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abortion, spontaneous
activated protein C resistance
advances in neurology
Africa
alopecia
AMPA receptor antibodies
ANA
ANA-negative systemic lupus erythematosus
anemia
angiography, cerebral
animal exposure
anorexia
anterior horn cell disease
anticardiolipin antibodies
anticoagulant, treatment
anticoagulant, treatment in CVD
antiphospholipid antibodies
antiphospholipid antibody syndrome
arteritides
arteritis, temporal
arthralgia
arthritis
asymptomatic
ataxia
ataxia, cerebellar
ataxic gait
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
autonomic dysfunction
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder, acute
biologic markers
blood dyscrasias, neurologic findings with
brain scan, abnormal
brainstem
brainstem, lesion of
cancer associated cognitive impairment
carcinoma
carcinoma of lung
CAT scan
CAT scan, abnormal
CAT scan, venography
catatonia
celiac disease, adult
celiac disease, childhood
central nervous system, infection of
cerebellar lesion
cerebral cortex
cerebral embolism
cerebral embolism, cardiac origin
cerebral infarction, hemorrhagic
cerebral venous infarction
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, complement of
cerebrospinal fluid, pressure increased
cerebrospinal fluid, red cells in
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, multiple
cerebrovascular accident, recurrent
cerebrovascular accident, three territory involvement
cerebrovascular accident, work up for
cerebrovascular accident, young adult
children
cholangitis
chorea
choreoathetosis
Clinical Pathologic Conference(C.P.C.)
cognition
collagen vascular disease
collapsin response mediator protein 5 IgG
complement
complement deficiency
complement, serum
complications
confusion
Coombs test, positive
cortical ribbon sign
cranial neuropathy, multiple
cytoid bodies
delusion
dementia
dermatitis herpetiformis
diarrhea
differential diagnosis
digital subtraction angiography
disorientation
DPPX, antibodies, encephalitis
dysarthria
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, facial
echocardiogram
electroencephalogram, abnormalities of
electrophoretic pattern, serum
embolism
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, etiology
encephalitis, viral
endocarditis
endocarditis, Libman-Sacks
eosinophilia
epidemiology of neurology
facial weakness
faciobrachial dystonic seizure
factor I, deficiency
Factor V Leiden
factor V, deficiency
falling
familial
fatigue
fever
flaccid paralysis
fluorescent treponema antibody absorption/false positive
foot drop
fragile-X syndrome
fragile-X syndrome, carrier
gamma amino butyric acid receptor antibody
gastrointestinal disease, neurologic complications
gender
genetic neurologic disorders
genetic screening
gluten ataxia
gluten sensitivity
gluten-free diet
growth retardation
hallucination
headache
headache, severe
headache, sudden onset of
hemorrhagic diathesis
heparin
hepatitis
herpes simplex encephalitis
HLA
hyperekplexia
hypergammaglobulinemia
hypocomplementemia
hypogonadism
hyponatremia
IgG4-related disease
immunosuppression
immunotherapy
insect sting
insomnia
intellectual deficit
intestinal biopsy
intracerebral hemorrhage
intracerebral hemorrhage, familial
intracerebral hemorrhage, work up
lacrimal gland enlargement
LE cell preparation
lenticular nucleus, lesion of, bilateral
leucine rich glioma inactivated 1 antibodies
leukocytosis
leukopenia
level of consciousness, decreased
limbic encephalitis
livedo reticularis
lupus anticoagulant
lymph node biopsy
lymphadenopathy
lymphoma involving CNS
malabsorption
malaise
memory, defect of recent
memory, impairment of
meningismus
meningitis
meningitis, aseptic
meningitis, bacterial
meningitis, chronic
meningitis, CSF findings in
meningitis, gram negative
meningitis, lupus
meningitis, meningococcal
meningitis, Mollaret's
meningitis, predisposing factors in
meningitis, recurrent
meningococcemia
meningoencephalitis
mental retardation
mental retardation, familial
mental status, abnormal
mesial temporal lobe
misdiagnosis
mitral valve lesion
mitral valve vegetation
monoclonal antibodies
mononeuropathy
mosquito
Mott cells
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, FLAIR
MRI, negative
MRI, venography
muscle pain
muscle weakness
myelitis
myelitis, transverse, recurrent
myocarditis
myoclonus
myositis
nausea and vomiting
neisseria meningitis
nephritis
nerve conduction studies
neurexin-3 alpha antibodies
neurologic complications of, systemic cancer
neurologic disease, diagnoses of
neurologic signs
neuromuscular disease, electrodiagnosis of
neuronal cell surface antigen
neurons
neuropathology
neuropathy
neuropathy, peripheral
night blindness
NMDA antagonists
nystagmus
optic neuritis
oral contraceptives
oral contraceptives, neurologic complications with
oral ulcerations
osteoporosis
pain, abdominal
papilledema
paranoia
parasitic infection, CNS
partial thromboplastin time, prolonged
pericarditis
personality change
petechiae
plasmacytosis
pleocytosis of cerebrospinal fluid
pleurisy
poliomyelitis-like illness
polymerase chain reaction
precipitating factors
pregnancy, neurologic complications in
prognosis
progressive neurologic disorder
protozoan infection
psychiatric problems in neurologic disorders
psychological testing
psychosis
ptosis
puberty
puberty, delayed
purpura
rash
rash, painful
Raynaud's phenomenon
recurrent
review article
risk factors
rituximab
salivary gland enlargement
schizophrenia
scotoma
sedimentation rate, elevated
seizure
serologic testing
serologic testing of cerebrospinal fluid
serologic testing, false negative
seronegative
short stature
skin, lesions in neurologic disorders
sleeping sickness
splenomegaly
steatorrhea
steroid
steroid psychosis
steroid therapy, CNS treatment and complications with
stool, loose
striatal encephalitis
striatum, lesion of
striatum, lesion of, bilateral
subcutaneous nodules
systemic illness
systemic inflammatory response syndrome
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
systemic lupus erythematosus, skin changes in
tachycardia
temporal artery, biopsy
temporal lobe, lesion
temporal lobe, lesion, bilateral
teratoma
teratoma, ovarian
thalamus
thalamus, lesion of
Three territory sign
thrombocytopenia
thrombophlebitis
thymoma
thyroiditis
travel, foreign
treatment of neurologic disorder
tremor
tropical disease
trypanosoma brucei gambiense
vasculitides
vasculopathy
viral infection
viral infection, CNS
visual fields, constricted
visual loss
visual loss, progressive
vitamin A
vitamin A deficiency
vitamin deficiency
walking frame
weakness
weight loss
West Nile fever
white matter disease
white matter disease, subcortical
x-linked mental retardation
Showing articles 700 to 750 of 1585 << Previous Next >>

