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acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

ACTH, ectopic syndrome of

acute intermittant porphyria

Addison's disease

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alpha glucosidase

alpha-fetoprotein

alveolar hypoventilation

Alzheimer's disease

aminoacidopathies

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

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, juvenile

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, myasthenic syndrome with

amyotrophic lateral sclerosis, Parkinson-dementia-complex

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 reflex, preserved

anterior horn cell disease

anterior interosseous neuropathy

anterior spinal artery infarction

anterior tibial muscle weakness

anti citrullinated antibody

anti Hu antibody

anticonvulsants

antiviral agents

aphasia, progressive, primary

apraxia of eye movements

arterial dissection

arterial dissection, aorta

arterial dissection, vertebral

arthrogryposis multiplex

ascending paralysis

aspartate aminotransferase

asthma, poliomyelitis-like syndrome with

ataxia telangiectasia

ataxia, cerebellar

ataxia, progressive

ataxia, truncal

athetosis, causes of

atlanto axial dislocation, congenital

autoimmune disease

autonomic dysfunction

axonal degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

Behcet's syndrome

Bence Jones protein

bitemporal visual field defect

bladder dysfunction

bone marrow biopsy

botulinum toxin

botulinum toxin, complications of

brachial amyotrophic diplegia

brachial neuritis

brainstem, lesion of

Brugada syndrome

bulbar palsy, acute

bulbar palsy, childhood

bulbar palsy, progressive

calcification, intracranial

calf hypertrophy

carcinoembryonic antigen

carcinoma of breast

carcinoma of lung

carpo-pedal spasm

CAT scan, abnormal

CAT scan, emission, abnormal

cauda equina, enhancement

cavernous sinus, syndrome

central core disease

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar vermis

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral peduncle

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, young adult

cerebrovascular disease, cardiovascular disease with

cervical collar

cervical spine injury

cervical spondylosis

Charcot-Marie-Tooth

chest x-ray, abnormal

chewing, impaired

Chinese paralytic syndrome

choreoathetosis

chromosomal abnormality

ciguatera poisoning

Clinical Pathologic Conference(C.P.C.)

