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Differential
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abdominal distention

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

acute disseminated encephalomyelitis

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

affect, inappropriate

agenesis of corpus callosum

Aicardi-Goutieres syndrome

Alexanders disease

Alexanders disease, adult onset

alpha glucosidase

altered states of consciousness

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, treatment of

AMPA receptor antibodies

amyloid angiopathy, cerebral

amyloid-related imaging abnormalities

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis-like syndrome

anesthesia, general

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, cerebral, false negative

angiography, cerebral, negative

animal exposure

ankylosing spondylitis

anterior horn cell disease

anterior tibial muscle weakness

antibodies to measles

antiphospholipid antibodies

antiviral agents

aphasia, global

arrhythmia, cardiac

arylsulfatase A

ascending paralysis

aspartate aminotransferase

ataxia telangiectasia

ataxia, cerebellar

ataxia, sensory

attention deficit disorder with hyperactivity

auditory evoked brainstem potentials

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

autonomic neuropathy

axonal degeneration

axonal spheroid

B 12 deficiency

bacterial infection

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basement membrane

basement membrane thickening

baylisascariasis

behavioral disorder

behavioral disorder, acute

Behcet's syndrome

biologic markers

bladder dysfunction

bone marrow biopsy

bone marrow infarction

bone marrow necrosis

bone marrow transplantation

brain biopsy, false negative

brainstem, atrophy

brainstem, lesion of

brucellosis, nervous system involvement with

bulbar palsy, progressive

burning paresthesia

calcification, intracranial

Canavan's disease

candida albicans

carbon monoxide poisoning

carbon monoxide poisoning, chronic

carboxyhemoglobin

cardiac arrest and resuscitation

carotid angiogram

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, hyperattenuation

CAT scan, spine

cataracts, congenital

cauda equina, enhancement

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar vermis

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral infarction

cerebral ischemia

cerebral vasculature

cerebral vasculature, calcification

cerebral venous thrombosis

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, recurrent

cerebrovascular accident, women

cerebrovascular disease

Charcot-Marie-Tooth

chasing the dragon

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

chilbran skin lesions

choreoathetosis

chorioretinitis

Clinical Pathologic Conference(C.P.C.)

cognitive delay

collapsin response mediator protein 5 IgG

congestive heart failure

contractures, joint

copper deficiency

corpus callosum

corpus callosum, infarction of

corpus callosum, lesion of

cortical blindness

cortical blindness, transient

cortical infarction

cortical ribbon sign

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

critical care unit

crying, pathologic

cultured skin fibroblasts

cyclophosphamide

cyst, parenchymal

deafness, bilateral

deafness, sudden

decerebrate posture

deep gray nuclei

degenerative diseases of CNS

Dejerine-Sottas syndrome

delayed dentition

dementia, childhood

dementia, frontal lobe type

dementia, frontotemporal

dementia, rapidly progressive

demyelinating disease

denervation of muscle

denervation potentials

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

diffuse idiopathic skeletal hyperostosis

diplopia, transient

disability, neurological

disseminated intravascular coagulation(DIC)

