Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abdominal distention
acquired immunodeficiency syndrome
acute disseminated encephalomyelitis
adverse drug reaction
affective disorders
agitation
alcoholism
algorithm
amblyopia
aminoacidopathies
aminoacidurias
amyloid angiopathy, cerebral
anemia
anemia, hemolytic
anemia, iron deficiency
anemia, megaloblastic
anesthesia, general
angiitis, granulomatous of CNS
angiitis, isolated of CNS
ankle edema
anorexia
anticonvulsants, untoward effects of
antiendomysial antibodies
areflexia
arsenic
arthralgia
ascending paralysis
ascites
ataxia
ataxia, cerebellar
ataxia, sensory
ataxic gait
athetosis
auditory evoked brainstem potentials
autoantibodies
autoimmune disease
autonomic dysfunction
autonomic neuropathy
B 12 deficiency
B 12 deficiency, infants
B 12 metabolism, defective
B12
B12 binding protein, abnormal
Babinski sign
bacterial infection
basal ganglia, lesion of
Behcet's syndrome
blepharospasm
blindness
blood dyscrasias, neurologic findings with
bone pain
brain atrophy
brain biopsy
brain fog
breast feeding
burning feet
burning feet, differential diagnosis of
burning hands
burning paresthesia
carbon monoxide poisoning
carotid artery disease
carotid artery stenosis
CAT scan
CAT scan, dementia
CAT scan, emission, abnormal
celiac disease, adult
central nervous system, infection of
central pontine myelinolysis
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral infarction
cerebral ischemia
cerebral venous thrombosis
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, prevention of
cerebrovascular disease, risk factors in
cervical spine
cervical spine injury
cervical spondylosis
chemotherapy, CNS treatment and complications with
children
chorea
chorea, causes of
choreoathetosis
Clinical Pathologic Conference(C.P.C.)
clubbing of fingers
cognition
colchicine
collagen vascular disease
coma
complications
concentration, impaired
confusion
congestive heart failure
controversies in neurology
copper deficiency
corpus callosum
corpus callosum, lesion of
cortical blindness
C-reactive protein, elevated
delusion
dementia
dementia, clinical diagnosis
dementia, diagnostic evaluation of
dementia, differential diagnosis of
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, reversible
dementia, treatment of
demyelinating disease
dental procedure, neurologic complications with
depression
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes mellitus
diarrhea
diet
differential diagnosis
dilantin
dilantin, toxicity
disability, neurological
dissociated sensory loss
distal muscle weakness
drug abuse
drug abuse, inhalation
drug abuse, neurologic complications of
drug induced neurologic disorders
dyspnea
dyspraxia
dysthyroidism
dystonia
dystonia, focal
ecchymoses
electrical sensation
electroencephalogram
electrophoretic pattern, serum
emotional lability
encephalitis, human immunodeficiency virus type 1
encephalitis, viral
encephalopathy
encephalopathy, Hashimoto's
epidemiology of neurology
ergotism
evidence-based research
evoked potentials
failure to thrive
falling
fatigue
fine motor function, impaired
folic acid
folic acid deficiency
foot drop
F-wave response
gait disorder
gastrectomy, neurologic complications following
gastric biopsy
gastric partitioning
gastric surgery
gastritis
gastrointestinal disease, neurologic complications
genetic neurologic disorders
genetic testing
girdle sensation
gliadin antibodies
gliomatosis cerebri
glossitis
glucose level, serum
glucose tolerance test, abnormal
gluten sensitivity
gluten-free diet
hallucination
hallucination, auditory
hand numbness
hand weakness
hearing loss
helicobacter pylori
hemichorea
hemorrhagic diathesis
hepatosplenomegaly
heralding manifestation
herniated disc, cervical
hip flexor weakness
Hispanics
histamine-2 receptor blockers
HLA
homocysteine, serum
homocystinuria
human immunodeficiency virus type 1
human immunodeficiency virus type 1, asymptomatic
hyperbilirubinemia
hyperesthesia
hyperhomocysteinemia
hyperpigmentation of skin
hyperreflexia
hypersegmented polys
hypertensive encephalopathy
hypocalcemia
hypogonadism
hypomagnesemia
hypopigmentation of skin
hypoproteinemia
hypoprothrombinemia
hypothermia
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
imbalance
inattention
incontinence, fecal
incoordination
infant, evaluation of
infantile tremor syndrome
intellectual deficit
intellectual deficit, treatable causes of
intellectual deterioration
intelligence quotient
internuclear ophthalmoplegia
internuclear ophthalmoplegia, unilateral
intestinal biopsy
