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Differential
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alpha-fetoprotein
alternating hemiplegia
alternating hemiplegia of childhood
alternating rapid movement
aminoacidurias
anti MAG antibodies
anti Yo antibody
aphasia
aphasia, children
apraxia, speech
aspiration
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
ataxic hemiparesis
attention deficit disorder with hyperactivity
attention span
autism
autoantibodies
Babinski sign
basal ganglia, degeneration
basilar artery stenosis
behavioral disorder
Benedict's solution test
bifid uvula
bradykinesia
brainstem, atrophy
brainstem, lesion of
calcification, intracranial
carcinoma
carcinoma of breast
carcinoma of ovary
CAT scan, emission, abnormal
catalepsy
cataplexy
cerebellar ataxia, children
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebral cortex
cerebral cortical atrophy
cerebral palsy
cerebral palsy, associated problems with
cerebral palsy, pure ataxic
cerebrospinal fluid, abnormal
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
chairbound
chemotherapy, CNS treatment and complications with
children
chorea
choreoathetosis
cleft palate
Clinical Pathologic Conference(C.P.C.)
cognition
complications
confusion
consanguinity
cortical-basal ganglionic degeneration
cranial nerve palsies
cranial nerve palsies, bilateral
cranial neuropathy, multiple
crying, pathologic
cryptococcal antigen
cryptococcal meningitis
cultured skin fibroblasts
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, presenile
demyelinating disease
developmental milestones, loss of
diagnostic criteria
dinitrophenylhydrazine(D.N.P.H.)reaction
diplegia, atonic
diplegia, spastic cerebral
diplopia
disability, neurological
disease modifying agents
dizziness
drooling
drowsiness
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dysphonia
dysplasia of C.N.S.
dyspraxia
dystonia
electroencephalogram
electromyogram
emotional lability
encephalitis
encephalitis, autoimmune
encephalopathy
encephalopathy, acute
epileptic encephalopathy
exome sequencing
eye movement, disorders of
facial nerve palsy
failure to thrive
falling
familial
FARS2 deficiency
ferric chloride test
fine motor function, impaired
foam cells
fungal infection
fungal infection, CNS
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
glabellar sign
grasp reflex
head nodding
headache
headache, intractable
hearing loss
hearing problems in children
heel-knee-shin test
hemiplegia
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
hyperreflexia
hypoglycorrhachia
hypotonia
iatrogenic neurologic disorders
imbalance
immunocompetent
immunodeficiency
immunomodulation
immunotherapy
inattention
incontinence, fecal
incoordination
infection
intellectual deficit
intellectual deficit, treatable causes of
intellectual deterioration
intelligence quotient
jaundice
karyotyping
Kayser-Fleischer ring
klippel feil syndrome
language disorders in children
laughing, pathologic
lethargy
leukemia
lipid storage disorder of CNS
liver disease
locked-in syndrome
lysosomal storage disease
maple syrup urine disease
masked facies
memory, impairment of
meningeal enhancement
meningeal enhancement, nodular
meningitis
meningitis, CSF cell count-normal
meningitis, fungal
meningitis, neutrophilic
meningitis, neutrophilic, persistent
mental retardation
mental status, abnormal
methotrexate
microcephaly
midbrain
midbrain, infarction of
midline defect in children
mimics
misdiagnosis
mitochondrial disease
monoclonal antibodies
monoparesis
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, angiography
MRI, contrast enhanced
MRI, disappearing lesion on
MRI, negative
MRI, nodular enhancement
multiple system atrophy
mutism
myelodysplasia
nasal speech
nausea and vomiting
negative
neurofibrillary degeneration
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neurologic symptoms
neuropathology
neuropathy
neurotoxic
neurotoxicity, acute
Niemann-Pick disease
ocular motility, disorders of
palatopharyngeal incompetence
paraneoplastic cerebellar degeneration
paraparesis, familial spastic
paraparesis, spastic
Parkinson disease
Parkinsonism syndrome
personality change
phenylketonuria
pleocytosis of cerebrospinal fluid
pleocytosis of cerebrospinal fluid, neutrophilic
pneumonia
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychosis
psychosis, childhood
psychosocial aspects
ptosis
ptosis, unilateral
pulmonary infection
pure motor hemiplegia
pursuit eye movements, abnormal
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
recurrent
release phenomena
remote effect of cancer on the nervous system
review article
rigidity
saccadic eye movements, abnormal
salivation, excessive
seizure
seizure, advice to parents and teachers regarding
seizure, children
seizure, psychosocial aspects of
seizure, treatment of
single photon emission computed tomography
skin, lesions in neurologic disorders
slit lamp examination
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
speech, loss of
spina bifida
splenomegaly
stare
stuttering
suck reflex
telangiectases
third nerve palsy
third nerve palsy, bilateral
third nerve palsy, partial
toe walking
tongue, impaired movements of
transient neurologic deficit
treatment of neurologic disorder
tremor
upgaze
upgaze, paralysis of
urinary incontinence
urine test for metabolic disorders
vertigo
walking, difficulty with
weight loss
wheelchair
wide based gait
Showing articles 100 to 150 of 15263 << Previous Next >>