distal muscle weakness

DPPX, antibodies, encephalitis

dropped head syndrome

drug abuse, inhalation

drug abuse, neurologic complications of

drug abuse, toxic screen In

dural sinus thrombosis

dysdiadochokinesia

dysferlinopathy

dyskinesia, facial

dystonia, children

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, diffuse slowing

electroencephalogram, periodic complexes

electron microscopy

emotional lability

encephalitis, autoimmune

encephalitis, etiology

encephalitis, focal

encephalitis, human immunodeficiency virus type 1

encephalitis, viral

encephalopathy, acute

encephalopathy, anoxic

encephalopathy, delayed

encephalopathy, metabolic

encephalopathy, post anoxic

encephalopathy, progressive

enzyme treatment

enzyme, muscle disease

epidemiology of neurology

episodic neurologic deficits

evoked potentials

exercise intolerance

exome sequencing

extraocular muscle lesion

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial weakness

facial weakness, bilateral

faciobrachial dystonic seizure

failure to thrive

feeding disorder

flail arm syndrome

fluorescein angiography

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, lesion of

frontal lobe, pathologic signs of

fundus, abnormality of

funduscopic exam

fungal infection, CNS

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gangliosidosis GM2

gastric partitioning

gastrointestinal disease, neurologic complications

gastrointestinal motility

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

genu of corpus callosum

gliomatosis cerebri

globus pallidus, hemorrhage

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glycogen storage disease

GM1 ganglioside antibodies

Gowers maneuver

Griscelli syndrome

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, sensory

hallucination, olfactory

hallucination, visual

head circumference

headache, positional

headache, recurrent

hearing loss, bilateral

hearing loss, sudden, bilateral

helminthic infection of CNS

hemiparesis, transient

hemiplegia, progressive

hemoglobin abnormality, neurologic complications of

hepatosplenomegaly

heralding manifestation

herpes simplex encephalitis

herpes simplex virus

herpes virus infection

hexosaminidase-A

high arched feet

high arched palate

highly active antiretroviral therapy

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

human immunodeficiency virus type 1

Huntington's chorea

hydroxyglutaric aciduria

hyperbaric oxygen

hyperhomocysteinemia

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypertensive encephalopathy

hypoglycorrhachia

hypomyelination

hypotension, systemic

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

immunosuppression

immunosuppressive agents

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

incontinence, fecal

infantile spasm

infectious mononucleosis

infectious mononucleosis, neurologic findings with

intellectual deficit

intellectual deterioration

interferon alpha

internal capsule

intestinal pseudoobstruction

intracerebral hemorrhage

intrathecal chemotherapy

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

joint hypermobility

Krabbe's disease

lactic dehydrogenase(LDH)

laminar necrosis, cortical

laughing, pathologic

leg weakness, bilateral

leg weakness, unilateral

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukemia, prophylactic treatment of CNS