cluster, geographic

cold temperature

compression neuropathy

conduction block

congenital heart disease

congenital myopathy

congestive heart failure

conversion reaction

cortical hand knob

coxsackievirus, myopathy with

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

Cushing's syndrome

cyclophosphamide

deep gray nuclei

degenerative diseases of CNS

Dejerine-Sottas syndrome

delay in diagnosis

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, lesion of

dermatomyositis

developmental milestones

developmental retardation

dexterity, impaired

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic mononeuropathy

diagnostic criteria

diaphragmatic paralysis

diaphragmatic paralysis, causes of

differential diagnosis

diplegia, atonic

diplegia, brachial

disability, neurological

distal muscle atrophy

distal muscle weakness

drug induced neurologic disorders

drug interactions

electrical injury of nervous system

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram, decremental response

electrophoretic pattern, serum

embolism, nucleus pulposus

emotional lability

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, central European

encephalitis, Japanese

encephalitis, paraneoplastic

encephalitis, Powassan

encephalitis, viral

encephalomyelitis

encephalomyeloneuritis

encephalopathy, anoxic

encephalopathy, neonatal

enterovirus infection of CNS

entrapment neuropathy

enzyme treatment

enzyme, muscle disease

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

ethics in neurology

evoked potentials

exercise intolerance

extremity, cold

eye movement, disorders of

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

fasciculation, benign

fatigable chewing

Fazio-Londe's disease

fine motor function, impaired

finger weakness

flaccid paralysis

flail arm syndrome

flu-like illness

football neurologic injuries

Friedreich's ataxia

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, lesion of

frontotemporal dementia, behavioral variant

F-wave response

gag reflex, depressed

gammaglobulin therapy, intravenous

gangliosidosis GM2

gastrectomy, neurologic complications following

gastroenteritis

gaze palsy, horizontal

gaze palsy, supranuclear

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genital ulcerations

glycogen storage disease

GM1 ganglioside

GM1 ganglioside antibodies

granular atrophy, cerebral cortex

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

hallucination, auditory

handlebar palsy

Hand-Schuller-Christian disease

heavy metal intoxication

hemifacial atrophy

heralding manifestation

heterochromia iridis

highly active antiretroviral therapy

history of neurology

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

Horner's syndrome

Horner's syndrome, etiologies of

human immunodeficiency virus type 1

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

Huntington's chorea

hyperadrenalism

hyperinsulinism

hyperparathyroidism

hyperpigmentation of skin

hyperthyroidism

hypogammaglobulinemia

hypoglycemic coma

hypokalemic alkalosis

hypokalemic periodic paralysis

hypoparathyroidism

hypotension, systemic

hypothalamus, disturbance of

hypotonia, infants

hypoxic encephalopathy

immunodeficiency

immunoelectrophoresis, serum

immunohistochemistry

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

infant, evaluation of

infantile neuronal degeneration

infantile tremor syndrome

inflexibility, mental

intellectual deficit

intellectual deterioration

intermittent positive pressure breathing

internal capsule

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

Isaacs syndrome

islet cell tumor

Jakob-Creutzfeldt disease

jaw jerk, abnormal

juvenile distal and segmental muscular atrophy

klippel feil syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

laboratory values, normal

lactic acidemia

laughing, pathologic

lead and the nervous system

leg weakness, bilateral

leg weakness, unilateral

leukemia, neurologic findings assoc.with

leukoencephalopathy

Lewy body disease, diffuse

lid closure, weakness of

life expectancy

life support, withdrawal of

life sustaining treatment

limbic encephalitis

locked-in syndrome

lumbar puncture

lumbosacral radiculopathy

lymphadenopathy

lymphadenopathy, hilar

lymphoma involving CNS

lysosomal storage disease

lysosomes, abnoral

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

Man-In-The-Barrel syndrome

masseter muscle wasting

median neuropathy

medical-legal aspects of neurology

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, neutrophilic

mental retardation

mental status, abnormal

metabolic disorder, primary

midbrain, lesion of

mitral valve lesion

molecular genetics

monoclonal antibodies

monoclonal gammopathy

monomelic amyotrophy

mononeuritis multiplex

mononeuropathy, motor

Motor Band Sign

motor neuron disease

motor neuron disease, juvenile form

motor neuron disease, misdiagnosis

motor neuron disease, spontaneous recovery

movement disorder

movement disorder, extrapyramidal

MRI, contrast enhanced

MRI, disappearing lesion on

MRI, gradient-echo

MRI, paramagnetic effect

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

multiple myeloma

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, progressive

muscle atrophy, static

muscle diseases, characteristics of

muscle hypertrophy

muscle twitching

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, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

