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Differential
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abortion, spontaneous
acetylcholine receptor antibody
acid maltase deficiency
acid maltase deficiency, adult
adverse drug reaction
agitation
algorithm
alpha glucosidase
Alzheimer's disease
Alzheimer's disease, treatment of
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, diagnosis of
ANA
anemia
angiokeratoma
anterior horn cell disease
anti basal ganglia antibodies
anti GQ1b IgG antibody
anti Hu antibody
anti Ro antibody
antibiotics
anticholinesterase
anticoagulant, treatment
antiphospholipid antibody syndrome
apoptosis
aspartate aminotransferase
aspirin
atomic bomb
autoantibodies
autoimmune disease
autoimmune encephalopathy
basal ganglia
basal ganglia, lesion of
bat bite
behavioral disorder
blindness
blindness, sudden
bone marrow transplantation
brain atrophy
brainstem, lesion of
carcinoma
carcinoma of lung
cardiomyopathy
caspases
cerebral edema
cerebral edema, vasogenic
cerebral venous thrombosis
cerebrospinal fluid, abnormal
cerebrospinal fluid, oligoclonal bands, absent
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, acute management of
cerebrovascular accident, intrauterine
cerebrovascular accident, severity
cerebrovascular accident, volume
cerebrovascular accident, young adult
channelopathy
chemotherapy, CNS treatment and complications with
cherry red spot
children
chloride channel dysfunction
chorea
choreoathetosis
chromosomal abnormality
chromosome 5
Clinical Pathologic Conference(C.P.C.)
cocaine
cognition
coma
coma, medically induced
comorbidities
complications
confusion
congestive heart failure
consanguinity
contractures, joint
cornea, opacification in infancy-causes of
cornea, opacity of
corpus callosum, lesion of
cortical dysplasia, focal
coumarin
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
cytochrome c oxidase
dabrafenib
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia, treatment of
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
developmental abnormality of brain
developmental retardation
diagnostic criteria
differential diagnosis
donepezil
drooling
drug abuse
dying
dysarthria
dysmorphic
dysostosis multiplex
dysphagia
dystonia
electroencephalogram, abnormalities of
emotional lability
encephalitis
encephalitis lethargica
encephalitis, autoimmune
encephalitis, focal
encephalitis, Rasmussen's
encephalomyelitis
encephalomyelitis, autoimmune
encephalopathy
encephalopathy, progressive
endocarditis, marantic
enzyme treatment
enzyme, defect
epidemiology of neurology
epilepsia partialis continua
extralimbic encephalitis
facial appearance, abnormal
false positive
familial
fasciculation
feeding disorder
fever
Fisher's syndrome
foot drop
football neurologic injuries
fucosidosis
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
ganglionitis
gangliosidosis GM1
gender
gene
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
glutamic acid decarboxylase, antibody
glycine receptor antibodies
glycogen storage disease
glycoprotein
growth retardation
Guillain Barre syndrome
hallucination
head circumference
headache
hearing loss
hemispherectomy
heparin
heparin, low-molecular-weight
hepatomegaly
hepatosplenomegaly
heralding manifestation
hiccoughs
Hurler's syndrome
hydrocephalus
hyperreflexia
hypersomnia
hypertonia
hypothalamus
hypothalamus, lesion of
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
immune checkpoint inhibitors
immune-related adverse events
immunohistochemistry
immunologic disease
immunosuppressive agents
immunotherapy
inborn errors of metabolism
infection, recurrent
intellectual deterioration
intelligence quotient
intrauterine
intrauterine growth retardation
intrauterine infection
iron, brain
karyotyping
kyphoscoliosis, neurologic causes of
laughing, pathologic
life expectancy
limbic encephalitis
lipid storage disorder of CNS
lissencephaly
livedo reticularis
lupus anticoagulant
lysosomal storage disease
lysosomes, abnoral
macrocephaly
malformation, CNS, congenital
megalencephaly
melanoma, malignant
memantine
memory, impairment of
mental retardation
mental status, abnormal
mesial temporal lobe
microangiopathy, brain
microcephaly
micrognathia
mimics
minocycline
misdiagnosis
molecular genetics
monoclonal antibodies
mortality
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, disappearing lesion on
MRI, eye of tiger sign
MRI, FLAIR
MRI, gradient-echo
MRI, paramagnetic effect
MRI, spinal cord
multiple organ failure
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
muscle biopsy
muscle cramp
muscle wasting, diffuse
myasthenia gravis
myasthenia gravis, drug induced
myasthenia gravis, unmasked
myelitis
myelitis, longitudinal
myelitis, transverse, recurrent
myocardial infarction
myoclonus
nasal bridge, wide
nausea and vomiting
neck weakness
negative
neoplasm, metastatic to CNS
neural tube defect
neuroaxonal dystrophy, infantile
neurologic disease
neurologic disease, diagnoses of
neuromyelitis optica (Devic's disease)
neuromyelitis optica spectrum disorder
neuromyelitis optica, IgG
neuronal cell death
neuronal degeneration
neuronal migration disorder
neuronopathy
neuronopathy, sensory
neurons
neuropathology
neuroprotective agents
nivolumab
NMDA antagonists
nursing home
obstetric complications
oculogyric crisis
ophthalmoplegia
optic chiasm
optic chiasm, lesion of
optic neuritis
optic neuritis, bilateral
optic neuritis, recurrent
pain
palliative care
PANK2 mutation
paraneoplastic ganglionopathy
Parkinson disease, postencephalitic
Parkinsonism syndrome
patient information and support
pembrolizumab
periaqueductal lesion
peripheral blood smear
perseveration
personality change
plasmapheresis
platelet inhibiting drugs
pleocytosis of cerebrospinal fluid
Pompe's disease of glycogen storage
postpartum
potassium channel antibodies
precipitating factors
pregnancy, neurologic complications in
premature infant
prenatal diagnosis by amniocentesis
prognosis
progressive encephalomyelitis with rigidity syndrome
progressive neurologic disorder
pseudobulbar palsy
psychological testing
psychological testing, children
rabies, nervous system involvement with
radiation therapy, CNS treatment and complications with
radiation, ionizing
radiation, ionizing, intrauterine
Raynaud's phenomenon
Red flags
remote effect of cancer on the nervous system
renal infarct
renal vein thrombosis
respiratory failure
review article
rigidity
schistocytes
scoliosis, neurologic association with
screening
sedimentation rate, elevated
seizure
seizure, children
seizure, focal
seizure, intractable
seizure, intractable, treatment of
seizure, prognosis in childhood
seizure, surgical treatment of
seizure, treatment of
serologic testing
seronegative
skin, lesions in neurologic disorders
SMN1 gene
somnolence
spinal cord
spinal cord degeneration
spinal cord, lesion of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
splenomegaly
status epilepticus
steroid therapy, CNS treatment and complications with
stiff man syndrome
stillbirth
Sturge-Weber syndrome
sudden death
sudden infant death syndrome
survival motor neuron gene
systemic lupus erythematosus
temporal lobe, lesion
temporal lobe, lesion, bilateral
temporal lobe, status
teratogenesis
teratogenic drugs
tetracycline
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
thrombophlebitis
thrombotic microangiopathy
thymoma
time is brain
tongue, enlarged
tonic spasms
trametinib
transient ischemic attack
treatment of neurologic disorder
ultrasonography
ultrasonography, head, fetus-neonate
urine test for metabolic disorders
valvulopathy
viral infection
visual loss
visual loss, sudden
water channel antibodies
weakness
weakness, fatiguable
weakness, generalized
weakness, proximal
white matter disease
workup
Showing articles 650 to 700 of 5610 << Previous Next >>

