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Differential
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airway obstruction
akathisia
amyloid plaques
arrhythmia, cardiac
ataxia
ataxia, progressive
autonomic dysfunction
bovine spongiform encephalopathy
brain atrophy
CAT scan, emission, abnormal
chewing movements
children
chorea
coma
confabulation
Creutzfeldt-Jakob disease, genetic
dementia
dementia, rapidly progressive
dementia, thalamic
dementia, transmissible
dysarthria
electromyogram
epidemic
epidemiology of neurology
exome sequencing
familial
fatal familial insomnia
genetic linkage
genetic neurologic disorders
genetic testing
genioglossus
Gerstmann-Straussler-Scheinker disease
hallucination
hypercapnia
hyperhidrosis
hypersomnia
hypertension
hyperthermia
hypoxia
immunotherapy
inattention
insight, loss
insomnia
intellectual deterioration
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, variant
kuru
memory, defect of recent
memory, impairment of
molecular genetics
mortality
movement disorder
MRI, abnormal
multiple system atrophy
myoclonic jerks
myoclonus
neurologic disease, diagnoses of
neuropathology
neuropathology, brain
next-generation sequencing
prion disease
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychosis
pyramidal tract dysfunction
respiratory failure
review article
sleep apnea
sleep pathology and physiology
snoring
spongy degeneration of brain
stuporous
sudden death
sudden infant death syndrome
tachycardia
thalamus, atrophy of
thalamus, lesion of
thalamus, lesion of-bilateral
tremor
weight loss
Showing articles 2050 to 2100 of 3377 << Previous Next >>

Gliomas of the Anterior Visual Pathway
Surv Ophthalmol 38:427-452, Dutton, J., 1994

Primary Central Nervous System Lymphoma
Ann Int Med 119:1093-1104, Fine,H.A.&Mayer,R.J., 1993

Autosomal Dominant Parkinsoniam with Benign Course and Typical Lewy-Body Pathology
Neurol 43:2222-2227, Golbe,L.I.,et al, 1993

DNA Diagnosis of Neurofibromatosis 2:Altered Coding Sequence of the Merlin Tumor Suppressor in an Extended Pedigree
JAMA 270:2316-2320, MacCollin,M.,et al, 1993

Inherited Primary Peripheral Neuropathies
JAMA 270:2326, 23301993., Lupski,J.R.,et al, 1993

Lissencephaly:A Human Brain Malformation Associated with Deletion of the LIS1 Gene Located at Chromosome 17p13
JAMA 270:2838-2842, Dobyns,W.B.,et al, 1993

Copper-Histidine Therapy for Menkes Disease
J Pediatr 123:828-830, Sarkar,B.,et al, 1993

The Mutations at nt 8993 of Mitochondrial DNA is a Common Cause of Leigh's Syndrome
Ann Neurol 34:827-834, Santorelli,F.M.,et al, 1993

A Neurological Gene Map
Arch Neurol 50:1269-1271, Rosenberg,R.N., 1993

Validity of Family History Data on Severe Headache and Migraine
Neurol 43:1954-1960, Ottman,R.,et al, 1993

Cryptococcal Meningitis and AIDS
Clin Inf Dis 17:837-842, Powderly,W.G., 1993

Eastern Equine Encephalomyelitis
Lancet 342:1281-1282, Freier,J.E., 1993

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

Pheochromocytomas, Multiple Endocrine Neoplasia Type 2, and Von Hippel-Lindau Disease
NEJM 329:1531-1538, Neumann,H.P.H.,et al, 1993

The Neurologic Syndrome of Vitamin E Deficiency:A Significant Cause of Ataxia
Neurol 43:2167-2169, Kayden,H.J., 1993

Risk Factors of Stroke Incidence and Mortality, A 12-Year Follow-up of the Oslo Study
Stroke 24:1484-1489, Haheim,L.L.,et al, 1993

Status Epilepticus at an Urban Public Hospital in the 1980s
Neurol 43:483-488, Lowenstein,D.H.&Alldredge,B.K., 1993

Aicardi's Syndrome:MR Appearance of Unusual Orbital and Ventricular Cystic Lesions
AJR 160:601-603, Mehta,r.C.,et al, 1993

New-Onset Seizures in an Elderly Hospitalized Population
Neurol 43:489-492, Ettinger,A.B.&Shinnar,S., 1993

Acquired Ocular Visual Impairment in Children, 1960-1989
Am J Dis Child 147:325-328, Robinson,G.C.&Jan,J.E., 1993

Molecular Genetic Advances in Fragile X Syndrome
J Pediatr 122:169-185, Tarleton,J.C.&Saul,R.A., 1993

