Neudle.com: chronic spinal muscle atrophy

Differential
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abdominal contractions

abducens nerve paralysis

acid maltase deficiency

acoustic nerve

acoustic neurinoma

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

acrocyanosis

ACTH, ectopic syndrome of

acute intermittant porphyria

acute necrotizing encephalitis

adult polyglucosan body disease

advance directives

advances in neurology

adverse drug reaction

Aicardi-Goutieres syndrome

alcohol intolerance

alcoholic polyneuropathy

altered states of consciousness

alveolar hypoventilation

Alzheimer's disease

aminoacidopathies

aminoacidurias

amphiphysin antibodies

amyloid angiopathy, cerebral

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, childhood

amyotrophic lateral sclerosis, cluster

amyotrophic lateral sclerosis, complications with

amyotrophic lateral sclerosis, conjugal

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, hospitalization

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, myasthenic syndrome with

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, post-encephalitic

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, sensory symptoms in

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis, work up

amyotrophic lateral sclerosis-like syndrome

aneurysm, cavernous sinus

aneurysm, internal carotid artery

angiography, cerebral, beaded vessels

angiography, cerebral, false negative

angiography, cerebral, negative

angiotensin-converting enzyme

animal exposure

ankle edema

ankylosing spondylitis

anorexia

anterior horn cell disease

anterior interosseous neuropathy

anterior tibial muscle weakness

anti citrullinated antibody

anti Hu antibody

antibodies to voltage-gated calcium channels

aphasia, progressive, primary

aphonia

apnea

apraxia

apraxia of eye movements

aqueduct of Sylvius, obstruction

arthrogryposis multiplex

asthma, poliomyelitis-like syndrome with

asymptomatic

ataxia

ataxia telangiectasia

atlanto axial dislocation, congenital

atonic bladder

atrioventricular block

autonomic dysfunction

Barkhof MR criteria for MS

basal cistern

basal ganglia

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

Bence Jones protein

benign congenital hypotonia

blood dyscrasias, neurologic findings with

bone marrow biopsy

Borrelia burgdorferi infection

botulinum toxin

botulinum toxin, complications of

brain biopsy, negative

brain scan

brainstem, infarction of

brainstem, lesion of

bright tongue sign

Brown Sequard syndrome

bulbar palsy, progressive

calcification, intracranial

calcium channel dysfunction

calf hypertrophy

camptocormia

cane

carbon monoxide poisoning

carcinoembryonic antigen

cardiovascular disease

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

cataracts, congenital

cauda equina

cauda equina, lesion of

cavernous sinus

cavernous sinus, lesion of

cavernous sinus, syndrome

CD4 counts

central core disease

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar vermis

cerebellum, neoplasms of

cerebral cortex

cerebral cortical atrophy

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure low

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, women

cerebrovascular accident, young adult

cervical myelopathy

cervical osteoarthritis

cervical osteophyte

cervical spine

cervical spine injury

cervical spine injury, treatment of

cervical spondylosis

cervical spondylosis, differential diagnosis of

cervical spondylosis, misdiagnosis

Charcot-Marie-Tooth

chemosis

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

chewing, impaired

chilbran skin lesions

children

chills

Chinese paralytic syndrome

chromosomal abnormality

chromosome 11

chromosome 3

chromosome 5

chronic polyneuritis, children

chronic progressive external ophthalmoplegia

cigarette smoking

ciguatera poisoning

cisterna magna

Clinical Pathologic Conference(C.P.C.)

