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abducens nerve paralysis
abducens nerve paralysis, bilateral
acute cerebellar ataxia
acute disseminated encephalomyelitis
Adies pupil
advances in neurology
adverse drug reaction
aggression
algorithm
altered states of consciousness
alternating rapid movement
AMPA receptor antibodies
amphiphysin antibodies
anemia
anemia, megaloblastic
antecedent illness
anti GQ1b IgG antibody
anti GT1aIgG antibody
anti Hu antibody
anti IgLON5
anti La antibody
anti Ma
anti MAG antibodies
anti mGluR1 encephalitis
anti Ri antibody
anti Ro antibody
anti Tr antibodies
anti Yo antibody
antiamphiphysin
antibiotics
antibodies to voltage-gated calcium channels
anticholinesterase
antiendomysial antibodies
antiganglioside antibodies
antineurofascin antibodies
antithyroid antibodies
anxiety
aphasia
areflexia
arthralgia
arthritis
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, paroxysmal
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
athetosis
atypical
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune cerebellar ataxia
autoimmune disease
autoimmune encephalopathy
autoimmune GFAP astrocytopathy
autonomic dysfunction
autonomic neuropathy
axonal degeneration
B 12 deficiency
Babinski sign
bacterial infection
ballismus, bilateral
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
behavioral disorder, acute
Behcet's syndrome
Bickerstaff's brainstem encephalitis
biologic markers
blindness
brachial neuritis
brainstem
brainstem, atrophy
brainstem, dysfunction
brainstem, lesion of
brucellosis, nervous system involvement with
Brudzinski's sign
bulbar dysfunction
bulbar palsy
bulbar palsy, acute
CA-125
calcium channel dysfunction
CAR syndrome
carbon monoxide poisoning
carcinoma
carcinoma of bladder
carcinoma of breast
carcinoma of cervix
carcinoma of lung
carcinoma of ovary
carcinoma of testis
carcinoma of uterus
CAT scan, abdomen
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, pelvis
celiac disease, adult
celiac disease, childhood
central core disease
central hypoventilation
central nervous system, infection of
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebellar peduncle
cerebellar vermis
cerebellitis
cerebellitis, autoimmune
cerebellum
cerebellum, disease of
cerebral cortex
cerebral edema
cerebral folate deficiency syndrome
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, proteincytologic dissociation
chairbound
chemical weapons
children
chloride channel dysfunction
chorea
choreoathetosis
choroid plexus
chromosomal abnormality
chronic fatigue syndrome
ciguatera poisoning
Clinical Pathologic Conference(C.P.C.)
cognition
collagen vascular disease
collapsin response mediator protein 5 IgG
coma
confusion
conjunctivitis
contactin associated protein like 1 antibodies
contactin associated protein like 2 antibodies
cortical ribbon sign
cranial nerve palsies
cranial nerve palsies, bilateral
cranial neuropathy
cranial neuropathy, multiple
cytokines
deep gray nuclei
DEET
delay in diagnosis
dementia
dementia, differential diagnosis of
dementia, rapidly progressive
dementia, treatment of
demyelinating disease
depression
dermatitis herpetiformis
dermatomyositis
diabetes mellitus
diagnostic criteria
diarrhea
differential diagnosis
diplopia
disorientation
distal muscle weakness
dizziness
down-beat nystagmus
DPPX
DPPX, antibodies
DPPX, antibodies, encephalitis
drowsiness
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dyskinesia
dyskinesia, buccal lingual facial
dysmetria
dysphagia
dystonia
electroencephalogram, abnormalities of
electroencephalogram, triphasic delta waves
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, etiology
encephalitis, paraneoplastic
encephalomyelitis
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, delayed
encephalopathy, Hashimoto's
encephalopathy, parainfectious
enteritis
Epstein-Barr virus
eye movement, disorders of
eye, pain in
face, numbness of
facial weakness
facial weakness, bilateral
falling
familial
familial hemiplegic migraine
fasciculation
fever
fine motor function, impaired
Fisher's syndrome
Fisher's syndrome, atypical
flaccid paralysis
flu-like illness
folic acid
folic acid deficiency
gait disorder
GALOP syndromes
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gammaglobulin therapy, intravenous, refractory
gangliosides
gastric biopsy
gastritis
gastrointestinal disease, neurologic complications
gaze palsy
gaze palsy, horizontal
gaze palsy, horizontal-bilateral
gaze palsy, vertical
genetic neurologic disorders
GFAP-IgG
gliadin antibodies
GluD2
glutamic acid decarboxylase, antibody
gluten ataxia
gluten sensitivity
gluten-free diet
growth retardation
Guillain Barre syndrome
Guillain Barre syndrome, axonal form
Guillain Barre syndrome, differential diagnosis of
Guillain Barre syndrome, ophthalmoplegia in
Guillain Barre syndrome, variant forms of
Gulf War syndrome
gynecomastia
hallucination
handwriting
head nodding
headache
hearing loss
heel-knee-shin test
hemifacial spasm
hemiparesis
hemiplegia
hemophagocytic lymphohistiocytosis, cerebromeningeal
hemophagocytosis
hepatitis
hepatomegaly
hepatosplenomegaly
heralding manifestation
HLA
hoarseness
Hodgkin's disease
Hodgkin's disease, neurologic involvement with
hot cross bun sign
hyperesthesia
hyperreflexia
hypersegmented polys
hyperthyroidism
hypertriglyceridemia
hypofibrinogenemia
hypoglycorrhachia
hypogonadism
hypokalemic periodic paralysis
hyporeflexia
hypothyroidism
IgG4-related disease
imbalance
immune-mediated pathogenesis
immunodeficiency
immunologic disease
immunology and the nervous system
immunomodulation
immunosuppression
immunosuppressive agents
immunotherapy
inappropriate antidiuretic(A.D.H.)hormone
incoordination
infection
insect repellent
insecticides
insomnia
intellectual deterioration
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intestinal biopsy