muscular dystrophy, neurogenic hypothesis of

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenic crisis

myasthenic syndrome

myelitis, longitudinal

myelitis, transverse

myelogram, cervical

myeloneuropathy

myelopathy, ischemic

myelopathy, carcinomatous

myelopathy, chronic progressive

myelopathy, necrotizing

myelopathy, radiation induced

myeloradiculitis

myeloradiculopathy

myocardial infarction

myocardial injury

myopathy, carcinomatous

myopathy, centronuclear

myopathy, critically ill

myopathy, distal

myopathy, mitochondrial

myopathy, neurogenic hypothesis of

myopathy, thyroid disease causing

myotonia congenita

myotonia dystrophica

myxedema, neurologic manifestations of

N-acetyl-L-aspartic acid

narcotic analgesics

nausea and vomiting

nemaline rod myopathy

neoplasm, hormone producing

neoplasm, hormone producing, ectopic

neoplasm, pituitary

nerve conduction studies

nerve conduction studies, motor

nerve growth factor

nerve root enhancement

neuralgia, intercostal

neuritis, causes of

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurofibromatosis 2

neurogenic bladder

neurogenic vs.myopathic atrophy

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic signs

neurologic symptoms

neurologic testing

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuronal degeneration

neuronal intranuclear inclusion disease

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, acute

neuropathy, amyloid

neuropathy, bicycle

neuropathy, diabetic

neuropathy, diphtheritic

neuropathy, hereditary peripheral

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, short-fiber

neuroprotective agents

neurotransmitter

newborn, evaluation of

next-generation sequencing

NMDA antagonists

nystagmus, primary position of gaze

nystagmus, rotary

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

oral ulcerations

otitis, neurologic complications with

owl's eye sign of spinal cord

pain, increased response

palatal myoclonus

palliative care

paralysis, acute

paralysis, acute areflexic

paralysis, asymmetric

paralysis, use-related

paraneoplastic ganglionopathy

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, flaccid

paraparesis, spastic

paraproteinemia

paraspinal muscle

parathyroid adenoma

paratrigeminal syndrome

Parkinson disease

Parkinson disease, motor neuron disease with

Parkinson disease, treatment of

Parkinsonism syndrome

Parkinsonism-dementia complex

paroxysmal neurologic deficits

patient information and support

periodic paralysis

periodic paralysis, thyrotoxic

peripheral vascular disease

peroneal muscle atrophy, causes of

peroxisomal disease

personality change

pheochromocytoma

phrenic nerve pacemaker

physical activity

physician assisted suicide

plasma cell dyscrasia

pleocytosis of cerebrospinal fluid

poison, mercury

poison, neurologic problems with

poliomyelitis, provocation

poliomyelitis-like illness

polyclonal gammopathy

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, critically ill

Pompe's disease of glycogen storage

pons, lesion of

positive sharp waves

post polio syndrome

posterior inferior cerebellar artery syndrome

posterior interosseous neuropathy

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

primary aldosteronism

primary lateral sclerosis

progressive neurologic disorder

progressive spinal muscular atrophy

proprioception, abnormal

proximal muscle atrophy

pseudoathetosis

pseudobulbar palsy

pseudohypertrophy

psychiatric problems in neurologic disorders

psychomotor retardation

pupil, abnormality in neurologic disorders

pyramidal tract

pyramidal tract dysfunction

quality of life

rabies, nervous system involvement with

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

rapidly progressing neurologic illness

recombinant DNA

Refsum's disease

rehabilitation for neurologic disorders

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal cell carcinoma

repetitive nerve stimulation

respiratory arrest

respiratory failure

respiratory tract infection

retinitis pigmentosa

retrograde axonal flow

reverse split hand sign

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

risk-benefit assessment

root lesion, nerve

Roussy Levy syndrome

saccadic eye movements, abnormal

salivation, excessive

scoliosis, neurologic association with

segmental demyelination

sensorineural hearing loss

sensory symptoms

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

serum alanine aminotransferase

shell fish poisoning

shoulder, subluxation

single photon emission computed tomography

skin, lesions in neurologic disorders

sleep pathology and physiology

Smell Identification Test

somatosensory evoked potentials

somatosensory evoked potentials, dermatomal

speech disorder

speech, loss of

spinal cord degeneration

spinal cord, cervical

spinal cord, compression of

spinal cord, infarction of

spinal cord, injury of

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, neoplasm

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 degeneration

sports medicine, neurology of

standing difficulty

stem cell transplantation

stereotyped behavior

sternocleidomastoid muscle

stiff man syndrome

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

subarachnoid hemorrhage

substantia nigra

superoxide dismutase

survival motor neuron gene

syphilis, neurologic complications with

tandem gait, ataxic

temporal lobe, atrophy

temporalis muscle wasting

tensilon test, false positive

thalamus, lesion of

thalamus, lesion of-bilateral

thoracic outlet syndromes

tick-borne encephalitis

Tolosa Hunt syndrome

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

travel, foreign

treatment of neurologic disorder

tremor, intention

triangle of Guillain and Mollaret

tricresylphosphate

trinucleotide repeats

Trousseau's sign

ulnar nerve, deep palmar branch of

ulnar neuropathy

unconsciousness

unconsciousness, episodic

unconsciousness, transient

upgaze, paralysis of

urea-cycle enzymopathies

urinary incontinence

urinary retention

vestibular function, tests of

viral infection

viral infection, CNS

viral isolation

visual field defect

Waldenstrom's macroglobulinemia

walking, difficulty with

watershed infarcts

weakness, acute

weakness, fatiguable

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

weaning from respirator, failure to

Werdnig-Hoffman disease

West Nile fever

whistle, inability to

white matter disease

winging of scapula

word-finding difficulty

X-linked bulbospinal neuronopathy

Showing articles 150 to 200 of 4340 << Previous Next >>

Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
NEJM 324:1381-1384, 1430-14321991., Siddique,T.,et al, 1991

Pick's Disease:A Case Clinically Resembling Amyotrophic Lateral Sclerosis
Neurol 41:1831-1833, Sam,M.,et al, 1991

Lymphoma, Motor Neuron Diseases, and Amyotrophic Lateral Sclerosis
Ann Neurol 29:78-86, Younger,D.S.,et al, 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Acute Paralytic Poliomyelitis Presenting as Guillain-Barre Syndrome
J Infection 22:129-133, Yohannan,M.D.,et al, 1991

Clinical Features and Associations of 560 Cases of Motor Neuron Disease
JNNP 53:1043-1045, Li,T.,et al, 1990

Selective Involvement of the Pyramidal Tract on Magnetic Resonance Imaging in Primary Lateral Sclerosis
Neurol 40:1799-1800, Marti-Fabregas,J.&Pujol,J., 1990

