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Differential
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achilles tendon, enlarged
Addison's disease
Adies pupil
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
adult polyglucosan body disease
algorithm
angiography, neurologic complications with
ankle reflex, absent
areflexia
artery of Adamkiewicz
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
behavioral disorder
bladder dysfunction
bone marrow transplantation
brainstem, atrophy
brainstem, lesion of
burning paresthesia
CAG repeats
cane
cardiomyopathy
CAT scan, abnormal
CAT scan, emission, abnormal
cataracts
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebral palsy
cerebrospinal fluid, lactic acid concentration
cerebrotendinous xanthomatosis
Charcot-Marie-Tooth
chenodeoxycholic acid
children
chromosomal abnormality
chromosome 2
chromosome 6
chromosome 9
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
cognition
consanguinity
corpus callosum, thinning
cultured skin fibroblasts
deep tendon reflexes
degenerative diseases of CNS
dementia
dementia, childhood
demyelinating disease
dentate nuclei, lesion of
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
diet
differential diagnosis
distal muscle atrophy
distal muscle weakness
Dravet syndrome
drug induced neurologic disorders
dysarthria
dysmetria
dysmorphic
dysphagia
ears of the Lynx MR sign
electroencephalogram, inflammatory disease
encephalopathy
epicanthal folds
epidemiology of neurology
epileptic encephalopathy
exome sequencing
eye movement, disorders of
facial appearance, abnormal
failure to thrive
falling
familial
FARS2 deficiency
fatty acid, elevated plasma content
fever
fine motor function, impaired
finger nose finger test
foot deformity
foot drop
frataxin
Friedreich's ataxia
gait disorder
gait, spastic
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
hammertoes
hand weakness
hearing loss
hepatomegaly
high arched feet
hyperreflexia
hypogonadism
hypomyelination
hypotonia
iatrogenic neurologic disorders
imbalance
impulsivity
inborn errors of metabolism
incoordination
intellectual deficit
intellectual deterioration
intrinsic hand muscles, wasting of
Jewish
lactic acidemia
leg weakness, bilateral
Leigh's disease
leukodystrophy
liver disease
Lorenzo's oil
meningitis, CSF cell count-normal
mental retardation
microcephaly
microdontia
middle cerebellar peduncle
middle cerebellar peduncle, lesion, bilateral
mimics
misdiagnosis
mitochondrial disease
molecular genetics
mortality
motor neuron disease
MRI
MRI, abnormal
myelin protein zero gene
myelomalacia
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
myoclonus, epilepsy
nerve conduction studies
neurologic disease, diagnoses of
neurologic signs
neuropathology
neuropathy
neuropathy, demyelinating
neuropathy, hereditary peripheral
next-generation sequencing
night blindness
numbness, extremity
nystagmus
nystagmus, rotary
ocular motility, disorders of
oculodentodigital dysplasia
optic ataxia
optic atrophy
orthostatic hypotension
pain, foot
paraparesis
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
paraplegia
paraplegia, acute
paraplegia, neonatal
paresthesias
past pointing
Pelizaeus Merzbacher
peroxisomal disease
personality change
pes cavus
polyglucosan body disease
polyneuropathy
pons, lesion of
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing, neurologic problems
psychomotor retardation
pupil
pupil, dilated and fixed, bilateral
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
release phenomena
review article
Romberg's sign
scissors gait
SCN1A gene
scoliosis
screening
seizure
seizure, children
seizure, familial
seizure, febrile
seizure, intractable
seizure, neonatal
seizure, tonic-clonic
skin, darkening of
sodium channel dysfunction
spastic ataxia
spastic diplegia
spastic paraplegia, type 11
spasticity
speech, loss of
spinal cord, infarction of
spinal cord, lesion of
spinocerebellar ataxia type 1
spinocerebellar degeneration
status epilepticus
steppage gait
stiff legs
striatonigral degeneration
striatonigral degeneration, infantile
subcortical U fibers
symmetric brain lesions
syndactyly
teeth, abnormal
testicular atrophy
titubation
toe walking
treatment of neurologic disorder
tremor
tremor, intention
trinucleotide repeats
umbilical artery catheterization
urinary incontinence
visual impairment
walking, difficulty with
weakness
weakness, progressive
wheelchair
white matter disease
xanthoma, tendon
Showing articles 850 to 900 of 1537 << Previous Next >>

