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Adies pupil
adverse drug reaction
aggression
AMPA receptor antibodies
amphiphysin antibodies
anemia
anti Hu antibody
anti La antibody
anti Ma
anti MAG antibodies
anti Ri antibody
anti Ro antibody
anti Yo antibody
antiamphiphysin
anxiety
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxia, truncal, associated with ocular oscillations
ataxic gait
atypical
autoantibodies
autoimmune disease
autonomic dysfunction
autonomic neuropathy
behavioral disorder
behavioral disorder, acute
brachial neuritis
brain biopsy
brainstem, lesion of
CAR syndrome
carcinoma
carcinoma of breast
carcinoma of cervix
carcinoma of lung
carcinoma of ovary
carcinoma of thyroid
carcinoma of uterus
CAT scan, abdomen
CAT scan, abnormal
CAT scan, emission, abnormal
CAT scan, false negative
CAT scan, pelvis
central nervous system, infection of
cerebellar degeneration
cerebellar lesion
cerebellar vermis
cerebellitis
cerebellum
cerebrospinal fluid, abnormal
cerebrospinal fluid, biochemical markers of CNS tumors
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
chest pain
chest x-ray, abnormal
children
Clinical Pathologic Conference(C.P.C.)
clonazepam
cognition
coinfection
collagen vascular disease
collapsin response mediator protein 5 IgG
contactin associated protein like 2 antibodies
cough
cranial nerve enhancement
cranial nerves
cranial neuropathy
cranial neuropathy, multiple
delay in diagnosis
dementia
depression
dermatomyositis
differential diagnosis
diplopia
disability, neurological
dizziness
down-beat nystagmus
drug induced neurologic disorders
dysarthria
dysmetria
electroencephalogram
electroencephalogram, abnormalities of
embolism, fat
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalitis, Powassan
encephalitis, St.Louis
encephalitis, viral
encephalomyelitis
encephalomyelitis, parainfectious
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, parainfectious
enterovirus
enterovirus infection of CNS
Epstein-Barr virus
eye movement, disorders of
face, numbness of
facial nerve palsy
falling
fever
gait disorder
gammaglobulin therapy, intravenous
gaze palsy
gaze palsy, horizontal
geographic location
GluD2
glutamic acid decarboxylase, antibody
handwriting
headache
headache, severe
hearing loss
heralding manifestation
Hodgkin's disease
Hodgkin's disease, neurologic involvement with
human immunodeficiency virus type 1
hyponatremia
idiopathic
imbalance
immunologic disease
immunology and the nervous system
immunosuppressive agents
immunotherapy
inappropriate antidiuretic(A.D.H.)hormone
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
irritability
leucine rich glioma inactivated 1 antibodies
leukopenia
limbic encephalitis
lip biopsy
Lyme disease
malignancy screen
malignancy, occult
meningeal enhancement
meningismus
meningitis
meningitis, aseptic
meningoencephalitis
meningoencephalomyelitis
mesial temporal lobe
midbrain, lesion of
mortality
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, negative
MRI, pelvis
myasthenia gravis, paraneoplastic
myasthenic syndrome
mycoplasma
mycoplasma pneumoniae
myelitis
myoclonic jerks
myoclonus
myopathy
nausea and vomiting
neuroblastoma
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic disease, multifocal
neuromuscular junction
neuromuscular junction, abnormality of
neuronal cell surface antigen
neuronopathy, sensory
neuroophthalmology
neuropathology
neuropathy
neuropathy, paraneoplastic
neuropathy, sensory
neurotoxin
NMDA antagonists
NMDA receptors
nystagmus
nystagmus, rotary
nystagmus, upbeating on upgaze
nystagmus, vertical
ocular flutter
onconeural antibodies
opsoclonus
opsoclonus, differential diagnosis of
opsoclonus-myoclonus syndrome
oscillopsia
ovarian tumor
ovary, enlarged
panic attacks
paraneoplastic brainstem encephalitis
paraneoplastic cerebellar degeneration
peripheral nerve, lesion of
personality change
photophobia
plasmapheresis
pleocytosis of cerebrospinal fluid
POEMS syndrome
poliomyelitis-like illness
polyneuropathy
pons, lesion of
prognosis
progressive neurologic disorder
pulmonary infiltrates
Purkinje cell
Purkinje cell surface antibody
Red flags
remote effect of cancer on the nervous system
respiratory tract infection
retinopathy
review article
rigidity
Schirmer test
screening
season
seroconversion
serologic testing
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
sleep
spinal cord, lesion of
staphylococcal protein A column therapy
steroid therapy, CNS treatment and complications with
stiff man syndrome
striatum, lesion of
striatum, lesion of, bilateral
systemic illness
temporal lobe, lesion
temporal lobe, lesion, bilateral
teratoma
teratoma, ovarian
thrombocytopenia
thymoma
tick bite
titubation
treatment of neurologic disorder
tremor
tremulousness
ultrasonography
vasculitides
vertigo
viral infection
viral infection, CNS
visual loss
walking, difficulty with
weight loss
West Nile fever
wheelchair
workup
Showing articles 600 to 650 of 1250 << Previous Next >>

