Neudle.com: muscle wasting diffuse

Differential
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abdominal distention

acid maltase deficiency

acid maltase deficiency, adult

aciduria

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

acrocyanosis

acute disseminated encephalomyelitis

acyclovir

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

Adies pupil

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

akinetic mute

albendazole

Alexanders disease

Alexanders disease, adult onset

algorithm

alpha glucosidase

altered states of consciousness

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, treatment of

AMPA receptor antibodies

amyloid angiopathy, cerebral

amyloidoma

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

ANA

anemia

anesthesia, general

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, cerebral, false negative

angiography, cerebral, negative

animal exposure

ankylosing spondylitis

anorexia

anterior horn cell disease

anterior tibial muscle weakness

antibiotics

antibodies to measles

antiphospholipid antibodies

aspartate aminotransferase

ataxia telangiectasia

ataxia, cerebellar

ataxia, sensory

ataxic gait

attention deficit disorder with hyperactivity

atypical

audiogram

auditory evoked brainstem potentials

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basement membrane

basement membrane thickening

baylisascariasis

behavioral disorder

behavioral disorder, acute

bone marrow infarction

bone marrow necrosis

bone marrow transplantation

brain biopsy, false negative

brucellosis, nervous system involvement with

bulbar palsy

bulbar palsy, progressive

calcification, intracranial

Canavan's disease

candida albicans

carbon monoxide poisoning

carbon monoxide poisoning, chronic

carboxyhemoglobin

carcinoma

cardiac arrest

cardiac arrest and resuscitation

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, hyperattenuation

CAT scan, spine

cataracts

cataracts, congenital

catatonia

cauda equina, enhancement

CD4 counts

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

cerebellum

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

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

cervical spine

Charcot-Marie-Tooth

chasing the dragon

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

chilbran skin lesions

Clinical Pathologic Conference(C.P.C.)

cocaine

cognition

cognitive delay

collapsin response mediator protein 5 IgG

coma

complications

confusion

congestive heart failure

corpus callosum, infarction of

corpus callosum, lesion of

cortical blindness

cortical blindness, transient

cortical infarction

cortical ribbon sign

cough

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

critical care unit

cry, abnormal

crying, pathologic

cultured skin fibroblasts

degenerative diseases of CNS

Dejerine-Sottas syndrome

delayed dentition

dementia

dementia, childhood

dementia, frontal lobe type

dementia, frontotemporal

dementia, rapidly progressive

demyelinating disease

denervation of muscle

denervation potentials

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

diarrhea

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

diffuse idiopathic skeletal hyperostosis

diplopia

diplopia, transient

disability, neurological

disseminated intravascular coagulation(DIC)

