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 3150 to 3200 of 5264 << Previous Next >>

Liver Function Disturbances in Guillain-Barre Syndrome:A Prospective Longitudinal Study in 100 Patients
Neurol 46:96-100, Oomes,P.G.,et al, 1996

Pilot Trial of Immunoglobulin Versus Plasma Exchange in Patients with Guillain-Barre Syndrome
Neurol 46:100-103, Bril,V.,et al, 1996

Wilson Disease:Findings at MR Imaging and CT of the Brain with Clinical Correlation
Radiology 198:531-536, van Wassenaer-van Hall,H.N.,et al, 1996

Cortical Hyperintensity on Proton Density-Weighted Images:An MR Sign of Cyclosporine-Related Encephalopathy
AJNR 17:337-344, Jansen,O.,et al, 1996

Reversible Encephalopathy with Cerebral Vasospasm in a Guillain-Barre Syndrome Patient Treated with Intravenous Immunoglobulin
Neurol 46:250-251, Voltz,R.,et al, 1996

Long-term Prognosis in Cerebral Venous Thrombosis:Follow-up of 77 Patients
Stroke 27:243-246, Preter,M.,et al, 1996

Thickening of the Carotid Wall:A Marker for Artherosclerosis in the Elderly?
Stroke 27:224-231, O'Leary,D.H.,et al, 1996

Idiopathic Dysautonomia Treated with Intravenous Gammaglobulin
Lancet 347:28-29, Heafield,M.T.E.,et al, 1996

Diagnostic Test for the Prader-Willi Syndrome by SNRPN Expression in Blood
Lancet 348:1068-1069, Wevrick,R.&Francke,U., 1996

Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
Neurol 47:1269-1277, Baser,M.E., 1996

Nonmotor Fluctuations in Patients with Parkinson's Disease
Neurol 47:1180-1183, Hillen,M.E.&Sage,J.I., 1996

Clinical and Pathological Features in Hydrocarbon-Induced Parkinsonism
Ann Neurol 40:922-925, Pezzoli,G.,et al, 1996

A Gene for Parkinson's Disease
BMJ 313:1278, Hawkes,C., 1996

Clinical Genetic Analysis of Parkinson's Disease in the Contursi Kindred
Ann Neurol 40:767-775, Golbe,L.I.,et al, 1996

Postpartum Neuralgic Amyotrophy
Neurol 47:1213-1219, Lederman,R.J.&Wilbourn,A.J., 1996

Neuralgic Amyothrophy Misdiagnosed as Diaphragmatic Rupture
Muscle & Nerve 19:1181-1182996., Beydoun,S.R.&Rodriquez,R., 1996

Radiation-Induced Brachial Plexopathy:MR and Clinical Findings
AJNR 17:1932-1936, Bowen,B.C.,et al, 1996

Bilateral Brachial Plexus Neuritis Following Parvovirus B19 and Cytomegalovirus Infection
Ann Neurol 40:928-932, Maas,J.J.,et al, 1996

Surgical Treatment for Trigeminal Neuralgia
BMJ 313:1027-1028, Walchenbach,R.&Voormolen,J.H.C., 1996

A Simplified Six-Item Checklist for Screening for Fragile X Syndrome in the Pediatric Population
J Pediatr 129:611-614, Giangreco,C.A.,et al, 1996

Patterns of Ordering Diagnostic Tests for Patients with Acute Low Back Pain
Ann Int Med 125:807-814, Carey,T.S.,et al, 1996

Idiopathic Acute Transverse Myelitis:MR Imaging Findings
Radiology 201:661-669, Tartaglino,L.M.,et al, 1996

Massive Nerve Root Enlargement in Chronic Inflammatory Demyelinating Polyneuropathy
JNNP 61:636-640, Schady,W.,et al, 1996

Intermittent Diplopia and Strabismus Caused by Ocular Neuromyotonia
Trans Am Ophthalmol Soc 94:207-223,223-226, Yee,R.D., 1996

Takayasu's Arteritis
Stroke Syndromes, Eds Bogousslavsky & Caplan, Cambridge Univ Press, Chp 48, p 439-442, Naritomi,H., 1995

