Neudle.com: hereditary peripheral neuropathy

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Differential
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abdominal distention

abducens nerve paralysis

acoustic nerve, vestibular division of

acral sensory symptoms

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

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 rapid movement

aminoacidopathies

amyloid angiopathy, cerebral

amyloidosis, oculoleptomeningeal, familial

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

ankle reflex, absent

anterior interosseous neuropathy

anterior tibial muscle weakness

apraxia of eye movements

Arnold Chiari malformation

arrhythmia, cardiac

arteritis, temporal

arthrogryposis multiplex

arthropathy, neuropathic

arylsulfatase A

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

atherosclerosis, premature

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

axonal degeneration

B 12 deficiency

bacterial infection

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

Bassen-Kornzweig syndrome

behavioral disorder

benign essential tremor

bicaudate index

biologic markers

bladder dysfunction

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, atrophy

brainstem, dysfunction

brainstem, lesion of

Brown-Vialetto-Van Laere syndrome

burning paresthesia

calcification, intracranial

caloric testing

carcinoembryonic antigen

carotid angiogram

carpal tunnel syndrome

CAT scan, abnormal

CAT scan, base of skull

CAT scan, metrizamide

CAT scan, myelogram with

cataracts, congenital

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 infarction, subcortical

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

cholesterol, HDL

chorea, familial

choreoathetosis

chromosomal abnormality

chronic progressive external ophthalmoplegia

cirrhosis, infancy

claudication, intermittent of cauda equina

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

Cockayne's syndrome

cold temperature

compression neuropathy

compression neuropathy, recurrent

conduction block

congestive heart failure

contractures, joint

cornea, abnormal

cornea, opacity of

corneal dystrophy

corpus callosum, lesion of

corpus callosum, thinning

cranial nerve enhancement

cranial nerve enlargement

cranial nerve palsies

cranial nerve palsies, familial

cranial nerve tumor

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cytochrome c oxidase

cytochrome c oxidase, deficiency

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

deep tendon reflexes

degenerative diseases of CNS

Dejerine-Sottas syndrome

dementia, childhood

dementia, rapidly progressive

demyelinating disease

denervation of muscle

dermatomyositis

developmental milestones, loss of

diabetes mellitus

differential diagnosis

diplegia, brachial

diplopia, transient

disability, neurological

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dopamine agonist

down-beat nystagmus

drug abuse, inhalation

drug induced neurologic disorders

dysdiadochokinesia

dyskinesia, buccal lingual facial

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electroencephalogram, inflammatory disease

electron microscopy

electronystagmography

electroretinograph

emergencies, neurologic

Emery-Dreifuss muscular dystrophy

endarterectomy, carotid

entrapment neuropathy

enzyme, muscle disease

epidemiology of neurology

episodic neurologic deficits

erythromelalgia

evoked potentials

exercise intolerance

exome sequencing

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 weakness

facial weakness, bilateral

failure to thrive

family planning

fatty acid, elevated plasma content

Fazio-Londe's disease

fetal alcohol syndrome

fine motor function, impaired

finger nose finger test

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

Friedreich's ataxia

frontal lobe, pathologic signs of

fundus, abnormality of

F-wave response

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic counselling

genetic diagnosis

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genu of corpus callosum

giant axonal neuropathy

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

Hallervorden Spatz disease

hearing problems in children

heavy metal intoxication

heel-knee-shin test

hemiparesis, transient

hemochromatosis

hemochromatosis, primary

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hepatic encephalopathy

hepatic failure

hepatitis C virus

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

high arched feet

Horner's syndrome

H-reflex testing

human immunodeficiency virus type 1

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

hyperinsulinism

hyperostosis cranialis interna

hypertriglyceridemia

hypofibrinogenemia

hypoglossal nerve paralysis

hypogonadism, hypogonadotropic

hypotension, systemic

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

intellectual deficit

intellectual deterioration

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracranial pressure, increased