distal muscle weakness

disulfiram

DPPX, antibodies, encephalitis

drooling

dropped head syndrome

drug abuse

drug abuse, inhalation

drug abuse, neurologic complications of

drug abuse, toxic screen In

dural sinus thrombosis

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, diffuse slowing

electroencephalogram, periodic complexes

encephalitis, autoimmune

encephalitis, etiology

encephalitis, focal

encephalitis, human immunodeficiency virus type 1

encephalitis, viral

encephalopathy

encephalopathy, acute

encephalopathy, anoxic

encephalopathy, delayed

encephalopathy, metabolic

encephalopathy, post anoxic

encephalopathy, progressive

enzyme treatment

enzyme, defect

enzyme, muscle disease

eosinophilia

epidemiology of neurology

episodic neurologic deficits

extraocular muscle lesion

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial weakness

facial weakness, bilateral

faciobrachial dystonic seizure

fluorescein angiography

foot deformity

foot drop

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

gait disorder

gait, spastic

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

ganglionitis

gangliosidosis GM2

gastric partitioning

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

genu of corpus callosum

globus pallidus, hemorrhage

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glycogen storage disease

GM1 ganglioside antibodies

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, sensory

hair analysis

hallucination

hallucination, olfactory

hallucination, visual

hearing loss, bilateral

hearing loss, sudden, bilateral

heart block

helminthic infection of CNS

hemiparesis

hemiparesis, transient

hemiplegia

hemiplegia, progressive

hemoglobin abnormality, neurologic complications of

hepatomegaly

hepatosplenomegaly

heralding manifestation

herpes simplex encephalitis

herpes simplex virus

herpes virus

herpes virus infection

hexosaminidase-A

high arched feet

high arched palate

highly active antiretroviral therapy

hoarseness

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

hospice

human immunodeficiency virus type 1

Huntington's chorea

hydrocephalus

hydroxyglutaric aciduria

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hyperreflexia

hypertension

hypertensive encephalopathy

hypotension, systemic

hypothermia

hypotonia

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

imbalance

immunosuppression

immunosuppressive agents

immunotherapy

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

infectious mononucleosis

infectious mononucleosis, neurologic findings with

insomnia

insular cortex

intellectual deficit

intellectual deterioration

interferon alpha

internal capsule

intestinal pseudoobstruction

intracerebral hemorrhage

intrathecal chemotherapy

intrauterine

intrinsic hand muscles, wasting of

irritability

Jakob-Creutzfeldt disease

lactic dehydrogenase(LDH)

laminar necrosis, cortical

laughing

laughing, pathologic

leg weakness, bilateral

leg weakness, unilateral

lenticular nucleus, lesion of, bilateral

lethargy

leucine rich glioma inactivated 1 antibodies

leukemia

leukemia, neurologic findings assoc.with

leukemia, prophylactic treatment of CNS

leukocyte enzyme abnormality

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy with calcification and cysts

