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Differential
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advance directives
advances in neurology
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, juvenile
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
amyotrophic lateral sclerosis-like syndrome
areflexia
arm weakness
aspiration
Babinski sign
basal ganglia, lesion of
BiPAP
botulinum toxin
Brugada syndrome
bulbar palsy
bulbar palsy, acute
bulbar palsy, progressive
CAG repeats
camptocormia
cerebral cortex
cerebral cortical atrophy
chewing, impaired
Clinical Pathologic Conference(C.P.C.)
clonus
complications
creatine phosphokinase(CPK)elevated
crying, pathologic
degenerative diseases of CNS
dementia
dementia, frontotemporal
dentatorubral-pallidoluysian atrophy
diabetes mellitus
differential diagnosis
distal muscle weakness
DNA probes
drooling
dying
dysarthria
dysphagia
dysphonia
dyspnea
electrocardiogram, abnormal
electromyogram
electromyogram, decremental response
emotional lability
epidemiology of neurology
familial
fasciculation
fatigable chewing
fatigue
fibrillations
flail arm syndrome
foot drop
fragile-X syndrome
frontal lobe, atrophy
gag reflex, depressed
gastrostomy
gastrostomy, percutaneous endoscopic
gene
gene mutation
genetic counselling
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genetic neurologic disorders
genetic screening
genetic testing
gynecomastia
hand weakness
hemiparesis
heralding manifestation
hoarseness
hospice
huntingtin
Huntington's chorea
hyperreflexia
hypertension
hyporeflexia
intellectual deficit
internal capsule
intrinsic hand muscles, wasting of
jaw clonus
jaw closure weakness
jaw jerk, abnormal
Kugelberg-Welander syndrome
laughing, pathologic
leg weakness, unilateral
life expectancy
liver disease
lobar atrophy
masseter muscle weakness
Mills syndrome
mimics
misdiagnosis
molecular genetics
motor neuron disease
MRI
MRI, abnormal
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
myocardial injury
myocytolysis
myopathy
myotonia dystrophica
nasal speech
neck weakness
neoplasm, primary intracranial
neoplasm, primary of CNS
neuroendocrinology
neurologic disease
neurologic disease, diagnoses of
neurologic symptoms
neuronal migration disorder
neuronopathy
neuropathology
neuropathology, brain
neuropathy
neuropathy, motor, multifocal
neuroprotective agents
pain
pain, management of chronic
palliative care
paraparesis, spastic
polymerase chain reaction
polymyositis
practice guidelines
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudobulbar palsy
pyramidal tract dysfunction
quality of life
repetitive nerve stimulation
respirator
respiratory failure
review article
riluzole
risk factors
salivation, excessive
sleep
sleep pathology and physiology
spasticity
speech disorder
spinal muscular atrophy
spinocerebellar ataxia type 1
spinocerebellar degeneration
standing difficulty
sudden death
temporal lobe, atrophy
temporalis muscle wasting
testicular atrophy
tongue, atrophy
tongue, fasciculations of
tongue, weakness
trauma
treatment of neurologic disorder
tremor
tremor, postural
trinucleotide repeats
tripping
walking, difficulty with
weakness
weakness, fatiguable
weakness, progressive
weight loss
white matter disease
X-linked bulbospinal neuronopathy
Showing articles 300 to 350 of 2602 << Previous Next >>

Classic & Generalized Variants of Pick's Disease, A Clinicopath, Ultrastruc & Immunocyto Study
Ann Neurol 16:467-480, Munoz-Garcia,D.,et al, 1984

Congenital Hydrocephalus & Eye Abnormalities with Severe Developmental Brain Defects:Warburg's Syndrome
Ann Neurol 16:60-65, Bordarier,C.,et al, 1984

Cerebro-ocular Dysgenesis (Walker-Warberg Syndrome) :Neuropathologic & Etiologic Analysis
Neurol 34:1531-1541, Williams,R.S.,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

Glutamate Dehydrogenase Deficiency in Patients with Olivopontocerebellar Atrophy
Neurol 33:1322-1326, Duvoisin,R.C.,et al, 1983

Syndromes of Amytrophic Lateral Sclerosis & Dementia:Relation to Transmissible Creutzfeldt-Jakob Disease
Ann Neurol 14:17-26, Salazar,A.M.,et al, 1983

Oligoclonal IgG Bands in Cerebrospinal Fluid in Various Neurological Diseases
Ann Neurol 13:434-439, Chu,A.B.,et al, 1983

Quadriceps Myopathy:A Varient of the Limb-Girdle Dystrophy Syndrome
JNNP 46:355-357, Swash,M.,et al, 1983

Acute Respiratory Failure in Motor Neuron Disease
Arch Neurol 40:30-32, Hill,R.,et al, 1983

Effect on Weakness & Spasticity in Amyotrophic Lateral Sclerosis of Thyrotropin-Releasing Hormone
Lancet 2:73-75, Engel,W.K.,et al, 1983

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

Neurodegenerative Disease of Infancy & Childhood
Ann Neurol 13:351-364, Dyken,P.,et al, 1983

Computed Tomography in Pick's Disease:Findings in a Family Affected in Three Consecutive Generations
J Comput Assist Tomogr 6:907-911, Groen,J.J.,et al, 1982

