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Differential
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abdominal cramps
acid maltase deficiency
acid maltase deficiency, adult
acral sensory symptoms
adrenoleukodystrophy
adrenomyeloneuropathy
adult polyglucosan body disease
adverse drug reaction
agalsidase alfa
agitation
alpha glucosidase
alternating rapid movement
aminoacidopathies
aminoacidurias
amniocentesis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, guamian type of
angina pectoris
angiokeratoma
anhidrosis
anterior horn cell disease
anterior tibial muscle weakness
anti GQ1b IgG antibody
anticonvulsants
anticonvulsants, selection of
antiviral agents
apraxia
areflexia
arm swing, reduced
Arnold Chiari malformation
arthropathy
arthropathy, neuropathic
arylsulfatase A
aspartate aminotransferase
aspiration
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
athetosis
atidarsagene autotemcel
attention
attention deficit disorder with hyperactivity
attention span
atypical
autoantibodies
autonomic dysfunction
axonal degeneration
axonal spheroid
Babinski sign
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar impression
Bassen-Kornzweig syndrome
behavioral disorder
bladder dysfunction
blindness
blood dyscrasias, neurologic findings with
bone marrow biopsy
bone marrow transplantation
bradykinesia
brain atrophy
brain biopsy
brain biopsy, complications of
brain biopsy, false negative
brain biopsy, indication
brainstem, infarction of
bulbar palsy
burning feet
burning feet, differential diagnosis of
burning hands
burning paresthesia
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, false negative
catalepsy
cataplexy
cataracts
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar atrophy, primary
cerebellar degeneration
cerebellar infarction
cerebral cortical atrophy
cerebral ischemia
cerebro hepato renal syndrome
cerebrospinal fluid, gammaglobulin of
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, cryptogenic
cerebrovascular accident, familial occurrence
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, young adult
cerebrovascular disease
cerebrovascular disease, cardiovascular disease with
cherry red spot
cherry red spot-myoclonus syndrome
children
chorea
choreoathetosis
chromosomal abnormality
chronic graft versus host disease
Clinical Pathologic Conference(C.P.C.)
coagulopathy
Cockayne's syndrome
cognition
cogwheel rigidty
complications
compression fracture
congestive heart failure
conjunctival biopsy
consanguinity
contractures, joint
cornea, abnormal
cornea, opacification in infancy-causes of
cornea, opacity of
corneal dystrophy
corpus callosum
corpus callosum, hypoplastic
corpus callosum, lesion of
creatine phosphokinase(CPK)elevated
creatinine, elevated
cry, abnormal
cultured skin fibroblasts
cystinosis
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, childhood
dementia, diagnostic evaluation of
dementia, presenile
dentatorubral-pallidoluysian atrophy
depression
developmental disability
developmental milestones, loss of
developmental retardation
diagnostic criteria
diarrhea
differential diagnosis
difficulty going down stairs
diplopia
disease modifying agents
distal muscle weakness
DNA probes
drooling
dropped head syndrome
drug induced neurologic disorders
dysarthria
dysmetria
dysmorphic
dysostosis multiplex
dysphagia
dystonia
dystonia, face
dystonia, focal
dystonic lipidosis
echocardiogram
efficacy
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
electronystagmography
electroretinograph
encephalitis, brainstem
encephalopathy
enzyme treatment
enzyme, defect
episodic disorders
episodic neurologic deficits
executive dysfunction
exercise intolerance
exome sequencing
eye movement, disorders of
Fabry's disease
facial appearance, abnormal
falling
familial
Farber's disease
fever
fine motor function, impaired
fingerprint bodies
Fisher's syndrome
foam cells
fracture, pathologic
Friedreich's ataxia
fucosidosis
fundus, abnormality of
gait disorder
gait, spastic
galactosidase
gangliosides
gangliosidosis GM1
gangliosidosis GM2
gangliosidosis, generalized
gargoylism
Gaucher's disease
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glucocerebrosidase
glycogen storage disease
glycoprotein
GM1 ganglioside
GM1 ganglioside antibodies
granular osmiphilic material
growth retardation
Guillain Barre syndrome, ophthalmoplegia in
Hallervorden Spatz disease
hallucination
hallucination, visual
hand pain
handwriting
head injury
hearing loss
heat intolerance
hemorrhagic diathesis
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
heralding manifestation
herpes virus infection
hexosaminidase-A
hexosaminidase-A and B
high arched feet
Hurler's syndrome
hydrocephalus
hyperreflexia
hypertonia
hypohidrosis
hypomyelination
hypotension, systemic
hypotonia
hypotonia, infants
imbalance
immunofluorescence
immunosuppression
inattention
inborn errors of metabolism
inborn errors of metabolism, screening
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intracytopasmic
incoordination
infection, recurrent
intellectual deficit
intellectual deterioration
intelligence quotient
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intrathecal medication
intrinsic hand muscles, wasting of
introverted
iridoplegia
Jakob-Creutzfeldt disease
jaundice
Jewish
Kearns-Sayre syndrome
klippel feil syndrome
