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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
congenital heart disease
congenital myopathy
congestive heart failure
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
degenerative diseases of CNS
delusion
dementia
dementia, age at onset
dementia, frontotemporal
dementia, presenile
developmental milestones
developmental retardation
diabetes mellitus
diagnostic criteria
differential diagnosis
distal muscle atrophy
distal muscle weakness
drooling
dying
dysarthria
dysphagia
dystonia
efficacy
emotional lability
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
enzyme treatment
enzyme, defect
epidemiology of neurology
exercise
eye movement, disorders of
facial weakness, bilateral
familial
fasciculation
floppy infant
fluency
foot drop
frontotemporal dementia, behavioral variant
gait disorder
gait, waddling
gene
gene mutation
gene therapy
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glycogen storage disease
growth retardation
hallucination
hand weakness
hemiparesis
hepatomegaly
heralding manifestation
history of neurology
hyperreflexia
hyporeflexia
hypotonia
hypotonia, infants
hypoxic encephalopathy
immunodeficiency
immunosuppression
inflexibility, mental
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
molecular genetics
monomelic amyotrophy
mortality
motor neuron disease
motor system
movement disorder
movement disorder, extrapyramidal
MRI, abnormal
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
myelomalacia
myopathy
myotonia congenita
neck weakness
nerve conduction studies
neurocutaneous disease
neuroendocrinology
neurologic disease, diagnoses of
neurologic evaluation
neuronal degeneration
neuropathology
neuropathy
newborn, evaluation of
next-generation sequencing
nusinersen
ocular motility, disorders of
pain, increased response
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 950 to 1000 of 7669 << Previous Next >>

Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992

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

Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 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

Provocation paralysis
Editorial, Lancet 340:1005-10061992., , 1992

Angelman Syndrome: Clinical Profile
J Child Neurol 7:270-280, Zori,R.T.,et al, 1992

A Clinical Study of Noonan Syndrome
Arch Dis Child 67:178-183, Sharland, M.,et al, 1992

Plasmapheresis in Children with Guillain-Barre Syndrome
Neurol 41:1928-1931, Lamont,P.J.,et al, 1991

Is Essential Tremor Benign?
Neurol 41:1982-1983, Busenbark,K.L.,et al, 1991

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

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
NEJM 325:1487-1498, Dalakas,M.C., 1991

Chronic Cardiomyopathy and WEakness or Acute Coma in Children with a Defect in Carnitine Uptake
Ann Neurol 30:709-716, Stanley,C.A.,et al, 1991

Intrathecal Immune Response in Patients with the Post-Polio Syndrome
NEJM 325:749-755, Sharief,M.K.,et al, 1991

Mutation of the Prion Protein in Libyan Jews with Creutzfeldt-Jakob Disease
NEJM 324:1091-1097, Hsiao,K.,et al, 1991

Clinical Follow-Up and Immunogenetic Studies of 32 Patients with Eosinophilia-Myalgia Syndrome
Lancet 337:1071-1074, Kaufman,L.D.,et al, 1991

Cognitive Abilities & School Performance of Extremely Low Birth Weight Children & Matched TermControls at Age 8
J Pediatr 118:751-760, Saigal,S.,et al, 1991

Effect of Very Low Brith Weight and Subnormal Head Size on Cognitive Abilities at School Age
NEJM 325:231-237, Hack,M.,et al, 1991

Eight-Year Outcome in Infants with Birth Weight of 500 to 999 Grams
Victorial Infant Collabor, Study Group, J Pediatr 118:761-767991., , 1991

Cerebral Edema Causing Death in Children with Maple Syrup Urine Disease
J Pediatr 119:42-45, Riviello,J.J.,et al, 1991

Prospective Observations of 100 High-Risk Neonates by High-Field MRI of CNS:II. Hypoxic-Ischemic Encephalopathy
Pediatrics 87:431-438, Keeney,S.E.,et al, 1991

Neurologic Outcome after Electroencephalographically Proven Neonatal Seizures
Pediatrics 88:583-596, Legido,A.,et al, 1991

Left-Handedness and Life Expectancy
Letters, NEJM 325:10411991., , 1991

Prediction of Non-Survival After Trauma:Innsbruck Coma Scale
Lancet 338:977-978, Benzer,A.,et al, 1991

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

Outcome in Children Who Nearly Drown:A British Isles Study
BMJ 302:931-933, Kemp,A.M.&Sibert,J.R., 1991

Clinical and Electrophysiological Aspects of Acute Paralytic Disease of Children and Young Adults in Northern China
Lancet 338:593-597, McKhann,G.M.,et al, 1991

Handesness and Life Span
NEJM 324:998, Halpern,D.F., 1991

Cognitive Dysfunction in MS, II. Impact on Employment and Social Functioning
Neurol 41:692-696, Rao,S.M.,et al, 1991

Clinical Characteristics of Patients in the Persistent Vegetative State
Arch Int Med 151:930-932, 855-8561991., Tresch,D.D.,et al, 1991

Acetazolamide-Responsive Vestibulocerebellar Syndrome:Clinical & Oculographic Features
Neurol 41:429-433, Baloh,R.W.&Winder,A., 1991

Progressive Motor Neuron Disease Associated with Electrical Injury
Muscle & Nerve 14:977-980991., Sirdofsky,M.D.,et al, 1991

Bicycle-Associated Head Injuries and Deaths in the US from 1984 to 1988, How Many Are Preventable?
JAMA 266:3016-3018, 30311991., Sacks,J.J.,et al, 1991

Handcuff Neuropathies
Neurol 41:145-147, Stone,D.A.&Laureno,R., 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

Dopa-Responsive Dystonia:Long-Term Treatment Response and Prognosis
Neurol 41:174-181, Nygaard,T.G.,et al, 1991

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

The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
Arch Neurol 47:1239-1242, Bromberg,M.B.,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 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

Neurological Sequelae of Cerebral Malaria in Children
Lancet 336:1039-1043, Brewster,D.R.,et al, 1990

Peripheral Neuropathy Associated with Eosinophilia-Myalgia Syndrome
Ann Neurol 28:522-528, Heiman-Patterson,T.D.,et al, 1990

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

Inherited Human Prion Diseases
Neurol 40:1820-1827, Hsiao,K.&Prusiner,S.B., 1990

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

Neurologic Sequelae of Domoic Acid Intoxication Due to the Ingestion of Contaminated Mussels
NEJM 322:1781-1787, Teitelbaum,J.S.,et al, 1990

Paralytic Shellfish Poisoning:A Case Report and Serial Electrophysiologic Observations
Neurol 40:1310-1312, Long,R.R.,et al, 1990



Showing articles 950 to 1000 of 7669 << Previous Next >>