intrinsic hand muscles, wasting of

Isaacs syndrome

Kearns-Sayre syndrome

klippel feil syndrome

Korsakoff's psychosis

Krabbe's disease

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lacunar infarction

laminectomy, cervical

laminectomy, lumbar

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

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

leukoencephalopathy

Lhermitte's sign

light-near dissociation, causes of

lipid storage disorder of CNS

lipomatosis, multiple symmetrical

liver transplantation

long thoracic nerve

lumbosacral plexopathy

lumbosacral plexus

lymphadenopathy

lymphoma involving CNS

lymphomatoid granulomatosis

macular degeneration

magnetic stimulation

magnetic stimulation, brain

Marinesco-Sjogren syndrome

McLeod syndrome

median neuropathy

memory, defect of recent

memory, impairment of

meningoencephalopathy

mental retardation

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

methylhydrazine derivatives

methylmalonic acid, serum

microhemorrhage, intracerebral

midbrain, atrophy

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

molecular genetics

monoamine oxidase inhibitors

monoclonal gammopathy

mononeuropathy multiplex

mononeuropathy, children

mononeuropathy, recurrent

motor neuron disease

movement disorder

movement disorder, extrapyramidal

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

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle diseases, characteristics of

muscle hypertrophy

muscle tenderness

muscle weakness

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

myelogram, cervical

myeloneuropathy

myelopathy, chronic progressive

myeloradiculopathy

myopathy, alcoholic

myopathy, carcinomatous

myopathy, distal

myopathy, distal, Welander's

myopathy, mitochondrial

myopathy, thyroid disease causing

myotonia dystrophica

nausea and vomiting

neoplasm, peripheral nerve

neoplasm, primary of CNS

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

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, burden

neurologic disease, diagnoses of

neuromuscular disease, electrodiagnosis of

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronopathy, sensory

neuropathology, brain

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

next-generation sequencing

night blindness

nitrogen mustard

numbness, extremity

nutritional deficiency

nystagmus, dissociated

nystagmus, gaze-evoked

nystagmus, vertical

ocular motility, disorders of

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy, hereditary

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

pain, abdominal

pain, neuropathic

paralysis, recurrent

paraparesis, familial spastic

paraparesis, spastic

paresthesias, feet

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

patient information and support

peroneal muscle atrophy, causes of

peroneal nerve, lesion of

peroxisomal disease

Perrault syndrome

pheochromocytoma

photosensitivity, skin

pigmentary retinopathy

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

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

progressive neurologic disorder

proximal muscle atrophy

pseudobulbar palsy

pseudoxanthoma elasticum

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

ptosis, bilateral

pulmonary function tests

pulmonary infection

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, scalloped

pyramidal tract

pyramidal tract dysfunction

pyridoxine deficiency

quadriplegia, transient

quality of life

radial nerve, palsy of

radiation hypersensitivity

ragged-red fibers

reading disorder, acquired

recombinant DNA

recruitment, reduced

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

retina, abnormal

retinal degeneration

retinitis pigmentosa

reversible neurologic disorder

riboflavin transporter deficiency

Riley-Day syndrome

root lesion, nerve

Roussy Levy syndrome

saccadic eye movements, abnormal

self-mutilation

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory loss, leg

sensory loss, truncal

sensory nerve action potentials

sensory polyneuropathy

serratus anterior muscle, weakness

shoulder, numbness

shoulder, pain in

Shy-Drager syndrome

single photon emission computed tomography

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray, abnormal

small vessel disease

small vessel disease, cerebral

somatosensory evoked potentials

spastic diplegia

speech disorder

speech disorder, childhood

speech disorder, non aphasic

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

spontaneous muscle activity

spontaneous remission

steroid therapy, CNS treatment and complications with

stiff man syndrome

striatum, lesion of

strokelike episodes

subarachnoid hemorrhage

subdural hematoma

substantia nigra

suprascapular neuropathy

symmetric brain lesions

systemic illness

tandem gait, ataxic

Tangier's disease

tapetoretinal degeneration

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

tomaculous neuropathy

tongue, enlarged

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

trigeminal nerve

trigeminal nerve, hypertrophy

trigeminal neuralgia

trinucleotide repeats

ulnar neuropathy

ultrasonography, nerve

upgaze, paralysis of

urinary incontinence

Usher's syndrome

vestibular areflexia

vestibular function, tests of

vibratory sensation, abnormal

vincristine neurotoxicity

viral infection

viral infection, CNS

viral isolation

visceral neuropathy

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss, congenital

vitamin deficiency

vitamin E deficiency

vitreous opacities

vocal cord paralysis

voice, abnormality of

Von Hippel Lindau

walking, difficulty with

walking, difficulty with in dark

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

xeroderma pigmentosa

X-linked neuropathy

Showing articles 3000 to 3050 of 5264 << Previous Next >>

CT-Guided Brachial Plexus Biopsy
AJNR 18:1420-1422, Cole,J.W.,et al, 1997

Gabapentin for Idiopathic Trigeminal Neuralgia:Report of Two Cases
Neurol 48:1467, Sist,T.,et al, 1997