CT and MR Findings of Neuroacanthocytosis
J Comput Assist Tomogr 21:221-222, Okamoto,K.,et al, 1997

Myotonic Dystrophy, The Role of Large Triplet Repeat Length in the Develop of Mental Retardation
Arch Neurol 54:251-254, Spranger,M.,et al, 1997

Cognitive Function and Academic Performance in Neurofibromatosis 1:North
K. N. , et al, Neurol 48:1121-11277., , 1997

Long-Term Cognitive Impairment Associated with Caudate Stroke
Stroke 28:970-975, Bokura,H.&Robinson,R.G., 1997

Serial Neuropsychological Assess & Magnetic Resonance Imagingf Analysis in Multiple Sclerosis
Arch Neurol 54:1018-1025, Hohol,M.J.,et al, 1997

Prevalence and Severity of Cognitive Impairment with and without Dementia in an Elderly Population
Lancet 349:1793-1796, Graham,J.E.,et al, 1997

A 44-Month Clinical-Brain MRI Follow-Up in a Patient with B12 Deficiency
Neurol 49:878-881, Stojsavljevic,N.,et al, 1997

Human Immunodeficiency Virus Infection and Stroke in Young Patients
Arch Neurol 54:1150-1153, Qureshi,A.I.,et al, 1997

Cat-Scratch Encephalopathy
Neurol 49:876-878, Wheeler,S.W.,et al, 1997

Primary Adhalinopathy (x-Sarcoglycanopathy) :Clin, Path & Genetic Correl in 20 Pts with Autosomal Recessive Muscular Dystrophy
Neurol 48:1227-1234, Eymard,B.,et al, 1997

Clinical Features of Perineuritis
Muscle & Nerve 20:1153-1157997., Sorenson,E.J.,et al, 1997

A Longitudinal Magnetic Resonance Imaging Study of Brain Changes in Adolescents with Anorexia Nervosa
Arch Pediatr Adolesc Med 151:793-797, Katzman,D.K.,et al, 1997

The X-Linked Infantile Spasms Syndrome (MIM 308350) Maps to Xp11. 4-Xpter in Two Pedigrees
Ann Neurol 42:360-364, Claes,S.,et al, 1997

