Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
acanthocytosis
acute necrotizing encephalitis
altered states of consciousness
aniridia
antiviral agents
areflexia
arrhythmia, cardiac
ataxia, cerebellar
autonomic dysfunction
autonomic neuropathy
autonomic neuropathy, idiopathic
baldness
Bassen-Kornzweig syndrome
behavioral disorder
blindness
brain biopsy
brain scan
brainstem, atrophy
calcification, intracranial
carcinoma of lung
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
cataracts, congenital
central nervous system, infection of
cerebellar ataxia, children
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar hypoplasia
cerebral cortical atrophy
cerebral palsy
cerebro hepato renal syndrome
cerebrospinal fluid, cytology
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, xanthochromia of
chorioretinitis
chromosome 28
clinodactyly
clubfoot as related to neurologic disease
Cockayne's syndrome
congenital heart disease
congenital infection, CNS
congenital infection, viral
congenital malformation
consanguinity
cornea, abnormal
cornea, opacity of
corpus callosum, hypoplastic
cultured skin fibroblasts
cyst, porencephalic
cytomegalic inclusion disease
cytosine arabinoside
deafmute
deafness
degenerative diseases of CNS
depression
depression, psychotic
dermatoglyphics
digits, abnormal
disability, neurological
dropped head syndrome
dwarfism
dysmorphic
ear, abnormal
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electron microscopy
encephalitis, brainstem
facial appearance, abnormal
facial nerve palsy
facial weakness
failure to thrive
familial
fever
foot deformity
Friedreich's ataxia
frontal balding
gargoylism
gene mutation
genetic neurologic disorders
genetic testing
glaucoma
glioblastoma multiforme(astrocytoma Gr.III)
gonadal dysgenesis
Guillain Barre syndrome
Hallgren's syndrome
hearing loss
heart block
hepatomegaly
herpes labialis
herpes simplex encephalitis
herpes simplex encephalitis, differential diagnosis of
herpes simplex encephalitis, recurrent
herpes simplex encephalitis, treatment of
herpes simplex myelitis
herpes simplex virus
herpes simplex virus infection, immunosuppressed patient
herpes simplex virus, human nervous system and
herpes simplex virus, localization of
herpes simplex virus, malignancy with
herpes simplex virus, pathogenesis of
herpes simplex virus, pathology of
herpes simplex, neurocutaneous lesions in
herpes virus
herpes zoster
herpes, genital
heterotopia
high arched palate
Hurler's syndrome
hydrocephalus
hypoglycorrhachia
hypotonia
immunofluorescent exam of CSF cells
immunosuppression
inborn errors of metabolism
inclusion bodies
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
infectious mononucleosis
interferon
interferon inducer
intracranial pressure, increased
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
iododeoxyuridine
Kearns-Sayre syndrome
keratoconus
Laurence-Moon-Bardet-Biedl syndrome
level of consciousness, decreased
limbic encephalitis
limbic system
lissencephaly
malformation, CNS, congenital
Marinesco-Sjogren syndrome
meningitis
meningitis, aseptic
mental retardation
mental status, abnormal
microcephaly
micropolygyria
micropthalmia
mongolism
monoamines
monoamines, brain
MRI
MRI, abnormal
mucopolysaccharidoses
multiple sclerosis
muscle biopsy
muscular dystrophy
myelitis
myelomalacia
myopathy
myopathy, mitochondrial
myopia
myotonia
myotonia dystrophica
myotonia dystrophica, classification
nasal bridge, wide
neck weakness
neoplasm, metastatic to CNS
neoplasm, primary intracerebral
neuritis
neurologic disease, diagnoses of
neuronal migration disorder
neuropathology
neuropathology, brain
neuropathy
neuropathy, hereditary peripheral
neuropathy, sensory
neuropathy, sensory, hereditary
nystagmus
nystagmus, congenital
nystagmus, pendular
obesity
ocular myopathy
ophthalmoplegia, progressive external
optic atrophy
optic nerve
optic nerve, hypoplasia of
pachygyria
paroxysmal nonkinesigenic dyskinesia
patent ductus arteriosus
peroxisomal disease
personality change
pleocytosis of cerebrospinal fluid
polycystic kidneys
polydactyly
polyinosinic cytidic acid(poly IC)
polyneuropathy, familial
pregnancy, neurologic complications in
prognosis
pseudoretinitis pigmentosa
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ragged-red fibers
remote effect of cancer on the nervous system
retinal dysplasia
retinitis pigmentosa
retinopathy
review article
rubella syndrome
rubella virus
schizophrenia
seizure
seizure, psychomotor-temporal lobe
skin, lesions in neurologic disorders
spasticity
Spielmeyer Vogt syndrome
steroid therapy, CNS treatment and complications with
subacute myelo-opticoneuropathy(S.M.O.N.)complex
subtemporal decompression
syndactyly
talk
transplacental virus infections
trauma
trigeminal neuralgia
trinucleotide repeats
Usher's syndrome
vaccination, neurologic complications with
viral infection
viral infection, CNS
visual field defect
visual fields, constricted
Walker-Warburg syndrome
weakness
white matter disease
x-linked mental retardation
Showing articles 0 to 50 of 1120 Next >>

Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
UptoDate 2022 Jan, Darras, B.T., 2022

Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients
Ann Neurol 44:720-730,713, Baumgartner,M.R.,et al, 1998

MR of Zellweger Syndrome
AJNR 18:1163-1170, Barkowich,A.J.&Peck,W.W., 1997

Bilat Periventricular Nodular Heterotopia with Mental Retard & Syndactyly in Boys:New X-Linked MR Synd
Neurol 49:1042-1047, Dobyns,W.B.,et al, 1997

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

The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990

Neurological and Developmental Findings in Children with Cataracts
Am J Dis Child 13:706-710, Pike,M.G.,et al, 1989

Cerebro-ocular Dysgenesis (Walker-Warberg Syndrome) :Neuropathologic & Etiologic Analysis
Neurol 34:1531-1541, Williams,R.S.,et al, 1984

A Familial Mitochondrial Myopathy With Central Defect in Neural Transmission
Arch Neurol 36:553-556, Barron,S.A.,et al, 1979

Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger
Ann Neurol 2:473, deLeon,G.A.,et al, 1977

Rubella Vaccination During Pregnancy
G. V. , et al, NEJM 295:3966., Quinman,Jr., 1976

Herpes Simplex & the Human Nervous System
Milit Med 140:765, Finelli,P.F., 1975

Pendular Nystagmus, In Ocular Differential Diagnosis
Lea & Febiger, Phila, 1975, p. 119., Roy,F.H., 1975

Genetic Counseling in Retinitis Pigmentosa
MCV Quart 8:283, Noah,V., 1972

Rubella, Clinical Manifestations & Management
Am J Dis Child 118:18-29, Cooper,L.Z.,et al, 1969

Congenital Rubella
Am J Dis Child 118:32-34, Menser,M.A.,et al, 1969

Subarachnoid Hemmorhage During Pregnancy and Puerperium:A Population-Based Study
Stroke 54:198-207, Korhonen,A., et al, 2023

Progressive Camptocormia with Head Drop and Dysphagia
JAMA Neurol 80:209-210, El-Wahsh,S., et al, 2023

Brain Calcification in a Young Woman With Seizures, Explore the Rare Differentials
Neurol 100:397-398, Menon,B.,et al, 2023

Neonatal Seizures
NEJM 388:1692-1700, Ropper.A.H., 2023

Tersons Syndrome
NEJM 388:e79, Sherman,S.V., 2023

Current and Emerging Issues in Wilsons Disease
NEJM 389:922-938, Roberts,E.A. & Schilsky, M.L., 2023

