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acid maltase deficiency
acid maltase deficiency, adult
advances in neurology
algorithm
alpha glucosidase
alpha-fetoprotein
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
amyotrophic lateral sclerosis, Parkinson-dementia-complex
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
anterior horn cell disease
aphasia
aphasia, progressive, primary
apraxia of eye movements
areflexia
arm weakness
aspartate aminotransferase
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
Babinski sign
behavioral disorder
bulbar palsy
calf hypertrophy
camptocormia
cane
carcinoembryonic antigen
carcinoma
cardiomyopathy
CAT scan, emission, abnormal
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar degeneration
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 5
cognition
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congenital myopathy
congestive heart failure
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
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efficacy
emotional lability
encephalopathy
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enzyme treatment
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epidemiology of neurology
exercise
eye movement, disorders of
facial weakness, bilateral
familial
fasciculation
floppy infant
fluency
foot drop
frontotemporal dementia, behavioral variant
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gait, waddling
gene
gene mutation
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genetic neurologic disorders
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history of neurology
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hypotonia
hypotonia, infants
hypoxic encephalopathy
immunodeficiency
immunosuppression
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intellectual deficit
intrinsic hand muscles, wasting of
jaw jerk, abnormal
Kugelberg-Welander syndrome
laughing, pathologic
leg atrophy
leg weakness, bilateral
leukemia
life expectancy
lobar atrophy
lymphoma
lysosomal storage disease
lysosomes, abnoral
mental retardation
Mills syndrome
mimics
misdiagnosis
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monomelic amyotrophy
mortality
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MRI, abnormal
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myotonia congenita
neck weakness
nerve conduction studies
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neuropathology
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newborn, evaluation of
next-generation sequencing
nusinersen
ocular motility, disorders of
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palliative care
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
Parkinsonism syndrome
Parkinsonism-dementia complex
pathology
patient information and support
personality change
Pompe's disease of glycogen storage
preclinical
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
progeria
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychomotor retardation
pyramidal tract dysfunction
radiation hypersensitivity
release phenomena
respiratory failure
review article
risk factors
safety
scoliosis
scoliosis, neurologic association with
screening
single photon emission computed tomography
skin, lesions in neurologic disorders
SMN1 gene
spastic ataxia
spasticity
spinal cord
spinal cord degeneration
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
telangiectases
tongue, enlarged
tongue, fasciculations of
trauma
treatment of neurologic disorder
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weakness, proximal
Werdnig-Hoffman disease
wheelchair
word-finding difficulty
workup
Showing articles 750 to 800 of 7771 << Previous Next >>

Motor Neuron Disease, Lymphoproliferative Disease, and Bone Marrow Biopsy
Muscle & Nerve 19:1334-1337996., Louis,E.D.,et al, 1996

Immunoassays Fail to Detect Antibodies Against Neuronal Calcium Channels in Amyotrophic Lateral Sclerosis Serum
Ann Neurol 40:695-700, 6911996., Arsac,C.,et al, 1996

Acute Myopathy of Intensive Care:Clinical, Electromyographic, and Pathological Aspects
Ann Neurol 40:645-654, Lacomis,D.,et al, 1996

Inclusion Body Myositis
JNNP 60:251-255, Garlepp,M.J.&Mastaglia,F.L., 1996

Motor Neuron Disease:A Paraneoplastic Process Associated with Anti-Hu Antibody and Small-Cell Lung Carcinoma
Ann Neurol 40:112-116, Verma,A.,et al, 1996

Opsoclonus
Semin Neurol 16:21-26, Averbuch-Heller,L.&Remler,B., 1996

Critical Illness Myopathy and Neuropathy
Lancet 347:1579-1582, Latronico,N.,et al, 1996

Clinicopath Conf
Tangier Disease, Case 16-1996, NEJM 334:1389-1394996., , 1996

Development of General Weakness in a Patient with Amyotrophic Lateral Sclerosis after Focal Botulinum Toxin Injection
Neurol 46:845-846, Mezaki,T.,et al, 1996

Twelfth-Nerve Palsy:Analysis of 100 Cases
Arch Neurol 53:561-566, Keane,J.R., 1996

Dose-Ranging Study of Riluzole in Amyotrophic Lateral Sclerosis
Lancet 347:1425-1431, Lacomblez,L.,et al, 1996

Skin Involvement in Amyotrophic Lateral Sclerosis
lancet 347:1226-1227, Kolde,G.,et al, 1996

Brain and Spinal Cord MRI in Motor Neuron Disease
JNNP 61:314-317, Thorpe,J.W.,et al, 1996

Amyotrophic Lateral Sclerosis and Occupational History
Arch Neurol 53:730-733, Strickland,D.,et al, 1996