Werner's Syndrome Associated with Spastic Paraparesis and Peripheral Neuropathy
Neurol 43:1252-1254, Umehara,F.,et al, 1993

Rapid Diagnosis of Herpes Simplex Virus Encephalitis by Using the Polymerase Chain Reaction
J Pediatr 123:376-380, Troendle-Atkins,J.,et al, 1993

Spastic Ataxia Associated with Human T-Cell Lymphotropic Virus Type II Infection
Ann Neurol 33:411-414, Harrington,W.J.,et al, 1993

Isolation of HTLV-II from Pt with Chronic, Prog Neurol Dis Clin Indistinguish from HAM/Tropical Spastic Paraparesis
Ann Neurol 33:392-396, Jacobson,S.,et al, 1993

Analysis of Dystrophin Expression after Activation of Myogenesis in Amniocytes, Chorionic-Villus Cells, and Fibroblasts
NEJM 329:915-920, Sancho,S.,et al, 1993

Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes (MELAS) :Clinical, Radiological, Pathol & Genetic Observ
Ann Neurol 34:25-31, Koo,B.,et al, 1993

Brainstem Glioma:I. Pathology, Clinical Features, and Therapy
J Child Neurol 8:112-128, Maria,B.L.,et al, 1993

Postoperative Chemotherapy & Dalayed Radiation in Children Less Than Three Years of Age with Malignant Brain Tumors
NEJM 328:1725-1731, 17801993., Duffner,P.K.,et al, 1993

Posterior Cranial Fossa Tumours in Childhood
Neuroradiology 35:274-278, Chang,T.,et al, 1993

MRI of Gangliocytoma of Cerebellum and Spinal Cord
J Comput Assist Tomogr 17:488-491, Furie,D.M.,et al, 1993

Relation Between Maternal Diet and Subsequent Primitive Neuroectodermal Brain Tumors in Young Children
NEJM 329:536-541, Bunin,G.R.,et al, 1993

TORCH Infections in the Newborn
Semin Neurol 13:106-115, Donley,D.K., 1993

Epilepsy and Pregnancy
BMJ 307:492-495, O'Brien,M.D.&Gilmour-White,S., 1993

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

A Controlled Trial of Diazepam Administered During Febrile Illnesses to Prevent Recurrence of Febrile Seizures
NEJM 329:79-84, Rosman,N.P.,et al, 1993

Outcome of Childhood Status Epilepticus and Lengthy Febrile Convulsions:Findings of National Cohort Study
BMJ 307:225-228, Verity,C.M.,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

Magnetic Resonance Imaging in Childhood Intractable Partial Epilepsies:Pathologic Correlations
Neurol 43:681-687, Kuzniecky,R.,et al, 1993

Sleep State and the Risk of Seizure Recurrence Following a First Unprovoked Seizure in Childhood
Neurol 43:701-706, Shinnar,S.,et al, 1993

Biologic Factors as Predictors of Social Outcome of epilepsy in Intellectually Normal Children:A Population-Based Study
J Pediatr 122:869-873, Camfield,C.,et al, 1993

New-Onset Seizures in Critically Ill Patients
Neurol 43:1042-1044, Wijdicks,E.F.M.&Sharbrough,F.W., 1993

Strokes in Children Due to Vertebral Artery Trauma
Neurol 43:2555-2558, Garg,B.P.,et al, 1993

Hippocampal Sclerosis in Children with Intractable Temporal Lobe Epilepsy:Detection with MR Imaging
AJR 161:1045-1048, Grattan-Smith,J.D.,et al, 1993