A 17-Year-Old Girl with Progressive Cognitive Impairment
Neurol 101:e1466-e1472, Zhao,B.,et al, 2023

New Onset Focal Tremor in Patient with Human Immunodeficienccy Virus
Clin Infect Dis 75:1861-1863, Finelli,P.F., 2022

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

Infantile and Childhood Hydrocephalus
NEJM 387:2067-2073, Whitehead,W.E.&Weiner,J.L., 2022

Multiple Cranial Nerve Gadolinium Enhancement in Norrie Disease
Ann Neurol 91:158-159, Jokela, M.,et al, 2022

Case Report of Lambl Excrescences in a Pediatric Patient with Multifocal Strokes
Neurol 99:73-76, Robertson, D.M.,et al, 2022

Spina Bifida
NEJM 387:444-450, Iskandar, B.J. & Finnell, R.H., 2022

Bilateral Hearing Loss and Constricted Visual Fields
BMJ 378:e070672, Sachdeva, G. & Shafquat, S., 2022

Spontaneous Subarachnoid Haemorrhage
Lancet 400:846-862, Claassen, J. & Park, S., 2022

Chorioretinopathy After Corticosteroid Treatment for Optic Neuritis
Neurol 96:e305-e306, Ling, J. and Micieli, J.A., 2021

CLOVES Syndrome
Neurol 96:e1487-e1488, Collins, M.,et al, 2021

A Rare Treatable and Under Recognized Cause of Recurrent Convexity Subarachnoid Hemorrhage:Lupus anticoagulant Hypoprothombinemia Syndrome
Ann Indian Acad Neurol 24:986-989, Jain, S.,et al, 2021

A 7-Year-Old Boy with Acute-Onset Altered Mental Status
Neurol 96:e2774-e2778, Wong, G.J.,et al, 2021

Congenital Cytomegalovirus Infection
BMJ 373:m1212, Pesch, M.H.,et al, 2021

Vessel Wall MR Imaging for the Detection of Intracranial Inflammatory Vasculopathies
Cardiovasc Diagn Ther 10:1108-1119, Edjlali,M.,et al, 2020

Acute Ischemic Stroke in Adolescents
Neurol 94:e158-e169, Rambaud, R.,et al, 2020

Feasibility, Safety, and Outcome of Endovascular Recanalization in Childhood Stroke
JAMA Neurol 77:25-34, Sporns, P.B.,et al, 2020

Delayed Leukoencephalopathy: A Rare Complication after Coiling of Cerebral Aneurysms
AJNR 41:286-292, Ikemura, A.,et al, 2020

Ondine Curse Syndrome Cause by Dorsolateral Medullary Stroke
Neurol 94:e1557-e1558, Fiedler, E. & Gill, R., 2020

Blurred Vision
BMJ 368:m569, Zhou, S.,et al, 2020

Bilateral Alopecia as Clue to Diagnosis of Gomez-Lopez-Hernandez Syndrome in a 38-Year-Old Man
Neurol 93:408-410, Kronlage,C.&Healy,D.G., 2019

Declining Malformation Rates with Changed Antiepileptic Drug Prescribing, An Observational Study
Neurol 93:e831-e840, Tomson,T.,et al, 2019

Characteristic Head Jerks in Congenital Oculomotor Apraxia due to Joubert Syndrome
Neurol 93:e1125-e1126, Borngraber, F.,et al, 2019

Muscular Dystrophies
Lancet 394:2025-2038, Mercuri, E.,et al, 2019

Fibromuscular Dysplasia and Its Neurologic Manifestations
JAMA Neurol 76:217-226, Touze, E.,et al, 2019

Management of Stroke in Neonates and Children
Stroke 50:e51-e96, Ferriero, D.M.,et al, 2019

Antiepileptic Drug Treatment Patterns in Women of Childbearing Age with Epilepsy
JAMA Neurol 76:783-790, Kim, H.,et al, 2019



Showing articles 0 to 50 of 1120 Next >>