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aceruloplasminemia
acetylcholine receptor antibody
Addison's disease
advances in neurology
adverse drug reaction
alcohol, neurologic complications with
alcoholism
amenorrhea
aminoacidurias
ammonia
amyloidosis
anatomy of
anemia
anemia, hemolytic
aneurysm, intracranial
ankle edema
ankle, swelling of
anorexia
anxiety
aorta, atherosclerosis
aphonia
Arnold Chiari malformation
artane
arthritis
ascites
aspartate aminotransferase
asymptomatic
ataxia
ataxia telangiectasia
ataxia, sensory
athetosis
athetosis, causes of
auditory evoked brainstem potentials
auditory evoked potentials
B 12 deficiency
Babinski sign
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar artery occlusion
behavioral disorder
Behcet's syndrome
benign essential tremor
blepharospasm
blood dyscrasias, neurologic findings with
bone marrow suppression
botulinum toxin
bradykinesia
brainstem, lesion of
burning feet
calcification, intracranial
carbon monoxide poisoning
carcinoma
carcinoma of pancreas
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
catatonia
caudate nucleus, lesion of
caudate nucleus, lesion of, bilateral
central nervous system, infection of
central pontine myelinolysis
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar lesion
cerebral cortex
cerebral cortical atrophy
cerebral infarction
cerebral infarction, hemorrhagic
cerebral venous thrombosis
cerebral venous thrombosis, deep
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
ceruloplasmin, serum
chelation therapy
children
China
cholelithiasis
chorea
chorea, causes of
choreoathetosis
chromosomal abnormality
cirrhosis
cirrhosis, causes of childhood
claustrum
Clinical Pathologic Conference(C.P.C.)
clubbing of fingers
coagulopathy
cogwheel rigidty
coma
confusion
consanguinity
copper
copper deficiency
copper metabolism, abnormal
cornea, abnormal
coronary artery bypass
corpus callosum
corpus callosum, lesion of
Cushing's syndrome
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
depression
diabetes mellitus
diabetic coma, diagnosis and treatment
diet
differential diagnosis
disability, neurological
disorientation
dissociated sensory loss
diuretic
DNA probes
DNA sequencing
dopa responsive dystonia
dopamine receptor, D2
drooling
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, causes of
dyskinesia, drug induced
dysphagia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, classification
dystonia, etiology of
dystonia, evaluation of
dystonia, face
dystonia, focal
dystonia, prevalence of
dystonia, symptomatic
dystonia, treatment of
DYT1 mutation
edema, pedal
electrolyte imbalance
electromyogram
emotional lability
encephalitis
encephalitis, Japanese
encephalitis, viral
encephalopathy
epidemiology of neurology
epistaxis
equinovarus
esophageal varices
evoked potentials
extrapyramidal
eye movement, disorders of
Fabry's disease
facial expression abnormality
Fahr disease
falling
familial
fatigue
ferritin, elevated
ferritinemia
flavivirus
fracture, long bone
Friedreich's ataxia
frontal lobe, lesion of
gait disorder
gastrectomy, neurologic complications following
gastric partitioning
gaze fixation, distractable
gene
gene mutation
gene therapy
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
gests antagoniste
Gilles de la Tourette syndrome
glioma
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
grimacing
gynecomastia
handwriting
head injury
head nodding
headache
hemorrhagic diathesis
hepatic encephalopathy
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), late onset
hepatolenticular degeneration(Wilson's disease), presymptomatic
hepatolenticular degeneration(Wilson's disease), screening for
hepatolenticular degeneration, non-Wilsonian
hepatomegaly
hepatosplenomegaly
heralding manifestation
Huntington's chorea
hyperadrenalism
hyperbilirubinemia
hyperglycemia
hyperparathyroidism
hyperthyroidism
hypoalbuminemia
hypochloremia
hypoglycemia
hypokalemia
hyponatremia
hypoparathyroidism
hypotension, systemic
hypothyroidism
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
impulsivity