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

Lyme Neuroborreliosis
Ann Neurol 37:691-702, Garcia-Monco,J.C.&Benach,J.L., 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Ependymomas of the Posterior Cranial Fossa:CT and MRI Findings
Neuroradiology 37:238-243, Tortori-Donati,P.,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

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

Brainstem Tumors in Patients with Neurofibromatosis Type 1:A Distinct Clinical Entity
Neurol 45:1897-1902, Molloy,P.T.,et al, 1995

Spectrum of Lateral Medullary Syndrome:Correlation Between Clinical Findings and Magnetic Resonance Imaging in 33 Subjects
Stroke 25:1405-1410, Kim,J.S.,et al, 1994

Restricted Acral Sensory Syndrome Following Minor Stroke
Stroke 25:2497-2502, Kim,J.S., 1994

Pure Dysarthria, Isolated Facial Paresis, or Dysarthria-Facial Paresis Syndrome
Stroke 25:1994-1998, Kim,J.S., 1994

Small Primary Intracerebral Hemorrhage:Clinical Presentation of 28 Cases
Stroke 25:1500-1506, Kim,J.S.,et al, 1994

The Syndrome of'Pure Akinesia'and Its Relationship to Progressive Supranuclear Palsy
Neurol 44:1025-1029, Riley,D.E.,et al, 1994

Diffuse Leukodystrophy with a Large-Scale Mitochondrial DNA Deletion
Lancet 343:1397-1398, Nakai,A.,et al, 1994

Cerebellar Infarction, Clinical and Anatomic Observations in 66 Cases
Stroke 24:76-83, Kase,C.S.,et al, 1993

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

Arginase Deficiency Presenting as Cerebral Palsy
Pediatrics 91:995-996, Scheuerle,A.E.,et al, 1993

Wallenberg's Lateral Medullary Syndrome
Arch Neurol 50:609-614, Sacco,R.L.,et al, 1993

Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
Neurol 42:1220-1224, 1992,, Rando,T.A.,et al, 1992

Neurological Complications Following Liver Transplantation
Ann Neurol 31:644-649, Stein,D.P.,et al, 1992

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

Chiari I Malformations:Clinical and Radiologic Reappraisal
Radiology 183:347-353, Elster,A.D.&Chen,M.Y.M., 1992

Midbrain Syndromes of Benedikt, Claude, and Nothnagel:Setting the Record Straight
Neurol 42:1820-1822, Liu,G.T.,et al, 1992

Cerebromeningeal Haemophagocytic Lymphohistiocytosis
Lancet 239:104-107, Henter,J.&Elinder,G., 1992

Infarction in the Anterior Rostral Cerebellum (the Territory of the Lateral Branch of the Superior Cerebellar Artery)
Neurol 41:253-258, Amarenco,P.,et al, 1991