Clinical Effectiveness of Lamotrigine and Plasma Levels in Essential and Symptomatic Trigeminal Neuralgia
Neurol 48:1714-1717, Lunardi,G.,et al, 1997

Neuro-Ophthalmic Manifestations of Lyme Disease
J Neuro-Ophthalmol 17:108-121, Balcer,L.J.,et al, 1997

Various Types of Hereditary Inclusion Body Myopathies Map to Chromosome 9p1-q1
Ann Neurol 41:548-551, Argov,Z.,et al, 1997

Gene Locus for Autosomal Recessive Distal Myopathy with Rimmed Vacuoles Maps to Chromosome 9
Ann Neurol 41:432-437, Ikeuchi,T.,et al, 1997

Familial Nature and Continuing Morbidity of the Amyotrophic Lateral Sclerosis-Parkinsonism Dementia Complex of Guam
Neurol 49:400-409, McGeer,P.L.,et al, 1997

Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
Neurol 49:568-572, Parboosingh,J.S.,et al, 1997

Calcium Channels in Neurological Disease
Ann Neurol 42:275-282, Greenberg,D.A., 1997

Comparison of First Degree Relatives and Spouses of Poeple with Chronic Tension Headache
BMJ 314:1092-1093, Ostergaard,S.,et al, 1997

Turning a Blind Eye
Lancet 349:1740, Bapat,V.N.&Tendolkar,A.G., 1997

Apolipoprotein E e4 Associated with Chronic Traumatic Brain Injury in Boxing
JAMA 278:136-140, Jordan,B.D.,et al, 1997

Brachial Neuritis Following Routine Childhood Immunizatioon for DTP:Two Cases & Review of Literature
Pediatrics 99:602-603, Hamati-Haddad,A.&Fenichel,G., 1997

Clinicopath Conf
Nonbact Thrombotic Endocarditis, Aortic Valve, with Cerebral, Renal & Splenic Emboli & Multiple Infa, cts, CA se 28-1997,NEJM 337:770-777,1997., 1997

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

Endolymphatic Sac Tumors, A Source of Morbid Hearing Loss in von Hippel-Lindau Disease
JAMA 277:1461-1466, Manski,T.J.,et al, 1997

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

Unusual Clinical Features and Early Brain MRI Lesions in a Family with Cerebral Autosomal Dominant Arteriopathy
Neurol 48:1200-1203, Malandrini,A.,et al, 1997

Inflammation, Aspirin, and the Risk of Cardiovascular Disease in Apparently Healthy Men
NEJM 336:973-979, 1014-10161997., Ridker,P.M.,et al, 1997

Atypical MRI Features of Wilson's Disease:High Signal in Globus Pallidus on T1-Weighted Images
Neuroradiology 39:171-174, Mochizuki,H.,et al, 1997

Offspring Recurrence Rates and Clinical Characteristics of Conjugal Multiple Sclerosis
Lancet 349:1587-1590, Robertson,N.P.,et al, 1997

Frataxin Gene of Friedreich's Ataxia is Targeted to Mitochondria
Ann Neurol 42:265-269, Priller,J.,et al, 1997

High-Frequency Unilateral Thalamic Stimulation in the Treatment of Essential and Parkinsonian Tremor
Ann Neurol 42:292-299, Koller,W.,et al, 1997

Clinical Characteristics of a Chromosome 17-Linked Rapidly Progressive Familial Frontotemporal Dementia
Arch Neurol 54:539-544, Basun,H.,et al, 1997

Clinical and Radiologic Findings in Progressive Facial Hemiatrophy (Parry-Romberg Syndrome)
AJNR 18:751-757, Cory,R.C.,et al, 1997

