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asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
autonomic dysfunction
biologic markers
brain atrophy
CAT scan, emission, abnormal
cerebellar ataxia, autosomal recessive
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, biochemical markers of CNS tumors
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children
controversies in neurology
dysarthria
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exome sequencing
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fatal familial insomnia
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genetic testing
glioma
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hypotonia
imbalance
immunotherapy
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lymphoma involving CNS
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molecular genetics
molecular markers
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MRI
MRI, abnormal
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MRI, negative
myelomalacia
neoplasm, primary intracerebral
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nerve conduction studies
neurologic disease, diagnoses of
polymerase chain reaction
prion disease
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
radiation therapy, CNS treatment and complications with
review article
saccadic eye movements, abnormal
seizure
sleep pathology and physiology
staggering
tandem gait, ataxic
temozolomide
thalamus, lesion of-bilateral
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
vitamin E deficiency
walking, difficulty with
white matter disease
workup
Showing articles 600 to 650 of 787 << Previous Next >>

Wilson Disease
Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992

Prenatal Diagnosis of Wilson's Disease by Analysis of DNA Polymorphism
NEJM 327:57, Cossu,P.,et al, 1992

Hypertensive Encephalopathy:Findings on CT, MR Imaging, and SPECT Imaging in 14 Cases
AJR 159:379-383, Schwartz,R.B.,et al, 1992

The First Decade of Molecular Genetics in Neurology:Changing Clinical Thought and Practice
Ann Neurol 32:207-214, Rowland,L.P., 1992

New Anatomical and Functional Imaging Methods
Ann Neurol 32:395-400, Prichard,J.W.&Brass,L.M., 1992

Advances in Neurology
NEJM 326:1608-1616, 1671-16761992., Gilman,S., 1992

Rasmussen's Encephgalitis:Neuroimaging Findings in Four Patints
AJR 158:1329-1332, Tien,R.D.,et al, 1992

Unstable DNA Sequence in Myotonic Dystrophy
Lancet 339:1125-1128, Harley,H.G.,et al, 1992

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

Genetic Diagnosis of Gaucher's Disease
Lancet 339:889-892, Mistry,P.K.,et al, 1992

Cerebral Brain Metabolism in Adult Dyslexic Subj Assessed with PET Scan During Auditory Task
ARch Neurol 49:734-739, Hagman,J.O.,et al, 1992

The Biology of Developmental Dyslexia
JAMA 268:912-915, Rumsey,J.M., 1992

Causal Heterogeneity in Isolated Lissencephaly
Neurol 42:1375-1388, Dobyns,W.B.,et al, 1992

Population Screening for Fragile X
Lancet 339:1210-1213, Turner,G.,et al, 1992

Blinded Clinical Evaluation of Positron Emission Tomography for Diagnosis of Probable Alzheimer's Disease
Neurol 42:765-770, Powers,W.J.,et al, 1992

MRI and SPECT in Amyotrophic Lateral Sclerosis, Demonstr of Upper Motor Neurone Invol by Neuroimaging
Neuroradiology 34:389-393, Udaka,F.,et al, 1992

Parkinson's Disease in Twins Studied with 18 F-Dopa and Positron Emission tomography
Neurol 42:1894-1900, Burn,D.J.,et al, 1992

Survival of Implanted Fetal Dopamine Cells & Neuro Improvement 12 to 46 Months after Transpl for Parkinson's
NEJM 327:1549-1555, 15891992., Freed,C.R.,et al, 1992

Bilateral Fetal Mesencephalic Grafting in Two Patients with Parkinsonism Induced by MPTP
NEJM 327:1556-1563, 15891992., Widner,H.,et al, 1992

Cerebral Glucose Metabolism in Parkinson's Disease with and without Dementia
Arch Neurol 49:1262-1268, Peppard,R.F.,et al, 1992

Serial Changes of Cerebral Glucose Metab & Caudate Size in Persons at Risk for Huntington's Dis
Arch Neurol 49:1161-1167, Grafton,S.T.,et al, 1992

Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria
Brain 115:495-520, Pringle,C.E.,et al, 1992

Angelman Syndrome: Clinical Profile
J Child Neurol 7:270-280, Zori,R.T.,et al, 1992