Severe Hypoglycaemia and Cognitive Impairment in Diabetes
BMJ 313:767-768, Deary,I.J., 1996

Diagnostic Test for the Prader-Willi Syndrome by SNRPN Expression in Blood
Lancet 348:1068-1069, Wevrick,R.&Francke,U., 1996

Prenatal Magnesium Sulfate Expos/Risk for CP or MR Among Very Low-Birth-Weight Child Aged 3-5 Yrs
JAMA 276:1805-1810, 18431996., Schendel,D.E.,et al, 1996

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

Whipple Disease Confined to the Central Nervous System in Childhood
AJNR 17:1589-1591, Duprez,T.P.J.,et al, 1996

Zoster Myelitis:Improvement with Antiviral Therapy in Two Cases
Neurol 47:929-931, deSilva,S.M.,et al, 1996

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

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

Reversibility of Cerebral Ventricular Enlargement in Anorexia Nervosa, Demonstrated by Quant MR
J Pediatr 128:296-301, Golden,N.H.,et al, 1996

Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
NEJM 334:362-366, Fadic,R.,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

Clinicopath Conf
Chronic Schistosoma Mansoni Infection Involving Large Intestine and Spinal Cord, Case 4-1996, NEJM 3, 4:2-389,1996., 1996

Subacute Measles Virus Encephalitis:A New & Fatal Opportunistic Infection in a Pt with AIDS
Neurol 46:586-587, Budka,H.,et al, 1996

Cognitive Dysfunction as the Major Presenting Feature of Becker's Muscular Dystrophy
Neurol 46:461-465, North,K.N.,et al, 1996

Clinical Heterogeneity of Adhalin Deficiency
Ann Neurol 39:196-202, Morandi,L.,et al, 1996

Wernicke's Encephalopathy After Vertical Banded Gastroplasty for Morbid Obesity
BMJ 312:434, Seehra,H.,et al, 1996

Optic Neuropathy
Neurol 46:315-322, Newman,N.J., 1996

MRI of White Matter Changes in the Sjogren-Larsson Syndrome
Neuroradiology 37:576-577, Hussain,M.Z.&Aihara,M., 1996

Clinicopath Conf
Focal Cortical Dysplasia, Case 7-1996, NEJM 334:586-592996., , 1996

Cognitive Impairment & Mortality in a Cohort of Elderly People
BMJ 312:608-611, Gale,C.R.,et al, 1996

Leukoencephalopathy-Related Cerebral Amyloid Angiopathy with Cystatin C Deposition
Stroke 27:1417-1419, Shimode,K.,et al, 1996

Reduced Response to Activated Protein C is Associated with Increased Risk for Cerebrovascular Disease
Ann Int Med 125:265-269, van der Bom,J.G.,et al, 1996

Cerebral Venous Sinus Thrombosis Associated with Factor V Gene Mutation
JNNP 61:204-205, Kimber,T.,et al, 1996

Carotid Artery Thrombus Associated with Severe Iron-Deficiency Anemia and Thrombocytosis
Stroke 27:1002-1005, Akins,P.T.,et al, 1996

Leukoencephalopathy Associated with Cobalamin Deficiency
Neurol 46:832-834, Chatterjee,A.,et al, 1996

Effect of Malnutrition after Acute Stroke on Clinical Outcome
Stroke 27:1028-1032, Davalos,A.,et al, 1996

Practice Parameters for the Diagnosis of Patients with Nervous System Lyme Borreliosis (Lyme Disease)
Neurol 46:619-627, 8811996., Halperin,J.J.,et al, 1996

Diagnosis of McArdle's Disease by Molecular Genetic Analysis of Blood
Neurol 47:579-580, El-Schahawi,M.,et al, 1996

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

The Relation of Transient Hypothyroxinemia in Preterm Infants to Neurologic Development at Two Years of Age
NEJM 334:821-827, 8571996., Reuss,M.L.,et al, 1996

Ethylene Oxide Neurotoxicity:A Cluster of 12 Nurses with Peripheral and Central Nervous System Toxicity
Neurol 46:992-998, Brashear,A.,et al, 1996

Maternal Phenylketonuria:Magnetic Resonance Imaging of the Brain in Offspring
J Pediatr 128:770-775, Levy,H.L.,et al, 1996

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Intellectual Impairment in Children Exposed to Polychlorinated Biphenyls in Utero
NEJM 335:783-789, Jacobson,J.L.,et al, 1996



Showing articles 700 to 750 of 1585 << Previous Next >>