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

leukoencephalopathy, toxic

leukostasis

levamisole

level of consciousness, decreased

Lewy body

Lewy body disease, diffuse

life expectancy

life support, withdrawal of

limbic encephalitis

lipid storage disorder of CNS

lobar atrophy

lymphohistiocytosis

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

lysosomes, abnoral

macrocephaly

malabsorption

Marinesco-Sjogren syndrome

masked facies

masseter muscle wasting

meconium staining

mediastinum, mass of

medulla oblongata, lesion of

megalencephaly

MELAS syndrome

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

meningeal gliomatosis

meningismus

meningitis

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

merosin

mesial temporal lobe

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methotrexate

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

methylglutaconic aciduria

microaneurysm, retinal

microangiopathy, brain

microangiopathy, retina

microcephaly

microhemorrhage, intracerebral

microinfarcts

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

MNGIE syndrome

molecular genetics

monoclonal antibodies

monoclonal gammopathy

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, cortical enhancement

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, gray matter enhancement

MRI, high signal foci on

MRI, hypointense signal foci on

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, susceptibility weighted

MRS

mucormycosis

multiple organ failure

multiple sclerosis

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, progressive

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

mutism

mycoplasma

mycoplasma pneumoniae

myelination of nervous system

myelitis, transverse, recurrent

myelomalacia

myeloneuropathy

myelopathy

myelopathy, chronic progressive

myopathy, critically ill

myopathy, drug-induced

myopathy, steroid induced

neoplasm, primary of CNS

neoplastic angioendotheliosis

nerve biopsy

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

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, painful

neuropathy, peripheral

neuropathy, sensory

neuroprotective agents

next-generation sequencing

NMDA antagonists

nutritional deficiency

nystagmus

obesity

occipital lobe, lesion of

old age, neurology of

opened mouth

ophthalmoplegia

opisthotonus

opportunistic infection

opportunistic infection, CNS

optic atrophy

optic chiasm, enlarged

optic nerve, enlarged

optic nerve, hypoplasia of

optic neuritis

optic neuritis, bilateral

optic neuropathy

optic neuropathy, nutritional

orthostatic hypotension

paraneoplastic ganglionopathy

paranoia

paraparesis

paraparesis, familial spastic

paraparesis, spastic

paresthesias

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

pathology

patient information and support

pediatric neurology

percussion induced muscle contraction

peroxisomal disease

persistent vegetative state

personality change

pes cavus

phenylketonuria

pleocytosis of cerebrospinal fluid

pneumonia

POLR3B

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, critically ill

polyneuropathy, critically ill, children

polyradiculoneuropathy

Pompe's disease of glycogen storage

pons, atrophy

pons, lesion of

posterior column disease

posterior leukoencephalopathy syndrome

posterior longitudinal ligament, ossification of

precipitating factors

pregnancy, neurologic complications in

prenatal

prenatal diagnosis by amniocentesis

primary lateral sclerosis

prognosis

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

proximal muscle atrophy

proximal myotonic myopathy

pruritus

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis

psychotic behavior

ptosis

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated, bilateral

pupil, dilated, episodic

pupil, tonic

pyramidal

pyramidal tract

pyramidal tract dysfunction

quadriparesis

quadriplegia

quadriplegia, transient

raccoon

radiation therapy, CNS treatment and complications with

radiculopathy

ragged-red fibers

rapidly progressing neurologic illness

rash

reading disorder, acquired

recurrent

release phenomena

remote effect of cancer on the nervous system

remternetug

respirator

respiratory failure

respiratory tract infection

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

retinal infarction

retinal lesion

retinal microvascular disease

retinopathy

retrovirus

reversible neurologic disorder

saccadic eye movements, abnormal

sarcoidosis

sarcoidosis, CNS

Schilder's disease

sedimentation rate, elevated

seizure

seizure, children

seizure, drug resistance

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory loss

sensory polyneuropathy

septicemia

serologic testing

serologic testing, false negative

sicca syndrome

sickle cell disease

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skew deviation

skin, lesions in neurologic disorders

sleep

sleep pathology and physiology

slit lamp examination

slow virus infection of CNS

small vessel disease

small-bowel resection

SMN1 gene

somatosensory evoked potentials

somnolence

spasticity

speech disorder, childhood

spinal cord

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

spondylosis

spongy degeneration of brain

spontaneous remission

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

suicide

superior sagittal sinus thrombosis

sural nerve

survival motor neuron gene

Susac's syndrome

sweating

symmetric brain lesions

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

teratoma, ovarian

thalamus, lesion of

thalamus, lesion of-bilateral

tone, muscle, increased

tongue, atrophy

tongue, biting

tongue, enlarged

tongue, fasciculations of

tongue, weakness

tonic cerebellar fits

toxic encephalopathy

transient neurologic deficit

trauma

treatment of neurologic disorder

trinucleotide repeats

tripping

unconsciousness

unconsciousness, transient

urinary incontinence

urine test for metabolic disorders

urine test in toxic screen

very long chain fatty acids

vibratory sensation, abnormal

visual acuity, decreased

visual loss

visual tracking

visuospatial disturbance

vitamin D

vitamin deficiency

vitamin E deficiency

Waldenstrom's macroglobulinemia

Walker-Warburg syndrome

walking, delayed

walking, difficulty with

weakness

weakness, acute

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

white matter disease, periventricular

white matter disease, subcortical

wide based gait

winging of scapula

word-finding difficulty

Showing articles 1900 to 1950 of 3822 << Previous Next >>

Management of Patients Receiving Interferon Beta-1b for MS:Report of a Consensus Conf
Neurol 46:12-18, Lublin,F.D.,et al, 1996

Delayed-Onset Progressive Movement Disorders after Static Brain Lesions
Neurol 46:68-74, Scott,B.L.,et al, 1996

Idiopathic Dysautonomia Treated with Intravenous Gammaglobulin
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Acute Rectus Muscle Palsy in Children as a Result of Orbital Myositis
J Pediatr 128:230-233, Pollard,F.,et al, 1996

Exacerbation of Myasthenia Gravis Associated with Cocaine Use
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Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
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Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996

A Reversible Posterior Leukoencephalopathy Syndrome
NEJM 334:494-500, Hinchey,J.,et al, 1996

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

Progressive Ataxia, Focal Seizures, and Malabsorption Syndrome in a 41 Year Old Woman
JNNP 60:225-230, Mumford,C.J.,et al, 1996

Progressive Familial Leukodystrophy of Late Onset
Neurol 46:429-434, Knopman,D.,et al, 1996

Trimethoprim and Sulfonamide-Associated Meningoencephalitis with MRI Correlates
Neurol 46:556-558, Blumenfeld,H.,et al, 1996

Age and Guillain-Barre Syndrome Severity
Muscle & Nerve 19:375-377996., Sheth,R.D.,et al, 1996

