Neudle.com: motor neuron disease

Differential
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abiotrophy

acid maltase deficiency

acid maltase deficiency, adult

acoustic neurinoma

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

ACTH, ectopic syndrome of

acute intermittant porphyria

Addison's disease

adult polyglucosan body disease

advance directives

advances in neurology

adverse drug reaction

akinetic mute

alcohol, neurologic complications with

alcoholic polyneuropathy

alveolar hypoventilation

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

animal exposure

ankle edema

ankle reflex, preserved

ankylosing spondylitis

anomic aphasia

anorexia

anterior horn cell disease

anterior interosseous neuropathy

anterior spinal artery infarction

anterior tibial muscle weakness

anti citrullinated antibody

anti Hu antibody

anti IgLON5

antibodies to voltage-gated calcium channels

aphasia, progressive, primary

apraxia of eye movements

arterial dissection, aorta

arterial dissection, vertebral

arthrogryposis multiplex

ascending paralysis

aspartate aminotransferase

aspartocyclase

aspiration

asthma

asthma, poliomyelitis-like syndrome with

asymptomatic

ataxia

ataxia telangiectasia

atlanto axial dislocation, congenital

autonomic dysfunction

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

behavioral disorder

Behcet's syndrome

Bence Jones protein

benign congenital hypotonia

benzodiazepine

biologic markers

BiPAP

bitemporal visual field defect

botulinum toxin, complications of

botulism

brachial amyotrophic diplegia

brainstem, infarction of

brainstem, lesion of

bright tongue sign

Brown Sequard syndrome

bulbar palsy, childhood

bulbar palsy, progressive

C0ORF72

cachexia

CAG repeats

calcification, intracranial

calcium channel dysfunction

carbon monoxide poisoning

carcinoembryonic antigen

CAT scan, emission, abnormal

catalepsy

cataracts

cauda equina

cauda equina, enhancement

cavernous sinus, syndrome

CD4 counts

central core disease

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar vermis

cerebellum, neoplasms of

cerebral cortex

cerebral cortical atrophy

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, oligoclonal IgM in

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, young adult

cerebrovascular disease, cardiovascular disease with

cervical collar

cervical osteoarthritis

cervical osteophyte

cervical rib

cervical spine

cervical spine injury

cervical spine injury, treatment of

cervical spondylosis

cervical spondylosis, differential diagnosis of

cervical spondylosis, misdiagnosis

Charcot-Marie-Tooth

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chewing, impaired

children

chills

Chinese paralytic syndrome

choking

chondroitin sulfate C

chorea

chorea, Sydenham's

choreoathetosis

chromosomal abnormality

chromosome 11

chromosome 5

chronic polyneuritis, children

Chvostek sign

ciguatera poisoning

climate change

Clinical Pathologic Conference(C.P.C.)

compression neuropathy

congenital heart disease

congenital myopathy

congestive heart failure

consanguinity

constipation

controversies in neurology

conversion reaction

cortical hand knob

cortical-basal ganglionic degeneration

coxsackievirus, myopathy with

CPAP

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

critical care unit

critical illness

crying, pathologic

cultured skin fibroblasts

degenerative diseases of CNS

Dejerine-Sottas syndrome

delay in diagnosis

delusion

dementia

dementia, age at onset

dementia, cerebrovascular disease causing

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

denervation of muscle

denervation potentials

dentate nuclei

dentate nuclei, lesion of

depression

dermatomyositis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic mononeuropathy