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
incoordination
intellectual deficit
intellectual deterioration
intracerebral hemorrhage
iron, brain
iron, serum, low
Jakob-Creutzfeldt disease
jaundice
jaw contractures
Kayser-Fleischer ring
L-dopa
Leigh's disease
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
lethargy
leukoencephalopathy
leukopenia
level of consciousness, decreased
lipid storage disorder of CNS
liver biopsy
liver disease
liver function enzymes
liver transplantation
lymphoma involving CNS
malabsorption
Marinesco-Sjogren syndrome
masked facies
mental retardation
mental status, abnormal
metabolic disorder, primary
metachromatic leukodystrophy
midbrain
midbrain, lesion of
mimics
misdiagnosis
molecular genetics
mood change
mortality
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, treatment of
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, face of giant panda sign on
MRI, false negative
MRI, gradient-echo
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, paramagnetic effect
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, susceptibility weighted
MRI, T1 weighted high signal foci
MRS
multiple sclerosis
multiple sclerosis, cognitive presenttion
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
muscle stiffness
myasthenia gravis
myeloneuropathy
myelopathy
myoclonus
myopathy
nausea and vomiting
neoplasm, intracranial
neoplasm, primary of CNS
neuroendocrinology
neurofibromatosis 1
neurologic complications of, burns
neurologic complications of, surgery
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuroophthalmology
neuropathology
neuropathy
neuropsychiatry
neurotoxin
nutritional deficiency
obesity
ocular motility, disorders of
oculogyric crisis
opened mouth
optic neuropathy
optic neuropathy, nutritional
organ transplantation
osmotic demyelination syndrome
pain, abdominal
pancreatitis
pancytopenia
paranoia
parenteral alimentation
Parkinson disease
Parkinson disease, misdiagnosis
Parkinsonism syndrome
penicillamine
pernicious anemia
personality change
phenylketonuria
phenylketonuria, adult onset
pheochromocytoma
polyneuropathy
polyradiculoneuropathy
pons, lesion of
porphyria
posterior column disease
postural abnormality
pregnancy, neurologic complications in
prognosis
proprioception, abnormal
prothrombin time, prolonged
pruritus
pseudobulbar palsy
psychiatric disorder
psychiatric manifestations of brain tumors
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, cause of
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract
quadriplegia
rehabilitation for neurologic disorders
remote effect of cancer on the nervous system
renal failure
renal stones
retinopathy
reversible neurologic disorder
review article
RFLPs
rheumatoid arthritis
rickets
rigidity
risk factors
risus sardonicus
salivation, excessive
schizophrenia
screening
seizure
sensory tricks
serum alanine aminotransferase
single photon emission computed tomography
skin, darkening of
slit lamp examination
somatosensory evoked potentials
speech disorder
speech, slowed
spinal cord, cervical
spinocerebellar degeneration
splenomegaly
spongy degeneration of brain
stimulation, deep brain
striatum, lesion of
striatum, lesion of, bilateral
subdural hematoma
suicide
swayback
symmetric brain lesions
syphilis, neurologic complications with
systemic illness
systemic lupus erythematosus
tardive dyskinesia
tardive dystonia
tetrathiomolybdate
thalamic tumors
thalamic tumors, bilateral
thalamus
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thiazide diuretic
thrombocytopenia
thrombus, mural
thymus and neuromuscular function
tongue, protrusion of
torticollis
treatment of neurologic disorder
tremor
tremor, intention
tremor, wing beating
trichopoliodystrophy
trientine dihydrochloride
unconsciousness
uric acid, low
urine test for metabolic disorders
urine, dark
viral infection
vitamin deficiency
Von Hippel Lindau
walking, difficulty with
weight loss
Wernicke's encephalopathy
white matter disease
work loss
writers cramp
writing
zinc
Showing articles 300 to 350 of 13505 << Previous Next >>

Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
NEJM 367:1921-1929, Ligt, J.,et al, 2012

Clinicopathologic Conference, Pancreatic Neuroendocrine Neoplasma, Insulinoma
NEJM 367:1637-1646, Case 32-2012, 2012

Clinical and Biomarker Changes in Dominantly Inherited Alzheimers Disease
NEJM 367:795-804,864, Bateman, R.J.,et al, 2012

Dopa-Responsive Dystonia Revisited
Arch Neurol 69:1558-1562, Tadic, V.,et al, 2012

Is It All Cerebral Toxoplasmosis?
Lancet 379:286, Mentzer,A.,et al, 2012

Cortical and Cerebellar Hypometabolism After Bilateral Antero-Inferior Cerebellar Artery Infarct
Neurol 78:69-70, Ayrignac, X.,et al, 2012

Brain Arteriovenous Malformation Multiplicity Predicts the Diagnosis of Hereditary Hemorrhagic Telangiectasia Quantitive Assessment
Stroke 43:72-78, Bharatha, A.,et al, 2012

�-Amyloid Burden in Healthy Aging
Neurol 78:387-395, Rodrigue,K.M.,et al, 2012

Subjective Cognition and Amyloid Deposition Imaging
Arch Neurol 69:223-229, Perrotin,A.,et al, 2012

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

Clinicalpathologic Conference, Vitamin B12 Deficiency due to Pernicious Anemia
NEJM 366:1626-1633, Case 13-2012, 2012

Predicting sites of New Hemorrhage with Amyloid Imaging in Cerebral Amyloid Angiopathy
Neurol 79:320-326, Gurol, M.E.,et al, 2012

Clinicopathologic Conference, Limbic Encephaitis with Antibodies to Leucine - Rich Glioma - inactivated 1 (LGI 1).
NEJM 365:1825-1833, Case 34-2011, 2011

Treat Alzheimer Disease Before It Is Symptomatic
Arch Neurol 68:1237-1238, , 2011

Longitudinal Change of Biomakers in Cognitive Decline
Arch Neurol 68:1257-1266,1237, Lo, R.Y.,et al, 2011

Longitudinal Assessment of A-beta and Cognition in Aging and Alzheimer Disease
Ann Neurol 69:181-192, Villemagne,V.L.,et al, 2011

Role of Brain Imaging in Early Parkinsonism
BMJ 324:d638, Breen,D.P.,et al, 2011

An unusual cause of stroke and hypoxia
BMJ 342:c7200, Bell, S.L. & Eveson, D.J., 2011

Frontotemporal brain sagging syndrome
Neurol 76:1377-1382, Wicklund, M.R.,et al, 2011

Screening for tumours in paraneoplastic syndromes: report of an EFNS Task Force
Eur J Neurol 18:19-27, Titulaer, M.J.,et al, 2011

From Jekyll to Hydeafter limbic subthalamic nucleus infarction
Neurol 77:82-84, Park, H.K.,et al, 2011

Presentation, Diagnosis, Pathophysiology, and Treatment of the Neurological Features of Sturge-Weber Syndrome
The Neurologist 17:179-184, Comi, A.M., 2011

Changing Concepts of Alzheimer Disease
JAMA 35:2458-2459, McKhann, G.M., 2011

Mild Cognitive Impairment
NEJM 362:2227-2234, Peterson, R.C., 2011

N-methyl-D-aspartate Receptor Autoimmune Encephalitis Presenting With Opsoclonus-Myoclonus
Arch Neurol 68:1069-1072, Smith, J.H.,et al, 2011

Combining MR Imaging, Positron-Emission Tomography, and CSF Biomarkers in the Diagnosis and Prognosis of Alzheimers Disease
AJNR 31:347-354, Walhovd, K.B.,et al, 2010

