Neudle.com: motor neuron disease reversible

Differential
(Click to cross reference)

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

advance directives

advances in neurology

adverse drug reaction

akinetic mute

algorithm

alveolar hypoventilation

Alzheimer's disease

aminoacidopathies

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, complications with

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, misdiagnosis

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis, work up

amyotrophic lateral sclerosis-like syndrome

analgesic

animal exposure

anorexia

anterior horn cell disease

anti citrullinated antibody

autonomic dysfunction

Babinski sign

Bagel sign

basal ganglia

basal ganglia, lesion of

basal ganglia, lesion, bilateral

brainstem, infarction of

brainstem, lesion of

bulbar palsy

bulbar palsy, acute

bulbar palsy, progressive

CAT scan, emission, abnormal

catalepsy

cataracts

CD4 counts

central nervous system, infection of

cerebellar atrophy, primary

cerebellar lesion

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrovascular accident

cervical collar

cervical spine

cervical spine injury

cervical spine injury, treatment of

cervical spondylosis

cervical spondylosis, differential diagnosis of

cervical spondylosis, misdiagnosis

children

chondroitin sulfate C

chorea

choreoathetosis

chromosomal abnormality

chromosome 5

Clinical Pathologic Conference(C.P.C.)

congenital heart disease

constipation

cortical-basal ganglionic degeneration

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, frontotemporal

developmental milestones, loss of

developmental retardation

diagnostic criteria

diaphragmatic paralysis

diarrhea

differential diagnosis

diplopia

disability, neurological

distal muscle atrophy

distal muscle weakness

electroencephalogram, abnormalities of

electromyogram

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, viral

enterovirus

enterovirus infection of CNS

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

facial weakness, bilateral

fine motor function, impaired

flaccid paralysis

flail arm syndrome

foot drop

gag reflex, depressed

gait disorder

gait, apraxic

gamma amino butyric acid

gammaglobulin therapy, intravenous

gangliosides

gastrostomy

gastrostomy, percutaneous endoscopic

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

GM1 ganglioside antibodies

Guillain Barre syndrome

Hallervorden Spatz disease

heralding manifestation

highly active antiretroviral therapy

human immunodeficiency virus type 1

iatrogenic neurologic disorders

immunosuppressive agents

immunotherapy

inborn errors of metabolism

infection

insomnia

intellectual deficit

intellectual deterioration

intermittent positive pressure breathing

internet

intrinsic hand muscles, wasting of

iron, brain

jaw clonus

jaw jerk, abnormal

juvenile distal and segmental muscular atrophy

Kugelberg-Welander syndrome

lactic acidemia

laminectomy, cervical

laughing, pathologic

L-dopa

leg weakness, bilateral

leg weakness, unilateral

leukodystrophy

life expectancy

life support, withdrawal of

life support, withholding of

life sustaining treatment

locked-in syndrome

lymphadenopathy

lysosomal storage disease

malaise

masked facies

medical-legal aspects of neurology

memory, impairment of

meningeal enhancement

meningismus

meningitis

meningitis, aseptic

meningitis, neutrophilic

mental status, abnormal

metabolic disorder, primary

motor neuron disease, misdiagnosis

motor neuron disease, spontaneous recovery

motor system

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, disappearing lesion on

MRI, negative

MRI, paramagnetic effect

MRI, ring sign

MRI, spinal cord

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, treatment of

multiple sleep latency test

multiple system atrophy

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle pain

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Duchenne

myasthenia gravis

myasthenia gravis, treatment of

myelitis

myelitis, longitudinal

myopathy, steroid responsive

nerve conduction studies

nerve conduction studies, motor

nerve growth factor

neurofibromatosis 1

neurofibromatosis 2

neurologic complications of, surgery

neurologic disease

neurologic disease, diagnoses of

neurologic signs

neurologic symptoms

neurologic testing

neuromuscular disease, electrodiagnosis of

neuronal degeneration

neuropathology, brain

neuropathy

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, peripheral

neuropathy, peripheral, treatment

neuroprotective agents

neurotransmitter

neutropenia

next-generation sequencing

ophthalmoplegia, total

opiate

oral ulcerations

orthopnea

owl's eye sign of spinal cord

pain, management of chronic

palliative care