intracerebral hemorrhage
inverted V sign
iron, serum, low
irritability
jaundice
laboratory values, normal
lactic dehydrogenase(LDH)
leg numbness
leg weakness, bilateral
leukoencephalopathy
leukoencephalopathy, differential diagnosis
Lhermitte's sign
limb shaking
limbic encephalitis
liver function enzymes
long bone lesion
low back pain
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
malabsorption
malabsorption syndrome
memory, defect of recent
memory, impairment of
mental status, abnormal
metabolic disorder, primary
metformin
methylmalonic acid, serum
methylmalonic acidemia
methylmalonic aciduria
midbrain, lesion of
migraine
mimics
Mini Mental Status Examination
misdiagnosis
mitochondrial disease
monoclonal gammopathy
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, high signal foci on
MRI, serial
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
multiple sclerosis
multiple sclerosis, differential diagnosis of
muscle weakness
myelitis, longitudinal
myeloma, osteosclerotic
myeloneuropathy
myelopathy
myelopathy, vacuolar
myoclonus
myopathy
nanging
neck trauma
neoplasm, primary of CNS
nerve conduction studies
neuritis
neuroendocrinology
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination
neurologic signs
neurologic symptoms
neuropathology
neuropathy
neuropathy, diabetic
neuropathy, painful
neuropathy, peripheral
neuropathy, sensory
neuropathy, small-fiber
neuropathy, small-fiber, painful sensory
neuropathy, toxic
neuropathy, work up for
neuropsychiatry
neurotoxic
neurotoxin
newborn, evaluation of
night sweats
nitrous oxide
normal
numbness, ascending
numbness, extremity
numbness, generalized
nutritional deficiency
nystagmus
obesity
old age, neurology of
optic atrophy
optic neuropathy
optic neuropathy, bilateral
optic neuropathy, nutritional
organomegaly
orthostatic hypotension
pain
pain, abdominal
pain, back
pain, leg
pain, neuropathic
pancytopenia
papilledema
paranoia
paraparesis
paraparesis, spastic
paraplegia
paresthesias
paresthesias, feet
paresthesias, generalized
paresthesias, hands
Parkinson disease
pellagra
peripheral blood smear
peripheral blood smear, abnormal
pernicious anemia
personality change
phenothiazine, dyskinesia associated with
phenylketonuria
plasma R binder deficiency
plasmacytoma
POEMS syndrome
polyneuropathy
polyradiculoneuropathy
position sensation, abnormal
posterior column disease
posterior leukoencephalopathy syndrome
posterior tibial nerve
posterior tibial nerve compression
practice guidelines
pregnancy, neurologic complications in
prevention of neurologic disorders
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
proprioception, abnormal
proton pump inhibitors
pseudoathetosis
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
psychosis, acute
psychotic behavior
pulmonary infiltrates
pyramidal tract
pyramidal tract dysfunction
pyridoxine deficiency
quadriparesis
radiation therapy, CNS treatment and complications with
Red flags
regional enteritis
remote effect of cancer on the nervous system
retinal hemorrhages
reversible neurologic disorder
review article
risk factors
Romberg's sign
sarcoidosis
sarcoidosis, CNS
sclerosis, bone
scotoma
scotoma, central
screening
seizure
sensory level
sensory loss
sensory loss, cutaneous
sensory loss, glove-stocking
shaking
sickle cell disease
skin, biopsy
skin, darkening of
skin, discoloration
skin, lesions in neurologic disorders
somatosensory evoked potentials
spasticity
speech, pressured
spinal cord
spinal cord, cervical
spinal cord, lesion of
splenomegaly
sprue
steatorrhea
substantia nigra
swayback
symmetric brain lesions
syncope
systemic illness
tachycardia
tangential
tarsal tunnel syndrome
tetany
thiamine
thiamine deficiency
thrombocytosis
thyroid function tests
thyroiditis
thyrotoxicosis
tongue, smooth
tongue, swelling
transcobalamin II, abnormal
transcobalamin II, hereditary absence of
transglutaminase antibodies
treatment of neurologic disorder
tremor
tremor, leg
tremor, orthostatic
ulcerative colitis
urinary incontinence
urine, dark
vascular endothelial growth factor
vasculitides
vasculopathy
vegetarianism
Venereal Disease Research Laboratory test
vertigo
vibratory sensation, abnormal
visual evoked response
visual loss
visual loss, slow
vitamin D deficiency
vitamin deficiency
vitamin supplementation
vitamin therapy
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weight loss
Wernicke's encephalopathy
Whipple's disease
white hair
white matter disease
wide based gait
word-finding difficulty
workup
writing
Showing articles 350 to 400 of 775 << Previous Next >>

