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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
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, rapidly progressive
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
developmental disability
developmental retardation
diabetes mellitus
diagnostic criteria
differential diagnosis
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
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
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 700 to 750 of 1991 << Previous Next >>

Dystonia and Chorea in Acquired Systemic Disorders
JNNP 65:436-445, Janavs,J.L.&Aminoff,M.J., 1998

The Human Genome Project,Application in the Diagnosis and Treatment of Neurologic Diseases
Arch Neurol 55:1287-1290, Evans,G.A., 1998

Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
NEJM 339:1994-2004, Johnson,R.T. & Gibbs,Jr.,C.J., 1998

Granulomatous Compressive Thoracic Myelopathy as the Initial Manifestation of Wegener's Granulomatosis
Neurol 51:1769-1770, Kelly,P.J.,et al, 1998

Localization of the Giant Axonal Neuropathy Gene to Chromosome 16q24
Ann Neurol 43:143-148, Flanigan,K.M.,et al, 1998

PCR-Based Strategy for Dx of Hered Neuropathy with Liability to Pressure Palsies & Charcot-Marie-Tooth Dis Type 1A
Neurol 50:760-763, Young,P.,et al, 1998

Neuroradiologic Findings in Marinesco-Sjogren Syndrome
AJNR 19:281-283, Georgy,B.A.,et al, 1998

Middle Cerebral Artery Main Stem Thrombosis in Two Siblings with Familial Thrombotic Thrombocytopenic Purpura
Neurol 50:1157-1160, Kelly,P.J.,et al, 1998

Detection of a Varient Protein in Hair:New Diagnostic Method in Portuguese Type Familial Amyloid Polyneuropathy
BMJ 316:1500-1501, Ando,Y.,et al, 1998

iH NMR Spectroscopy Studies of Huntington's Disease, Correlations with CAG Repeat Numbers
Neurol 50:1357-1365, Jenkins,B.G.,et al, 1998

Patients with Features Similar to Huntington's Disease, Without CAG Expansion in Huntingtin
Neurol 51:215-220, Rosenblatt,A.,et al, 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Tourette Syndrome:Update and Review of the Literature
The Neurologist 4:188-195, Feigin,A.&Clarke,H., 1998

Hereditary Cerebral Cavernous Angiomas:Clinical and Genetic Features in 57 French Families
Lancet 352:1892-1897, Labauge,P.,et al, 1998

Inherited Prothrombotic States and Ischaemic Stroke in Childhood
JNNP 65:508-511, Ganesan,V.,et al, 1998

Sneddon's Syndrome:Neuro-Ophthalmologic Manifestations in a Possible Autosomal Recessive Pattern
Neurol 51:1185-1187, Rehany,U.,et al, 1998

The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

Factor V Leiden Mutation is a Risk Factor for Cerebral Venous Thrombosis,A Case-Control Study of 55 Patients
Stroke 29:2507-2510, Ludemann,P.,et al, 1998

Initial and Follow-up Screening for Aneurysms in Families with Familial Subarachnoid Hemorrhage
Neurol 51:1125-1130, Raaymakers,T.W.M.,et al, 1998

Dipsticks and Convulsions
Lancet 352:1824, Koch,H., 1998

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Parkinson's Disease
NEJM 339:1044-1053,1130-1143, Lang,A.E.&Lozano,A.M., 1998

Is There a Familial Carpal Tunnel Syndrome? An Evaluation and Literature Review
Muscle & Nerve 21:1533-1536, Gossett,J.G.&Change,P.F., 1998

High-signal Basal Ganglia on T1-Weighted Images in a Patient with Sydenham's Chorea
Neuroradiology 11:704-709, Ikuta,N.,et al, 1998

Morvan's Fibrillary Chorea: A Paraneoplastic Manifestation of Thymoma
JNNP 65:857-862, Lee,E.K.,et al, 1998

Posterior Cerebral Artery Syndromes
, Caplan,L.R. &Bogousslavsky,J., 1998

Risk of Harboring an Unruptured Intracranial Aneurysm
Stroke 29:359-362, Ronkainen,A.,et al, 1998

Genetic Studies on Chromosome 12 in Late-Onset Alzheimer Disease
JAMA 280:619-622, 6521998., Wu,W.S.,et al, 1998

Evidence for an Alzheimer Disease Susceptability Locus on Chromosome 12 and for Further Locus Heterogeneity
JAMA 280:614-618, 6521998., Rogaeva,E.,et al, 1998

Familial Aggregation in Frontotemporal Dementia
Neurol 50:1541-1545, Stevens,M.,et al, 1998

Neurological Channelopathies, Dysfunctional Ion Channels May Cause Many Neurological Diseases
BMJ 316:1104-1105, Rose,M.R., 1998

Case-Control Study of Risk Factors of Creutzfeldt-Jacob Disease in Europe During 1993-95
Lancet 351:1081-1085, Van Duijn,C.M.,et al, 1998

Inclusion Body Myositis in Twins
Neurol 51:598-600, Amato,A.A.&Shebert,R.T., 1998

Familial Idiopathic Intracranial Hypertension with Spinal and Radicular Pain
Arch Neurol 55:854-856, Santinelli,R.,et al, 1998

A Woman Who Trembled, Then Had Chorea
Lancet 351:1326, Nagoaka,T.,et al, 1998

Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
Neurol 50:853-855, Nygaard,T.G.&Wooten,G.F., 1998

Hereditary Form of Parkinsonism-Dementia
Ann Neurol 43:768-781, Muenter,M.D.,et al, 1998

Facial Nerve is Liable to Pressure Palsy
Neurol 51:320-322, Foloni,T.E.,et al, 1998

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
NEJM 338:1119-1126, Krivit,W.,et al, 1998

Mucolipidosis Type IV; Characteristic MRI Findings
Neurol 51:565-569, Frei,K.P.,et al, 1998

Transdural Spinal Cord Herniation:Imaging and Clinical Spectra
AJNR 19:1337-1344, 11851998., Watters,M.R.,et al, 1998

Epilepsies in Twins:Genetics of the Major Epilepsy Syndromes
Ann Neurol 43:435-445, Berovic,S.F.,et al, 1998

Genetic Analysis Enables Definite and Rapid Diagnosis of Cerebrotendinous Xanthomatosis
Neurol 51:865-867, Chen,W.,et al, 1998

CADASIL in a North American Family:Clinical, Pathological, and Radiologic Findings
Neurol 51:844-849, Desmond,D.W.,et al, 1998

CAG Repeat Number Correlates with the Rate of Brainstem and Cerebellar Atrophy in Machado-Joseph Disease
Neurol 51:882-884, Abe,Y.,et al, 1998

Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
Neurol 51:1666-1671, Moseley,M.L.,et al, 1998

Reduced Penetrance,Variable Expressivity,and Genetic Heterogeneity of Familial Atrial Septal Defects
Circulation 97:2043-2048, Benson,D.W.,et al, 1998

Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
Ann Neurol 43:288-296, Onokera,O.,et al, 1998

Reduction in Voice Tremor Under Thalamic Stimulation
Neurol 50:796-798, Carpenter,M.A.,et al, 1998



Showing articles 700 to 750 of 1991 << Previous Next >>