Classic Amyotrophic Lateral Sclerosis With Dementia
Arch Neurol 39:681-683, Wilkstrom,J.,et al, 1982

Distal Myopathy, Histochemical & Ultrastructural Studies
Arch Neurol 39:367-371, Kumamoto,T.,et al, 1982

Enigmatic Dyspnoea:An Unusual Presentation of Motor-Neuron Disease
Lancet 1:933-935, Nightingale,S.,et al, 1982

Long-Term Management of Respiratory Failure in Amyotrophic Lateral Sclerosis
Ann Neurol 12:18-23, Sivak,E.,et al, 1982

Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
Arch Neurol 39:657-660, D'Alessandro,R.,et al, 1982

Amyotrophic Lateral Sclerosis & Paraproteinemia
Neurol 32:896-898, Krieger,C.,et al, 1982

Nonfamilial Amyotrophy with Dementia, etc
Advances in Neurology, Human Motor Neuron Diseases, Ed. Rowland, Raven Press, NY 1982 vol 36, p 173., Tyler,H.R., 1982

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Progressive Pontobulbar Palsy With Deafness
Arch Neurol 38:186-190, Brucher,J.M.,et al, 1981

Motor Neuron Disease:Decremental Responses to Repetitive Nerve Stimulation
Neurol 31:202-204, Bernstein,L.P.,et al, 1981

Preservation of the Phrenic Motorneurons in Werdnig-Hoffman Disease
Ann Neurol 9:506-510, Kuzuhara,S.,et al, 1981

Circulating Immune Complexes in Neurologic Disease
Neurol 31:1402-1407, Noronha,A.B.C.,et al, 1981

Vitamin E Deficiency in Werdnig-Hoffmann Disease
Ann Neurol 10:266-268, Shapira,Y.,et al, 1981

Management of Hypoventilation in Motor Neuron Disease Presenting with Respiratory Insufficiency
Ann Neurol 7:188-191, Sivak,E.D.,et al, 1980

Juvenile Muscular Atrophy Localized to Arms
Arch Neurol 37:297-299, Singh,N.,et al, 1980

Myotonic Dystrophy
In Harrison's Principles of Internal Medicine, 9th Ed, McGraw-Hill Book Co, NY 206180., Adams,R.D.,et al, 1980

Quadriceps Myopathy in Two Brothers
Rhode Island Med J 62:125, Finelli,P.F., 1979

Use of the ECG in the Diagnosis of Childhood Spinal Muscular Atrophy
Arch Neurol 36:317-318, Russman,B.S.,et al, 1979

Spirometry in Amyotrophic Lateral Sclerosis
Arch Neurol 36:74-80, Fallat,R.J.,et al, 1979

Age & Cerebrospinal-Fluid Protein in Motor-Neuron Disease
NEJM 300:437-438, Guiloff,R.J.,et al, 1979

Double-Blind Study of Modified Neurotoxin in Motor Neuron Disease
Neurol 29:77-81, Tyler,H.R., 1979

Haemophilic Neuromyopathy
JNNP 42:600-605, Defaria,C.R.,et al, 1979

Presenile Dementia With Motor Neuron Disease in Japan, A New Entity
Arch Neurol 36:592-593, Mitsuyama,Y.,et al, 1979

Amyotrophic Lateral Sclerosis With Ophthalmoplegia; A Cliniocopathologic Study
Arch Neurol 36:615-617, Harvey,D.G.,et al, 1979

Clinical Pathological Conference
Amyotrophic Lateral Sclerosis, Case Record 46-1979, NEJM 301:1104-1111979., , 1979

Clinical Features of Subcortical Arteriosclerotic Encephalopathy (Binswanger Disease)
Neurol 28:1206-1215, Caplan,L.R.,et al, 1978

Abnormal Iris Vasculature in Myotonic Dystrophy
Arch Neurol 35:224, Stern,L.Z.,et al, 1978

Sparing of the Onufrowicz Nucleus in Sacral Anterior Horn Lesions
Ann Neurol 4:245-249, Iwata,M.,et al, 1978

Peripheral Neuropathy in Myotonic Dystrophy
Arch Neurol 35:741-745, Olson,N.D.,et al, 1978

Distal Chronic Spinal Muscular Atrophy Involving the Hands
JNNP 41:653-658, O'Sullivan,D.J.,et al, 1978

Amyotrophic Lateral Sclerosis
Arch Neurol 35:638-642, Rosen,A.D., 1978

Cellular Immunity In Guamanians with Amyotrophic Lateral Sclerosis & Parkinsonism-Dementia
NEJM 299:680-685, Hoffman,P.M.,et al, 1978

Diaphragmatic Paralysis in Motor Neuron Disease
Neurol 28:18, Parhad,I.M.,et al, 1978

Free Amino Acid Levels in Amyotrophic Lateral Sclerosis
Ann Neurol 3:305, Patten,B.M.,et al, 1978

Juvenile Type of Distal & Segmental Muscular Atrophy of Upper Extremities
Ann Neurol 3:429, Sobue,I.,et al, 1978



Showing articles 300 to 350 of 2602 << Previous Next >>