Krabbe's disease
kyphoscoliosis, neurologic causes of
lactic acidemia
Lafora's disease
laughing
laughing, pathologic
Laurence-Moon-Bardet-Biedl syndrome
lead poisoning
learning disability, in children
Leigh's disease
leukocyte enzyme abnormality
leukocyte peroxidase
leukodystrophy
leukoencephalopathy
leukoencephalopathy, hereditary diffuse
Lewy body disease, diffuse
life expectancy
limb-girdle weakness
lipid storage disorder of CNS
liver disease
lymphadenopathy
lymphocyte fingerprint profiles
lysosomal storage disease
lysosomes, abnoral
macrocephaly
macular degeneration
marche a petits pas
Marinesco-Sjogren syndrome
megalencephaly
memory, defect of recent
memory, impairment of
meningitis, chronic
mental retardation
MERRF syndrome
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
metachromatic leukodystrophy, juvenile
metachromatic leukodystrophy, late-infantile
microcephaly
miglustat
mimics
Mini Mental Status Examination
misdiagnosis
mitral valve prolapse
molecular genetics
mongolism
monoclonal antibodies
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, hypointense signal foci on
MRI, negative
MRI, serial
MRS
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, differential diagnosis of
muscle biopsy
muscle spasm
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy, Duchenne
myelomalacia
myeloneuropathy
myelopathy
myocardial infarction
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy
myopathy, metabolic
myopathy, mitochondrial
myopathy, vacuolar
myopia
N-acetyl-L-aspartic acid
N-acetyl-L-leucine
negative
neonatal screening, genetic neurologic disorders
neoplasm, primary of CNS
neuraminidase deficiency
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neuroaxonal leukodystrophy
neurofibrillary degeneration
neurogenic bladder
neuroichthyosis
neurolipidosis IV
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic testing
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathic pain scale
neuropathology
neuropathy
neuropathy, ataxic
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, painful
neuropathy, small-fiber
neuropathy, small-fiber, painful sensory
neurosis
next-generation sequencing
Niemann-Pick disease
night blindness
nystagmus
nystagmus, dissociated
one and a half syndrome
ophthalmoplegia
ophthalmoplegia, acute
ophthalmoplegia, bilateral, acute
ophthalmoplegia, plus syndrome
ophthalmoplegia, progressive external
ophthalmoplegia, total
optic atrophy
optic nerve
optic neuropathy
optokinetic nystagmus, abnormal
osteopetrosis
overlap syndrome
pain
pain, neuropathic
papillitis
paranoia
paraparesis, familial spastic
Parkinson disease, postencephalitic
Parkinsonism syndrome
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
patient in waiting
pediatric neurology
peroxisomal disease
pes cavus
photophobia
pigmentary retinopathy
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polyneuropathy
Pompe's disease of glycogen storage
Pompe's disease, infantile
precipitating factors
preclinical
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
proteinuria
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychomotor retardation
psychosis
pupil, abnormality in neurologic disorders
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract
quadriparesis
quadriplegia
radiculopathy
rectal biopsy
refractive errors
Refsum's disease
remote effect of cancer on the nervous system
renal failure
respiratory failure
respiratory tract infection
retina, abnormal
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
retropulsion
review article
rigidity
safety
salivation, excessive
Salla disease
Sandhoff's disease
schizophrenia
scoliosis, neurologic association with
screening
sea-blue histiocytes
seizure
seizure, children
seizure, laughing as manifestation
seizure, paradoxical
seizure, treatment of
sensorineural hearing loss
serologic testing
short stature
sick sinus syndrome
skin, biopsy
skin, lesions in neurologic disorders
skull x-ray, abnormal
slit lamp examination
slurred speech
small vessel disease
spasticity
speech, delayed development of
sphingomyelin
spinal cord, compression of
spinocerebellar degeneration
splenomegaly
startle reaction
stem cell transplantation
storage disease of CNS
strabismus
stuttering
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subdural hematoma
systemic illness
tandem gait, ataxic
tapetoretinal degeneration
Tay-Sachs disease
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
toe walking
tone, muscle, increased
tongue, enlarged
treatment of neurologic disorder
tremor
tremor, intention
tripping
tuberous sclerosis
Unverricht-Lundborg disease
urea-cycle enzymopathies
urinary incontinence
urinary sulfatidase excretion
urine test for metabolic disorders
Usher's syndrome
vasculopathy
ventricular enlargement
vertebral-basilar insufficiency
vertigo
vestibulopathy
viral infection, CNS
vision, failure of in childhood
visual acuity, decreased
visual field defect
visual fields, constricted
visual loss
visual loss, progressive
visual loss, slow
visual loss, transient
visuospatial disturbance
Von Hippel Lindau
walking, delayed
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
Werdnig-Hoffman disease
West disease
wheelchair
white matter disease
whole genome sequencing
wide based gait
writing
Showing articles 750 to 800 of 895 << Previous Next >>

