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abdominal protrusion
abortion, spontaneous
acanthocytosis
agenesis of aqueduct of Sylvius
alpha-fetoprotein
aneurysm
aneurysm, asymptomatic
aneurysm, intracranial
angiography, cerebral
aniridia
anterior tibial muscle weakness
antibodies to voltage-gated calcium channels
apraxia of eye movements
aqueduct of Sylvius, stenosis
aqueductal stenosis
areflexia
arenavirus
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, congenital
ataxia, paroxysmal
ataxia, sensory
ataxia, truncal
ataxic gait
bacterial endocarditis, neurologic manifestations of
Balint's syndrome
Bassen-Kornzweig syndrome
blindness
blindness, sudden
blood cultures
blue tongue virus
brain biopsy
brainstem, atrophy
brainstem, lesion of
bulbar palsy
bulbar palsy, progressive
calcification, intracranial
calcification, periventricular
calcium channel dysfunction
carcinoembryonic antigen
carcinoma
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
cataracts, congenital
central core disease
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hypoplasia
cerebellar infarction
cerebellar lesion
cerebellar vermis
cerebral cortical atrophy
cerebral embolism
cerebral infarction
cerebral infarction, hemorrhagic
cerebral ischemia
cerebral palsy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, red cells in
cerebrovascular accident
cerebrovascular accident, bilateral
children
chloride channel dysfunction
chorea
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 11
Clinical Pathologic Conference(C.P.C.)
Coats syndrome
Cockayne's syndrome
coma
congenital infection, CNS
congenital infection, viral
congenital malformation
congenital myopathy
congenital paresis
consanguinity
contactin associated protein like 1 antibodies
contactin associated protein like 1 auto antibodies.(CNTN1)
cornea, abnormal
cyst
cyst, parenchymal
cyst, porencephalic
cyst, subcortical
Dandy Walker malformation
Dandy Walker malformation, adult
deafmute
deafness
degenerative diseases of CNS
dementia
dental procedure, neurologic complications with
diabetes mellitus
difficulty climbing stairs
distal muscle weakness
drooling
dwarfism
dysarthria
dysphagia
dyspnea
dystonia
electroencephalogram, abnormalities of
electromyogram
electron microscopy
embolism
embolism, septic
embolism, systemic
embryogenesis
encephalitis
encephalitis, viral
encephalopathy
endocarditis
endocarditis, neurologic manifestations with
endocarditis, subacute bacterial
endovascular therapy
eye movement, disorders of
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
familial
familial hemiplegic migraine
fever
fibrillations
foot deformity
foot drop
Friedreich's ataxia
gait disorder
gait, spastic
gammaglobulin therapy, intravenous, refractory
gargoylism
gene
gene mutation
genetic linkage
genetic neurologic disorders
Gillespie syndrome
glaucoma
growth retardation
Hallgren's syndrome
hand flapping
head circumference
headache
hearing loss
heart block
hematoma, intracerebral
hepatosplenomegaly
herpes simplex virus
histochemistry of muscle
Hurler's syndrome
hydranencephally
hydrocephalus
hydrocephalus, congenital
hydrocephalus, non-communicating(obstructive)
hydrocephalus, treatment of
hypokalemic periodic paralysis
hypotonia
immunodeficiency
immunohistochemistry
immunosuppression
incoordination
influenza A virus
intellectual deterioration
intracerebral hemorrhage
intrauterine
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
iris, abnormal
jittery baby
juvenile paresis
Kearns-Sayre syndrome
keratoconus
Laurence-Moon-Bardet-Biedl syndrome
leukemia
lid closure, weakness of
lymphocytic choriomeningitis
lymphoma
maculopathy
malformation, CNS, congenital
malignant hyperpyrexia
Marinesco-Sjogren syndrome
mental retardation
microcephaly
migraine
migraine, hemiplegic
mimics
misdiagnosis
mitral valve lesion
mitral valve prolapse
mitral valve regurgitation
monoclonal gammopathy
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
mucopolysaccharidoses
multiple system atrophy
mumps virus
muscle biopsy
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, differential diagnosis of
muscular dystrophy, facioscapulohumeral
myasthenic syndrome
mycotic aneurysm
myelomalacia
myeloschisis
myoclonic jerks
myoclonus, epilepsy
myopathy
myopia
myotonia congenita
nausea and vomiting
neck pain
nemaline rod myopathy
nemaline rod myopathy, adult onset
neonatal infection, viral
neuritis
neurocutaneous disease
neuroendocrinology
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuropathology
neuropathology, brain
neuropathy
neuropathy, autoimmune
nodopathy, autoimmune
nystagmus
obesity
occipital lobe, infarction
occipital lobe, infarction, bilateral
ocular motility, disorders of
ocular myopathy
old age, neurology of
optic ataxia
pachygyria
pain, neuropathic
papilledema
paramyotonia congenita
paraspinal muscle
paraspinal muscle weakness
parietal lobe, infarction
paroxysmal neurologic deficits
parvovirus
pathology
periodic paralysis
personality change
pleocytosis of cerebrospinal fluid
polydactyly
Poretti-Boltshauser syndrome
posterior cerebral artery occlusion
posterior fossa, lesion of
potassium channel antibodies
potassium channel dysfunction
progeria
prognosis
progressive neurologic disorder
pseudoaneurysm
pseudoretinitis pigmentosa
psychiatric disorder
psychomotor retardation
radiation hypersensitivity
rapidly progressing neurologic illness
respiratory failure
retinal degeneration
retinitis pigmentosa
retinopathy
review article
rituximab
rubella encephalitis
rubella encephalitis, progressive
rubella syndrome
rubella virus
rubeola virus
schizophrenia
seizure
serologic testing
serologic testing of cerebrospinal fluid
shunt procedure, ventricular
shunt procedure, ventriculo-peritoneal
simultanagnosia
skin, lesions in neurologic disorders
sloped shoulders
slow virus infection of CNS
sodium channel dysfunction
spasticity
Spielmeyer Vogt syndrome
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 6
standing difficulty
stem cell transplantation
stooped posture
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subarachnoid hemorrhage
superior cerebellar artery infarction
sweating
telangiectases
teratogenesis
teratogenesis, viral
thrombectomy
thyroiditis
titubation
transplacental virus infections
transverse smile
treatment of neurologic disorder
unconsciousness
urinary incontinence
Usher's syndrome
vasculitides
vertigo
viral infection
viral infection, CNS
viral isolation
virus, slow
visual field defect
visual fields, constricted
visual loss
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
weight loss
wheelchair
white matter disease
wide based gait
winging of scapula
Showing articles 1150 to 1200 of 2289 << Previous Next >>