Treatment of Patients with Neuropathy and Anti-MAG IgM M-Proteins
Ann Neurol 24:93-97, Nobile-Orazio,E.,et al, 1988

Serum Antibodies to GM1 Ganglioside in Amytrophic Lateral Sclerosis
Neurol 38:1457-1461, Pestronk,A.,et al, 1988

Commentary on Guidelines for the Determination of Brain Death in Children
Ann Neurol 24:789-791, Shewmon,D.A., 1988

MR of Neuronal Migration Anomalies
AJR 150:179-187, Barkovich,A.J.,et al, 1988

Paraneoplastic Syndromes Involving the Eyes
In Walsh & Hoyt's Clin Neuro-ophthal, 4th ed, Williams & Wilkins, Vol 3, p 1735-1746, Miller,N.R., 1988

Cholesterol Crystal Embolization:A Review of 221 Cases in the English Literature
Angiology 38:769-784, Fine,M.J.,et al, 1987

MR Imaging of Heterotopic Gray Matter
J Comput Assist Tomogr 11:878-879, Hayden,S.A.,et al, 1987

Neuroleptic Malignant Syndrome:Review and Analysis of 115 Cases
Biol Psychiatry 22:1004-1020, Addonizio,G.,et al, 1987

Neurological Clues from Environmental Neurotoxins
BMJ 295:346-347, Martyn,C.N., 1987

Motor Neuron Disease in the US, 1971 & 1973-1978:Patterns of Mortality & Associated Conditions at Time of Death
Neurol 37:1339-1343, Leone,M.,et al, 1987

Hypomelanosis of Ito, Wood's Light & Magnetic Resonance Imaging as Diagnostic Measures
Arch Neurol 43:848-850, Ardinger,H.H.&Bell,W.E., 1986

Bone-Marrow Transplantation for Neurovisceral Storage Disorders
Editorial, Lancet 2:788-7891986., , 1986

Enzyme Replacement in Nervous Tissue After Allogeneic Bone-Marrow Transplantation for Fucosidoisis in Dogs
Lancet 2:772-774, Taylor,R.M.,et al, 1986

Giant Cell Arteritis as a Cause of Death
JAMA 255:493-496, Save-Soderbergh,J.,et al, 1986

Cerebral Venous Thrombosis-A Review of 38 Cases
Stroke 16:199-213, Bousser,M.,et al, 1985

Developmental Dyslexia:Four Consecutive Patients with Cortical Anomalies
Ann Neurol 18:222-233, Galaburda,A.M.,et al, 1985

