlations with Sural Nerve Biopsy
AJNR 21:1793-1798,1779, Cellerini,M.,et al, 2000

Cardiac Dysfunction in Neuromuscular Diseases
The Neurologist 6:67-82, Pourmand,R., 2000

Hereditary Recurrent Focal Neuropathies, Clinical and Molecular Features
Neurol 54:546-551, Stogbauer,F.,et al, 2000

The Roussy-Levy Family:From the Original Description to the Gene
Ann Neurol 46:770-773, Plante-Bordeneuve,V.,et al, 1999

Hypertrophy of Multiple Cranial Nerves and Spinal Roots in Chronic Inflammatory Demyelinating Neuropathy
JNNP 67:685-687, Duarte,J.,et al, 1999

MR Imaging of Dejerine-Sottas Disease
AJNR 20:378-380, Make,D.D.,et al, 1999

Compression of Spinal Cord and Cauda Equina in Charcot-Marie-Tooth Disease Type 1A
Neurol 52:890-891, Butefisch,C.,et al, 1999

Is There a Familial Carpal Tunnel Syndrome? An Evaluation and Literature Review
Muscle & Nerve 21:1533-1536, Gossett,J.G.&Change,P.F., 1998

PCR-Based Strategy for Dx of Hered Neuropathy with Liability to Pressure Palsies & Charcot-Marie-Tooth Dis Type 1A
Neurol 50:760-763, Young,P.,et al, 1998

Detection of a Varient Protein in Hair:New Diagnostic Method in Portuguese Type Familial Amyloid Polyneuropathy
BMJ 316:1500-1501, Ando,Y.,et al, 1998

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

Facial Nerve is Liable to Pressure Palsy
Neurol 51:320-322, Foloni,T.E.,et al, 1998

Localization of the Giant Axonal Neuropathy Gene to Chromosome 16q24
Ann Neurol 43:143-148, Flanigan,K.M.,et al, 1998

Neurogenic Muscle Hypertrophy
Muscle & Nerve 19:811-818996., Gutmann,L., 1996

Clinicopath Conf
Tangier Disease, Case 16-1996, NEJM 334:1389-1394996., , 1996

Mapping of Hereditary Neuralgic Amyotrophy (Familial Brachial Plexus Neuropathy) to Distal Chromosome 17q
Neurol 46:1128-1132, Pellegrino,J.E.,et al, 1996

Phenotypic Heterogen in Hered Neurop with Liability to Press Palsies Assoc with Chromosome 17p11. 2-12 Delet
Neurol 46:1133-1137, Pareyson,D.,et al, 1996

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

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

Isolated Vitamin E Deficiency
Muscle & Nerve 19:1161-1165996., Jackson,C.E.,et al, 1996

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

Clin Electrophy & Molec Correl in 13 Families with Hered Neurop with Liabil to Press Palsies & Chromosome 17p11. 2 Deletion
Neurol 45:2018-2023, Gouider,R.,et al, 1995

Acute Anterior Interosseous Neuropathy in Pt with Hereditary Neuropathy with Liability to Press Palsies:Clin & EMG Study
Muscle & Nerve 18:1329-1331995., Felice,K.J., 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Hereditary Sensory and Autonomic Neuropathy with Cataracts, Mental Retardation, and Skin Lesions:Five Cases
Neurol 45:1405-1408, Heckmann,J.M.,et al, 1995

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

DNA Analysis in Finnish Patients with Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)
JNNP 57:1260-1262, Silander,K.,et al, 1994

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

A Sproadic Form of Hereditary Neuropathy with Liability to Pressure Palsies:Clin, Electrodiag & Molecular Genetic Findings
Neurol 44:753-755, Reisecker,F.,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

Cerebral Involvement in McLeod Syndrome
Neurol 44:117-120, Danek,A.,et al, 1994

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

Hered Neuralgic Amyotrophy & Hered Neuropathy with Liability to Pressure Palsies:Distinct Clin, Electrophy & Genetic Entities
Neurol 44:2250-2252, Gouider,R.,et al, 1994

Hereditary Neuralgic Amyotrophy & Hereditary Neuropathy with Liability to Pressure Palsies:Distinct Genetic Dis
Neurol 44:2253-2257, Chance,P.F.,et al, 1994

Erythromelalgia:Association with Hereditary Sensory Neuropathy and Response to Amitriptyline
Neurol 43:621-622, Herskovitz,S.,et al, 1993

Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
Neurol 33:4-9, Nishino,H.,et al, 1993

Inherited Primary Peripheral Neuropathies
JAMA 270:2326, 23301993., Lupski,J.R.,et al, 1993

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

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

Showing articles 50 to 100 of 5139 << Previous Next >>