diagnostic criteria

diaphragmatic paralysis

diaphragmatic paralysis, causes of

diarrhea

diet

differential diagnosis

difficulty climbing stairs

disability rating scale, neurological

disability, neurological

distal muscle atrophy

distal muscle weakness

dropped head syndrome

drowning

drug induced neurologic disorders

electrical injury of nervous system

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram

electromyogram, decremental response

electron microscopy

electrophoretic pattern, serum

embolism

embolism, nucleus pulposus

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, central European

encephalitis, Japanese

encephalitis, paraneoplastic

encephalitis, Powassan

encephalitis, viral

encephalocele

encephalomyelitis

encephalomyeloneuritis

encephalopathy

encephalopathy, anoxic

encephalopathy, neonatal

encephalopathy, post anoxic

endocarditis, subacute bacterial

enolase

enterovirus

enterovirus infection of CNS

entrapment neuropathy

enzyme treatment

enzyme, defect

enzyme, muscle disease

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

ethics in neurology

euthanasia

evidence-based research

evoked potentials

excitotoxin

executive dysfunction

eye movement, disorders of

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, causes of

facial pain

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

falling

familial

fasciculation

fasciculation, benign

fatigable chewing

fatigue

Fazio-Londe's disease

feeding disorder

fever

fibrillations

fine motor function, impaired

football neurologic injuries

free radical

Friedreich's ataxia

frontal behavioral spatial syndrome

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, lesion of

frontotemporal dementia, behavioral variant

F-wave response

gag reflex, depressed

gamma amino butyric acid

gammaglobulin therapy, intravenous

ganglionitis

gangliosides

gangliosidosis GM2

gastrectomy, neurologic complications following

gastroenteritis

gastrostomy

gastrostomy, percutaneous endoscopic

gaze palsy

gaze palsy, horizontal

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

glycogen storage disease

GM1 ganglioside

GM1 ganglioside antibodies

granular atrophy, cerebral cortex

grasp reflex

growth retardation

guanidine

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

Gulf War syndrome

Guyon's canal

gynecomastia

Hallervorden Spatz disease

hallucination

hallucination, auditory

hand weakness

handlebar palsy

Hand-Schuller-Christian disease

heavy metal intoxication

hemiplegia, progressive

hepatomegaly

heralding manifestation

herniated disc

herpes simplex encephalitis

herpes simplex encephalitis, diagnosis of

herpes zoster

herpes zoster, oticus

heterochromia iridis

highly active antiretroviral therapy

hippocampus

histochemistry

histochemistry of muscle

Hodgkin's disease, neurologic involvement with

Horner's syndrome

Horner's syndrome, etiologies of

hospice

human immunodeficiency virus type 1

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

hyperpigmentation of skin

hypogammaglobulinemia

hypoglycemia

hypoglycemic coma

hypokalemia

hypokalemic alkalosis

hypokalemic periodic paralysis

hypotension, systemic

hypothalamus

hypothalamus, disturbance of

hypoxic encephalopathy

iatrogenic neurologic disorders

immunization, neurologic complications with

immunodeficiency

immunoelectrophoresis, serum

immunohistochemistry

immunologic disease

immunosuppression

immunosuppressive agents

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, ubiquitin

inclusion body myositis

incontinentia pigmenti

India

infant, evaluation of

infantile neuronal degeneration

infantile tremor syndrome