Are There Really Alternatives to the Use of Fetal Tissue from Elective Abortions in Transplant Research?
NEJM 327:1592-1595, Garry,D.J.,et al, 1992

Degeneration of the Posterior Columns of the Spinal Cord:Postmortem MRI and Histopathology
J Comput Assist Tomogr 16:865-867, Okumura,R.,et al, 1992

Wegener's Granulomatosis Mimicking Temporal Arteritis
Neurol 41:1694-1695, Palaic,M.,et al, 1991

Neurodegenerative Diseases of Childhood:MR and CT Evaluation
J Comput Assist Tomogr 15:210-222, Mirowitz,S.A.,et al, 1991

Autoimmune Aetiology for Acquired Neuromyotonia (Isaacs'Syndrome)
Lancet 338:75-77, Sinha,S.,et al, 1991

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

Autoantibodies and Rheumatic Disorders in a Neurology Inpatient Population:A Prospective Study
Am J Med 90:479-488, Olsen,M.L.,et al, 1991

Thyroid-Associated Eye Disease:Clinical Management
Lancet 338:29-32, Fells,P., 1991

N-Methyl-D-Aspartate Antagonists in the Treatment of Parkinson's Disease
Arch Neurol 48:977-981, Greenamyre,J.T.&O'Brien,C.F., 1991

Immunosuppressive Treatment in Multifocal Motor Neuropathy
Ann Neurol 30:397-401, Feldman,E.L.,et al, 1991

The Spectrum of Lissencephaly:Report of Ten Patients Analyzed by Magnetic Resonance Imaging
Ann Neurol 30:139-146, Barkovich,A.J.,et al, 1991

The Diagnosis of Childhood Neurodegenerative Disorders Presenting as Dementia in Adults
Neurol 41:794-798, Coker,S.B., 1991

Recovery of Motor Function after Spinal-cord Injury-A Randomized, Placebo-Contrlled Trial with GM-1 Ganglioside
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Muscle Carnitine Deficiency in Patients Using Valproic Acid
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Tissue Plasminogen Activator Plus Glutamate Antagonist Improves Outcome after Embolic Stroke
Arch Neurol 48:1235-1238, Zivin,J.A.&Mazzarella,V., 1991

