Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
aminoacidopathies
areflexia
ataxia
ataxia, truncal
Babinski sign
basal ganglia, lesion of
basal ganglia, lesion, bilateral
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, proteincytologic dissociation
children
Clinical Pathologic Conference(C.P.C.)
degenerative diseases of CNS
developmental milestones
developmental milestones, loss of
developmental retardation
dystonia
encephalopathy
enzyme, defect
exome sequencing
eye movement, disorders of
familial
genetic neurologic disorders
genetic testing
hepatomegaly
hyperreflexia
hypotonia
inborn errors of metabolism
lactic acidemia
Leigh's disease
metabolic acidosis
metabolic disorder, primary
metabolic disorder, primary-screening tests
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
mitochondrial disease
mitral valve lesion
mitral valve prolapse
MRI
MRI, abnormal
MRI, diffusion weighted
myoclonic jerks
myoclonus
myoclonus, epilepsy
neuromuscular disease, electrodiagnosis of
nystagmus
nystagmus, rotary
ophthalmoplegia
ophthalmoplegia, plus syndrome
ophthalmoplegia, progressive external
optic atrophy
pons, lesion of
precipitating factors
progressive infantile poliodystrophy
psychomotor retardation
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
ragged-red fibers
recurrent
respiratory tract infection
review article
seizure
seizure, children
spasticity
speech, loss of
status epilepticus
striatonigral degeneration
striatonigral degeneration, infantile
symmetric brain lesions
titubation
treatment of neurologic disorder
tremor
tremor, intention
weakness
Showing articles 400 to 450 of 800 << Previous Next >>

Ischemic Core and Penumbra in Human Stroke
Stroke 30:93-99, Kaufmann,A.M.,et al, 1999

Cerebral Injury After Cardiac Surgery,Identification of a Group of Extraordinary Risk
Stroke 30:514-522, Wolman,R.L.,et al, 1999

Long-Term Evaluation of Bilateral Fetal Nigral Transplantation in Parkinson Disease
Arch Neurol 56:179-187, Hauser,R.A.,et al, 1999

Spastic Paraparesis after Anaesthesia
Lancet 353:554, Lee,P.,et al, 1999

Oculogyric Crisis as an Initial Manifestation of Wilson's Disease
Neurol 52:714-715, Lee,M.S.,et al, 1999

Sjogren-Larsson Syndrome, Clinical and MRI/MRS Findings in FALDH-Deficient Patients
Neurol 52:1345-1352,1307, Van Domburg,P.H.M.F.,et al, 1999

Hyperintense Basal Ganglia on T1-Weighted MR Imaging
AJR 172:1109-1115, Lai,P.H.,et al, 1999

Globus Pallidus Deep Brain Stimulation for Generalized Dystonia:Clinical and PET Investigation
Neurol 53:871-874, Kumar,R.,et al, 1999

Nuclear Medicine in Neurology and Psychiatry
Lancet 354:1107-1111, Costa,D.C.,et al, 1999

Diagnosis and Treatment of Wilson's Disease
Semin Neurol 19:261-270, Brewer,G.J.,et al, 1999

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

Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients
Ann Neurol 44:720-730,713, Baumgartner,M.R.,et al, 1998

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

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

MRI of Spinal Cord and Brain Lesions in Subacute Combined Degeneration
Neuroradiology 11:716-719, Katsaros,V.K.,et al, 1998

Oral or Parenteral Therapy for B12 Deficiency
Lancet 352:1721-1722, Elia,M., 1998

Permanent Cortical Damage Detected by Flumazenil Positron Emission Tomography in Acute Stroke
Stroke 29:454-461, Heiss,W.,et al, 1998

Imaging the Brain, Part 1 & 2
NEJM 338:812-820, 889-8961998., Gilman,S., 1998

Wobbly Handwriting
Lancet 351:336, Rosario,M.A.F.,et al, 1998

A Case of Subacute Combined Degeneration:MRI Findings
Neuroradiology 40:398-400, Yamada,K.,et al, 1998

Acute Leukoencephalopathies:Differential Diagnosis and Investigation
The Neurologist 4:148-166, Weinshenker,B.G.,et al, 1998

Hypothalamic Activation in Cluster Headache Attacks
Lancet 352:275-278, 2531998., May,A.,et al, 1998

A Man Who Lost Weight and His Sight
Lancet 351:1174-1175, Moschos,M.&Droutsas,D., 1998

Limbic Encephalitis:Comparison of FDG PET and MR Imaging Findings
AJR 170:1659-1660, Provenzale,J.M.,et al, 1998

Myelopathy Caused by Nitrous Oxide Toxicity
AJNR 19:894-896, 9941998., Pema,P.J.,et al, 1998

PET with 18 Fluorodeoxyglucose and Hexamethylpropylene Amine Oxime SPECT in Late Whiplash Syndrome
Neurol 51:345-350, 3361998., Bicik,I.,et al, 1998

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

Cerebral Manifestation of Wilson's Disease Successfully Treated with Liver Transplantation
Neurol 51:863-865, Bax,R.T.,et al, 1998

X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

Characterizing the Target of Acute Stroke Therapy
Stroke 28:866-872, Fisher,M., 1997

Atypical MRI Features of Wilson's Disease:High Signal in Globus Pallidus on T1-Weighted Images
Neuroradiology 39:171-174, Mochizuki,H.,et al, 1997

A 44-Month Clinical-Brain MRI Follow-Up in a Patient with B12 Deficiency
Neurol 49:878-881, Stojsavljevic,N.,et al, 1997

Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
Neurol 49:568-572, Parboosingh,J.S.,et al, 1997

Measurement of Acetylcholinesterase by PET in the Brains of Healthy Controls & Pts with Alzheimer's Disease
Lancet 349:1805-1809, Iyo,M.,et al, 1997

Genetic Testing of Children at Risk for Huntington's Disease
Neurol 49:1048-1053, Nance,M.A.,et al, 1997

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

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

Sympathetic Cardioneuropathy in Dysautonomias
NEJM 336:696-702, 7211997., Goldstein,D.S.,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

A Simplified Six-Item Checklist for Screening for Fragile X Syndrome in the Pediatric Population
J Pediatr 129:611-614, Giangreco,C.A.,et al, 1996

Acute Phenytoin Toxicity Followed by Seizure Breakthrough From a Ticlopidine-Phenytoin Interaction
Arch Neurol 53:1191-1192, Privitera,M.&Welty,T.E., 1996

Maternal Phenylketonuria:Magnetic Resonance Imaging of the Brain in Offspring
J Pediatr 128:770-775, Levy,H.L.,et al, 1996

Preclinical Evidence of Alzheimer's Disease in Persons Homozygous for the e4Allele for Apolipoprotein E
NEJM 334:752-758, 7911996., Reiman,E.M.,et al, 1996

Ticlopidine Impairs Phenytoin Clearance:A Case Report
Neurol 46:1172-1173, Riva,R.,et al, 1996

The Inherited Ataxias and the New Genetics
JNNP 61:327-332, Hammans,S.R., 1996

Treatment of Wilson Disease with Ammonium Tetrathiomolybdate
Arch Neurol 53:1017-1025, Brewer,G.J.,et al, 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Clinical, Neuroimaging, and Pathologic Features of Progressive Nonfluent Aphasia
Ann Neurol 39:166-173, Turner,R.S.,et al, 1996

Trinucleotide Repeat Length and Clinical Progression in Huntington's Disease
Neurol 46:527-531, Brandt,J.,et al, 1996



Showing articles 400 to 450 of 800 << Previous Next >>