Electrographic Seizures in Preterm & Full-Term Neonates:Clin Corr Brain Lesions, Risk for Sequelae
Pediatrics 91:128-134, Scher,M.S.,et al, 1993

Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease)
NEJM 329:241-245, Tsujino,S.,et al, 1993

Brief Report:Deletion of the Dystrophin Muscle-Promoter Region Associated with X-Linked Dilated Cardiomyopathy
NEJM 329:921-925, 9601993., Muntoni,F.,et al, 1993

Spinal Fluid Cells and Protein in Amyotrophic Lateral Sclerosis
Arch Neurol 50:489-491, Norris,F.H.,et al, 1993

Hereditary Motor-Sensory Neuropathy (Charcot-Marie-Tooth Disease) with Nerve Deafness:A New Variant
J Pediatr 123:431-434, Hamiel,O.P.,et al, 1993

Charcot-Marie-Tooth Disease Type 1A:Association with a Spontaneous Point Mutation in the PMP22 Gene
NEJM 329:96-101, Roa,B.B.,et al, 1993

Niemann-Pick Disease Type C:Diagnosis and Outcome in Children, with Particular Reference to Liver disease
J Pediatr 123:242-247, Kelly,D.A.,et al, 1993

Acetylcholine Receptor Antibodies in Juvenile Myasthenia Gravis
Neurol 43:977-982, Andrews,P.I.,et al, 1993

Molecular Genetic Characterization of an X-Linked Form of Leigh's Syndrome
Ann Neurol 33:652-655, Matthews,P.M.,et al, 1993

Leber's Hereditary Optic Neuropathy as a Cause of Severe Visual Loss in Childhood
Pediatrics 91:988-989, Moorman,C.M.&Elston,J.S., 1993

Atypical Leber's Hereditary Optic Neuropathy with Molecular Confiramtion
Arch Neurol 50:470-473, Weiner,N.C.,et al, 1993

Leber's Hereditary Optic Neuropathy, New Genetic Considerations
Arch Neurol 50:540-548, Newman,N.J., 1993

Identical Twins with Similar Onset of Parkinson's Disease:A Case Report
Neurol 43:1159-1161, Pahwa,R.,et al, 1993

The Nonenvironmental Basis for Rising Mortality from Parkinson's Disease
Arch Neurol 50:653-656, Riggs,J.E., 1993

Functional Abilities at Age 4 Years of Children Born Before 29 Weeks of Gestation
BMJ 306:1715-1718, Johnson,A.,et al, 1993

Dural Puncture and Headache, Avoid the First but Treat the Second
BMJ 306:874-876, Reynolds,F., 1993

Delirium
JNNP 56:742-751, Taylor,D.&Lewis,S., 1993

Long-Term Survival of Veterans with Traumatic Spinal Cord Injury
Arch Neurol 50:909-914, Samsa,G.P.,et al, 1993

Acute Ischemic Stroke from Fibrocartilaginous Embolism to the Middle Cerebral Artery
Stroke 24:738-740, Toro-Gonzalez,G.,et al, 1993

Spinal Epidural Abscess, Optimizing Patient Care
Arch Int Med 153:1713-1721, Maslen,D.R.,et al, 1993

Seizure Characteristics in Chromosome 20 Benign Familial Neonatal Convulsions
Neurol 43:1355-1360, Ronen,G.M.,et al, 1993

Status Epilepticus:The Interaction of Epilepsy and Acute Brain Disease
Neurol 43:1473-1478, Barry,E.&Hauser,W.A., 1993

Life Threatening Focal Status Epilepticus Due to occult Cortical Dysplasia
Arch Neurol 50:695-700, Desbiens,R.,et al, 1993

Treatment of Convulsive Status Epilepticus
Recommendations of the Epilepsy Foundation of America's Working Group on Status Epilepticus, JAMA 27, :54-859,1993., 1993

Felbamate:A Double-Blind Controlled Trial in Presurgical Evaluation of Partial Seizures
Neurol 43:693-696, Bourgeois,B.,et al, 1993

Head Injury
JNNP 56:440-447, Miller,J.D., 1993

Progr Myoclonus Epilepsy of Unverricht-Lundborg Type:Clin & Molecular Genetic Study from US 4 Affected Sibs
Neurol 43:2284-2286, Lehesjoki,A.E.,et al, 1993

Twin Birth is Not a Risk Factor for Seizures
Neurol 43:2515-2519, Berkovic,S.F.,et al, 1993

Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
JAMA 270:1569-1575, Brown,W.,et al, 1993



Showing articles 2050 to 2100 of 3377 << Previous Next >>