The Woman Who Needed a Pet
Surv Ophthalmol 51:592-595, Atchison,M.,et al, 2006

Tuberculosis Meningitis Mimics Malignancy Like Lesion in Fluroine-18-FDG PET Scan and Gallium Scan
Ann Nucl Med Sci 19:275-278, Chang,W.-D.,et al, 2006

The Tuberous Sclerosis Complex
NEJM 355:1345-1356, Crino,P.B.,et al, 2006

Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Frequently Missed Diagnosis?
Neurol 67:1519, Koppel,S.,et al, 2006

PET of Brain Amyloid and Tau in Mild Cognitive Impairment
NEJM 355:2652-2663, Small,G.W.,et al, 2006

Detection of Unknown Primary Tumor in a Patient with Cerebellar Metastasis Using FDG PET-CT: Case Report
No Shinkei Geka 34:1027-1032, Ishiguro,T.,et al, 2006

Whole-Body MRI and PET-CT in the Management of Cancer Patients
Eur Radiol 16:1216-1225, Schmidt,G.P.,et al, 2006

Multiple Diagnostic Tests Are Needed to Assess Multiple Causes of Dementia
Arch Neurol 63:144-146,146, Rikkert,M.G.M.O.,et al, 2006

Alexander Disease, Ventricular Garlands and Abnormalities of the Medulla and Spinal Cord
Neurol 66:494-498,468, van der Knaap,M.S.,et al, 2006

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

Chronic Disorders of Consciousness
Lancet 367:1181-1192, Bernat,J.L., 2006

Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
NEJM 354:2584-2592, Case 18-2006, 2006

Finding the Causes of Inherited Neuropathies
Arch Neurol 63:812-816, Scherer,S.S., 2006

Clinicopath Conf, Von Hippel Lindau Disease, Adrenal Pheochromocytoma, Brain-Stem and Spinal Cord Hemangioblastoma
NEJM 355:394-402, Case 23-2006, 2006

Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
NEJM 355:831-839, Case 26-2006, 2006

Dystonia
NEJM 355:818-829, Tarsy,D. &Simon,D.K., 2006

Episodic Neurologic Dysfunction with Migraine and Reversible Imaging Findings After RadiationRRH
Neurol 67:676-678, Pruitt,A.,et al, 2006

Diagnosis of Neurolymphomatosis with FDG PET
Neurol 67:722-723, Rosso,S.M.,et al, 2006

Fragile X Premutation With Atypical Symptoms at Onset
Arch Neurol 63:1135-1138, Cellini,E.,et al, 2006

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

The role of radiotracer imaging in Parkinson disease
Neurol 64:208-215, Ravina, B., et al, 2005

Genetic Screening for a Single Common LRRK2 Mutation in Familial Parkinson's Disease
Lancet 365:410-412, Nichols, W.C., et al, 2005

Unusual Variants of Alexander's Disease
Ann Neurol 57:327-338, van der Knaap,M.S., et al, 2005

Clinicopath Conf, Neurofibromatosis Type 1, with Multiple Spinal Neurofibromas
NEJM 352:1800-1808, Case 13-2005, 2005