infection

infectious mononucleosis, neurologic findings with

inflexibility, mental

initiative, lack of

injection, intramuscular

insomnia

intellectual deficit

intellectual deterioration

intermittent positive pressure breathing

internal capsule

internet

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

jaw clonus

jaw jerk, abnormal

Jewish

juvenile distal and segmental muscular atrophy

klippel feil syndrome

Klumpke palsy

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

laboratory values, normal

lactic acidemia

laminectomy, cervical

language disorder in adults

lead and the nervous system

lead poisoning

leg atrophy

leg weakness, bilateral

leg weakness, unilateral

leprosy

leukemia

leukemia, neurologic findings assoc.with

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

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

lumbosacral radiculopathy

Lyme disease

lymphadenopathy

lymphadenopathy, hilar

lymphoma

lymphoma involving CNS

lysosomal storage disease

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

Man-In-The-Barrel syndrome

masked facies

masseter muscle wasting

median neuropathy

medical-legal aspects of neurology

MELAS syndrome

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningismus

meningitis

meningitis, aseptic

meningitis, neutrophilic

meningoencephalitis

mental retardation

mental status, abnormal

metabolic disorder, primary

Millard Gubler syndrome

Mills syndrome

mimics

minimally conscious state

miosis

misdiagnosis

misdirection

mitochondrial disease

mitochondrial encephalomyopathy

monoclonal antibodies

monoclonal gammopathy

monomelic amyotrophy

mononeuritis multiplex

mononeuropathy

mononeuropathy, motor

monoparesis

Montreal cognitive assessment

motor neuron disease, juvenile form

motor neuron disease, misdiagnosis

motor neuron disease, spontaneous recovery

motor system

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, paramagnetic effect

MRI, ring sign

MRI, serial

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

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 sleep latency test

multiple system atrophy

mumps virus

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

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

muscular dystrophy, neurogenic hypothesis of

mutism

myasthenia gravis

myasthenia gravis, diagnosis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, treatment of

myelitis, longitudinal

myelopathy, carcinomatous

myelopathy, chronic progressive

myelopathy, necrotizing

myelopathy, radiation induced

myeloradiculitis

myeloradiculopathy

myocardial infarction

myopathy, carcinomatous

myopathy, centronuclear

myopathy, critically ill

myopathy, distal

myopathy, mitochondrial

myopathy, neurogenic hypothesis of

myopathy, quadriceps

myopathy, steroid responsive

myopathy, thyroid disease causing

myxedema, neurologic manifestations of

N-acetyl-L-aspartic acid

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, hormone producing

neoplasm, hormone producing, ectopic

neoplasm, pituitary

neoplasm, primary intracerebral

neoplasm, primary of CNS

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

nerve growth factor

nerve root enhancement

neuralgia

neuralgia, intercostal

neuritis, causes of

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurofibromatosis 2

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, tempo

neurologic evaluation

neurologic signs

neurologic symptoms

neurologic testing

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuromyotonia

neuron specific enolase

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal intranuclear inclusion disease