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

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

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

Lateral Medullary Infarction
Stroke, Pathophysiology, Diagnosis and management, Churchhill Livingstone, NY 3rd Ed, Ch 22, p. 534, Amarenco,P.,et al, 1998

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

CSF Antigliadin Antibodies and the Ramsay Hunt Syndrome
Neurol 49:1131-1133, Chinnery,P.F.,et al, 1997

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

Multiple-System Atrophy is Genet Distinct from Ident Inherited Causes of Spinocerebellar Degen
Neurol 49:1598-1604, Brandmann,O.,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

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

Autoantibodies to Glutamic Acid Decarboxylase in Three Patients With Cerebellar Ataxia, Late-Onset Insulin-Dependent Diabetes Mellitus, and Polyendocrine Autoimmunity
Neurol 49:1026-1030, Saiz,A.,et al, 1997

Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
Neurol 48:482-485, Zhou,Y.X.,et al, 1997

Familial episodic Ataxia:Clinical Heterogeneity in Four Families Linked to Chromosome 19p
Ann Neurol 41:8-16, 41997., Baloh,R.W.,et al, 1997

Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997

Is There a Gulf War Syndrome? Searching for Syndromes by Factor Analysis of Symptoms
JAMA 227:215-222, 2591997., Haley,R.W.,et al, 1997

Self-Reported Exposure to Neurotoxic Chemical Combinations in the Gulf War:A Cross-Sectional Epidemiologic Study
JAMA 227:231-237, 2591997., Haley,R.W.&Kurt,T.L., 1997

Familial Idiopathic Brain Calcification with Autosomal Dominant Inheritance
Neurol 48:645-649, Kobari,M.,et al, 1997

CIDP:Clinical Features & Responses to Trtm in 67 Consecutive Pts with/without a Monoclonal Gammopathy
Neurol 48:321-328, Gorson,K.G.,et al, 1997

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

Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
Neurol 49:1243-1246, 11961997., Stevanin,G.,et al, 1997

Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl
NEurol 49:1247-1251, Geschwind,D.H.,et al, 1997

Ataxia and Slurred Speech after Artesunate Treatment for Falciparum Malaria
NEJM 336:1328, Miller,L.G.&Panosian,C.B., 1997

Clinicopath Conf
Hodgkin's Disease, Paraneoplastic Cerebellar Degeneration, Case 21-1997, NEJM 337:115-12297., , 1997

Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997

A 36-Year-Old Woman Recuperating From a Stroke
JAMA 277:1970-1976, Alexander,M., 1997

Pure or Predominant Sensory Stroke Due to Brain Stem Lesion
Stroke 28:1761-1764, Kim,J.S.&Bae,Y.H., 1997

Clinicopath Conf
Progressive Supranuclear Palsy, Case 26, 1997, NEJM 337:549-55697., , 1997

Phenotypic Variability in Friedreich Ataxia:Role of the Associated GAA Triplet Repeat Expansion
Ann Neurol 41:675-682, Montermini,L.,et al, 1997

Frataxin Gene of Friedreich's Ataxia is Targeted to Mitochondria
Ann Neurol 42:265-269, Priller,J.,et al, 1997

Balance in the Healthy Elderly
Arch Neurol 54:976-981, Camicioli,R.,et al, 1997

Pain After Thalamic Stroke:Right Diencephalic Predominance and Clinical Features in 180 Patients
Neurol 48:1196-1199, Nasreddine,Z.S.&Saver,J.L., 1997

Calcium Channels in Neurological Disease
Ann Neurol 42:275-282, Greenberg,D.A., 1997

Rapid Spongiform Degeneration of the Cerebrum and Cerebellum in Creutzfeldt-Jakob Encephalitis:Serial MR Findings
AJNR 18:583-586, Tzeng,B-C.,et al, 1997

Age on Onset, Sex, & Cardiomyopathy as Predictors of Disability and Survival in Friedreich's Disease
Neurol 47:1260-1264, DeMichele,G.,et al, 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Total Alopecia, Diabetes Mellitus, and Falls
Lancet 348:1420, Mueller-Schoop,J.W., 1996

Cytomegalovirus Encephalitis
Ann Int Med 125:577-578, Arribas,J.R.,et al, 1996

Diagnostic Guidelines in Central Nervous System Whipple's Disease
Ann Neurol 40:561-568, Louis,E.D.,et al, 1996

Clinicopath Conf
Q Fever, Acute (with Cerebellar and Meningeal Involvement) , Case 38-1996, NEJM 335:1829-1834., , 1996

Isolated Vitamin E Deficiency
Muscle & Nerve 19:1161-1165996., Jackson,C.E.,et al, 1996

Progressive Ataxia, Focal Seizures, and Malabsorption Syndrome in a 41 Year Old Woman
JNNP 60:225-230, Mumford,C.J.,et al, 1996

A Man with Weight Loss, Ataxia, and Confusion for 3 Months
Lancet 347:448, Beversdorf,D.,et al, 1996



Showing articles 600 to 650 of 1250 << Previous Next >>