intracranial pressure, increased
intubation
iridoplegia
irritability
Jakob-Creutzfeldt disease
kelch-like protein 11 antibodies
Kernig's sign
lateropulsion
laughing, pathologic
leg spasms, painful
leg weakness, bilateral
lethargy
leucine rich glioma inactivated 1 antibodies
leukemia, neurologic findings assoc.with
leukopenia
level of consciousness, decreased
limbic encephalitis
lip biopsy
listeriosis, CNS
liver function enzymes
lymphadenopathy
lymphadenopathy, hilar
lymphoma
lymphoma involving CNS
malabsorption
malignancy screen
malignancy, occult
malignant hyperpyrexia
memory, impairment of
meningeal enhancement
meningismus
meningitis
meningoencephalitis
meningoencephalomyelitis
mental status, abnormal
mesial temporal lobe
mestinon
midbrain, lesion of
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
migraine, hemiplegic
mimics
misdiagnosis
monoclonal antibodies
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion tensor
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, lumbosacral plexus
MRI, negative
MRI, pelvis
MRI, serial
MRI, spinal cord
multiple sclerosis
muscle cramp
muscle pain
muscle spasm
muscle spasm, face
myasthenia gravis, paraneoplastic
myasthenic syndrome
mycoplasma
mycoplasma pneumoniae
myelitis
myelitis, autoimmune
myelitis, longitudinal
myelopathy
myelopathy, chronic progressive
myoclonus
myoclonus, segmental
myopathy
myotonia
myotonia congenita
nasal speech
nausea and vomiting
nephrotic syndrome
nerve agents
nerve root enhancement
nerve root hypertrophy
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic disease, multifocal
neurologic signs
neuromuscular junction
neuromuscular junction, abnormality of
neuronal cell surface antigen
neuronopathy, sensory
neuroophthalmology
neuropathology
neuropathy
neuropathy, ataxic
neuropathy, autoimmune
neuropathy, paraneoplastic
neuropathy, peripheral, treatment
neuropathy, sensory
neuropathy, toxic
neurotoxic
neurotoxin
neutropenia
NMDA antagonists
NMDA receptors
node of Ranvier
nodopathy, autoimmune
nonresponsive
numbness, ascending
numbness, extremity
nystagmus
nystagmus, dissociated
nystagmus, primary position of gaze
nystagmus, upbeating on upgaze
nystagmus, vertical
ocular flutter
ocular motility, disorders of
oculocephalic reflex
old age, neurology of
olivary degeneration, hypertrophic
onconeural antibodies
one and a half syndrome
ophelia syndrome
ophthalmoplegia
ophthalmoplegia, acute
ophthalmoplegia, bilateral, acute
ophthalmoplegia, postinfectious
ophthalmoplegia, progressive external
ophthalmoplegia, total
opisthotonus
opsoclonus
opsoclonus, differential diagnosis of
opsoclonus-myoclonus syndrome
optic atrophy
optic neuropathy
oral ulcerations
oscillopsia
osteoporosis
ovarian tumor
ovary, enlarged
overlap syndrome
palatal myoclonus
pancytopenia
panic attacks
papilledema
papillitis
paralysis
paramyotonia congenita
paraneoplastic brainstem encephalitis
paraneoplastic cerebellar degeneration
parasomnia
paresthesias
paresthesias, generalized
paresthesias, hands
parietal lobe, lesion of
Parkinsonism syndrome
Parkinsonism, freezing phenomena in
parotid gland neoplasm
paroxysmal neurologic deficits
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
periodic paralysis
peripheral nerve, lesion of
perivascular enhancement
pernicious anemia
personality change
plasmapheresis
pleocytosis of cerebrospinal fluid
POEMS syndrome
poison, organophosphate
polyneuropathy
pons, lesion of
positional head-hanging test
post infectious cerebellar ataxia
postinfectious
potassium channel antibodies
potassium channel dysfunction
practice guidelines
precipitating factors
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ptosis
ptosis, bilateral
puberty
puberty, delayed
pupil, abnormality in neurologic disorders
Purkinje cell
purkinje cell cytoplastic autoantibody
Purkinje cell surface antibody
pursuit eye movements, abnormal
pyramidal tract dysfunction
quadriparesis
quadriplegia
rapidly progressing neurologic illness
recurrent
Red flags
remote effect of cancer on the nervous system
respirations in CNS disease
respirator
respiratory failure
respiratory tract infection
retinopathy
retropulsion
reversible neurologic disorder
review article
rheumatoid arthritis factor(R.A.factor)
rhomboencephalopathy
rigidity
risk factors
rituximab
saccadic eye movements, abnormal
salivation, excessive
scannig speech
Schirmer test
screening
sedimentation rate, elevated
seizure
seizure, intractable
seminoma
serologic testing
serologic testing, false negative
seronegative
short stature
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
skin, lesions in neurologic disorders
sleep apnea, obstructive
sleep pathology and physiology
sodium channel dysfunction
somnolence
speech disorder
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 6
splenomegaly
standing difficulty
staphylococcal protein A column therapy
startle reaction
status epilepticus
steroid
steroid responsive encephalopathy
steroid therapy, CNS treatment and complications with
stiff man syndrome
strabismus
striatal encephalitis
stuporous
superior cerebellar peduncle
systemic illness
systemic lupus erythematosus
tandem gait, ataxic
tauopathy
temporal lobe
temporal lobe, lesion
temporal lobe, lesion, bilateral
teratoma
teratoma, ovarian
thrombocytopenia
thymoma
thyroiditis
tinnitus
titubation
transglutaminase antibodies
treatment of neurologic disorder
tremor
tremor, intention
tremor, jaw
tremor, postural
tremulousness
triangle of Guillain and Mollaret
tuberculosis
uveitis
vaccination, neurologic complications with
vertigo
vestibulopathy
viral infection
visual loss
vitiligo
vocal cord paralysis
walking, difficulty with
war
weakness
weakness, progressive
weight loss
wheelchair
wide based gait
workup
Showing articles 400 to 450 of 2532 << Previous Next >>