Patterns of Sensory Dysfunction in Lateral Medullary Infarction, Clinical-MRI Correlation
Neurol 49:1557-1563, Kim,J.S.,et al, 1997

Adult-Onset Krabbe Disease with Mutation in the Galactocerebrosidase Gene, MRI of Corticospinal Tract Demyelin
Neurol 49:1392-1399, Satoh,J.-I.,et al, 1997

"Idiopathic"Cranial Hypertrophic Pachymeningitis Responsive to Antiotuberculous Therapy:Case Report
Neurosurg 41:965-971, Parney,I.F.,et al, 1997

Sympathetic Cardioneuropathy in Dysautonomias
NEJM 336:696-702, 7211997., Goldstein,D.S.,et al, 1997

Linkiage of Locus for Cerebral Cavernous Hemagiomas to Chromosome 7q in 4 Families of Mexican-American Descent
Neurol 48:752-757, Polymeropoulos,M.H.,et al, 1997

Familial Intracranial Aneurysms
Lancet 349:380-384, Ronkainen,A.,et al, 1997

Pathogenesis of Acute Monocular Blindness from Leaking Anterior Communicating Artery Aneurysms
Neurol 48:680-683, Chan,J.W.,et al, 1997

Pupil-Involving Third-Nerve Palsy and Carotid Stenosis:Rapid Recovery Following Endarterectomy
Ann Neurol 41:273-276, Balcer,L.J.,et al, 1997

Vascular Events During Follow-up in Patients with Aortic Arch Atherosclerosis
Stroke 28:36-39, Mitusch,R.,et al, 1997

Giant Lambl Excrescences:An Unusual Source of Cerebral Embolism
Arch Neurol 54:41-44, Nighoghossian,N.,et al, 1997

The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
JAMA 277:832-836, Post,S.G.,et al, 1997

Clin Features of Early-Onset Alzheimer Disease in Large Kindred with an E280A Presenilin-1 Mutation
JAMA 277:793-799, Lopera,F.,et al, 1997

Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
Neurol 48:482-485, Zhou,Y.X.,et al, 1997

Familial episodic Ataxia:Clinical Heterogeneity in Four Families Linked to Chromosome 19p
Ann Neurol 41:8-16, 41997., Baloh,R.W.,et al, 1997

Hereditary Frontotemporal Dementia is Linked to Chromosome 17q21-q22:Genetic & Clinicopath Study of 3 Dutch Families
Ann Neurol 41:150-159, Heutnik,P.,et al, 1997

Frontotemporal Dementia is on the MAP
Ann Neurol 41:139-140, Wilhelmsen,K.C., 1997

X-Linked Vacuolated Myopathy:Membrane Attack Complex Depos on Muscle Fiber Membr with Calcium Accumul on Sarcolemma
Ann Neurol 41:117-120, Louboutin,J.P.,et al, 1997

Prognosis in Familial ALS:Progr & Surv in Pts with glu100gly & ala4val Mutations in Cu, Zn Superoxide Dismutase
Neurol 48:55-57, Juneja,T.,et al, 1997

HTLV-Associated Myelopathy in a Cohort of HTLV-I and HTLV-II Infected Blood Donors
neurol 48:315-320, Murphy,E.L.,et al, 1997

Proximal Myotonic Myopathy with MRI White Matter Abnormalities of the Brain
Neurol 48:33-37, Hund,E.,et al, 1997

Appropriate Number of Plasma Exchanges in Guillain-Barre Syndrome
French Coop Grp on Plasma Exchange in GBS, Ann Neurol 41:298-306, 287997., , 1997

Adult Botulism
Muscle & Nerve, 20:100-10297., Shapiro,B.E.,et al, 1997

Familial Idiopathic Brain Calcification with Autosomal Dominant Inheritance
Neurol 48:645-649, Kobari,M.,et al, 1997

HLA Typing in Acute Optic Neuritis, Relation to MS & Magnetic Resonance Imaging Findings
Arch Neurol 54:76-80, Frederiksen,J.L.,et al, 1997

Correlation of Clinical, Magnetic Resonance Imaging, and Cerebrospinal Fluid Findings in Optic Neuritis
Ann Neurol 41:392-398, Jacobs,L.D.,et al, 1997

Showing articles 3000 to 3050 of 5264 << Previous Next >>