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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
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 1250 to 1300 of 1991 << Previous Next >>

Pimozide Treatment of Sydenham's Chorea
Neurol 40:186, Shannon,K.&Fenichel,G.M., 1990

Presymptomatic and Prenatal Diagnosis in Myotonic Dystrophy by Genetic Linkage Studies
Neurol 40:671-676, Speer,M.C.,et al, 1990

Autosomal Dominant Cramping Disease
Arch Neurol 47:810-812, Ricker,K.&Moxley,R.T., 1990

Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
Lancet 336:271-273, Melki,J.,et al, 1990

Spinal Muscular Atrophies
Editorial, Lancet 336:280-2811990., , 1990

Genetic Linkage of Hereditary Motor & SensoryNeuro Type I (Charcot-Marie-Tooth Disease) to Chrom 1 & 17
Neurol 40:1450-1453, Defesche,J.C.,et al, 1990

Anderson-Fabry Disease
Editorial, Lancet 336:24-251990., , 1990

Cranial MR in Phenylketonuria
J Comput Assist Tomogr 14:458-460, Shaw,D.W.W.,et al, 1990

Acute Intermittent Porphyria
JAMA 264:1290-1293, 1315-13161990., Sack,G.H., 1990

Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus
NEJM 322:1652-1669, Arn,P.H.,et al, 1990

Progressive Myopathy in Hyperkalemic Periodic Paralysis
Arch Neurol 47:1013-1017, Bradkey,W.G.,et al, 1990

Hematologic Disorders and Ischemic Stroke
Stroke 21:1111-1121, Hart,R.G.&Kanter,M.C., 1990

A Familial Syndrome of Dystonia, Blepharospasm, and Pigmentary Retinopathy
Neurol 40:1359-1363, Coppeto,J.R.&Lessel,S., 1990

Tangier Disease in a Black Patient:An Unusual Clinical Presentation
Am J Med 89:105-108, Lo,W.D.,et al, 1990

Hereditary Motor and Sensory Neuropathies and Hereditary Spastic Paraplegia:A Magnetic Stimulation Study
Ann Neurol 28:43-49, Claus,D.,et al, 1990

Familial Multiple Symmetric Lipomatosis with Peripheral Neuropathy
Neurol 40:1246-1250, Chalk,C.H.,et al, 1990

Effectiveness of Sodium Valproate in the Treatment of Sydenham's Chorea
Neurol 40:1140-1141, Daoud,A.S.,et al, 1990

Hyperostosis Cranialis Interna
NEJM 322:450-463, Manni,J.J.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Adrenomyeloneuropathy Presenting as Addison's Disease in Childhood
NEJM 322:13-16, 54-551990., Sadeghi-Nejad,A.&Senior,B., 1990

Movement Disorders in Alcoholism:A Review
Neurol 40:741-746, Neiman,J.,et al, 1990

The Triumph of Linkage Analysis, Editorial
Ann Neurol 27:111-113, Rosenberg,R.N., 1990

Screening for Prolonged Incubation of HTLV-1 in Relatives of British Patients with Tropical Spastic Paraparesis
BMJ 300:300-304, Cruickshank,J.K.,et al, 1990

Intracranial Hemorrhage in Patients with Polycystic Kidney Disease
Stroke 21:291-294, Ryu,S.J., 1990

Cerebrotendinous Xanthomatosis:Clinical and MRI Study (A Case Report)
JNNP 53:76-78, Fiorelli,M.,et al, 1990

Premature Stroke in a Family with Lupus Anticoagulant and Antiphospholipid Antibodies
Stroke 21:66-71, Ford,P.M.,et al, 1990

The Dystonias
BMJ 300:139-144, Marsden,C.D.&Quinn,N.P., 1990

Dystonia Gene in Ashkenazi Jewish Population is Located on Chromosome 9q32-34
Ann Neurol 27:114-120, Kramer,P.L.,et al, 1990

Transmission and Age-At-Onset Patterns in Familial Alzheimer's Disease:Evidence for Heterogeneity
Neurol 40:395-403, Farrer,L.A.,et al, 1990

A Disorder of Azonal Development, Necrotizing Myopathy, Cardiomyopathy, and Cataracts:A New Familial Disease
Ann Neurol 27:193-199, Lyon,G.,et al, 1990

Joubert Syndrome:A Clinico-Radiological Study
Neuroradiology 31:502-506, Kendall,B.,et al, 1990

Improved Molecular-Genetic Diagnosis of Leber's Hereditary Optic Neuropathy
NEJM 323:1488-1489, Johns,D.R., 1990

Hypoxic-Ischemic Damage of the Basal Ganglia
Mov Disord 5:219-224, Hawker, K. & Lang, A.E., 1990

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989

Follow-up and Diagnostic Reappraisal of 75 Patients with Leber's Congenital Amaurosis
Am J Ophthalmol 107:624-631, Lambert,S.R.,et al, 1989

REcurrent Familial Brachial Plexus Palsies as the ONly Clinical Expression of'Tomaculous'Neuropathy
Eur Neurol 29:61-66, Martinelli,P.,et al, 1989

Friedreich Ataxia
In Rowland, L. P. Merritt's Textbook of Neurology, 8th Ed, Lea & Febiger, Phila, Ch 13, p627, Rosenberg,R.N., 1989

Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
Neurol 39:1446-1452, Farlow,M.R.,et al, 1989

Familial Patterns of Narcolepsy
lancet 2:1376-1379, Guilleminault,C.,et al, 1989

Cardioembolic Stroke in Primary Oxalosis with Cardiac Involvement
DiPasquale. G. , et al, Stroke 20:1403-14069., , 1989

Acute and Chronic Effects of Propranolol and Primidone in Essential Tremor
Neurol 39:1587-1588, Koller,W.C.&Vetere-Overfield,B., 1989

Tourette's Syndrome:Current Concepts
Neurol 39:1625-1630, Kurland,R., 1989

Adult-Onset Adrenoleukodystrophy Manifesting as Dementia
Am J Med 87:481-483, Panegyres,P.K.,et al, 1989

Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
Ann Neurol 26:699-708, Hold,I.J.,et al, 1989

Familial X-linked Myalgia and Cramps:A Nonprogressive Myopathy Associated with a Deletion in the Dystrophin Gene
Neurol 39:1277-1280, Gospe,S.M.,et al, 1989

Homing in on Wilson's Disease
Editorial, Lancet 1:822-8231989., , 1989

Diagnosis of Gerstmann-Straussler Syndrome in Familial Dementia with Prion Protein Gene Analysis
Lancet 2:15-17, Collinge,J.,et al, 1989

Clinicopath Conf
HTLV-I Infection, with Adult T-Cell Lymphoma and Tropical Spastic Paraparesis, Case 36-2989, NEJM 32, :6675,1989., 1989

HTLV-I-Associated Myelopathy with Adult T-Cell Leukemia
Neurol 39:1129-1131, Kawai,H.,et al, 1989

HTLV-I Myeloneuropathy in the Solomon Islands
NEJM 321:615-616, Ajdukiewicz,A.,et al, 1989



Showing articles 1250 to 1300 of 1991 << Previous Next >>