Clinicopath Conf,Cerebral Amyloid Angiogpathy and Giant-Cell Inflammatory Reaction to Beta 4-Amyloid and Vasculitis, Case 10-2000
NEJM 342:957-965, , 2000

Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000

Rhombencephalitis Caused by West Nile Fever Virus
Neurol 55:153, Nichter,C.A. et al, 2000

Evolution of Sporadic Olivopontocerebellar Atrophy Into Multiple System Atrophy
Neurol 55:527-532, Gilman,S. et al, 2000

Spinocerebellar Ataxia Type 8
Neurol 55:649-657, Day,J.W. et al, 2000

Niemann-Pick Disease Type C: Two Cases and an Update
Movement Disorders 15:1199-1203, Uc,E.Y.,et al, 2000

Cerebellar Ataxia Associated with Subclinical Celiac Disease Responding to Gluten-Free Diet
Neurol 53:1606-1608, Pellecchia,M.T.,et al, 1999

Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
NEJM 341:901-908, , 1999

Neurologic Complications in Children with Enterovirus 71 Infection
NEJM 341:936-942, Huang,C-C.,et al, 1999

N-Acetylcysteine Therapy for Unverricht-Lundborg Disease
Neurol 52:426-427, Selwa,L.M., 1999

Clinical and MRI Findings in Spinocerebellar Ataxia Type 5
Neurol 53:1355-1357, Stevanin,G.,et al, 1999