PANK2 mutation

paralysis, acute

paralysis, acute areflexic

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paresthesias

Parkinson disease

Parkinson disease, atypical

Parkinson disease, axial symptoms

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinsonism syndrome

paroxysmal neurologic deficits

patient information and support

penguin silhouette sign

peroxisomal disease

personality change

phrenic nerve pacemaker

physician assisted suicide

placebo

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poliomyelitis

poliomyelitis-like illness

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

pregnancy, neurologic complications in

prevention of neurologic disorders

primary lateral sclerosis

prognosis

progressive neurologic disorder

progressive supranuclear palsy

proximal muscle atrophy

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychomotor retardation

pyramidal tract dysfunction

quadriparesis

quadriplegia

quality of life

radiation therapy, salivary gland

rapidly progressing neurologic illness

rash

recombinant DNA

REM sleep

REM sleep behavior disorder

remote effect of cancer on the nervous system

respiratory tract infection

retinitis pigmentosa

retrocollis

retrovirus

reverse split hand sign

review article

RFLPs

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

risk-benefit assessment

saccadic eye movements, abnormal

safety

salivation, excessive

scoliosis

scoliosis, neurologic association with

seizure, treatment of

sensory symptoms

sequencing difficulty

serologic testing

serologic testing of cerebrospinal fluid

serum alanine aminotransferase

sinemet

skin, lesions in neurologic disorders

sleep

sleep apnea

sleep offset paralysis

sleep onset paralysis

sleep paralysis

sleep pathology and physiology

speech disorder, childhood

spinal cord

spinal cord degeneration

spinal cord, cervical

spinal cord, compression of

spinal cord, injury of

spinal cord, injury, management of

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spondylosis

sports medicine, neurology of

stem cell transplantation

survival motor neuron gene

thyrotropin-releasing hormone

tongue, atrophy

tongue, fasciculations of

tracheostomy

trauma

treatment of neurologic disorder

tremor

tripping

unconsciousness

unconsciousness, episodic

unconsciousness, transient

undiagnosed

urea-cycle enzymopathies

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

web sites

weight gain

weight loss

Werdnig-Hoffman disease

West Nile fever

wheelchair

workup

Showing articles 900 to 950 of 10627 << Previous Next >>

Explanation & Management of Neurological Disability
BMJ 294:1203-1205, Critchley,E.M.R.&Mitchell,J.D., 1987

Lyme Disease:Cause of a Treatable Peripheral Neuropathy
Neurol 37:1700-1706, Halperin,J.J.,et al, 1987

Prediction of Early Beneficial Response to Plasma Exchange in Guillain-Barre Syndrome
Arch Neurol 44:295-298, Gruener,G.,et al, 1987

Alternating Hemiplegia of Childhood
Int Pediatr 2:115-119, Aicardi,J., 1987

Acute Arsenic Intoxication Presenting as Guillain-Barre-Like Syndrome:Donofrio
P. D. , et al, Muscle & Nerve 10:114-120, , 1987

Immobilization Hypercalcemia Associated with Landry-Guillain-Barre Syndrome
Arch Int Med 146:1567-1571, Maythaler,J.M.,et al, 1986

Alzheimer's Disease, Parkinson's Disease, & Motoneurone Disease:Abiotropic Interaction Between Ageing & Environment
Lancet 2:1067-1068, Calne,D.B.,et al, 1986

Amyotrophic Lateral Sclerosis, Associated Clinical Disorders & Immunological Evaluations
Arch Neurol 43:234-238, Appel,S.H.,et al, 1986

Familial Adult Motor Neuron Disease:Amyotrophic Lateral Sclerosis
Neurol 36:511-517, Mulder,D.W.,et al, 1986

Neonatal Paralytic Poliomyelitis
Arch Neurol 43:192-194, Bergeisen,G.H.,et al, 1986

A Long-Term Follow-Up Study of Patients with Post-Poliomyelitis Neuromuscular Symptoms
NEJM 314:959-963, Dalakas,M.C.,et al, 1986

From Benign Fasciculations & Cramps to Motor Neuron Disease
Neurol 36:997-998, Shepherd-Fleet,W.&Watson,R.T., 1986

Delayed Postirradiation Lower Motor Neuron Syndrome
Ann Neurol 19:308-309, Gallego,J.,et al, 1986

Primary Amyloidosis with Peripheral Neuropathy & Signs of Motor Neuron Disease
Neurol 36:1125-1127, Abarbanel,J.M.,et al, 1986

Lathyrism:Evidence for Role of the Neuroexcitatory Aminoacid BOAA
Lancet 2:1066-1067, Spencer,P.S.,et al, 1986

Brain Abscess, A Study of 45 Consecutive Cases
Medicine 65:415-431, Chun,C.H.,et al, 1986

Location of the Gene for X-Linked Spinal Muscular Atrophy
Neurol 36:1595-1598, Fischbeck,K.H.,et al, 1986

Late Sequelae of Poliomyelitis
Editorial, Lancet 2:1195-11961986., , 1986

Slow Resolution of Multifocal Weakness & Fasciculation:A Reversible Motor Neuron Syndrome
Neurol 36:1260-1263, Chad,D.A.,et al, 1986

