Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
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 600 to 650 of 1744 << Previous Next >>

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

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

Long-Term Follow-Up of Levodopa Responsiveness in Generalized Dystonia
Arch Neurol 55:1320-1323, Dewey,R.B.,et al, 1998

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

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

The Genetics of Alzheimer Disease, Current Status and Future Prospects
Arch Neurol 55:294-296, Blacker,D.&Tanzi,R.E., 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

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

Long-Term Effect of Botulinum Toxin in Impairment and Functional Health in Cervical Dystonia
Neurol 50:1461-1463, Brans,J.W.M.,et al, 1998

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,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

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

Idiopathic Granulomatous Angiitis of the CNS Manifesting as Diffuse White Matter Disease
Neurol 49:1696-1699, Finelli,P.F.,et al, 1997

Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
BMJ 315:856-857, Fox,N.C.,et al, 1997

A News Locus for Hemiplegic Migraine Maps to Chromosome 1q31
Neurol 49:1231-1238, 11931997., Gardner,K.,et al, 1997

Complete Genomic Screen in Late-Onset Familial Alzheimer Disease, Evidence for a New Locus on Chromosome 12
JAMA 278:1237-1241, 12821997., Pericak-Vance,M.A.,et al, 1997

Genetic Testing for Alzheimer Disease, Practical and Ethical Issues
Arch Neurol 54:1226-1229, Roses,A.D., 1997

Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
Lancet 350:1511-1515, 14901997., Joutel,A.,et al, 1997

Adult-Onset Krabbe's Disease in Siblings with Novel Mutations in the Galactocerebrosidase Gene
Ann Neurol 41:111-114, Bernardini,G.L.,et al, 1997

Familial Idiopathic Brain Calcification with Autosomal Dominant Inheritance
Neurol 48:645-649, Kobari,M.,et al, 1997

The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
JAMA 277:832-836, Post,S.G.,et al, 1997

Clin Features of Early-Onset Alzheimer Disease in Large Kindred with an E280A Presenilin-1 Mutation
JAMA 277:793-799, Lopera,F.,et al, 1997

Hereditary Frontotemporal Dementia is Linked to Chromosome 17q21-q22:Genetic & Clinicopath Study of 3 Dutch Families
Ann Neurol 41:150-159, Heutnik,P.,et al, 1997

Frontotemporal Dementia is on the MAP
Ann Neurol 41:139-140, Wilhelmsen,K.C., 1997

Familial Acephalgic Migraines
Neurol 48:776-777, Shevell,M.I., 1997



Showing articles 600 to 650 of 1744 << Previous Next >>