Visual Loss after Neurosurgical Repair of Paraclinoid Aneurysms
Ophthalmol 102:905-910, Rizzo,J.F.,III, 1995

Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
J Med Genet 32:25-31, Twist,E.C.,et al, 1995

Painful Oculomotor Palsy Caused by Posterior-Draining Dural Carotid Cavernous Fistulas
Arch Ophthalmol 113:1045-1049, Acierno,M.D.,et al, 1995

Lambert-Eaton Myasthenic Syndrome:Clinical Diagnosis,Immune-Mediated Mechanisms,and Update on Therapies
Ann Neurol 37:S63-S73, Sanders,D.B., 1995

Site of Autonomic Dysfunction in a Patient with Ross'Syndrome and Postganglionic Horner's Syndrome
Neurol 45:2094-2096, Wolfe,G.I.,et al, 1995

Spinocerebellar Ataxias and Ataxins
NEJM 333:1351-1353, Rosenberg,R.N., 1995

Brainstem Ocular Motility Defects and AIDS
Am J Ophthalmol 106:437-442, Hamed,L.M.,et al, 1995

Clinicopath Conf
Multiple Myeloma with Bilateral Carpal Tunnel Syndrome Probably Due to Secondary Amyloid Deposit, Ca, e38-1995,NEJM 333:1625-1630,1995., 1995

Acute, Painful, Pupil-involving Third Nerve Palsy in Chronic Inflammatory Demyelinating Polyneuropathy
Neurol 45:846-847, Arroyo,J.G.&Horton,J.C., 1995

The Restoration of IVIg Efficacy by Plasma Exchange in CIDP
Neurol 45:1628-1629, Berger,A.R.,et al, 1995

Sciatic Endometriosis:MR Evaluation
AJNR 16:1399-1401, Cottier,J-P.,et al, 1995

Familial Subarachnoid Hemorrhage:Distinctive Features and Patterns of Inheritance
Ann Neurol 38:929-934, Bromberg,J.E.C.,et al, 1995

Clinicopath Conf
Intravascular Lymphomatosis, Case 31-1995, NEJM 333:992-999995., , 1995

Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
Ann Neurol 38:817-824, Hutchinson,M.,et al, 1995

Clinical Spectrum of CADASIL:A Study of 7 Families
Lancet 346:934-939, Chabriat,H.,et al, 1995

New Phenotype of the Cerebral Autosomal Dominant Arteriopathy Mapped to Chromosome 19:Migraine as the Prominent Clinical Feature
JNNP 59:579-585, Verin,M.,et al, 1995

Familial Aorto-Cervicocephalic Arterial Dissections and Congenitally Bicuspid Aortic Valve
Stroke 26:1935-1940, Schievink,W.I.&Mokri,B., 1995

Combined System Disease after Nitrous Oxide Anesthesia:A Case Report
Neurol 45:1224-1225, McMorrow,A.M.,et al, 1995

Pain and Remote Weakness in Limbs Injected with Botulinum Toxin A for Writer's Cramp
Lancet 346:154-156, Sheean,G.L.,et al, 1995

Transient Trochlear Nerve Palsy Following Anterior Temporal Lobectomy for Epilepsy
Neurol 45:1465-1468, Jacobson,D.M.,et al, 1995

Dopamine, Dystonia, and the Deficient Co-Factor
Lancet 345:1130, Williams,A.C., 1995

Kindreds of Dominantly Inherited Parkinson's Disease:Keys to the Riddle
Ann Neurol 38:355-356, Duvoisin,R.C.&Golbe,L.I., 1995

A Greek-American Kindred with Autosomal Dominant, Levodopa-Responsive Parkinsonism and Anticipation
Ann Neurol 38:373-378, 3551995., Markopoulou,K.,et al, 1995

Multiple System Atrophy presenting as Parkinsonism:Clinical Features and Diagnostic Criteria
JNNP 59:144-151, Albanese,A.,et al, 1995

X-Linked Pure Familial Spastic Paraparesis
Arch Neurol 52:665-669, Cambi,F.,et al, 1995

Showing articles 3150 to 3200 of 5264 << Previous Next >>