Lower Motor Neuron Disease in a Patient with Autoantibodies Against Gangliosides GM1 and GD1b:Improvement with Immunotherapy
Neurol 40:842-844, Shy,M.E.,et al, 1990

Polyclonal IgM Anti-GM1 Ganglioside Antibody in Patients with Motor Neuron Disease and Variants
Ann Neurol 27:558-563, Salazar-Grueso,E.F.,et al, 1990

Immunologic Reactivity Against Borrelia Burgdorfi in Patients with Motor Neuron Disease
Arch Neurol 47:586-594, Halperin,J.J.,et al, 1990

Non Alzheimer's Disease Forms of Cerebral Atrophy
Editorial, JNNP 53:929-9311990., Neary,D., 1990

Anti-GM1 IgM Antibodies in Motor Neuron Disease and Neuropathy
Neurol 40:1747-1750, Nobile-Orazio,E.,et al, 1990

Phenotypic Heterogeneity of Spinal Muscular Atrophy Mapping to Chromosome 5q11. 2-12. 3 (SMA5q)
Neurol 40:1831-1836, Munsat,T.L.,et al, 1990

What Causes Motoneuron Disease?
Editorial, Lancet 336:1033-10351990., , 1990

Misdiagnosis in Patients with Amyotrophic Lateral Sclerosis
Arch Int Med 150:2301-2305, Belsh,J.M.&Schiffman,P.L., 1990

HIV-Related Neuromuscular Syndrome Simulating Motor Neuron Disease
Neurol 40:544-546, Verma,R.K.,et al, 1990

The Spectrum of Neurologic Disease Associated with Anti-GM1 Antibodies
Neurol 40:1067-1072, Sadiq,S.A.,et al, 1990

Neuronal Intranuclear Inclusion Disease in a Child:Diagnosis by Rectal Biopsy
Ann Neurol 27:103-106, Goutieres,F.,et al, 1990

Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
Lancet 336:271-273, Melki,J.,et al, 1990

Spinal Muscular Atrophies
Editorial, Lancet 336:280-2811990., , 1990

Paraneoplastic Motor Neuron Disease and Renal Cell Carcinoma:Improvement after Nephrectomy
Neurol 40:960-962, Evans,B.K.,et al, 1990

The Remote Effects of Cancer on the Nervous System
in Neurol Manif of Systemic Dis, W. B. Saunders, Co, Phila, Neurologic Clinics 7:579-603, Dropcho,E.J., 1989

HTLV-1 Associated Myelopathy and Polymyositis in a US Native
Neurol 39:1572-1575, Evans,B.K.,et al, 1989

Rising Mortality From Motoneuron Disease in the USA, 1962-84
Lancet 1:710-712, Lilienfeld,D.E.,et al, 1989

Respiratory Complications and Their Management in Motor Neuron Disease
Brain 112:1155-1170, Howard,R.S.,et al, 1989

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989

Motoneuron Disease:A Disorder Secondary to Solvent Exposure?
Lancet 1:73-76, 82-831989., Hawkes,C.H.,et al, 1989

The Molecular Genetic Revolution, Its Impact on Clinical Neurology
Arch Neurol 45:1366-1376, Payne,C.S.&Roses,A.D., 1988

Motoneuron Disease and Past Poliomyelitis in England and Wales
Lancet 1:1319-1322, Martyn,C.N.,et al, 1988

Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease
Springer-Verlag, NY, p289988., Swash,M.&Schwartz,M.S., 1988

Amyotrophic Lateral Sclerosis Presenting with Sleep Hypopnea Syndrome
Chest 93:1309-1312, Carre,P.C.,et al, 1988

Serum Antibodies to GM1 Ganglioside in Amytrophic Lateral Sclerosis
Neurol 38:1457-1461, Pestronk,A.,et al, 1988

Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988

Motor Neuron Disease & Paraproteinemia
Neurol 37:335-337, Rudnicki,S.,et al, 1987

Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
Neurol 37:446-450, Larsen,R.,et al, 1987

Neurological Clues from Environmental Neurotoxins
BMJ 295:346-347, Martyn,C.N., 1987

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

Motor Neuron Disease in the US, 1971 & 1973-1978:Patterns of Mortality & Associated Conditions at Time of Death
Neurol 37:1339-1343, Leone,M.,et al, 1987

Clinincopath Conf
Progressive Muscular Atrophy & Diabetic Neuromuscular Disease, Case 21-1987, NEJM 316:1326-13357., , 1987

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

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

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

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

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

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

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

Showing articles 150 to 200 of 4340 << Previous Next >>