leukocyte enzyme abnormality

leukoencephalopathy

leukoencephalopathy with calcification and cysts

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

leukoencephalopathy, toxic

level of consciousness, decreased

Lewy body disease, diffuse

life expectancy

life support, withdrawal of

limbic encephalitis

lipid storage disorder of CNS

lymphohistiocytosis

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

lysosomes, abnoral

Marinesco-Sjogren syndrome

masseter muscle wasting

meconium staining

mediastinum, mass of

medulla oblongata, lesion of

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

meningeal gliomatosis

meningitis, aseptic

meningitis, bacterial

meningitis, basilar

meningitis, eosinophilic

meningitis, leukemic

meningitis, melanomatous

meningitis, Mollaret's

meningitis, recurrent

meningitis, treatment of

meningoencephalitis

mental retardation

mental status, abnormal

mesial temporal lobe

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

methylglutaconic aciduria

microaneurysm, retinal

microangiopathy, brain

microangiopathy, retina

microhemorrhage, intracerebral

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoclonal antibodies

monoclonal gammopathy

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, contrast enhanced

MRI, cortical enhancement

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, functional

MRI, gradient-echo

MRI, gray matter enhancement

MRI, high signal foci on

MRI, hypointense signal foci on

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

multiple organ failure

multiple sclerosis

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, progressive

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, congenital, Ullrich

muscular dystrophy, LAMA2

muscular dystrophy, limb-girdle

mycoplasma pneumoniae

myelination of nervous system

myelitis, transverse, recurrent

myeloneuropathy

myelopathy, chronic progressive

myoclonic jerks

myopathy, acute

myopathy, critically ill

myopathy, drug-induced

myopathy, steroid induced

myotonia dystrophica

nausea and vomiting

neoplasm, primary of CNS

neoplastic angioendotheliosis

nerve conduction studies

nerve root enhancement

neurexin-3 alpha antibodies

neuroaxonal leukodystrophy

neurogenic bladder

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic disease, tempo

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neurological intensive care

neuromuscular disease, electrodiagnosis of

neuronal cell surface antigen

neuronal degeneration

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, painful

neuropathy, peripheral

neuropathy, sensory

neuroprotective agents

neurotoxicity, acute

next-generation sequencing

NMDA antagonists

nutritional deficiency

occipital lobe, lesion of

old age, neurology of

ophthalmoplegia

opportunistic infection

opportunistic infection, CNS

optic chiasm, enlarged

optic nerve, enlarged

optic nerve, hypoplasia of

optic neuritis, bilateral

optic neuropathy

optic neuropathy, nutritional

orthostatic hypotension

pain, abdominal

pain, total body

paralysis, recurrent

paraneoplastic ganglionopathy

paraparesis, familial spastic

paraparesis, spastic

Parkinson disease

Parkinson disease, differential diagnosis of

Parkinson disease, L-dopa nonresponsive

Parkinson disease, misdiagnosis

Parkinson disease, tremor, absence of

Parkinsonism syndrome

PAS positive material in the brain

patient information and support

pediatric neurology

percussion induced muscle contraction

peroxisomal disease

persistent vegetative state

personality change

phenylketonuria

pleocytosis of cerebrospinal fluid

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy, critically ill

polyneuropathy, critically ill, children

polyradiculoneuropathy

Pompe's disease of glycogen storage

pons, lesion of

posterior column disease

posterior leukoencephalopathy syndrome

posterior longitudinal ligament, ossification of

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

primary lateral sclerosis

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

proximal muscle atrophy

proximal myotonic myopathy

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychotic behavior

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated, bilateral

pupil, dilated, episodic

pyramidal tract

pyramidal tract dysfunction

quadriplegia, transient

radiation therapy, CNS treatment and complications with

ragged-red fibers

rapidly progressing neurologic illness

reading disorder, acquired

release phenomena

remote effect of cancer on the nervous system

respiratory failure

respiratory tract infection

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

retinal infarction

retinal microvascular disease

reversible neurologic disorder

Rosenthal fibers

saccadic eye movements, abnormal

sarcoidosis, CNS

Schilder's disease

sedimentation rate, elevated

seizure, children

seizure, drug resistance

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory polyneuropathy

serologic testing

serologic testing, false negative

sickle cell disease

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

sleep pathology and physiology

slit lamp examination

slow virus infection of CNS

small vessel disease

small-bowel resection

somatosensory evoked potentials

speech disorder, childhood

spinal cord degeneration

spinal cord, cervical

spinal cord, compression of

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinal stenosis

spinal stenosis, cervical canal

splenium of corpus callosum

spongy degeneration of brain

spontaneous remission

standing difficulty

startle myoclonus

startle reaction

steroid therapy, CNS treatment and complications with

stimulant drugs

striatal encephalitis

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subarachnoid hemorrhage

subdural hematoma

superior sagittal sinus thrombosis

survival motor neuron gene

Susac's syndrome

symmetric brain lesions

systemic illness

tandem gait, ataxic

Tay-Sachs disease

teeth, abnormal

teeth, number of in infants

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

teratoma, ovarian

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

tone, muscle, increased

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, weakness

tonic cerebellar fits

toxic encephalopathy

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

tremor, resting

trichopoliodystrophy

trigeminal neuralgia

trinucleotide repeats

unconsciousness

unconsciousness, transient

urinary incontinence

urine test for metabolic disorders

urine test in toxic screen

vasospasm, cerebral

vertebral infarction

very long chain fatty acids

vibratory sensation, abnormal

viral infection

viral infection, CNS

vision, blurred

visual acuity, decreased

visual tracking

visuospatial disturbance

vitamin deficiency

vitamin E deficiency

Waldenstrom's macroglobulinemia

Walker-Warburg syndrome

walking, delayed

walking, difficulty with

weakness, acute

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

Whipple's disease

white matter disease

white matter disease, periventricular

white matter disease, subcortical

wide based gait

winging of scapula

word-finding difficulty

X-linked neuropathy

Showing articles 1950 to 2000 of 3822 << Previous Next >>

Atrophy of Bilateral Extraocular Muscles
J Neuro-Ophthalmol 16:286-288, Okamoto,K.,et al, 1996

Psychiatric Features in Diffuse Lewy Body Disease:A Clinicopath Study Using Alzheimer's & PD Groups
Neurol 47:1148-1152, Klatka,L.A.,et al, 1996

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

Motor Neuron Disease, Lymphoproliferative Disease, and Bone Marrow Biopsy
Muscle & Nerve 19:1334-1337996., Louis,E.D.,et al, 1996

Immunoassays Fail to Detect Antibodies Against Neuronal Calcium Channels in Amyotrophic Lateral Sclerosis Serum
Ann Neurol 40:695-700, 6911996., Arsac,C.,et al, 1996

Lambert-Eaton Myasthenic Syndrome Presenting with Severe Respiratory Failure
Muscle & Nerve 19:1328-1333996., Nicolle,M.W.,et al, 1996

Phenylketonuria:Findings at MR Imaging & Localized in Vivo H-1 MR Spectroscopy of Brain in Pts with Early Treatment
Radiology 201:413-420, Pietz,J.,et al, 1996

