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amyotrophic lateral sclerosis

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amyotrophic lateral sclerosis, differential diagnosis

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diabetes mellitus

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differential diagnosis

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disability rating scale, neurological

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ethics in neurology

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hypotonia, infants

hypoxic encephalopathy

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inflexibility, mental

intellectual deficit

intermittent positive pressure breathing

internal capsule

intrinsic hand muscles, wasting of

jaw jerk, abnormal

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

laminectomy, cervical

laughing, pathologic

leg weakness, bilateral

leg weakness, unilateral

leukemia, neurologic findings assoc.with

leukoencephalopathy

lid closure, weakness of

life expectancy

life support, withdrawal of

life sustaining treatment

limbic encephalitis

locked-in syndrome

medical-legal aspects of neurology

mental status, abnormal

minimally conscious state

molecular genetics

monomelic amyotrophy

motor neuron disease

motor neuron disease, spontaneous recovery

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

muscle atrophy, progressive

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscular dystrophy

myelitis, longitudinal

myelitis, transverse

myelopathy, ischemic

myeloradiculitis

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narcotic analgesics

nausea and vomiting

nerve conduction studies

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neurologic complications of, surgery

neurologic disease

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neurologic symptoms

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neuropathology, brain

neuroprotective agents

next-generation sequencing

old age, neurology of

owl's eye sign of spinal cord

pain, increased response

pain, management of chronic

palliative care

paralysis, acute

paralysis, acute areflexic

paraneoplastic ganglionopathy

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, flaccid

paraparesis, spastic

paraspinal muscle

Parkinsonism syndrome

Parkinsonism-dementia complex

patient information and support

persistent vegetative state

personality change

phrenic nerve pacemaker

physician assisted suicide

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poliomyelitis-like illness

polymerase chain reaction

positive sharp waves

practice guidelines

pregnancy, neurologic complications in

primary lateral sclerosis

progressive neurologic disorder

progressive spinal muscular atrophy

proximal muscle atrophy

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary embolism

pulmonary function tests

pyramidal tract

pyramidal tract dysfunction

quality of life

rapidly progressing neurologic illness

release phenomena

remote effect of cancer on the nervous system

repetitive nerve stimulation

respiratory arrest

respiratory failure

respiratory tract infection

salivation, excessive

scoliosis, neurologic association with

sensory symptoms

serologic testing, false negative

single photon emission computed tomography

sleep pathology and physiology

speech disorder

spinal cord degeneration

spinal cord, compression of

spinal cord, injury of

spinal cord, injury, management of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

stereotyped behavior

superoxide dismutase

survival motor neuron gene

thalamus, lesion of

tick-borne encephalitis

tongue, atrophy

tongue, fasciculations of

treatment of neurologic disorder

unconsciousness

viral infection

viral infection, CNS

walking, difficulty with

weakness, generalized

weakness, progressive

weaning from respirator, failure to

Werdnig-Hoffman disease

West Nile fever

word-finding difficulty

Showing articles 200 to 250 of 6941 << Previous Next >>

Home Ventilation for ALS Patients:Outcomes, Costs, and Patient, Family and Physician Attitudes
Neurol 43:438-443, Moss,A.H.,et al, 1993

Motor Neuron Diseases and Amyotrophic Lateral Sclerosis:GM1 Antibodies and Paraproteinemia
Neurol 43:418-420, Sanders,K.A.,et al, 1993

Signal Loss in the Motor Cortex on Magnetic Resonance Images in Amyotrophic Lateral Sclerosis
Ann Neurol 33:218-222, Ishikawa,K.,et al, 1993

Amyotrophic Lateral Sclerosis:Hyperintensity of the Corticospinal Tracts on MR of Spinal Cord
AJR 160:604-606, Friedman,D.P.&Tartaglino,L.M., 1993

Lymphocytic Infiltrates in the Spinal Cord in Amyotrophic Lateral Sclerosis
Arch Neurol 50:30-36, Engelhardt,J.I.,et al, 1993

Rapidly Progressive Aphasic Dementia and Motor Neuron Disease
Ann Neurol 33:200-207, Caselli,R.J.,et al, 1993

Polyglucosan Body Disease Simulating Amyotrophic Lateral Sclerosis
Neurol 43:785-790, McDonald,T.D.,et al, 1993

Single-Photon Emission Computed Tomographic Investigation of Patients with Motor Neuron Disease
Neurol 43:1569-1573, Abe,K.,et al, 1993