The Bioloigcal Basis for the Treatment of Acute Stroke
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Myasthenia Gravis in Mothers and Their Newborns
Clin Obstet Gynecol 34:82-99, Plauche,W.C., 1991

Stroke-Like Syndrome, Mineralizing Microangiopathy, and Neuroaxonal Dyst with Intrathecal Methotrexate
Neurol 41:1847-1848, Phanthumchinda,K.,et al, 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

Focal Neuronal Migration Disorders and Intractable partial Epilepsy:A Study of 30 Patients
Ann Neurol 30:741-749, Palmini,A.,et al, 1991

Focal Neuronal Migration Disorders and Intractable Partial Epilepsy:Results of Surgical Treatment
Ann Neurol 30:750-757, Palmini,A.,et al, 1991

MRI in the Diagnosis of Heterotopic Gray Matter, Report of Three Cases First Discovered in Adulthood
Neuroradiology 33:527-528, Zisch,R.&Artmann,W., 1991

Neonatal Lupus Erythematosus Simulating Transient Myasthenia Gravis at Presentation
J Pediatr 118:417-419, Rider,L.G.,et al, 1991

Calcium Channel Autoantibodies in the Lambert-Eaton Myashenic Syndrome
Ann Neurol 29:307-314, Leys,K.,et al, 1991

Anti-Ri:An Antibody Associated with Paraneoplastic Opsoclonus and Breast Cancer
Ann Neurol 29:241-251, Luque,F.A.,et al, 1991

Serum Antibodies to GM1 and GM3-gangliosides in Systemic Lupus Erythematosus with Chronic Inflammatory Demyelinating Polyradiculoneuropathy
Acta Neurol Scand 83:399-402, Sindern,E.,et al, 1991

Diagnostic Value of Anti-Neuronal Antibodies for Paraneoplastic Disorders of the Nervous System
JNNP 53:940-943, Moll,J.W.B.,et al, 1990

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

Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
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Epilepsy and Disorders of Neuronal Migration
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Inherited Human Prion Diseases
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Anti-GM1 IgM Antibodies in Motor Neuron Disease and Neuropathy
Neurol 40:1747-1750, Nobile-Orazio,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

A Clinical Triad to Diagnose Paraneoplastic Retinopathy
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Autoantibody Synthesis in the Central Nervous System of Patients with Paraneoplastic Syndromes
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Magnetic Resonance Imaging and Neurobehavioral Correlates in Schizencephaly
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The Spectrum of Neurologic Disease Associated with Anti-GM1 Antibodies
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Perinatal Loss and Neurological Abnormalities Among Children of the Atomic Bomb
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Progress in Tuberous Sclerosis
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Autoantibodies to Gaba-Ergic Neurons & Pancreatic Beta Cells in Stiff-Man Syndrome
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Neuronal Intranuclear Inclusion Disease in a Child:Diagnosis by Rectal Biopsy
Ann Neurol 27:103-106, Goutieres,F.,et al, 1990

High-Intensity Basal Ganglia Lesions on T1-Weighted MR Images in Neurofibromatosis
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Rapid Detection of Creutzfeldt-Jakob Disease and Scrapie Prion Porteins
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Adult Phosphorylase b Kinase Deficiency
Ann Neurol 28:529-538, Clemens,P.R.,et al, 1990

Specificity of Calcium Channel Autoantibodies in Lambert-Eaton Myasthenic Syndrome
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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

Cancer-Associated Retinopathy (Car Syndrome) with Antibodies Reacting with Retinal, Optic-Nerve, and Cancer Cells
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Antineural Autoantibodies in Patients with Paraneoplastic Cerebellar Degeneration
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Anticerebellar Antibodies in Neurologically Normal Patients with Ovarian Neoplasm
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Bilateral Central Macrogyria:Epilepsy, Pseudobulbar Palsy, and Mental Retardation-A Migration Disorder
Ann Neurol 25:547-554, Kuzniecky,R.,et al, 1989



Showing articles 750 to 800 of 895 << Previous Next >>