Cognitive Dysfunction as the Major Presenting Feature of Becker's Muscular Dystrophy
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Clinical Heterogeneity of Adhalin Deficiency
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Diagnosis of Merosin (Laminin-2) Deficient Congenital Muscular Dystrophy by Skin Biopsy
Lancet 347:582-584, Sewry,C.A.,et al, 1996

From Enigmatic to Problematic:The New Molecular Genetics of Childhood Spinal Muscular Atrophy
Neurol 46:335-340, Crawford,T.O., 1996

Lewy Body Disease and Dementia
Arch Int Med 156:487-493, Kalra,S.,et al, 1996

Another Kind of Knapsack Palsy
Neurol 46:585-586, Pringle,C.E.,et al, 1996

MRI of White Matter Changes in the Sjogren-Larsson Syndrome
Neuroradiology 37:576-577, Hussain,M.Z.&Aihara,M., 1996

A 64-Year-Old Man with Diabetes and Ascending Paraplegia
Lancet 347:516, Gliemroth,J.,et al, 1996

Autonomic Ganglionitis with Severe Hypertension, Migraine, and Episodic but Fatal Hypotension
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Infarction of Superior Cerebellar Artery Presenting as Cerebellar Symptoms
Stroke 27:1679-1681, Terao,S.,et al, 1996

Meningeal Gliomatosis Presenting as Multiple Cerebral Infarcts:A Case Report
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Risk of Stroke During Long-Term Anticoagulant Therapy in Patients After Myocardial Infarction
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Significant Progression of White Matter Lesions and Small Deep (Lacular) Infarcts in Patients with Stroke
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Palliative Care in Neurology
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Restless Legs Syndrome and Leg Cramps in Fibromyalgia Syndrome:A Controlled Study
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Leukoencephalopathy Associated with Cobalamin Deficiency
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Campylobacter Jejuni Infection and Anti-GM1 Antibodies in Guillain-Barre Syndrome
Ann Neurol 40:181-187, Jacobs,B.C.,et al, 1996

Antiamphiphysin Antibodies with Small-Cell Lung Carcinoma and Paraneoplastic Encephalomyel; itis
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HIV Encephalitis Presenting with Severe Generalized Chorea
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Intravenous Immunoglobulin Treatment of Neurological Disease
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A Woman with a Relapsing Psychosis Who Got Better with Prednisone
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Cost-Effectiveness Analysis:What Is It and How Will It Influence Neurology
Ann Neurol 39:818-823, Holloway,R.G., 1996

The"Gulf War Syndrome"-Is There Evidence of Dysfunction in the Nervous System
JNNP 60:449-451, Jamal,G.A.,et al, 1996

Pure Motor Hand Weakness
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A New Variant of Creutzfeldt-Jakob Disease in the UK
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Creutzfeldt-Jakob Disease in a Young Woman
Lancet 347:945-948, Tabrizi,S.J.,et al, 1996

Subacute Sclerosing Panencephalitis:Evaluation with CT and MR
AJNR 17:761-772, Brismar,J.,et al, 1996

Wegener Granulomatosis:CT and MR Findings
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Cytomegalovirus Infection and Guillain-Barre Syndrome:The Clinical, Electrophysiologic, and Prognostic Features
Neurol 47:668-673, Visser,L.H.,et al, 1996

Prospective Evaluation of MRI Lumbosacral Nerve Root Enhancement in Acute Guillain-Barre Syndrome
Neurol 47:813-817, Gorson,K.C.,et al, 1996

Intravenous IgG in Guillain-Barre Syndrome
BMJ 313:376-377, Hughes,R.A.C., 1996

Lyme Radiculoneuritis Treated with Intravenous Immunoglobin
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Sustained Myoglobinuria:The Presenting Manifestation of Dermatomyositis
Neurol 47:119-123, Rose,M.R.,et al, 1996

Multiple Mitochondrial DNA Deletions in Sporadic Inclusion Body Myositis:A Study of 56 Patients
Ann Neurol 39:789-795, Santorelli,F.M.,et al, 1996

Is Chronic Respiratory Failure in Neuromuscular Diseases Worth Treating
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Erroneous Diagnosis Corrected After 28 Years
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Showing articles 1900 to 1950 of 3822 << Previous Next >>