collapsin response mediator protein 5 IgG

coma

complications

compression neuropathy

concussion

conduction block

confusion

congenital heart disease

congenital myopathy

congestive heart failure

conjunctivitis

constipation

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

conversion reaction

corpus callosum

corpus callosum, lesion of

corpus callosum, thinning

cortical hand knob

cortical-basal ganglionic degeneration

coxsackievirus, myopathy with

CPAP

cranial nerve enlargement

cranial nerve palsies

cranial nerves

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cyst, cortical parenchyma

cysticercosis, cerebral

cysticercosis, intraventricular

cysticercosis, subarachnoid

cytomegalic inclusion disease

degenerative diseases of CNS

Dejerine-Sottas syndrome

delay in diagnosis

delusion

dementia

dementia, age at onset

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

demyelinating disease

denervation of muscle

denervation potentials

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

depression, psychotic

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic mononeuropathy

diagnostic criteria

diaphragmatic paralysis

diaphragmatic paralysis, causes of

diet

differential diagnosis

difficulty climbing stairs

diffuse idiopathic skeletal hyperostosis

diphtheria

diplegia, atonic

diplopia

disability rating scale, neurological

disability, neurological

distal muscle atrophy

distal muscle weakness

DNA probes

dopamine

down-beat nystagmus

down-beat nystagmus, primary position of gaze

drooling

dropped head syndrome

dysthyroid ocularmyopathy

dysthyroidism

dystonia

dystonia, children

dystrophic calcification

dystrophin

ears of the Lynx MR sign

efficacy

electrical injury of nervous system

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

electromyogram, decremental response

electron microscopy

electrophoretic pattern, serum

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalitis, recurrent

encephalopathy, anoxic

encephalopathy, neonatal

encephalopathy, post anoxic

endemic area

endocarditis, subacute bacterial

enterovirus

enterovirus infection of CNS

entrapment neuropathy

enzyme, muscle disease

epidemiology of neurology

episodic neurologic deficits

erythema migrans

ethics in neurology

euthanasia

evidence-based research

extraocular muscle enlargement

eye movement, disorders of

eye, pain in

face, numbness of

facial nerve palsy

facial nerve palsy, bilateral

facial pain

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failed medical management

Fazio-Londe's disease

feeding disorder

fever

fibrillations

fine motor function, impaired

football neurologic injuries

fourth ventricle, cyst

fragile-X syndrome

free radical

Friedreich's ataxia

frontal behavioral spatial syndrome

frontal lobe, atrophy

frontotemporal dementia, behavioral variant

fundus, abnormality of

funduscopic exam

gadolinium

gag reflex, depressed

gammaglobulin therapy, intravenous

ganglionitis

gangliosides

gastrostomy

gastrostomy, percutaneous endoscopic

gaze palsy

gaze palsy, horizontal

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

girdle sensation

glioblastoma multiforme(astrocytoma Gr.III)

glioma

glutamic acid

GM1 ganglioside antibodies

granulomatous disease

Graves ophthalmopathy

gray matter

growth retardation

guanidine

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

headache, progressive

headache, severe

health insurance

hearing loss

hearing loss, bilateral

hearing loss, sudden, bilateral

heart block

heavy metal intoxication

helminthic infection of CNS

hemangioma

hemianopia, homonymous

hemiparesis

hemiplegia

hemiplegia, progressive

heralding manifestation

herniated disc

herpes labialis

herpes simplex encephalitis

herpes simplex encephalitis, diagnosis of

herpes simplex encephalitis, differential diagnosis of

herpes simplex encephalitis, recurrent

herpes simplex encephalitis, treatment of

herpes simplex myelitis

herpes simplex virus

herpes simplex virus infection, immunosuppressed patient

herpes simplex virus, human nervous system and

herpes simplex virus, localization of

herpes simplex virus, malignancy with

herpes simplex virus, pathogenesis of

herpes simplex virus, pathology of

herpes simplex, neurocutaneous lesions in

herpes virus

herpes zoster

herpes, genital

highly active antiretroviral therapy

Hodgkin's disease, neurologic involvement with

hospice

human immunodeficiency virus type 1

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

hydrocephalus, non-communicating(obstructive)