The Spectrum of Cerebellar Infarctions
Neurol 41:973-979, Amarenco,P., 1991

Wilson Disease:Clinical Presentation, Treatment, and Survival
Ann Int Med 115:720-726, Stremmel,W.,et al, 1991

Microangiopathy of the Brain, Retina, and Ear:Improvement without Immunosuppressive Therapy
Stroke 22:933-937, Gordon,D.L.,et al, 1991

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

Sarcoidosis of the Nervous System, A Clinical Approach
Arch Int Med 151:1317-1321, Sharma,Om.P.&Sharma,A.D., 1991

Neurological and Neuropsychiatric Spectrum of Wilson's Disease:A Prospective Study of 45 Cases
J Neurol 238:281-287, Oder,W.,et al, 1991

Neurologic Manifestations of Giant Cell Arteritis
Am J Med 89:67-72, Reich,K.A.,et al, 1990

Progressive Rubella Panencephalitis
In Handbk of Clin Neurol, Vinken & Bruyn, Ed, N Holland Publ Co, 56:405-416, Wolinsky,J.S., 1990

Cerebral Palsy Diplegia:Improvements for Walking
BMJ 299:1115-1116, Patrick,J., 1989

Clinicopath Conf
Subacute Cerebellar Degeneration, Cystadenocarcinoma of Ovary, (with Paraneoplastic Syndrome) , Case, 34-1EJM 321:524-535,1989., 1989

Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
BMJ 298:1019-1020, Boyd,K.&Patterson,V., 1989

MR Imaging of a Group I Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988

Lacunar Syndromes Due to Brainstem Infarct & Haemorrhage
JNNP 51:509-515, Huang,C.Y.,et al, 1988

Clinicopath Conf
Adenocarcinoma of Lung, with Metastasis to Meninges of Brain, Spinal Cord & Optic Nerves, Case Recor, 14-1EJM 318:903-915,1988., 1988

The Clinical and Computed Tomographic Features of Cerebellar Peduncular Hemorrhage
Neurol 38:1485-1487, Wizer,B.,et al, 1988

Clinical Assessment of 31 Patients with Wilson's Disease, Correlations with Struct. Changes on MRI
Arch Neurol 44:365-370, Starosta-Rubinstein,S.,et al, 1987

Clinical & Magnetic Resonance Features of Primary Intracranial Arachnoid Cysts
Ann Neurol 21:342-348, Gandy,S.E.&Heier,L.A., 1987

Partial Dorsal Mesencephalic Hemorrhages:Report of Three Cases
Neurol 36:529-533, Sand,J.J.,et al, 1986

The Clinical Features & Natural History of the Steele-Richardson-Olszewski Syndrome (Prog Supranuclear Palsy)
Neurol 36:1005-1006, Maher,E.R.,et al, 1986

Improved Neurologic Function After Long-Term Correction of Vitamin E Deficiency in Children with Chronic Cholestasis
NEJM 313:1580-1586, Sokol,R.J.,et al, 1985

Alexander's Disease, A Disease of Astrocytes
Brain 108:367-385, Borrett,D.&Becker,L.E., 1985

Nervous System Complications of Relapsing Polychondritis
Neurol 33:513-515, Sundaram,M.B.M.,et al, 1983

Herpes Zoster-Associated Encephalitis:Clinicopathologic Report of 12 Cases and Review of the Literature
Medicine 62:81-95, Jemsek,J.,et al, 1983

Self-Limited Granulomatous Angiitis of the Cerebellum
Ann Neurol 5:490-492, Beresford,H.R.,et al, 1979

Neurologic Disturbances in Pagets Disease of Bone:Response to Calcitonin
Neurol 29:448-457, Chen,J.R.,et al, 1979

Azorean Disease of the Nervous System
NEJM 296:1505, Romanul,F.C.A.,et al, 1977



Showing articles 100 to 150 of 15263 << Previous Next >>