Thalamic Ischemia in Transient Global Amnesia:A SPECT Study
Neurol 41:1748-1752, Goldenberg,G.,et al, 1991

Visual Loss in Tuberous Sclerosis
Neurol 41:1915-1917, Dotan,S.A.,et al, 1991

Clinical Genetics and Genetic Counseling in Alzheimer Disease
Ann Int Med 115:601-606, Breitner,J.C.S., 1991

More Bad Luck for the X Chromosome:Thalassaemia/Mental Retardation
Lancet 338:1562-1563, , 1991

Myasthenia Gravis in Mothers and Their Newborns
Clin Obstet Gynecol 34:82-99, Plauche,W.C., 1991

Depletion of Muscle Mitochondrial DNA in AIDS Patients with Zidovudine-Induced Myopathy
Lancet 337:508-510, Arnaudo,E.,et al, 1991

Widespread Functional Effects of Discrete Thalamic Infarction
Arch Neurol 48:178-182, Szelies,B.,et al, 1991

Genetice of Cerebrovascular Disease
Stroke 22:276-280, Alberts,M.J., 1991

Anomalous Molecular Form of Acetylcholinesterase in CSF in Histologically Diagnosed Alzheimer's Disease
Lancet 337:447-450, Navaratnam,D.S.,et al, 1991

N-Isopropyl-p- (123I) Iodoamphetamine SPECT in MELAS Syndrome:Comparison with CT & MR Imaging
J Comput Assist Tomogr 15:77-82, Satoh,M.,et al, 1991

Diagnosis and Management of Hormone-Secreting Pituitary Adenomas
NEJM 324:822-831, Klibanski,A.&Zervas,N.T., 1991

Cesarean Section Before Onset of Labor & Motor Function in Infants with Meningomyelocele Diag Antenatally
NEJM 324:662-666, 6901991., Luthy,D.S.,et al, 1991

Sensitivity of Ultrasound in Detecting Spina Bifida
Letter, NEJM 324:769-7721991., , 1991

Diagnosis and Management of Neural-Tube Defects Today
NEJM 324:690-691, Hobbins,J.C., 1991

Assessment:Positron Emission Tomography
Report of Therapeutics & Technology Assessment Subcommittee of the AAN, Neurol 41:163-16791., , 1991

PET:Its Clinical Role in Neurology
JNNP 54:1-5, Brooks,D.J., 1991

Glucosephosphate Isomerase as a CSF Marker for Leptomeningeal Metastasis
Neurol 41:395-398, Newton,H.B.,et al, 1991

Identification of Early Recurrence of Primary Central Nervous System Tumors by (18F) Fluorodeoxyglucose PET
Ann Neurol 29:347-355, 3451991., Glantz,M.J.,et al, 1991

Posterior Cortical Dementia with Alexia:Neurobehavioural, MRI, and PET Findings
JNNP 54:443-448, Freedman,L.,et al, 1991

Positron Emission Tomography in Progressive Supranuclear Palsy
Arch Neurol 48:389-391, Bhatt,M.H.,et al, 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Frontal Lobe Degeneration:Clinical, Neuropsychologicaland SPECT Characteristics
Neurol 41:1374-1382, Miller,B.L.,et al, 1991

Mutation of the Prion Protein in Libyan Jews with Creutzfeldt-Jakob Disease
NEJM 324:1091-1097, Hsiao,K.,et al, 1991

SPECT and MR Imaging in Herpes Simplex Encephalitis
J Comput Assist Tomogr 15:811-815, Schmidbauer,M.,et al, 1991

Prevalence and Incidence of Becker Muscular Dystrophy
Lancet 337:1022-1024, Bushby,K.M.D.,et al, 1991

Mitochondril Encephalopathies:Molecular Genetic Diagnosis from Blood Samples
Lancet 337:1311-1313, Hammans,S.R.,et al, 1991

Regional Cerebal Blood Flow and Cognitive Function in Pts with Chronic Liver Disease
Lancet 337:1250-1253, O'Carroll,R.E.,et al, 1991



Showing articles 600 to 650 of 787 << Previous Next >>