hydrocephalus, transient

hypercalcemia

hypercapnia

hyperparathyroidism

hyperpyrexia, CNS disorder causing

hypertrophic intracranial pachymeningitis

hypogammaglobulinemia

hypokalemic alkalosis

hypothalamus, disturbance of

hypoxic encephalopathy

iatrogenic neurologic disorders

immunoelectrophoresis, serum

immunofluorescent exam of CSF cells

immunohistochemistry

immunologic disease

immunology and the nervous system

immunosuppression

immunosuppressive agents

immunotherapy

impotence

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

inclusion body myositis

incontinence, fecal

infant, evaluation of

infantile tremor syndrome

infectious mononucleosis

inflexibility, mental

intermittent positive pressure breathing

internal capsule

internet

intestinal pseudoobstruction

intracranial hypertension, benign

intracranial pressure, increased

intranasal medication

intrauterine

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Kearns-Sayre syndrome

klippel feil syndrome

Korsakoff's psychosis

Kugelberg-Welander syndrome

lactic acidemia

laminectomy, cervical

lathyrism

laughing, pathologic

lead and the nervous system

Leber's hereditary optic neuropathy

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leptospirosis

leucine rich glioma inactivated 1 antibodies

leukemia

leukemia, neurologic findings assoc.with

leukodystrophy

leukoencephalopathy

level of consciousness, decreased

Lewy body disease, diffuse

lid closure, weakness of

life expectancy

life support, withdrawal of

life support, withholding of

life sustaining treatment

lymphadenopathy, hilar

lymphocytic meningoradiculitis

lymphoma

lymphoma involving CNS

lysosomal storage disease

Madonna facies

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malignancy screen

malignancy, occult

masseter muscle weakness

median neuropathy

medical-legal aspects of neurology

MELAS syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, cysticercosis

meningitis, eosinophilic

meningitis, fungal

meningitis, fungal-negative CSF culture

meningitis, leptospira

meningitis, recurrent

meningoencephalitis

meningoencephalopathy

meningomyelitis

mental retardation

mental status, abnormal

MERRF syndrome

metabolic disorder, primary

methotrexate

methylhydrazine derivatives

Mexican

Mexico

microangiopathy, brain

microangiopathy, retina

microcephaly

micropthalmia

Millard Gubler syndrome

Mills syndrome

mimics

minimally conscious state

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mobility

mobility aids

molecular genetics

monoamine oxidase inhibitors

monoamines

monoamines, brain

monoclonal antibodies

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

monomelic amyotrophy

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

mononeuropathy, motor

motor neuron disease, juvenile form

motor neuron disease, spontaneous recovery

motor system

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, cranial nerves

MRI, diffusion weighted

MRI, FLAIR

MRI, functional

MRI, gradient-echo

MRI, high signal foci on

MRI, muscle

MRI, paramagnetic effect

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, susceptibility weighted

MRS

multiple myeloma

multiple sclerosis

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle strength, testing

muscle tenderness

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

mutism

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, limb-girdle

myasthenia gravis, paraneoplastic

myasthenia gravis, treatment of

myasthenic crisis

myasthenic syndrome

myelinolysis, extrapontine

myelitis

myelitis, longitudinal

myelopathy, carcinomatous

myelopathy, chronic progressive

myelopathy, necrotizing

myocardial infarction

myopathy, carcinomatous

myopathy, centronuclear

myopathy, distal

myopathy, mitochondrial

myopathy, proximal

myopathy, quadriceps

myopathy, thyroid disease causing

myositis

myotonia congenita

myotonia dystrophica

N-acetyl-L-aspartic acid

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, hormone producing

neoplasm, hormone producing, ectopic

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

nephritis

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

nerve growth factor

nerve hypertrophy

nerve root enhancement

nerve root hypertrophy

neuritis, causes of

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurogenic bladder

neurogenic vs.myopathic atrophy

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic disease, incurable

neurologic disease, multifocal

neurologic disease, tempo

neurologic evaluation

neurologic examination

neurologic signs

neurologic symptoms

neurologic testing

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuromyotonia

neuronal cell surface antigen

neuronal degeneration

neuronal migration disorder

neuronopathy

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy, diphtheritic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, vasculitic, systemic

