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Differential
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acanthocytosis
advances in neurology
akathisia
alcohol
alcohol, neurologic complications with
algorithm
alpha-fetoprotein
alternating hemiplegia
alternating hemiplegia of childhood
Alzheimer's disease
Alzheimer's disease, familial
aminoacidopathies
aminoacidurias
amyotrophic chorea-acanthocytosis
amyotrophic lateral sclerosis
anemia
anemia, hemolytic
anxiety
aphonia
apraxia
apraxia of eye movements
areflexia
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
athetosis
athetosis, causes of
ATP1A3 gene
autonomic dysfunction
Babinski sign
baclofen
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
benign essential tremor
bicaudate index
biotin
blindness
blood dyscrasias, neurologic findings with
brain atrophy
brainstem, atrophy
brainstem, lesion of
CAG repeats
calcification, intracranial
carbamazepine
carcinoembryonic antigen
carcinoma
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
catalepsy
cataracts
caudate nucleus
caudate nucleus, atrophy
caudate nucleus, lesion of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebral cortical atrophy
cerebrovascular accident
ceruloplasmin, serum
chewing movements
children
chorea
chorea, causes of
chorea, familial
chorea, familial benign
chorea, senile
chorea, treatment of
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 11
chromosome 12
chromosome 19
chromosome 2
cirrhosis
cirrhosis, causes of childhood
Clinical Pathologic Conference(C.P.C.)
clonazepam
cognition
confabulation
consanguinity
contractures, joint
copper metabolism, abnormal
cortical blindness
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
deafness
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, presenile
dementia, rapidly progressive
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
developmental disability
developmental retardation
diabetes mellitus
diagnostic criteria
differential diagnosis
disease modifying agents
distal muscle atrophy
DNA probes
drooling
dying
dysarthria
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, causes of
dyskinesia, drug induced
dysphagia
dysphasia
dyssynergia cerebellaris myoclonica
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, face
dystonia, paroxysmal
dystonia, treatment of
dystonic reaction, acute
electroencephalogram, abnormalities of
electromyogram
electron microscopy
emotional lability
employment
encephalopathy
enzyme, defect
epileptic encephalopathy
episodic neurologic deficits
equinovarus
ethics in neurology
exercise intolerance
exome sequencing
eye movement, disorders of
failure to thrive
falling
familial
fasciculation
fatal familial insomnia
fever
flunarizine
fragile-X syndrome
Friedreich's ataxia
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gilles de la Tourette syndrome
gliosis
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glutaric acidemia
glutaric aciduria
grimacing
growth retardation
Hallervorden Spatz disease
hammertoes
handwriting
health insurance
hearing loss
hemiplegia
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
heralding manifestation
huntingtin
Huntington's chorea
Huntington's chorea, genetic counselling
Huntington's chorea, late onset
Huntington's chorea, membrane abnormality
Huntington's chorea, misdiagnosis of
Huntington's chorea, presymptomatic detection of
Huntington's chorea, sporadic form
Huntington's disease, children
hyperekplexia
hyperreflexia
hypertonia
hyporeflexia
hypotonia
imbalance
immunodeficiency
immunosuppression
impulsivity
inattention
inborn errors of metabolism
incoordination
infantile bilateral striatal necrosis
insight, loss
insomnia
intellectual deficit
intellectual deterioration
internet
iron, brain
Jakob-Creutzfeldt disease
jaundice
karyotyping
Kayser-Fleischer ring
lactic acidemia
lenticular nucleus, lesion of, bilateral
Lesch-Nyhan syndrome
leukemia
leukodystrophy
lip, biting
lipid storage disorder of CNS
liver disease
liver function enzymes
liver transplantation
lymphocyte capping, diminished
lymphoma
lysosomal storage disease
manic-depressive
McLeod syndrome
memory, defect of recent
memory, impairment of
meningitis, carcinomatous
mental retardation
mental status, abnormal
metabolic disorder, primary
microcephaly
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
Minamata disease
misdiagnosis
mitochondrial disease
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
movement disorder, hyperkinetic
movement disorder, paroxysmal
movement disorder, treatment of
MRI
MRI, abnormal
MRI, eye of tiger sign
MRI, FLAIR
MRI, gradient-echo
MRI, paramagnetic effect
MRI, susceptibility weighted
multiple system atrophy
muscle stiffness
muscle weakness
muscular dystrophy
muscular dystrophy, Duchenne
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy
myotonia dystrophica
neoplasm, primary intracranial
neoplasm, primary of CNS
neurocutaneous disease
neurodegeneration with brain iron accumulation
neuroendocrinology
neurofibromatosis 1
neurofibromatosis 2
neurologic disease
neurologic disease, diagnoses of
neurologic history
neurologic testing
neuronal migration disorder
neuronopathy, sensory
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, peripheral
neurotoxin
neurotransmitter
next-generation sequencing
Niemann-Pick disease
nystagmus
nystagmus, gaze-evoked
nystagmus, monocular
ocular motility, disorders of
old age, neurology of
opened mouth
ophthalmoplegia
optic atrophy
optokinetic nystagmus, abnormal
palilalia
pancytopenia
PANK2 mutation
Parkinson disease
Parkinson disease, dystonia with
Parkinsonism syndrome
paroxysmal dystonic choreoathetosis
paroxysmal hemiplegia
paroxysmal kinesigenic dyskinesia
paroxysmal neurologic deficits
pathology
penicillamine
peroxisomal disease
personality change
photosensitivity, skin
poison, mercury
poison, neurologic problems with
POLG1 gene
polymerase chain reaction
pons, atrophy
pontocerebellar atrophy
precipitating factors
prevention of neurologic disorders
prion disease
progeria
prognosis
progressive neurologic disorder
progressive pallidum atrophy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
putamen, lesion of
pyramidal tract
pyramidal tract dysfunction
quadriplegia
radiation hypersensitivity
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
recombinant DNA
recurrent
retinitis pigmentosa
review article
RFLPs
rigidity
salivation, excessive
schizophrenia
screening
sea-blue histiocytes
seizure
seizure, stimulus sensitive
self-mutilation
sensorineural hearing loss
short stature
single photon emission computed tomography
skin, lesions in neurologic disorders
sleep pathology and physiology
slit lamp examination
spasticity
speech disorder
speech disorder, childhood
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 16
spinocerebellar degeneration
splenomegaly
startle reaction
status epilepticus
stereotypy
striatum, lesion of
striatum, lesion of, bilateral
striopallidodentate calcifications, familial idiopathic
substantia nigra
suicide
tardive dyskinesia
Tay-Sachs disease
telangiectases
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
tic
tongue, biting
torticollis
toxins, nervous system
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, wing beating
trinucleotide repeats
urea-cycle enzymopathies
uric acid, low
visual evoked response
walking, difficulty with
weight loss
wheelchair
white matter disease
wide based gait
workup
writers cramp
xeroderma pigmentosa
X-linked bulbospinal neuronopathy
Showing articles 1450 to 1500 of 2019 << Previous Next >>

