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Differential
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abdominal cramps
abdominal reflex, absent
acute disseminated encephalomyelitis
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
ageusia
akinetic mute
alcohol
Alexanders disease
Alexanders disease, adult onset
aminoacidopathies
aminoacidurias
amnestic syndrome
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, prognosis
anatomy of
angiitis
angiitis, granulomatous of CNS
angiitis, isolated of CNS
angina pectoris
anhidrosis
anosmia
anti MAG antibodies
antispasticity drugs
aphasia
arteriopathy
asterixis
asymptomatic
ataxia
ataxia, cerebellar
ataxic gait
attention deficit disorder with hyperactivity
autonomic dysfunction
Babinski sign
baclofen
basal ganglia, infarction
basal ganglia, lesion of
behavioral disorder
benign essential tremor
beta adrenergic blocker
bladder dysfunction
blink reflex
bone marrow transplantation
brain biopsy
brainstem
brainstem, infarction of
brainstem, lesion of
burning paresthesia
calcification, intracranial
Canavan's disease
CAT scan
CAT scan, abnormal
CAT scan, demyelinating disease
CAT scan, serial
catecholamine
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral infarction
cerebral infarction, small, deep
cerebral infarction, subcortical
cerebral ischemia
cerebral palsy
cerebral venous infarction
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cell count
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, immunoglobulins of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, multiple
cerebrovascular accident, nonvascular territory
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease, cardiovascular disease with
Charcot-Marie-Tooth
children
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
cognition
congenital malformation
congestive heart failure
corneal dystrophy
cortical blindness
cortical blindness, transient
crying, pathologic
cyst, porencephalic
cystinuria
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, cerebrovascular disease causing
dementia, presenile
dementia, subcortical
dementia, thalamic
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
depression
diabetes mellitus
diagnostic criteria
diarrhea
differential diagnosis
dilantin
diplopia
disability, neurological
dopamine
drug induced neurologic disorders
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dysphagia
dystonia
dystonia musculorum deformens
echocardiogram
echolalia
electrical sensation
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electron microscopy
ELISA
emotional lability
encephalitis
encephalitis, viral
encephalomalacia
encephalopathy
encephalopathy, metabolic
enzyme, defect
evoked potentials
exercise intolerance
eye, pain in
Fabry's disease
facial nerve palsy
facial weakness
facial weakness, bilateral
Fahr disease
familial
fatigue
fever
flexor spasm
gadolinium
gait disorder
gamma amino butyric acid
gamma amino butyric acid-mimetic drug
gamma knife therapy
gangliosidosis GM2
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gilles de la Tourette syndrome
glioma
glutaric acidemia
granular osmiphilic material
haloperidol
head injury
head nodding
headache
hearing loss
hearing loss, bilateral
heavy metal intoxication
hemianopia
hemianopia, transient
hemiparesis
hemiparesis, transient
hemiplegia
hepatic encephalopathy
hepatic encephalopathy, treatment of
hepatolenticular degeneration(Wilson's disease)
hiccoughs
HLA
holoprosencephaly
homovanillic acid
hormone replacement
human immunodeficiency virus type 1
human T-lymphotropic virus type I(HTLV-I)
hydrocephalus
hyperreflexia
hypersomnia
hypertension
hyperthyroidism
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
incoordination
intellectual deficit
intellectual deterioration
interferon
interferon beta 1-a
interferon beta 1-b
intrathecal antispasticity drugs
iron, brain
Japan
Krabbe's disease
lactic acidemia
lacunar infarction
laughing, pathologic
L-dopa
Leber's hereditary optic neuropathy
Leigh's disease
Leigh's disease, adult variety
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
level of consciousness, decreased
Lhermitte's sign
lipid storage disorder of CNS
liver disease
Lorenzo's oil
low birth weight
magnetic susceptibility
malformation, CNS, congenital
maple syrup urine disease
MELAS syndrome
mental retardation
metabolic disorder, primary
metachromatic leukodystrophy
metronidazole
microhemorrhage, intracerebral
migraine
