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advances in neurology
adverse drug reaction
alcohol
alcohol, neurologic complications with
algorithm
aminoacidurias
amyloidosis
amyotrophic lateral sclerosis
anemia
anemia, hemolytic
anterocollis
anticholinergic drugs
aphonia
artane
arthrogryposis multiplex
athetosis
athetosis, causes of
attention deficit disorder with hyperactivity
Babinski sign
basal ganglia
basal ganglia, lesion, bilateral
benign essential tremor
bent spine syndrome
biopterin deficiency
blepharospasm
botulinum toxin
bradykinesia
Brueghel's syndrome
camptocormia
carbamazepine
CAT scan
CAT scan, abnormal
CAT scan, muscle
catecholamine
cerebral ischemia
cerebral palsy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrovascular accident
Charcot-Marie-Tooth
children
chorea
chorea, causes of
chorea, treatment of
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 14
cirrhosis
cirrhosis, causes of childhood
Clinical Pathologic Conference(C.P.C.)
clonazepam
cogwheel rigidty
complications
conversion reaction
creatine phosphokinase(CPK)elevated
dementia
depression
dermatomyositis
developmental retardation
diurnal variation
dopa responsive dystonia
dopamine
drug induced neurologic disorders
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, causes of
dyskinesia, drug induced
dysphagia
dysphonia
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, classification
dystonia, etiology of
dystonia, evaluation of
dystonia, face
dystonia, focal
dystonia, laryngeal
dystonia, painful
dystonia, post traumatic
dystonia, prevalence of
dystonia, symptomatic
dystonia, treatment of
DYT1 mutation
efficacy
electromyogram
encephalitis, brainstem
epidemiology of neurology
equinovarus
familial
gait disorder
gamma amino butyric acid
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
gests antagoniste
Gilles de la Tourette syndrome
globus pallidus
globus pallidus, lesion of, bilateral
Guillain Barre syndrome
Hallervorden Spatz disease
handwriting
head nodding
head tilt
hepatic encephalopathy
hepatic encephalopathy, treatment of
hepatitis
hepatolenticular degeneration(Wilson's disease)
homovanillic acid
Huntington's chorea
hyperekplexia
hyperreflexia
iron, brain
Kayser-Fleischer ring
klippel feil syndrome
kyphosis
laminectomy
laminectomy, lumbar
laterocollis
L-dopa
leg spasms
leg spasms, painful
low back pain
migraine
migraine, children
misdiagnosis
molecular genetics
monoamines
mononeuropathy
motor neuron disease
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, treatment of
MRI, abnormal
MRI, eye of tiger sign
MRI, gradient-echo
MRI, paramagnetic effect
MRI, susceptibility weighted
multiple sclerosis
muscle biopsy
muscle diseases, characteristics of
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenic crisis
myopathy
myopathy, carcinomatous
myopathy, metabolic
myopathy, thyroid disease causing
myositis
myotonia dystrophica
nerve conduction studies
neuritis, causes of
neurodegeneration with brain iron accumulation
neurologic complications of, surgery
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuropathy
neuropathy, diabetic
neurotransmitter
norepinephrine
obsessive-compulsive disorder
old age, neurology of
pain
pancytopenia
PANK2 mutation
paraspinal muscle
paraspinal muscle weakness
Parkinson disease
Parkinson disease, juvenile
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinsonism syndrome
paroxysmal dystonic choreoathetosis
paroxysmal kinesigenic dyskinesia
paroxysmal neurologic deficits
patient information and support
penicillamine
phenylketonuria
poliomyelitis
polymyositis
polyneuropathy
porphyria
postoperative neurologic complications
postural abnormality
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychosis
radiculopathy
reflex sympathetic dystrophy
retrocollis
reversible neurologic disorder
review article
rigidity
Riley-Day syndrome
salivation, excessive
sarcoidosis
schizophrenia
scoliosis
seizure
seizure, stimulus sensitive
sensory tricks
sinemet
slit lamp examination
spastic dysphonia
speech disorder
speech disorder, non aphasic
splenomegaly
startle reaction
stiff man syndrome
stimulation, deep brain
stooped posture
tardive dyskinesia
tardive dystonia
tetrabenazine
tic
toe walking
tonic foot response
torticollis
torticollis, benign paroxysmal
torticollis, familial
torticollis, infants and children
torticollis, post traumatic
trauma
treatment of neurologic disorder
tremor
tremor, jaw
tremor, leg
tremor, post traumatic
tremor, postural
tremor, treatment of
tremor, voice
uric acid, low
vasospasm, cerebral
walking, difficulty with
weakness, progressive
Werdnig-Hoffman disease
wheelchair
workup
writers cramp
Showing articles 1150 to 1200 of 1744 << Previous Next >>

Intrathecal Baclofen for Severe Spinal Spasticity
NEJM 320:1517-1521, 1553-15551989., Penn,R.D.,et al, 1989

Treatment of Spastic Paresis
NEJM 320:1553-1555, Young,R.R., 1989

Continuous Levodopa Infusions to Treat Complex Dystonia in Parkinson's Disease
Neurol 39:888-891, Sage,J.I.,et al, 1989