Superficial Siderosis of the Central Nervous System,A Late Complication of Cerebellar Tumors
Neurol 52:163-169, Anderson,N.E.,et al, 1999

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
Neurol 52:1472-1478, Nardocci,N.,et al, 1999

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999

Multiple Sclerosis in Children Under 6 Years of Age
Neurol 53:478-484, Ruggieri,M.,et al, 1999

Clinicopath Conf,Multifocal Inflammatory Leukoencephalopathy Related to Combination Chemo with Fluorouracil/levamisole
NEJM 341:512-519, Case 24-1999, 1999

Dancing Eyes-Dancing Feet
Lancet 354:390, Imtiaz,K.E.&Vora,J.P., 1999

Leukoencephalopathy and Raised Brain Lactate from Heroin Vapor Inhalation ("Chasing the Dragon")
Neurol 53:589-1048, Kriegstein,A.R., et al, 1999

Subcotical Arteriosclerotic Encephalopathy (Binswangers Disease)
, Ghika,J. &Bogousslavsky, J., 1998

Adult Brainstem Gliomas
Neurol 51:1136-1139, Landolfi,J.C.,et al, 1998

Clinical,Radiological,Neurophysiological,and Neuropathological Characteristics of Gluten Ataxia
Lancet 352:1582-1585, Hadjivassiliou,M.,et al, 1998

Acute Inflammatory Demyelinating Polyradiculopathy in Children:Clinical and Electrodiagnostic Studies
Ann Neurol 44:350-356, Delanoe,C.,et al, 1998

Myelopathy Caused by Nitrous Oxide Toxicity
AJNR 19:894-896, 9941998., Pema,P.J.,et al, 1998

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Clinical Usefulness of Magnetic Resonance Imaging in Multiple System Atrophy
JNNP 65:65-71, Schrag,A.,et al, 1998

CAG Repeat Number Correlates with the Rate of Brainstem and Cerebellar Atrophy in Machado-Joseph Disease
Neurol 51:882-884, Abe,Y.,et al, 1998

Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
Neurol 51:1666-1671, Moseley,M.L.,et al, 1998

Ataxic Hemiparesis,Critical Appraisal of a Lacunar Syndrome
Stroke 29:2549-2555, Gorman,M. J.,et al, 1998

Neuroradiologic Findings in Marinesco-Sjogren Syndrome
AJNR 19:281-283, Georgy,B.A.,et al, 1998

Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
BMJ 316:582-586, 5641998., Crimlisk,H.L.,et al, 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,et al, 1998

Lateral Medullary Infarction
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Cerebellar Degeneration Associated With Human Immunodeficiency Virus Infection
Neurol 50:244-251, Tagliati,M.,et al, 1998

Hypophosphatemia-Induced Neuropathy: Clinical and Electrophysiologic Findings
Muscle Nerve 21:650-652, Siddiqui,M.F. &Bertorini,T.E., 1998

Usefulness of CT and MR Imaging in the Diagnosis of Acute Wernickes Encephalopathy
AJR 171:1131-1137, Antunez, E.,et al, 1998

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998

Susac Syndrome
Medicine 77:3-11, Papo,T.,et al, 1998

Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
Ann Neurol 43:288-296, Onokera,O.,et al, 1998

Chronic Progressive Leukoencephalopathy in Adult Celiac Disease
Neurol 50:820-822, Beyenburg,S.,et al, 1998

New Variant Creutzfeldt-Jakob Disease:Neurological Features and Diagnostic Tests
Lancet 350:903-907, Zeidler,M.,et al, 1997

Friedreich's Ataxia GAA Repeat Expansion in Pts with Recessive or sporadic Ataxia
Neurol 49:1004-1009, Geschwind,D.H.,et al, 1997

Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
Neurol 49:1617-1620, Ragno,M.,et al, 1997

Atrophy of Cerebellum & Brainstem in Dentatorubral Pallidoluysian Atrophy, CAG Repeat Size on MRI Findings
Neurol 49:1605-1612, Koide,R.,et al, 1997

Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
BMJ 315:856-857, Fox,N.C.,et al, 1997

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

Ocular Findings in Ramsay Hunt Syndrome
J Neuro-Ophthalmol 17:199-201, Mansour,A.M.&Bailey,B.J., 1997

Adult-Onset Neimann-Pick Type C Disease, Clinical, Biochemical and Genetic Study
Arch Neurol 54:1536-1541, Lossos,A.,et al, 1997

The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
Neurol 49:1009-1013, Lorenzetti,D.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997



Showing articles 400 to 450 of 2532 << Previous Next >>