neuronal loss

neuronopathy

neuronopathy, sensory

neurons

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy, diphtheritic

neuropathy, hereditary peripheral

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, short-fiber

neuropathy, toxic

neuroprotective agents

newborn, evaluation of

next-generation sequencing

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, vertical

obsessive-compulsive disorder

occupational neurologic disorders

occupational neuropathies

ocular motility, disorders of

oculogyric crisis

old age, neurology of

olivary degeneration, hypertrophic

Onufrowicz nucleus

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, progressive external

ophthalmoplegia, total

opiate

Oppenheim muscular dystrophy

optic atrophy

oral ulcerations

organ transplantation

orthopnea

osteomalacia

otitis, neurologic complications with

owl's eye sign of spinal cord

pain, increased response

pain, leg

pain, management of chronic

paralysis, acute areflexic

paralysis, asymmetric

paralysis, use-related

paraneoplastic ganglionopathy

paranoia

paraoxonase

paraparesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

paratrigeminal syndrome

paresthesias

Parkinson disease

Parkinson disease, atypical

Parkinson disease, axial symptoms

Parkinson disease, L-dopa nonresponsive

Parkinson disease, motor neuron disease with

Parkinson disease, postencephalitic

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinsonism syndrome

Parkinsonism-dementia complex

paroxysmal neurologic deficits

pathologic reflex

pathology

patient information and support

penguin silhouette sign

penicillamine

periarteritis nodosa

periodic paralysis

periodic paralysis, thyrotoxic

peripheral vascular disease

peroneal muscle atrophy, causes of

peroxisomal disease

perseveration

persistent vegetative state

phrenic nerve pacemaker

physical activity

physical therapy

physician assisted suicide

Pick bodies

Pick's disease

placebo

plasma cell dyscrasia

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, mercury

poison, neurologic problems with

poliomyelitis

poliomyelitis vaccine

poliomyelitis, neonatal

poliomyelitis, provocation

poliomyelitis-like illness

polyclonal gammopathy

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, critically ill

polysomnogram

Pompe's disease of glycogen storage

posterior fossa, differential diagnosis of lesions of

posterior inferior cerebellar artery syndrome

posterior interosseous neuropathy

practice guidelines

preclinical

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

pressure sores

prevention of neurologic disorders

primary aldosteronism

primary lateral sclerosis

progeria

prognosis

progranulin

progressive muscular dystrophy

progressive neurologic disorder

progressive spinal muscular atrophy

progressive supranuclear palsy

proprioception

proprioception, abnormal

proximal muscle atrophy

pseudoathetosis

pseudobulbar palsy

pseudohypertrophy

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pulmonary function tests

pupil

pupil, abnormality in neurologic disorders

pyramidal tract

pyramidal tract dysfunction

rabies, nervous system involvement with

radial nerve, palsy of

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

radiation therapy, salivary gland

radiculitis

radiculopathy

ragged-red fibers

rapidly progressing neurologic illness

rehabilitation for neurologic disorders

release phenomena

REM sleep

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal cell carcinoma

renal stones

repetitive nerve stimulation

respirator

respiratory arrest

respiratory depression

respiratory failure

respiratory tract infection

retinal degeneration

retinitis pigmentosa

retrocollis

retrograde axonal flow

retropulsion

retrovirus

reverse split hand sign

review article

RFLPs

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

risk-benefit assessment

rubeola, encephalitis

saccadic eye movements, abnormal

safety

salivation, excessive

sarcoidosis

scleroderma

scoliosis

scoliosis, neurologic association with

scooters

screening

sedation

segmental demyelination

seizure

seizure, children

seizure, treatment of

semantic dementia

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory loss

sensory symptoms

sensory testing

sequencing difficulty

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

serum alanine aminotransferase

shell fish poisoning

short stature

shoulder, subluxation

sinemet

single photon emission computed tomography

single-fiber electromyography

skin, biopsy

skin, lesions in neurologic disorders

sleep

sleep apnea

sleep apnea, obstructive

sleep offset paralysis

sleep onset paralysis

sleep paralysis

sleep pathology and physiology

smell

Smell Identification Test

SMN1 gene

solvent

somatosensory evoked potentials