Interventional Neuroradiology
BMJ 311:789-792, Taylor,W.&Rodesch,G., 1995

Clinicopath Conf
Granulomatous Angiitis of CNS, Case 33-1995, NEJM 333:1135-1143995., , 1995

Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
NEJM 333:1313-1318, 13511995., Gotoda,T.,et al, 1995

Neurologic Aspects of Inflammatory Bowel Disease
Neurol 45:416-421, Lossos,A.,et al, 1995

Clinicopathological Study of 35 Cases of Multiple System Atrophy
JNNP 58:160-166, Wenning,G.K.,et al, 1995

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
Neurol 45:311-317, Barth,P.G.,et al, 1995

Leukoencephalopathy with Swelling & A Discrepantly Mild Clinical Course in Eight Children
Ann Neurol 37:324-334, van der Knaap,M.S.,et al, 1995

A Novel Mutation in Exon 3 of the Proteolipid Protein Gene in Pelizaeus-Merzabacher Disease
Neurol 45:394-395, Pratt,V.M.,et al, 1995

'Anesthesia Paresthetica':Nitrous Oxide-Induced Cobalamin Deficiency
Neurol 45:1608-1610, 14351995., Kinsella,L.J.&Green,R., 1995

Hereditary Sensory and Autonomic Neuropathy with Cataracts, Mental Retardation, and Skin Lesions:Five Cases
Neurol 45:1405-1408, Heckmann,J.M.,et al, 1995

Neurological Multisystem Manifestation in Multiple Symmetric Lipomatosis:A Clinical and Electrophysiological Study
Muscle & Nerve 18:693-698995., Naumann,M.,et al, 1995

Folic Acid and the Prevention of NEural Tube Defects
BMJ 310:1019-1020, Wald,N.J.&Bower,C., 1995

Ischemic Stroke and Intracranial Multifocal Cerebral Arteriopathy in Williams Syndrome
J Pediatr 126:945-958, Soper,R.,et al, 1995

Cerebral Artery Stenosis in Williams Syndrome Causes Strokes in Childhood
J Pediatr 126:943-945, Kaplan,P.,et al, 1995

MRI in Acute Hemiplegia of Childhood
J Comput Assist Tomogr 19:492-494, Connolly,B.,et al, 1995

PET Studies on the Dopaminergic Sys & Striatal Opioid Binding in the OPCA Variant of Multiple System Atrophy
Ann Neurol 37:568-573, Rinne,J.O.,et al, 1995