Cerebral Lateralization, Biological Mechanisms, Associations, & Pathology:I
Arch Neurol 42:428-459, 4271985., Geschwind,N.&Galaburda,A.M., 1985

Takayasu Arteritis, A Study of 32 North American Patients
Medicine 64:89-99, Hall,S.,et al, 1985

Cysticercosis-Review of 230 Patients
Bull Clin Neurosci 50:76-101, McCormick.G.F., 1985

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

Hypomelanosis of Ito (incontinentia pigmenti achromians) :Macrocephaly & Gray Matter Heterotopias
Neurol 32:1013-1016, Ross,D.L.,et al, 1982

Brain Abnormalities in Infants with Fotter Syndrome (oligohydramnios tetrad)
Neurol 31:1571-1574, Grunnet,M.L.,et al, 1981

Prognosis in Giant-cell Arteritis
BMJ 282:269-270, Graham,E.,et al, 1981

Progressive Pontobulbar Palsy With Deafness
Arch Neurol 38:186-190, Brucher,J.M.,et al, 1981

Infantile Neuronal Degeneration Masquerading as Werdnig-Hoffmann Disease
Ann Neurol 8:317-324, Steiman,G.S.,et al, 1980

Fetal Methylmercury Poisoning:Clinical & Toxicological Data on 29 Cases
Ann Neurol 7:348-353, Marsh,D.O.,et al, 1980

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Agenesis of the Corpus Callosum:A Study of the Frequency of Associated Malformations
Ann Neurol 6:349-354, Parrish,M.L.,et al, 1979

The Aicardi Syndrome:Report of 4 Cases & Review of the Literature
Ann Neurol 5:475-482, Bertoni,J.M.,et al, 1979

Cytoarchitectonic Abnormalities in Developmental Dyslexia:A Case Study
Ann Neurol 6:94-100, Galaburda,A.M.,et al, 1979

Prenatal Genetic Diagnosis in 3000 Amniocenteses
NEJM 300:157-163, Golbus,M.S.,et al, 1979

Human Brain, (Cytoarchitectonic Left-Right Asymmetries in the Temporal Speech Region)
Arch Neurol 35:812-817, Galaburda,A.M.,et al, 1978

Chronic Hexosaminidase A & B Deficiency
et al. , Ann Neurol 2:156977., Goldie,W.D., 1977

EEG Recognition of Aicardi's Syndrome
Arch Neurol 34:563, Fariello,R.G.,et al, 1977

Epidemiology of Motor-Neuron Diseases
NEJM 288:1047, Bobwick,A.R.,et al, 1973

Atrioventricular-Node Inflammation-Mechanism of Sudden Death in Protracted Meningococcemia
NEJM 286:1091, Robboy,S., 1972

Abnormal Hemoglobin as a Cause of Neurolic Disease
Neurol 12:114, Greer,M.,et al, 1962

Cerebral Hemorrhage In Leukemia
Arch Neurol 2:439-451, Groch,S.N.,et al, 1960

Cerebellar Ataxia in Children
Handout & References., Gilbert,J.J., 1850

Niemann-Pick Type C Disease
www.UpToDate.com, Nov, Schiffmann, R., 2026

A 49-Year-Old Man with Meningoencephalitis and Persistent Altered Mental Status
Neurol 106:e214777, Hariswar,P.T.,et al, 2026

Clinical Insights Into CASPR1 and CASPR1/Contactin1 Com-lex Autoimmune Nodopathies
Neurol 106:e214403, Paramasivan,N.K.,et al, 2026

Clinical Manifestations of Primary CNS T-Cell Lymphoma, Retrospective Study of Histopathologic, Molecular, and Neuroimaging Fetures
Neurol 106:e24744, Muller,K.J.,et al, 2026

Frequency of AQP4 and MOG Antibodies in Patients with Optic Neuritis Fulfilling Minimal New Multiple Sclerosis MRI Criteria
Neurol 106:e214753, Deschamps,R.,et al, 2026

Patterns and Factors Associated with Cerebral Infarction on MRi in Tuberculous Meningitis: Secondary Anlysis of the ACT-TBM Trial
Stroke 57:856-864, Chandu,M.,et al, 2026

Syphilis as an Important Modern-Day Risk Factor for Intracranial Vasculopathy and Ischemic Stroke:A Teaching Case
Stroke 57:e108-e111, Higham-Kessler,C.,et al, 2026

Clinicopathologic Conference, non-islet-Cell Tumor hypoglycemia Due to a Benign Cellular Smooth-Muscle Tumor of the Abdomen
NEJM 394:1216-1225, Case 9-2026, 2026

A 35-Year-Old Man with Recurrent Asymmetric Lumbosacral and Cervical Plexopathy
Neurol 106:e214910, Tayade,K.S., et al, 2026

Cerebral Syphilitic Vasculitis Presenting with Recurrent Stroke
Stroke 57:e197-e198, Yilmaz,E.,et al, 2026

Inflammatory Myopathies
NEJM 394:1925-1938, AllenBach,Y. & Benveniste,O., 2026



Showing articles 650 to 700 of 5610 << Previous Next >>