somatosensory evoked potentials, dermatomal

speech disorder, childhood

speech, loss of

spina bifida

spinal cord

spinal cord degeneration

spinal cord, cervical

spinal cord, compression of

spinal cord, infarction of

spinal cord, injury of

spinal cord, injury, management of

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, infants and children

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

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spirometry

spondylosis

spongy degeneration of brain

sports medicine, neurology of

standing difficulty

stem cell tourism

stem cell transplantation

stereotyped behavior

sternocleidomastoid muscle

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

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

subarachnoid hemorrhage

sudden infant death syndrome

suicide

superoxide dismutase

survival motor neuron gene

symptomatic

synucleinopathy

syphilis, neurologic complications with

temporal lobe, atrophy

temporalis muscle wasting

tensilon test

tensilon test, false positive

thalamus, lesion of-bilateral

thalidomide

Thies's sign

thoracic outlet syndromes

thrombophlebitis

thyrotoxicosis

thyrotropin-releasing hormone

tick bite

tick paralysis

tick-borne encephalitis

Tolosa Hunt syndrome

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

tonsillectomy

torticollis

torticollis, infants and children

toxins, nervous system

treatment of neurologic disorder

triangle of Guillain and Mollaret

tricresylphosphate

trigger finger

trinucleotide repeats

ulnar nerve, deep palmar branch of

ulnar neuropathy

unconsciousness

unconsciousness, episodic

unconsciousness, transient

undiagnosed

upgaze, paralysis of

urea-cycle enzymopathies

urinary incontinence

urinary retention

uveitis

vaccination, neurologic complications with

vaccine

valium

vasculopathy

venous thrombosis, non-cerebral

ventricular enlargement

vestibular function, tests of

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

Waldenstrom's macroglobulinemia

walking frame

walking, difficulty with

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

Werdnig-Hoffman disease

West disease

West Nile fever

wheelchair

whistle, inability to

white matter disease

wide based gait

winging of scapula

word-finding difficulty

workup

wrist drop

xerostomia

X-linked bulbospinal neuronopathy

Showing articles 100 to 150 of 2918 << Previous Next >>

Kennedy Disease
Arch Neurol 60:893-894, Paparounas,K.,et al, 2003

ALS Patients on TPPV
Neurol 61:135-137, Hayashi,H. &Oppenheimer,E.A., 2003

Polymyositis Masquerading as Motor Neuron Disease
Arch Neurol 60:1001-1003, Ryan,A.,et al, 2003

Occurrence of Amyotrophic Lateral Sclerosis Among Gulf War Veterans
Neurol 61:742-749, Horner,R.D.,et al, 2003

Excess Incidence of ALS in Young Gulf War Veterans
Neurol 61:750-756, Haleyl,R.W., 2003

Multiple Sclerosis Presenting as Lower Motor Neuron Wasting and Weakness of the Distal Upper Extremity
Neurol 61:1303-1304, Chong,P.S.T.,et al, 2003

Serial MRI Findings in a Case of Primary Lateral Sclerosis
Neurol 58:647-649, Smith,C.D., 2002

Familial Amyotrophic Lateral Sclerosis
Muscle Nerve 25:135-159, Hand,C.K. &Rouleau,G.A., 2002

Euthanasia and Physician-Assisted Suicide Among Patients with Amyotrophic Lateral Sclerosis in the Netherlands
NEJM 346:1638-1644, Veldink,J.H.,et al, 2002

Results of Radiotherapy for Drooling in Amyotrophic Lateral Sclerosis
Neurol 58:1308, Stalpers,L.J.A. &Moser,E.C., 2002

Mimic Syndromes in Sporadic Cases of Progressive Spinal Muscular Atrophy
Neurol 58:1593-1596, Visser,J.,et al, 2002

The Final Month of Life in Patients with ALS
Neurol 59:428-431, Ganzini,L.,et al, 2002

Poliomyelitis Due to West Nile Virus
NEJM 347:1280-1281, Glass,J.D.,et al, 2002

West Nile Virus Encephalitis
NEJM 347:1225-1226, Peterson,L.R.,et al, 2002

A Poliomyelitis-like Syndrome from West Nile Virus Infection
NEJM 347:1279-1280, Leis,A.A., et al, 2002

Early Symptom Progression Rate is Related to ALS Outcome
Neurol 59:99-103, Chio,A.,et al, 2002

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002

Nonpoliovirus Poliomyelitis Simulating Guillain-Barre Syndrome
Arch Neurol 58:1460-1464, Gorson,K.C.&Ropper,A.H., 2001

Hospitalization in Amyotrophic Lateral Sclerosis, Causes, Costs, and Outcomes
Neurol 56:753-757, Lechtzin,N.,et al, 2001

Inclusiong Body Myositis Mimicking Motor Neuron Disease
Arch Neurol 58:1253-1256, Dabby,R.,et al, 2001

An ALS-Like Syndrome with New HIV Infection and Complete Response to Antiretroviral Therapy
Neurol 57:1094-1097,945, MacGowan,D.J.L.,et al, 2001

Reversible ALS-Like Disorder in HIV Infection
Neurol 57:995-1001,945, Moulignier,A.,et al, 2001

Recessive Ataxia With Ocular Apraxia
Arch Neurol 58:201-205,173, Barbot,C.,et al, 2001

Amyotrophic Lateral Sclerosis
NEJM 344:1688-1700, Rowland,L.P. & Shneider,N.A., 2001