Metabolic Patterns Associated with the Clinical Response to Galantamine Therapy
Arch Neurol 62:721-728, Mega,M.S.,et al, 2005

Proton MR Spectroscopy in Wilson Disease: Analysis of 36 Cases
AJNR 26:1066-1071, Lucato,L.T.,et al, 2005

Diffusion-Weighted Imaging and Proton MR Spectroscopy of White Matter Abnormalities in a Case of Phenylketonuria
Eur J Radiol Extra 54: 5-9, Teksam,M.,et al., 2005

A Positron Emission Tomographic Study in Spontaneous Migraine
Arch Neurol 62:1270-1275, Afridi,S.K.,et al, 2005

Spectrum of Mutations in Biopsy-Proven CADASIL: Implications for Diagnostic Strategies
Arch Neurol 62:1091-1094, Peters,N.,et al, 2005

A New Cause of Limbic Encephalopathy
Brain 128:1745-1746, Darnell,R.B., et al, 2005

Treatment-Responsive Limbic Encephalitis Identified by Neuropil Antibodies: MRI and PET Correlates
Brain 128:1764-1777, Ances,B.M., et al, 2005

Unknown Primary Tumors: Detection with Dual-Modality PET/CT--Initial Experience
Radiology 234:227-234, Gutzeit,A.,et al, 2005

Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
Lancet Neurol 4:239-248, Shahwan, A., et al, 2005

Serial 18F-fluoro-2-deoxy-D-glucose Positron Emmission Tomography and Magnetic Resonance Imaging of Paraneoplastic Limbic Encephalitis
Arch Neurol 61:1785-1789, Scheid,R.,et al, 2004

Neuro-Ophthalmic Findings in the Visual Variant of Alzheimers Disease
Ophthalmology 111:376-381, Lee,A.G. &Martin,C.O., 2004

Neuroprotection in Parkinson Disease, Mysteries, Myths, and Misconceptions
JAMA 291:358-364, Schapira,A.H.V.&Olanow,C.W., 2004

Aromatic L-Amino Acid Decarboxylase Deficiency
Neurol 62:1058-1065, Pons,R.,et al, 2004

Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
Arch Neurol 61:875-880, Smith,C.O.,et al, 2004

Clinical Correlation of Brain MRI and MRS Abnormalities in Patients with Wilson Disease
Neurol 63:638-643, Page,R.A.,et al, 2004

Best Measure of Ischemic Penumbra: Positron Emission Tomography
Stroke 34:2534-2535, Heiss,W.-D., 2003

Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
Neurol 60:1413-1417, Pearl,P.L.,et al, 2003

von Hippel-Lindau Disease
Lancet 361:2059-2067, Lonser,R.R.,et al, 2003

Antivonvulsants for Creutzfeldt-Jakob Disease?
Lancet 361:224, Fioel,A.,et al, 2003

Prenatal Diagnosis Requests for Huntington's Disease when the Father is at Risk, and Does Not Want to Know His Genetic Status: Clinical, Legal, and Ethical Viewpoints
BMJ 326:331-333, Tassicker,R.,et al, 2003

Neuroimaging and Early Diagnosis of Alzheimer Disease: A Look to the Future
Radiology 226:315-336, Petrella,J.R.,et al, 2003

Practice Parameter: Evaluation of the Child with Global Developmental Delay
Neurol 60:367-380, Shevell,M.,et al, 2003

A Study of Persistent Post-Concussion Symptoms in Mild Head Trauma Using Positron Emission Tomogrophy
JNNP 74:326-332, Chen,S.H.A.,et al, 2003

Treatment of Wilson Disease With Ammonium Tetrathiomolybdate, III. Initial Therapy in a Total of 55 Neurologically Affected Patients and Follow-up With Zinc Therapy
Arch Neurol 60:379-385, Brewer,G.J.,et al, 2003

Severe Intoxication After Phenytoin Infusion: A Preventable Pharmacogenetic Adverse Reaction
Neurol 60:1395-1396, Citerio,G.,et al, 2003

Neonatal Epileptic Encephalopathy
Lancet 361:1614, Clayton,P.T.,et al, 2003



Showing articles 350 to 400 of 775 << Previous Next >>