Motor Neuron Disease & Plasma Cell Dyscrasia
Neurol 36:1429-1436, Shy,M.E.,et al, 1986

Effect of Near Normoglycaimia for Two Yrs on Progression of Early Diabetic Retinopathy, Nephropathy, & Neuropathy
BMJ 293:1195-1199, Dahl-Jorgensen,K.,et al, 1986

Neurologic Complications in Oral Polio Vaccine Recipients
J Pediatr 108:878-881, Gaebler,J.W., 1986

Classification of Peripheral Neuropathy:The Long and the Short of It
Muscle & Nerve 9:711-719986., Sabin,T.J., 1986

Post-Polio Syndrome
J Med Assoc Ga 74:510-511, Bailey,A.A., 1985

Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis
Ann Neurol 18:614-617, Wolf,B.,et al, 1985

Guillain-Barre Syndrome:Management of Respiratory Failure
Neurol 35:1662-1665, Ropper,A.H.&Kehne,S.M., 1985

Wernicke's Encephalopathy
NEJM 312:1035-1039, Reuler,J.B.,et al, 1985

Progressive Dementia, Visual Deficits, Amyotrophy, & Microinfarcts
Neurol 35:789-796, Kaplan,J.G.,et al, 1985

Sarcoidosis & Its Neurological Manifestations
Arch Neurol 42:909-917, Stern,B.J.,et al, 1985

Amyotrophic Lateral Sclerosis:Part 1. Clinical Features, Pathology, & Ethical Issues in Management
Ann Neurol 18:271-280, Tandan,R.,et al, 1985

Amytrophic Lateral Sclerosis:Part 2, Etiopathogenesis
Ann Neurol 18:419-431, Tandan,R.,et al, 1985

Isolation of LAV/HTLV-III From a Patient with Amyotrophic Lateral Sclerosis
NEJM 313:324-325, Hoffman,P.M.,et al, 1985

ALS & Pet Exposure
Neurol 35:717-720, Tarras,S.,et al, 1985

Plasmapheresis & Acute Guillain-Barre Syndrome
The Guillain-Barre Syndrome Study Group, Neurol 35:1096-11041985., , 1985

Clinical Findings in Four Children with Biotinidase Deficiency Detected Through a Statewide Neonatal Screening Program
NEJM 313:16-19, 43-441985., Wolf,B.,et al, 1985

Leukaemia & the Central Nervous System
Editorial, Lancet 1:1196-11981985., , 1985

Improved Neurologic Function After Long-Term Correction of Vitamin E Deficiency in Children with Chronic Cholestasis
NEJM 313:1580-1586, Sokol,R.J.,et al, 1985

Sino-Orbital Aspergillosis Associated with Total Ophthalmoplegia
Laryngoscope 95:190-192, Yumoto,E.,et al, 1985

Pathological Laughter & Crying
In Frederiks, J. A. M. (Ed) Handbook of Clinical Neurology, Elsevier Science Publ, 45:219, Poeck,K., 1985

Cysticercosis-Review of 230 Patients
Bull Clin Neurosci 50:76-101, McCormick.G.F., 1985

Nystagmus in Motor Neuron Disease:Clinicopathological Study of Two Cases
Ann Neurol 16:71-77, Kushner,M.J.,et al, 1984

Sudden Infant Death Syndrome Caused by Poliomyelitis
Arch Neurol 41:775-777, Dunne,J.W.,et al, 1984

Inhibition of Terminal Axonal Sprouting by Serum From Patients with Amyotrophic Lateral Sclerosis
NEJM 311:933-939, Gurney,M.E.,et al, 1984

Familial Occurrence of Amyotrophic Lateral Sclerosis, Parkinsonism, & Dementia
Ann Neurol 16:642-648, Schmitt,H.P.,et al, 1984

Controlled Trial of Plasma Exchange in Acute Inflammatory Polyradiculoneuropathy
Lancet 1:877-879, Greenwood,R.J.,et al, 1984

Monomelic Amyotrophy
Arch Neurol 41:388-394, Gourie-Devi,M.,et al, 1984

Benign Focal Amyotrophy
Arch Neurol 41:678-679, Riggs,J.E.,et al, 1984

Conjugal Amyotrophic Lateral Sclerosis
Ann Neurol 14:699, Paolino,E.,et al, 1983

Adult Polyglucosan Body Disease:Clinical & Nerve Biopsy Findings in Two Cases
Ann Neurol 13:440-444, Vos,A.L.M.,et al, 1983

Amyotrophic Lateral Sclerosis & Pet Exposure
NEJM 309:244-245, Schenkman,M.,et al, 1983

Showing articles 900 to 950 of 10627 << Previous Next >>