Clinicopath Conf., Brain Abscess, Pulmonary Arteriovenous Malformation Due to Hereditary Hemorrhagic Telangiectasia
NEJM 362:1326-1333, Case 10-2010, 2010

Pediatric Moyamoya Disease: An Analysis of 410 Consecutive Cases
Ann Neurol 68:92-101, Kim,S.-K., et al, 2010

Huntingtons Disease
BMJ 341:34-40, Novak,M.J. &Tabrizi,S.J., 2010

3-Methylglutaconic Aciduria Type I Redefined: A Syndrome With Late-Onset Leukoencephalopathy
Neurol 75:1079-1083, Wortmann,S.B.,et al, 2010

Clinical and Neuroimaging Findings of Cree Leukodystrophy: A Retrospective Case Series
AJNR 31: 1418-1423, Harder,S.,et al, 2010

Vitamin B12-Responsive Severe Leukoencephalopathy and Autonomic Dysfunction in a Patient With "Normal" Serum B12 Levels
JNNP 81:1369-1371, Graber,J.J.,et al, 2010

Imaging Manifestations of Progressive Multifocal Leukoencephalopathy
Clinical Radiol 65:431-439, Shah,R.,et al, 2010

Comparison of Clinical, Familial, and MRI Features of CADASIL and NOTCH3-Negative Patients
Neurol 74:57-63, Pantoni,L.,et al, 2010

Positron Emission Tomography-Computed Tomography in Paraneoplastic Neurologic Disorders: Systematic Analysis and Review
Arch Neurol 67:322-329, McKeon,A.,et al, 2010

FDG-PET a Pivotal Imaging Modality for Diagnosis of Stroke-Onset Intravascular Lymphoma
Arch Neurol 67:366-367, Yamada,S.,et al, 2010

A 31-Year-Old Woman with a Transformed Low-Grade Glioma
JAMA 303:967-976, Warnke,P.C., 2010

Diffuse Brain Stem Glioma
Arch Neurol 67:368-369, Renard,D.,et al, 2010

Clinicopath Conf, The POEMS Syndrome, with Demyelinating Neuropathy and Solitary Pharmacytoma of Bone
NEJM 362:929-940, Case 7-2010, 2010

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

Acute Limbic Encephalitis and Glutamic Acid Decarboxylase Antibodies:A Reality?
J Neurosci 287:69-71, Blanc,F.,et al, 2009

Clinical and Mutational Spectrum of Neurofibromatosis Type 1-Like Syndrome
JAMA 302:2111-2118, 2150, 2170, Messian,L.,et al, 2009

Sarcoidosis
BMJ 339:620-625, Dempsey,O.,et al, 2009

Practice Parameter: Evaluation of the Child with Microcephaly (An Evidence-Based Review): Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society
Neurol 73:887-897, Ashwal,S.,et al, 2009

Conversion of Amyloid Positive and Negative MCI to AD over 3 Years: An 11C-PIB PET Study
Neurol 73:754-760, 744, Okello,A.,et al, 2009

Akinetopsia in the Posterior Cortical Variant of Alzheimer Disease
Neurol 73:731-732, Tsai,P. &Mendez,M.F., 2009

Association of Parental Dementia With Cognitive and Brain MRI Measures in Middle-Aged Adults
Neurol 73:2071-2078, 2054, Debette,S.,et al, 2009

Pittsburg Compound B Imaging and Prediction of Progression From Cognitive Normality to Symptomatic Alzheimer Disease
Arch Neurol 66:1469-1475, Morris,J.,et al, 2009

Practice Parameter: Evaluation of Distal Symmetric Polyneuropathy: Role of Laboratory and Genetic Testing (An Evidence-Based Review)
Nuerol 72:185-192, England,J.D.,et al, 2009

Conventional MRI and NOTCH3 Gene Screening in Sporadic CADASIL
Neurol 72:469-471, Liguori,M.,et al, 2009



Showing articles 300 to 350 of 13505 << Previous Next >>