Chronic Myelopathies Associated with HTLV-I, A Clinical, Serologic, and Immunovirologic Study of 10 Patients in France
Arch Neurol 46:255-260, Gout,O.,et al, 1989

Predisposing Locus for Alzheimer's Disease on Chromosome 21
Lancet 1:352-355, Goate,A.M.,et al, 1989

Mitochondrial DNA and Genetic Disease
Editorial, Lancet 1:250-2511989., , 1989

Familial Idiopathic Striopallidodentate Calcifications
Neurol 39:381-385, Ellie,E.,et al, 1989

Endemic Fluorosis with Spinal Cord Compression, A Case Report and Review
Arch Int Med 149:697-700, Fisher,R.L.,et al, 1989

Occurrence of Both Neurofibromatosis 1 and 2 in the Same Individual with a Rapidly Progressive Course
Neurol 39:282-283, Sadeh,M.,et al, 1989

Hereditary Sensory Neuropathy with Deafness:A Familial Multisystem Atrophy
Neurol 39:244-248, Horoupian,D.S., 1989

Acute Profound Dystonia in Infants with Glutaric Acidemia
Pediatrics 83:228-234, Bergman,I.,et al, 1989

Ethanol and the Nervous System
NEJM 321:442-454, Charness,M.E.,et al, 1989

Primary Progressive Cerebellar Ataxia
Neuroradiology 31:16-18, Bradac,G.B.,et al, 1989

Concurrence of Multiple Sclerosis and Inflammatory Bowel Disease
NEJM 321:762-763, Sadovnick,A.D.,et al, 1989

Neurofibromatosis and Other Disorders Among Children with CNS Tumors and Their Families
Neurol 39:487-492, Baptiste,M.,et al, 1989

The Diagnosis of Neurofibromatosis-1 in the Child Under the Age of 6 Years
Am J Dis Child 143:717-719, Obringer,A.C.,et al, 1989

Adrenoleukodystrophy
JAMA 262:1504-1506, Ladenson,P.W., 1989

Hereditary Long Q-T Syndrome Presenting as Epilepsy:Electroencephalography Laboratory Diagnosis
Ann Neurol 25:514-516, Gospe,S.M.&Choy,M., 1989

Problems in Genetic Prediction for Huntington's Disease
Lancet 2:601-603, Morris,M.J.,et al, 1989

Uptake of Presymptomatic Predictive Testing for Huntington's Disease
Lancet 2:603-605, Craufurd,D.,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

Detection of Human T-Cell Leukemia/Lymphoma Virus Type I in a Transfusion Recipient with Chronic Myelopathy
Neurol 39:841-844, Saxton,E.H.,et al, 1989

Lyme Disease
NEJM 321:586-596, Steere,A.C., 1989

Rippling Muscle Disease
Arch Neurol 46:405-408, Ricker,K.,et al, 1989

Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989

Respiratory Muscle Weakness in Charcot-Marie-Tooth Disease, A Field Study
Arch Int med 149:1389-1391, Nathanson,B.N.,et al, 1989

Hereditary Motor & Sensory Neuropathy with Optic Atrophy, Ultrastructural and Morphometic Observations
Arch Neurol 46:973-977, Sommer,C.&Schroder,J.M., 1989

Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I
Neurol 39:1173-1177, Rosen,S.A.,et al, 1989

Late Onset of Distinct Neurologic Syndromes in Galactosemic Siblings
Neurol 39:741-742, Friedman,J.H.,et al, 1989

Magnetic Resonance Imaging in a Family with Hereditary Cerebral Arteriovenous Malformations
Arch Neurol 46:184-187, Allard,J.C.,et al, 1989

Molecular Genetics of Amyloid Neuropathy in Europe
Lancet 1:524-526, Holt,I.J.,et al, 1989

Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
Medicine 68:1-29, Lamiell,J.M.,et al, 1989

Bilateral Opercular Polymicrogyria
Ann Neurol 25:90-92, Becker,P.S.,et al, 1989

Treatment of Focal Dystonias of the Hand with Botulism Toxin Injections
JNNP 52:355-363, Cohen,L.G.,et al, 1989

Post-Traumatic Tremor
Neurol 39:103-106, Biary,N.,et al, 1989

Life-Threatening Cranial Dystonia Following Trihexyphenidyl Withdrawal
Movement Disorders 4:349-353, Gimenez-Roldan,S.,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

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

Refsum Disease
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989

Peripheral Neuropathy in Amyotrophic Chorea-Acanthocytosis
Ann Neurol 26:583-587, Vista,G.,et al, 1989

Dyslexia
Editorial, Lancet 2:719-7201989., , 1989

MRI in Cockayne Syndrome Type 1
Neuroradiology 31:276-277, Boltshauser,E.,et al, 1989

Demyelinating Diseases
In Rowlands Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, p. 749, Sibley,W.A.,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

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

Paroxysmal Cerebellar Ataxia
Aust NZ J Med 19:113-117, Feeney,G.F.&Boyle,R.S., 1989



Showing articles 1150 to 1200 of 1744 << Previous Next >>