Carbamazepine Withdrawal:Effects of Taper Rate on Seizure Frequency
Neurol 43:2280-2284, Malow,B.A.,et al, 1993

Intractable Seizures in Infancy and Early Childhood
Neurol 43 (suppl-5) :S2-S37993., Moshe,S.L.&Dulac,O., 1993

Hippocampal Sclerosis in Epilepsy and Childhood Febrile Seizures
Lancet 342:1391-1394, Kuks,J.B.M.,et al, 1993

Congenital Bilateral Perisylvian Syndrome:Study of 31 Patients
Lancet 341:608-612, Kuzniecky,R.,et al, 1993

Risk of Intracranial Hemorrhage & Adverse Outcomes-Cocaine Expose in 323 Very Low Birth Wt Infants
J Pediatr 122:438-445, Dusick,A.M.,et al, 1993

Neurologic Prognosis of Cytomegalovirus Polyradiculomyelopathy in AIDS
Neurol 43:493-499, Cohen,B.A.,et al, 1993

Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
Neurol 33:4-9, Nishino,H.,et al, 1993

Intramedullary Spinal Sarcoidosis:Clinical and Magnetic Resonance Imaging Characteristics
Neurol 43:333-337, Junger,s.S.,et al, 1993

Coxiella (Q fever) -Associated Myelopathy
Neurol 43:338-342, Hwang,Y.M.,et al, 1993

Experience with Screening Newborns for Duchenne Muscular Dystrophy in Wales
BMJ 306:357-360, 3491993., Bradley,D.M.,et al, 1993

Ornithine Transcarbamylase Deficiency Presenting with Strokelike Episodes
J Pediatrics 122:423-425, Christodoulou,J.,et al, 1993

Neuroradiological Manifestations of Focal Polymorphic Delta Activity in Children
Arch Neurol 50:181-184, Maytal,J.,et al, 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

Epilepsy in the First 10 Years of Life:Findings of the Child Health & Education Study
BMJ 305:857-861, Verity,C.M.,et al, 1992

Spontaneous Resolution of a Postirradiation Lumbosacral Plexopathy
Neurol 42:2224-2225, Enevoldson,T.P.,et al, 1992

Risk Factors for Early Intraventricular Hemorrhage in Low Birth Weight Infants
J Pediatr 121:776-783, Ment,L.R.,et al, 1992

Cerebral Infarction Complicating Hemorrhagic Shock and Encephalopathy Syndrome
Pediatrics 90:626-628, Bratton,S.L.&Jardine,D.S., 1992

Outlook for the Child with a Cephalocele
Pediatrics 90:914-919, Brown,M.S.,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

Human T Lymphotropic Virus Type I-Assoc Myelopathy, A Rpt of 10 Pts Born in US
Arch Neurol 49:1113-1118, Sheremata,W.A.,et al, 1992

Chronic Myelopathy Associated with Human T-Lymphotropic Virus Type I (HTLV-I)
Ann Int Med 117:933-946, Gessain,A.&Gout,O., 1992

Vascular Dysplasia in Down Syndrome:A Possible Relationship to Moyamoya Disease
Brain Dev 14:248-251, Mito,T.&Becker,L.E., 1992

Multiple Sclerosis with Very Late Onset
Neurol 42:1907-1910, Hooge,J.P.&Redekop,W.K., 1992

Lupus-Related Myelopathy:Report of Three Cases and Review of the Literature
JNNP 55:830-835, Provenzale,J.&Bouldin,T.W., 1992

Three-and Four-Year Cognitive Outcome in Children with Noncortical Brain Tumors & Whole-Brain RT
Ann Neurol 32:551-554, Radcliffe,J.,et al, 1992

Superior Sagittal Sinus Thrombosis in a Child with Protein S Deficiency
Neurol 42:2303-2305, Prats,J.M.,et al, 1992

The Role of Transeophageal Echocardiography in the Acute Onset of Paraplegia
Stroke 23:1660-1661, Walsh,D.V.,et al, 1992



Showing articles 850 to 900 of 1537 << Previous Next >>