misdiagnosis
mitochondrial disease
monoamines
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, complications with
MRI, contrast enhanced
MRI, demyelinating disease
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, negative
MRI, paramagnetic effect
MRI, serial
MRI, spinal cord
MRI, T1 weighted high signal foci
MRI, volumetry
multiple sclerosis
multiple sclerosis, asymptomatic
multiple sclerosis, chronic progressive
multiple sclerosis, clinical patterns
multiple sclerosis, conjugal
multiple sclerosis, diagnosis of
multiple sclerosis, differential diagnosis of
multiple sclerosis, etiology of
multiple sclerosis, familial
multiple sclerosis, linoleic acid in
multiple sclerosis, misdiagnosis
multiple sclerosis, parental transmission
multiple sclerosis, pathogenesis
multiple sclerosis, prognosis
multiple sclerosis, risk factors for
multiple sclerosis, spinal form
multiple sclerosis, treatment of
muscle biopsy
myelin basic protein gene
myelinolysis, extrapontine
myelitis
myelitis, longitudinal
myelitis, transverse
myelomalacia
myelopathy
myelopathy, chronic progressive
myocardial infarction
myoclonus
mysoline
nausea and vomiting
neurochemistry
neurogenic bladder
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neuromyelitis optica (Devic's disease)
neuromyelitis optica spectrum disorder
neuromyelitis optica, IgG
neuropathology
neuropathy
neuropathy, peripheral
neurotransmitter
norepinephrine
Notch3 gene
nystagmus
obsessive-compulsive disorder
occipital lobe, infarction
occipital lobe, lesion of
old age, neurology of
optic atrophy
optic atrophy, bilateral
optic atrophy, hereditary
optic nerve, hypoplasia of
optic neuritis
optic neuritis, bilateral
optic neuropathy
optic neuropathy, bilateral
optic neuropathy, hereditary
palatal myoclonus
palilalia
paraparesis
paraparesis, spastic
paraparesis, spastic, tropical
paraplegia
paratrigeminal syndrome
paresthesias
Parkinson disease
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
PAS positive
PAS positive material in the brain
Pelizaeus Merzbacher
periventricular leukomalacia
phenylketonuria
phenylketonuria, adult onset
pimozide
pleocytosis of cerebrospinal fluid
poison, neurologic problems with
polymerase chain reaction
pons, lesion of
posterior cerebral artery territory infarction
posterior leukoencephalopathy syndrome
premature infant
prevention of neurologic disorders
primary lateral sclerosis
prognosis
propranolol
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
pyramidal tract dysfunction
quadriparesis
quadriplegia
quality of life
radiation therapy, stereotactic
ragged-red fibers
Red flags
regional enteritis
renal stones
retrovirus
reversible neurologic disorder
review article
rigidity
Riley-Day syndrome
risk factors
Rosenthal fibers
Sandhoff's disease
Schilder's disease
scotoma
scotoma, central
seizure
seizure, children
seizure, neonatal
sensorineural hearing loss
sick sinus syndrome
skin, biopsy
skin, lesions in neurologic disorders
smell
spasticity
spasticity, treatment of
speech disorder
speech, loss of
spinal cord
spinal cord, injury of
spinal cord, injury, management of
spinal cord, lesion of
spontaneous remission
steroid therapy, CNS treatment and complications with
stimulation, deep brain
symmetric brain lesions
systemic lupus erythematosus
tardive dyskinesia
taste
Tay-Sachs disease
temporal lobe, lesion, bilateral
thalamic tumors
thalamic tumors, bilateral
thalamotomy
thalamus
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine deficiency
thyrotoxicosis
tic
tinnitus
tongue, impaired movements of
top of the basilar syndrome
torticollis
transient ischemic attack
transient ischemic attack, recurrent
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, classification
tremor, differential diagnosis of
tremor, intention
tremor, jaw
tremor, leg
tremor, rubral
tremor, surgical treatment of
tremor, thalamic stimulation for suppression of
tremor, treatment of
twins
ulcerative colitis
uremia
urinary frequency
urinary incontinence
urinary urgency
vasculitides
vasculopathy
vasospasm, cerebral
vertigo
vertigo, episodic
very long chain fatty acids
viral infection
viral infection, CNS
vision loss, sequential
visual acuity, decreased
visual evoked response
visual loss
visual loss, progressive
visual loss, sudden
visual loss, transient
walking, difficulty with
water channel antibodies
weakness
Wernicke's encephalopathy
white matter disease
workup
Showing articles 0 to 50 of 5354 Next >>

Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
AJNR 38:1467-1474, Bond, K.M.,et al, 2017

Neuromyelitis Optica Spectrum Disorders
UpToDate, May, Glisson,C.C., 2016

Familial Neuromyelitis Optica
Neurol 75:310-315, Matiello,M., et al, 2010

Clinicopath Conf, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)
NEJM 360:1656-1665, Case 12-2009, 2009

Parental Transmission of MS in a Population-Based Canadian Cohort
Neurol 69:1208-1212,1202, Herrera,B.M.,et al, 2007

Differential Diagnosis of Bilateral Thalamic Lesions
Clin Neuroradiol 17:3-22, Linn,J.,et al, 2007

Multiple Sclerosis in Twins From Continental Italy and Sardinia: A Nationwide Study
Ann Neurol 59:27-34, Ristori,G.,et al, 2006

Metabolic Disease and Stroke: MELAS
emedicine.com, Mandava,P.,et al, 2006

Migraine and Cerebral White Matter Lesions
The Neurologist 11:19-29, Gladstone,J.P. &Dodick,D.W., 2005

Adrenoleukodystrophy
JAMA 294:3131-3134, Moser,H.W.,et al, 2005

Familial Multiple Sclerosis and Other Inherited Disorders of the White Matter
The Neurologist 10:201-215, Kalman,B. &Leist,T.P., 2004

Patients with Multiple Sclerosis and Risk of Type 1 Diabetes Mellitus in Sardinia,Italy: A Cohort Study
Lancet 359:1461-1465,1450, Marrosu,M.G.,et al, 2002

Phenylketonuria Presenting in Adulthood as Progressive Spastic Paraparesis With Dementia
JNNP 71:795-797, Kasim,S.,et al, 2001

Disability and Quality of Life in Charcot-Marie-Tooth Disease Type 1
JNNP 70:548-550, Pfeiffer,G.,et al, 2001

Functional Outcomes After Gamma Knife Thalamotomy for Essential Tremor and MS-Related Tremor
Neurol 55:443-446, Niranjan,A. et al, 2000

Multiple Sclerosis
NEJM 343:938-952, Noseworthy,J.H. et al, 2000

Conjugal Multiple Sclerosis: Population-Based Prevalence and Recurrence Risks in Offspring
Ann Neurol 48:927-931, Evers,G.C.,et al, 2000

De Novo Mutation in the Notch3 Gene Causing CADASIL
Ann Neurol 47:388-391, Joutel,A.,et al, 2000

A Comparison of Continuous Thalamic Stimulation and Thalamotomy for Suppression of Severe Tremor
NEJM 342:461-468,505, Schuurman,P.R.,et al, 2000

Familial Neuromyelitis Optica (Devics Syndrome) with Late Onset in Japan
Neurol 55:318-320, Yamakawa,K.,et al, 2000

Primary and Transitional Progressive MS,A Clinical and MRI Cross-Sectional Study
Neurol 52:839-845, Stevenson,V.L.,et al, 1999

The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Offspring Recurrence Rates and Clinical Characteristics of Conjugal Multiple Sclerosis
Lancet 349:1587-1590, Robertson,N.P.,et al, 1997

Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
Lancet 350:1511-1515, 14901997., Joutel,A.,et al, 1997

Idiopathic Granulomatous Angiitis of the CNS Manifesting as Diffuse White Matter Disease
Neurol 49:1696-1699, Finelli,P.F.,et al, 1997

Evidence for Genetic Basis of Multiple Sclerosis
Lancet 347:1728-1730, Sadovnick,A.D.,et al, 1996

Clinical and Subclinical Neurological Involvement in Children of Conjugal Multiple Sclerosis Patients
Multiple Sclerosis 1:170-172, Constantinescu,C.S.,et al, 1996

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

Tourette's Syndrome:A Model Neuropsychiatric Disorder
JAMA 273:498-501, Hyde,T.M.&Weinberger,D.R., 1995

The British Isles Survey of Multiple Sclerosis in Twins
Neurol 44:11-15, Mumford,C.J.,et al, 1994

Clin & Path Features of an Autosomal Dominant, Adult-Onset Leukodystrophy Simul Chronic Progressive MS
Arch Neurol 51:757-766, Schwankhaus,J.D.,et al, 1994

The Relationship of Essential Tremor to Other Movement Disorders:Report on 678 Patients
Ann Neurol 35, 717-7231994., Koller,W.C.,et al, 1994

Spinal Fluid Cells and Protein in Amyotrophic Lateral Sclerosis
Arch Neurol 50:489-491, Norris,F.H.,et al, 1993

A Population-Based Study of Multiple Sclerosis in Twins:Update
Ann Neurol 33:281-285, Sadovnick,A.D.,et al, 1993

Genetic Susceptibility in Familial Multiple Sclerosis not Linked to the Myelin Basic Protein Gene
Lancet 341:1179-1181, Rose,J.,et al, 1993

Familial Multiple Sclerosis:MRI Findings in Clinically Affected and Unaffected Siblings
JNNP 55:883-886, Teinari,P.J.,et al, 1992

Genetic Susceptibility to Multiple Sclerosis Linked to Myelin Basic Protein Gene
Lancet 340:987-991, Tienari,P.J.,et al, 1992

Multiple Sclerosis in 54 Twinships:Concordance Rate is Independent of Zygosity
French Res. Gr. of MS, Ann Neurol 32:724-727, 7222., , 1992

Twinning and Neurologic Morbisity
Am J Dis Child 146:1110-1113, Scheller,J.M.&Nelson,K.B., 1992

Recurrent Encephalopathy and Seizures in a US Native with HTLV-I-Associated Myelopathy/Tropical Spastic Paraparesis
Neurol 42:658-661, Smith,C.R.,et al, 1992

Myelopathy Associated with Human T Cell Lymphotropic Virus Type 1 in a White European Native to England
BMJ 305:453, Ali,A.&Rudge,P., 1992

Occurrence of MS-Like Illness in Women Who Have a Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutation
Brain 115:979-989, Harding,A.E.,et al, 1992

Is Essential Tremor Benign?
Neurol 41:1982-1983, Busenbark,K.L.,et al, 1991

Conjugal Multiple Sclerosis:A Clinical and Laboratory Study
Neurol 41:1320-1321, Finelli,P.F., 1991

MRI in Familial Multiple Sclerosis
Neurol 40:900-903, Lynch,S.G.,et al, 1990

A Comparison of Sporadic and Familial Multiple Sclerosis
Neurol 40:1354-1358, Weinshenker,B.G.,et al, 1990

Excessive Muscular Fatigue in Patients with Spastic Paraparesis
Neurol 40:1271-1274, Miller,R.G.,et al, 1990

Multiple Sclerosis Sibling Pairs:Clustered Onset and Familial Predisposition
Neurol 40:1546-1552, Doolittle,T.H.,et al, 1990



Showing articles 0 to 50 of 5354 Next >>