Poliomyelitis:Hyperintensity of the Anterior Horn Cells on MRI Images of the Spinal Cord
AJR 161:863-865, Malzberg,M.S.,et al, 1993

Clinicopath Conf
Acquired Demyelinating Neuropathy, ? CIDP, ? Motor Neuropathy with Multifocal Conduction Blocks, Cas, 41-1EJM 329:1182-1190,1993., 1993

Brain Imaging in Late-Onset CM2 Gangliosidosis
Neurol 43:2055-2058, Streifler,J.Y.,et al, 1993

Conjugal Amyotrophic Lateral Sclerosis:Report of a Young Married Couple
Neurol 43:2378-2380, Cornblath,D.R.,et al, 1993

Amyotrophic Lateral Sclerosis:T2 Shortening in Motor Cortex at MR Imaging
Radiology 189:843-846, Oba,H.,et al, 1993

Evidence for a Dopaminergic Deficit in Sporadic Amyoptrophic Lateral Sclerosis on Positron Emission Scanning
Lancet 324:1016-1018, Takahashi,H.,et al, 1993

Differential Diagnosis of Guillain-Barre Synd, In Guillain-Barre Synd
Thieme Med Publ, Ch 3, p 42993., Parry,G.J., 1993

MRI and SPECT in Amyotrophic Lateral Sclerosis, Demonstr of Upper Motor Neurone Invol by Neuroimaging
Neuroradiology 34:389-393, Udaka,F.,et al, 1992

Serum Antibodies to L-Type Calcium Channels in Patients with Amyotrophic Lateral Sclerosis
NEJM 327:1721-1728, 17521992., Smith,R.G.,et al, 1992

Decreased Glutamate Transport by the Brain and Spinal Cord in Amyotrophic Lateral Sclerosis
NEJM 326:1464-1468, 14931992., Rothstein,J.D.,et al, 1992

Intrafamilial Heterogeneity in Hereditary Motor Neuron Disease
Neurol 42:1488-1492, Applebaum,J.S.,et al, 1992

Amyotrophic Lateral Sclerosis and Lymphoma:Bone Marroe Examination and Other Diagnostic Tests
Neurol 42:1101-1102, Rowland,L.P.,et al, 1992

Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
Ann Neurol 32:404-407, Boylan,K.B.&Cornblath,D.R., 1992

Motor Neurone Disease
BMJ 304:459-460, Norris,F.H., 1992

Multifocal Demyelinating Motor Neuropathy:Cranial Nerve Involvement and Immunoglobulin Therapy
Neurol 42:506-509, Kaji,R.,et al, 1992

Multifocal Motor Neuropathy with Conduction Block:Is It a Distinct Clinical Entity?
Neurol 42:497-505, Lange,D.J.,et al, 1992

GM-1 Ganglioside for Spinal-Cord Injury
NEJM 326:493, Schonhofer,P.S., 1992

Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria
Brain 115:495-520, Pringle,C.E.,et al, 1992

Olfactory Impairment in Motor Neuron Disease:A Pilot Study
JNNP 54:927-928, Elian,M., 1991

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

Parental Sex Effect in Familial Amyotrophic Lateral Sclerosis
Neurol 41:1292-1294, Leone,M., 1991

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

Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
Neurol 41:823-828, Olney,R.K.,et al, 1991

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

Prognostic Significance of Conjugate Eye Deviation in Stroke Patients
Stroke 22:200-202, Tijssen,C.C.,et al, 1991

Progressive Motor Neuron Disease Associated with Electrical Injury
Muscle & Nerve 14:977-980991., Sirdofsky,M.D.,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

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

Clinical Uses of Intravenous Immunoglobulins
Ann Int Med 112:278-292, Berkman,S.A.,et al, 1990

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

How Frequently Does Classic Amyotrophic Lateral Sclerosis Develop in Survivors of Poliomyelitis
Neurol 40:172-174, Armon,C.,et al, 1990

Amyotrophic Lateral Sclerosis:A Case-Control Study Following Detection of a Cluster in a Small Wisconsin Community
Arch Neurol 47:38-41, Sienko,D.G.,et al, 1990

Neuromuscular Blockade
Lancet 335:382-384, , 1990

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

2-Amino-3- (methylamino) -Propanoic Acid (BMAA) in Cycad Flour:An Unlikely Cause of ALS & Parkinsonism-Dementia of Guam
Neurol 40:767-772, Duncan,M.W.,et al, 1990

Showing articles 200 to 250 of 6941 << Previous Next >>