neuroprotective agents

newborn, evaluation of

next-generation sequencing

nystagmus, primary position of gaze

nystagmus, rotary

occupational neurologic disorders

ocular motility, disorders of

old age, neurology of

olivary degeneration, hypertrophic

onconeural antibodies

Onufrowicz nucleus

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, progressive external

opiate

Oppenheim muscular dystrophy

opsoclonus-myoclonus syndrome

orthostatic hypotension

osmotic demyelination syndrome

osteomalacia

owl's eye sign of spinal cord

pain, increased response

pain, management of chronic

paralysis, asymmetric

paraneoplastic cerebellar degeneration

paraneoplastic ganglionopathy

paranoia

paraoxonase

paraparesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraproteinemia

parasitic infection, CNS

Parkinson disease, L-dopa nonresponsive

Parkinson disease, motor neuron disease with

Parkinson disease, treatment of

Parkinsonism syndrome

Parkinsonism-dementia complex

paroxysmal neurologic deficits

pathology

patient information and support

pelvic mass

penicillamine

periodic paralysis

periodic paralysis, thyrotoxic

peripheral nerve, lesion of

pernicious anemia

peroxisomal disease

persistent vegetative state

personality change

pes cavus

photophobia

phrenic nerve pacemaker

physical activity

physical therapy

physician assisted suicide

Pick's disease

pigmentary retinopathy

placebo

plasma cell dyscrasia

plasmapheresis

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, mercury

poison, neurologic problems with

poliomyelitis

polyclonal gammopathy

polyglucosan body

polyglucosan body disease

polyinosinic cytidic acid(poly IC)

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, variant form

polyneuropathy, chronic inflammatory demyelinating-pure motor syn

polyneuropathy, chronic inflammatory demyelinating-sens atax var

polyneuropathy, chronic inflammatory demyelinating-variant forms

porphyria

positive sharp waves

post polio syndrome

posterior fossa, differential diagnosis of lesions of

posterior inferior cerebellar artery syndrome

posterior interosseous neuropathy

posterior longitudinal ligament, ossification of

practice guidelines

preclinical

pregnancy, neurologic complications in

prenatal

pressure sores

prevention of neurologic disorders

primary lateral sclerosis

progressive multifocal leucoencephalopathy

progressive muscular dystrophy

progressive neurologic disorder

progressive spinal muscular atrophy

progressive supranuclear palsy

proprioception, abnormal

proptosis

proximal muscle atrophy

pseudobulbar palsy

pseudohypertrophy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary function tests

pyramidal tract

pyramidal tract dysfunction

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

radiation therapy, salivary gland

remote effect of cancer on the nervous system

renal cell carcinoma

renal stones

renal transplantation

repetitive nerve stimulation

respirations in CNS disease

respirator

respiratory arrest

respiratory depression

respiratory failure

respiratory tract infection

retinal artery occlusion

retinal branch artery occlusion

rheumatoid arthritis, neurologic complications of

risk-benefit assessment

rubella virus

saccadic eye movements, abnormal

safety

salivation, excessive

sarcoidosis

sarcoidosis, CNS

scleroderma

scleroderma, neurologic involvement with

scoliosis

scoliosis, neurologic association with

seizure, psychomotor-temporal lobe

seizure, treatment of

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory loss

sensory loss, cutaneous

sensory symptoms

sensory testing

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

serum alanine aminotransferase

shell fish poisoning

short stature

shoulder, subluxation

shunt procedure, ventricular

single photon emission computed tomography

sinuses, diseases of

sinusitis

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, lesions in neurologic disorders

sleep

sleep apnea

sleep pathology and physiology

smell

Smell Identification Test

SMN1 gene

somatosensory evoked potentials

somatosensory evoked potentials, dermatomal

somnolence

spastic ataxia

spastic paraplegia, type 11

spastic paraplegia, type 7

spasticity

speech disorder

speech disorder, childhood

spinal cord degeneration

spinal cord, biopsy

spinal cord, cervical

spinal cord, compression of

spinal cord, enlargement

spinal cord, injury of

spinal cord, injury, management of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, intramedullary

spinal cord, pathologic exam of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinal stenosis