Linkage of Familial Amyotrophic Lateral Sclerosis with Frontotemporal Dementia to Chromosome 9q21-q22
JAMA 284:1664-1669, Hosler,B.A.,et al, 2000

A 44-Year-Old Woman with Difficulty Walking
JAMA 284:2632-2639, Iezzoni,L.I., 2000

Amyotrophic lateral Sclerosis Mimic Syndromes, A Population-Based Study
Arch Neurol 57:109-113, Traynor,B.J.,et al, 2000

Poliomyelitic-Like Illness in Central European Encephalitis
Neurol 55:299-302, Schellinger,P.D. et al, 2000

Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000

Injections of Botulinum Toxin A Into the Salivary Glands Improve Sialorrhoea in Amyotrophic Lateral Sclerosis
JNNP 69:121-123, Giess,R. et al, 2000

The Split Hand in ALS has a Cortical Basis
J Neurol Sci 180:66-70, Weber,M.,et al, 2000

Disorders of Upper & Lower Motor Neurons
Neurol in Clin Practice, 3rd Ed., Butterworth, Boston: Ch. 78 p. 2007, Mitasumoto,H., 2000

Botulinum Toxin is a Useful Treatment in Excessive Drooling of Saliva
JNNP 67:697, Bhatia,K.P.,et al, 1999

An Algorithm for ALS Diagnosis and Management
Neurol 53:S58-S62, Swash,M., 1999

Adult-Onset Nemaline Myopathy:Another Cause of Dropped Head
Muscle & Nerve 22:1146-1150, Lomen-Hoerth,C.,et al, 1999

Atypical Form of Amyotrophic Lateral Sclerosis
JNNP 66:581-585, Sasaki,S.&Iwata,M., 1999

Practice Parameter:The Care of the Patient with Amyotrophic Lateral Sclerosis (An Evidence-Based Review), Report of the Quality Standards Subcommittee of the AAN
Neurol 52:1311-1323, Miller,R.G.,et al, 1999

A Prospecitve Study of Preferences and Actual Treatment Choices in ALS
Neurol 53:278-283,248, Albert,S.M.,et al, 1999

Clinicopath Conf:Lymphoplasmocytic Lymphoma with Motor Neuronopathy,Waldenstrom's Macroglobulinemia
NEJM 340:1661-1669, , 1999

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999

Safety and Factors Related to Survival After Percutaneous Endoscopic Gastrostomy in ALS
Neurol 53:1123-1125, Chio,A.,et al, 1999

Brachial Amyotrophic Diplegia, A Slowly Progressive Motor Neuron Disorder
Neurol 53:1071-1076, Katz,J.S.,et al, 1999

Olfactory Dysfunction in Guamanian ALS,Parkinsonism,and Dementia
Neurol 51:1672-1677, Ahlskog,J.E.,et al, 1998

Attitudes of Patients with Amyotrophic Lateral Sclerosis and Their Care Givers Toward Assisted Suicide
NEJM 339:967-973,987, Ganzini,L.,et al, 1998

Steroid-Responsive Myopathy with Deficient Chondroitin Sulfate C in Skeletal Muscle Conn Tissue
Neurol 50:526-529, Al-Lozi,M.T.,et al, 1998

MR Findings of Werdnig-Hoffmann Disease in Two Infants
AJNR 19:550-552, Hsu,C.,et al, 1998

Distal Hereditary Upper Limb Muscular Atrophy
JNNP 64:217-220, Gross,D.W.,et al, 1998

Estimation of Brainstem Neuronal Loss in ALS with in Vivo Proton Magnetic Resonance Spectroscopy
Neurol 50:72-77, Cwik,V.A.,et al, 1998

Risk of Amyotrophic Lateral Sclerosis & History of Physical Activity, A Population Study
Arch Neurol 55:201-206, Longstreth,W.T.,et al, 1998

Toward Earlier Diagnosis of Amyotrophic Lateral Sclerosis, Revised Criteria
Neurol 50:768-772, Ross,M.A.,et al, 1998

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