Three Get Ready
Arch Neurol 53:1222-1223, Goldblatt,D., 1996

Riluzole
Lancet 348:795-799, Wokke,J., 1996

Inclusion Body Myositis:Clinical and Pathological Boundaries
Ann Neurol 40:581-586, Amato,A.A.,et al, 1996

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

Acute Myopathy of Intensive Care:Clinical, Electromyographic, and Pathological Aspects
Ann Neurol 40:645-654, Lacomis,D.,et al, 1996

Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
Ann Neurol 40:782-791, Pegoraro,E.,et al, 1996

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

Needle Electromyography in the Thoracic Paraspinal Muscles of Motor Neuron Disease
No to Shinkei-Brain & Nerve 48:637-642996., Kyuno,K.,et al, 1996

Pediatric Ulnar Mononeuropathy:Report of 21 Electromyography-Documented Cases & Review of Literature
J Child Neurol 11:116-120, Felice,K.J.&Jones,H.R., 1996

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

Gait Disorders in Older Adults
J Am Geriatr Soc 44:434-452, Alexander,N.B., 1996

White Matter MR Hyperintensities in Adult Patients with Congenital Rubella
AJNR 17:99-103, Barton Lane,E.,et al, 1996

Brain Edema after Carotid Surgery
Neurol 46:175-181, Breen, J.C.,et al, 1996

A Case of Creutzfeldt-Jakob Disease (CJD) Started with Monoparesis of the Left Arm
Rinshi Shinkeigaku 36:1245-1248, Obi, T.,et al, 1996

Neurosyphilis in HIV-Positive and HIV-Negative Patients: Neuroimaging Findings
AJNR 16:703-711, Brightbill,T.C.,et al, 1995

The Electrophysiological Study of Diff Dx Between ALS & Cervical Spondylotic Myelopathy
EMG & Clin Neurophysiology 35:231-238995., Kang,D.X.&Fan,D.S., 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340, LeForestier,N.,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

Acquired Neuromyotonia:Evidence for Autoantibodies Directed Against K+Channels of Peripheral Nerves
Ann Neurol 38:714-722, 7011995., Shillito,P.,et al, 1995

Neuromuscular Effects of Papuan Taipan Snake Venom
Ann Neurol 38:916-920, Connolly,S.,et al, 1995

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

Clinicopath Conf
Granulomatous Angiitis of CNS, Case 33-1995, NEJM 333:1135-1143995., , 1995

Campylobacter Jejuni Infection and Guillain-Barre Syndrome
NEJM 333:1374-1379, 14151995., Rees,J.H.,et al, 1995

Inclusion Body Myositis and Myopathies
Ann Neurol 38:705-713, Griggs,R.C.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995

Clinicopath Conf
Progressive Muscular Atrophy, Case 36-1995, NEJM 333:1406-1412995., , 1995

Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
Lancet 1458-1463, Barrett,T.G.,et al, 1995

Apolipoprotein E E4 in Inclusion Body Myositis
Ann Neurol 38:957-959, Garlepp,M.J.,et al, 1995

MR Findings in Methanol Intoxication
AJNR 16:1783-1786, Gaul,H.P.,et al, 1995

Oral Sumatriptan-Associated Transmural Myocardial Infarction
Neurol 45:2274-2276, O'Connor,P.&Gladstone,P., 1995

Effect of GPi Pallidotomy on Motor Function in Parkinson's Disease
Lancet 346:1383-1387, Lozano,A.M.,et al, 1995

Leptomeningeal Dissemination of Malignant Glioma Simulating Cerebral vasculitis:Case Report with Angiographic & Path
Stroke 26:2366-2370, Herman,C.,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

Prognosis for Survival After an Initial Stroke
Stroke 26:2011-2015, Lai,S.M.,et al, 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

Neurological Correlated of Fetal Cocaine Exposure:Transient Hypertonia of Infancy and Early Childhood
Pediatrics 96:1070-1077, Chiriboga,C.A.,et al, 1995

Cranial MR in Wilson Disease:Abnormal White Matter in Extrapyramidal and Pyramidal Tracts
AJNR 16:2021-2027, van Wassenaer-van Hall,H.N.,et al, 1995

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Lambert-Eaton Myasthenic Syndrome (LEMS) in Association with Lymphoproliferative Disorders
Muscle & Nerve 18:715-719995., Argov,Z.,et al, 1995

Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
Ann Neurol 38:450-454, Wokke,J.H.J.,et al, 1995

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995

Showing articles 1950 to 2000 of 3822 << Previous Next >>