Eval of the Circle of Willis with Three-Dimentional CT Angiography in Pts with Suspected Intracran Aneurysms
AJNR 16:1571-1578, 15791995., Alberico,R.A.,et al, 1995

Intracranial Arteries:Prospective Blinded Comparative Study of MR Angiography and DSA in 50 patients
Radiology 195:451-456, Klaus,W.S.,et al, 1995

Midcervical Central Cord Syndrome:Numb & Clumsy Hands Due to Midline Cervical Disc Protrusion at C3-4 Intervert Level
JNNP 58:607-613, Nakajima,M.&Hirayama,K., 1995

Reversible Downbeat Nystagmus and Ataxia in Felbamate Intoxication
Neurol 45:845, Hwang,T.L.,et al, 1995

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
Neurol 45:1739-1743, Shulman,L.M.,et al, 1995

Spinocerebellar Ataxias and Ataxins
NEJM 333:1351-1353, Rosenberg,R.N., 1995

Familial Subarachnoid Hemorrhage:Distinctive Features and Patterns of Inheritance
Ann Neurol 38:929-934, Bromberg,J.E.C.,et al, 1995

CT & MRI of Intracavernous Carotid Art Aneurysm with Occlusion of Cervical Internal Carotid Art
J Comput Assist Tomogr 19:1006-1007, Holemans,J.A.&Cox,T.C., 1995

Is Blood Pressure Really a Trigger for the Circadian Rhythm of Subarachnoid Hemorrhage?
Stroke 26:1805-1810, Kleinpeter,G.,et al, 1995

Dopa-Responsive parkinsonism Phenotype of Machado-Jospeh Disease:Confirmation of 14q CAG Expansion
Ann Neurol 48:684-687, Tuite,P.J.,et al, 1995

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995

Folate Levels and Neural Tube Defects:Implications for Prevention
JAMA 274:1698-1702, 17171995., Daly,L.E.,et al, 1995

Detection and Assessment of Intracranial Aneurysms:Value of CT Angiography with Shaded Surface Display
AJR 165:1497-1502, Liang,E.Y.,et al, 1995

Management of Acoustic Neuroma
BMJ 311:1141-1144, Wright,A.&Bradford,R., 1995

Anterior Communicating Artery Aneurysm Paraparesis Syndrome:Clinical Manifestations and Pathologic Correlates
Neurol 45:45-50, Greene,K.A.,et al, 1995

Rerupture of Cerebral Aneurysms During Angiography
AJNR 16:539-542, Saitoh,H.,et al, 1995

Stroke in Pregnancy and the Puerperium:What Magnitude of Risk
JNNP 58:129-131, Grosset,D.,et al, 1995

A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
Ann Neurol 37:289-293, 2851995., Vahedi,K.,et al, 1995

Correlation Between CAT Scan Abnormalities & Neuropsychological Function in Children with Symptomatic HIV Disease
Arch Neurol 52:39-44, Brouwers,P.,et al, 1995

Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995

Postvaricella Basal Ganglia Infarction in Children
AJNR 16:449-452, Silverstein,F.S.&Brunberg,J.A., 1995

Improvement of Paraneoplastic Opsoclonus-Myoclonus After Protein A Column Therapy
NEJM 332:192, Nitschke,M.,et al, 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Intracranial Aneurysms:MR Angiographic Screening in 400 Asymptomatic Individuals with Increased Familial Risk
Radiology 195:35-40, Ronkainen,A.,et al, 1995

Cranial MRI in Ataxia-Telangiectasia
Neuroradiology 37:77-82, Sardanelli,F.,et al, 1995

Endocarditis-Related Cerebral Aneurysms:Radiologic Changes with Treatment
AJNR 16:745-748, Corr,P.,et al, 1995

Outcome in Familial Subarachnoid Hemorrhage
Stroke 26:961-963, Bromberg,J.E.C.,et al, 1995

Subarachnoid Haemorrhage Presenting as Head Injury
BMJ 310:1186-1187, Sakas,D.E.,et al, 1995

Cognitive Outcome After Aneurysm Rupture:Relationship to Aneurysm Site and Perioperative Complications
Neurol 45:875-882, Tidswell,P.,et al, 1995

Sudden Death From Aneurysmal Subarachnoid Hemorrhage
Neurol 45:871-874, Schievink,W.I.,et al, 1995

Syndromes of Pontine Base Infarction:A Clinical-Radiological Correlation Study
Stroke 26:950-955, Kim,J.S.,et al, 1995



Showing articles 1150 to 1200 of 2289 << Previous Next >>