Familial Recurrent Bell's Palsy with Ocular Motor Palsies
Neurol 37:1369-1371, Aldrich,M.S.,et al, 1987

Hereditary Motor & Sensory Neuropathy, X-Linked:A Half Century Follow-Up
Neurol 37:1460-1465, Rozear,M.P.,et al, 1987

Long Term Exposure to Hydrogen Sulphide Producing Subacute Encephalopathy in a Child
BMJ 294:614, Gaitonde,U.B.&Sellar,R.J., 1987

Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
Neurol 37:446-450, Larsen,R.,et al, 1987

Normal Caudate Glucose Metabolism in Persons at Risk for Huntington's Disease
Arch Neurol 44:254-257, Young,A.B.,et al, 1987

Reduced Cerebral Glucose Metabolism in Asymptomatic Subjects at Risk for Huntington's Disease
NEJM 316:357-362, Mazziotta,J.C.,et al, 1987

Disorders of the Autonomic Nervous System:Part 1. Pathophysiology & Clinical Features
Ann Neurol 21:419-430, McLeod,J.G.&Tuck,R.R., 1987

Familial Cavernous Malformations of the Central Nervous System & Retina
Ann Neurol 21:578-583, Dobyns,W.B.,et al, 1987

Von Hippel-Lindau Disease in an Adolescent
Pediatrics 79:632-637, Seitz,M.L.,et al, 1987

CT in Ceroid Lipofuscinosis
Neurol 37:1025-1026, Dunn,D.W., 1987

Adult Polycystic Kidney Disease & Intracranial Aneurysms
BMJ 295:526, Saifuddin,A.&Dathan,J.R.E., 1987

Childhood Stroke Associated with Protein C or S Deficiency
J Pediatr 111:562-564, Israels,S.J.&Seshia,S.S., 1987

Analysis of Risk Factors for Stroke in a Cohort of Men Born in 1913
NEJM 317:521-526, Welin,L.,et al, 1987

Mendelian Etiologies of Stroke
Ann Neurol 22:175-192, Natowicz,M.&Kelley,R.I., 1987

Huntington's Disease:Deterioration in Clinical State During Treatment with ACE Inhibitor
BMJ 294:1659-1660, Goldblatt,J.&Bryer,A., 1987

Neurofibromatosis
Editorial, Lancet 1:663-6641987., , 1987

Renal Cell Carcinoma in von Hippel-Lindau Syndrome
Am J Med 82:236-238, Malek,R.S.,et al, 1987

Adrenoleukodystrophy:Dietary Oleic Acid Lowers Hexacosanoate Levels
Ann Neurol 21:230-231, 232-2391987., Rizzo,W.B.,et al, 1987