spinal stenosis, cervical canal

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

stem cell transplantation

steppage gait

stereotyped behavior

sternocleidomastoid muscle

steroid

steroid therapy, CNS treatment and complications with

subacute myelo-opticoneuropathy(S.M.O.N.)complex

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

subarachnoid hemorrhage

subdural hematoma

subtemporal decompression

survival motor neuron gene

temporal lobe, atrophy

temporalis muscle wasting

tensilon test

tensilon test, false positive

term infant

testicular atrophy

thalamus, lesion of

thalamus, lesion of-bilateral

thoracic outlet syndromes

thrombocytopenia

thrombophlebitis

thyrotropin-releasing hormone

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

torticollis

tracheostomy

transplacental virus infections

trauma

travel, foreign

treatment of neurologic disorder

tremor

tremor, jaw

tremor, postural

triangle of Guillain and Mollaret

tricresylphosphate

trigeminal nerve

trigeminal nerve, hypertrophy

trigeminal neuralgia

trigger finger

trinucleotide repeats

tripping

tumor necrosis factor inhibitor

ubiquitin

ulcers, fingertip

ulnar nerve

ulnar nerve, deep palmar branch of

ulnar neuropathy

unconsciousness

upgaze, paralysis of

urea-cycle enzymopathies

venous thrombosis, non-cerebral

vertigo

vertigo, positional

vibratory sensation, abnormal

vinblastine

vincristine neurotoxicity

viral infection

viral infection, CNS

viral isolation

visual acuity, decreased

visual loss

vitamin deficiency

vocal cord paralysis

Waldenstrom's macroglobulinemia

walking frame

walking, difficulty with

weakness

weakness, fatiguable

weakness, generalized

weakness, infant

weakness, progressive

weaning from respirator, failure to

web sites

Weber's syndrome

weight loss

Werdnig-Hoffman disease

West Nile fever

wheelchair

Whipple's disease

whistle, inability to

white matter disease

wide based gait

winging of scapula

word-finding difficulty

X-linked bulbospinal neuronopathy

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Pseudoulnar Palsy From a Small Infarct of the Precentral Knob
Neurol 54:2185, Phan,T.G.,et al, 2000

Congenital Muscular Dystrophy with Rigid Spine Syndrome:A Clinical, Pathological, Radiological, and Genetic Study
Ann Neurol 47:152-161, 143, Flanigan,K.M.,et al, 2000

Nitrous Oxide Anesthesia-Associated Myelopathy
ArchNeurol 57:380-382, Marie,R.,et al, 2000

Clinical Features of Nipah Virus Encephalitis Among Pig Farmers in Malaysia
NEJM 342:1229-1235, Goh,K.J.,et al, 2000

Motor Strokes Sparing the Leg
Arch Neurol 57:513-518, de Freitas,G.R.,et al, 2000

Prevalence of Progressive Supranuclear Palsy and Multiple System Atrophy:A Cross-Sectional Study
Lancet 354:1771-1775, Schrag,A.,et al, 1999

Autosomal Dominant Myofibrillar Myopathy with Arrhythmogenic Right Ventricular Cardiomyopathy Linked to Chromosome 10q
Ann Neurol 46:684-692,681, Melberg,A.,et al, 1999

Intravenous Immunoglobulin in the Treatment of Autoimmune Neuromuscular Diseases:Present Status and Practical Therapeutic Guidelines
Muscle & Nerve 22:1479-1497, Dalakas,M.C., 1999

A Sartorial Challenge
Lancet 354:996, Reading,P.J.,et al, 1999

Importance of Dural Ectasia in Phenotypic Assessment of Marfan's Syndrome
Lancet 354:910-913, 878, Fattori,R.,et al, 1999

Colour Doppler Imaging for Diagnosis of Intracranial Hypotension
Lancet 354:826-829, Chen,C-C.,et al, 1999

HTLV-I-Associated Myelopathy:Acute Progression and Atypical MR Findings
AJNR 20:1417-1421, Shakudo,M.,et al, 1999

Polymerase Chain Reaction in the Diagnosis and Management of Central Nervous System Infections
Arch Neurol 56:1215-1219, DeBiasi,R.L.&Tyler,K.L., 1999

Multiple Sclerosis, Side Effects of Interferon Beta Therapy and Their Management
Neurol 53:1622-1627, Walther,E.U.&Hohlfeld,R., 1999

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

Neurologic Complications in Children with Enterovirus 71 Infection
NEJM 341:936-942, Huang,C-C.,et al, 1999

Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
NEJM 341:1037-1044, 1077, Andreu,A.L.,et al, 1999

MR Findings in AIDS-Associated Myelopathy
AJNR 20:1412-1416,1387, Chong,J.,et al, 1999

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