Avoiding False Positive Diagnoses of Motor Neuron Disease:Lessons from the Scottish Motor Neuron Disease Register
JNNP 60:147-151, Davenport,R.J.,et al, 1996

Diagnosing Motor Neurone Disease
BMJ 312:650-651, Chancellor,A.M., 1996

Motor Neuron Disease
BMJ 313:244, Shneerson,J.M., 1996

Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996

AAEM Case Report#13:Diabetic Amyotrophy
Muscle & Nerve 19:939-945996., Chokroverty,S.&Sander,H.W., 1996

Cerebrovascular Complications of Fabry's Disease
Ann Neurol 40:8-17, Mitsias,P.&Levine,S.R., 1996

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Campylobacter Jejuni Infection and Anti-GM1 Antibodies in Guillain-Barre Syndrome
Ann Neurol 40:181-187, Jacobs,B.C.,et al, 1996

Neurogenic Muscle Hypertrophy
Muscle & Nerve 19:811-818996., Gutmann,L., 1996

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

A New Variant of Creutzfeldt-Jakob Disease in the UK
Lancet 347:921-925, 915, 916, 91796., Will,R.G.,et al, 1996

Creutzfeldt-Jakob Disease in a Young Woman
Lancet 347:945-948, Tabrizi,S.J.,et al, 1996

Prospective Evaluation of MRI Lumbosacral Nerve Root Enhancement in Acute Guillain-Barre Syndrome
Neurol 47:813-817, Gorson,K.C.,et al, 1996

Neurological Complications of HIV Infection
Lancet 348:445-452, Price,R.W., 1996

Stroke and Automobile Accidents
Conn Med 60:145-147, Finelli,P.F.&Lee,N., 1996

Pure Motor Hand Weakness
Semin Neurol 16:75-81, Lewis,R.A., 1996

The Epilepsy of Trisomy 9p
Neurol 47:821-824, Stern,J.M., 1996

Natural Evolution of Late Shiplash Syndrome Outside the Medicolegal Context
Lancet 347:1207-1211, Schrader,H.,et al, 1996

Phenotypic Heterogen in Hered Neurop with Liability to Press Palsies Assoc with Chromosome 17p11. 2-12 Delet
Neurol 46:1133-1137, Pareyson,D.,et al, 1996

Treatment of Advanced Parkinson's Disease by Posterior GPi Pallidotomy:1-Year Results of a Pilot Study
Ann Neurol 40:355-366, 3411996., Baron,M.S.,et al, 1996

Acute Stroke with Atrial Fibrillation:The Copenhagen Stroke Study
Stroke 27:1765-1769, Jorgensen,H.S.,et al, 1996

Stroke Severity in Atrial Fibrillation:The Framingham Study
Stroke 27:1760-1764, Lin,H.J.,et al, 1996

Motor Neuron Disease with Parkinsonism
Arch Neurol 53:987-991, Qureshi,A.I.,et al, 1996

Age on Onset, Sex, & Cardiomyopathy as Predictors of Disability and Survival in Friedreich's Disease
Neurol 47:1260-1264, DeMichele,G.,et al, 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Late Juvenile Metachromatic Leukodystrophy Treated with Bone Marrow Transplantation:A 4-Year Follow-up Study
Neurol 46:254-256, Navarro,C.,et al, 1996

Acute Rectus Muscle Palsy in Children as a Result of Orbital Myositis
J Pediatr 128:230-233, Pollard,F.,et al, 1996

Familial Hemiplegic Migraine, Nystagmus and Cerebellar Atrophy
Ann Neurol 39:100-106, Elliott,M.A.,et al, 1996

Autonomic Ganglionitis with Severe Hypertension, Migraine, and Episodic but Fatal Hypotension
Neurol 47:817-821, Lee,H.C.,et al, 1996

The Syndrome of Posterior Choroidal Artery Territory Infarction
Ann Neurol 39:779-788, Neau,J.&Bogousslavsky,J., 1996

Age and Guillain-Barre Syndrome Severity
Muscle & Nerve 19:375-377996., Sheth,R.D.,et al, 1996

Valproic Acid Hepatic Fatalities. III. U. S. Experience Since 1986
Neurol 46:465-469, Bryant,A.E.&Dreifuss,F., 1996

Fatal Insomnia in a Case of Familial Creutzfeldt-Jakob Disease with the Codon 200Lys Mutation
Neurol 46:758-761, Chapman,J.,et al, 1996

Long-Term Outcome After Whiplash Injury:A 2-Year Follow-up Consid Injury Mech & Somatic, Radiologic, & Psychosoc Findings
Medicine 74:281-299, Radanov,B.P.,et al, 1995



Showing articles 750 to 800 of 7771 << Previous Next >>