A New Dietary Therapy for Adrenoleukodystrophy:Biochemical & Preliminary Clinical Results in 36 Patients
Ann Neurol 21:230-231, 240-2491987., Moser,A.B.,et al, 1987

Familial Occurrence of Spontaneous Dissection of the Internal Carotid Artery
Stroke 18:246-251, Mokri,B.,et al, 1987

Cerebral Amyloid Angiopathy, A Critical Review
Stroke 18:311-324, Vinters,H.V., 1987

Movement Disorders & AIDS
Neurol 37:37-41, Nath,A.,et al, 1987

Myelopathies & Retroviral Infections
Ann Neurol 21:113-115, Johnson,R.T.&McArthur,J.C., 1987

Tropical Spastic Paraparesis:HTLV-I Antibodies in Patients from the Seychelles
NEJM 316:51, Roman,G.C.,et al, 1987

Endemic Tropical Spastic Paraparesis Associated with HTLV-I:A Clinical & Seroepidem Study of 25 Cases
Ann Neurol 21:123-130, Vernant,J.C.,et al, 1987

Chronic Progressive Myelopathy Associated with Elevated Antibodies to HTLV-I & Adult T-Cell Leukemialike Cells
Ann Neurol 21:117-121, Osame,M.,et al, 1987

Antibody to Human T-Lymphotropic Virus Type I In West-Indian-Born UK Residents with Spastic Paraparesis
Lancet 1:415-416, Newton,M.,et al, 1987

Evidence That the Gene for Tuberous Sclerosis is on Chromosome 9
Lancet 1:659-661, Fryer,A.E.,et al, 1987

Clinical Assessment of 31 Patients with Wilson's Disease, Correlations with Struct. Changes on MRI
Arch Neurol 44:365-370, Starosta-Rubinstein,S.,et al, 1987

Caffeine & Tremor
Neurol 37:169-172, Koller,W.,et al, 1987

Tourette Syndrome
Editorial, Lancet 1:3081987., , 1987

Dementia of the Alzheimer Type:Clinical & Family Study of 22 Twin Pairs
Neurol 37:359-363, Nee,L.E.,et al, 1987

Involuntary Movement & Bacterial Meningitis
Editorial, Lancet 1:142-1431987., , 1987

Prenatal Diagnosis & Detection of Carriers with DNA Probes in Duchenne's Muscular Dystrophy
NEJM 316:985-993, 1018-10201987., Darras,B.T.,et al, 1987

Alternating Hemiplegia of Childhood
Int Pediatr 2:115-119, Aicardi,J., 1987

Hereditary Neuropathy with Liability to Pressure Palsies
In Handbk of Clin Neurol, Elsevier Sci Publ Co, NY 51:551-562987., Cherry,S.&Mayer,R.F., 1987

Lyme Disease, A Neuro-Ophthalmologic View
J Clin Neuro-ophthalmol 7:185-190, MacDonald,A.B., 1987

Carbamazepine Side Effects in Children and Adults
Pellock. J. M. , Epilepsia 28:S64-S707., , 1987

Phosphorylase Deficiency
In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986

Facioscapulohumeral Dystrophy, in Myology, Basic & Clinical
McGraw-Hill Book Co, NY, p1251986., Munsat,T.L., 1986

Acid Maltase Deficiency
Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986

Location of the Gene for X-Linked Spinal Muscular Atrophy
Neurol 36:1595-1598, Fischbeck,K.H.,et al, 1986

Lathyrism:Evidence for Role of the Neuroexcitatory Aminoacid BOAA
Lancet 2:1066-1067, Spencer,P.S.,et al, 1986

Transketolase Abnormality in Tolazamide-Induced Wernicke's Encephalopathy
Neurol 36:1508-1510, Mukherjee,A.B.,et al, 1986

Ornithine Transcarbamylase Deficiency-A Cause of Bizarre Behavior in a Man
NEJM 315:744-747, DiMagno,E.P.,et al, 1986

Adult-Onset Autosomal Dominant Limb-Girdle Muscular Dystrophy
Ann Neurol 20:240-248, Chutkow,J.G.,et al, 1986

Gerstmann-Straussler-Scheinker Disease:Autopsy Study of a Familial Case
Ann Neurol 20:540-543, Vinters,H.V.,et al, 1986

Identical Twins with Hereditary Hemorrhagic Telangiectasia Concordant for Cerebrovascular Arteriovenous Malformations
Am J Med 81:931-934, Lesser,B.A.,et al, 1986

The Inheritance of Gilles De La Tourette's Syndrome & Associated Behaviors
NEJM 315:993-997, Pauls,D.L.&Leckman,J.F., 1986

Arteriovenous Malformation Presenting as Hemidystonia
Neurol 36:1590-1593, Friedman,D.I.,et al, 1986



Showing articles 1450 to 1500 of 2019 << Previous Next >>