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Differential
(Click to cross reference)
abdominal migraine
acrochordon
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
affect, inappropriate
agnosia, color
agnosia, visual
akathisia
alcoholism
alexia
alexia without agraphia
Alzheimer's disease
Alzheimer's disease, visual variant
amnesic stroke
anatomy of
anemia
anemia, megaloblastic
angiotensin-converting enzyme
ankle, swelling of
anorexia
anosmia
aphasia
argyria
arrhythmia, cardiac
arthralgia
ascites
aspartate aminotransferase
ataxia
ataxia, cerebellar
ataxic gait
autoantibodies
autonomic dysfunction
B 12 deficiency
behavioral disorder
bladder dysfunction
blindness
bone marrow transplantation
brain biopsy
brain natriuretic peptide
burning hands
burning legs
burning paresthesia
burning skin
calf hypertrophy
carbon monoxide poisoning
cardiomyopathy
cardiovascular disease
CAT scan, abnormal
CAT scan, angiography
CAT scan, emission
CAT scan, emission, abnormal
cerebellum, disease of
cerebral artery, encasement
cerebral embolism
cerebral embolism, cardiac origin
cerebral infarction
cerebral infarction, hemorrhagic
cerebral peduncle
cerebrovascular accident
cerebrovascular accident, bilateral
cerebrovascular accident, women
cervical spondylosis
children
cirrhosis
Clinical Pathologic Conference(C.P.C.)
color desaturation
color vision
color vision, impaired
color vision, impaired, cerebral
color vision, impaired, sudden onset
coma
complications
confusion
contractures, joint
corpus callosum
corpus callosum, infarction of
cortical blindness
creatine phosphokinase(CPK)elevated
critical care unit
crying, pathologic
cultured skin fibroblasts
cyclic vomiting
cyclic vomiting syndrome
dantrolene sodium
deafness
decerebrate posture
delay in diagnosis
dementia
dementia, childhood
demyelinating disease
depression
depth perception, impaired
dermal sinus tract
dermoid
developmental retardation
dexterity, impaired
diabetes insipidus
diagnostic criteria
diamond on quadriceps
diastematomyelia
diet
differential diagnosis
difficulty climbing stairs
dimple
disconnection syndrome
dizziness
drug induced neurologic disorders
drug interactions
dysarthria
dyschromatopsia
dysphagia
dyspnea
dyspraxia
dysraphism, spinal
dystonia
dystrophin
electroencephalogram, abnormalities of
electromyogram
encephalopathy
encephalopathy, post anoxic
epidemiology of neurology
ergotamine
ergotism
erythromelalgia
exercise
facial weakness
falling
familial
fatigue
fatty acid, elevated plasma content
fever
fibrillations
fine motor function, impaired
gadolinium
gait disorder
gait, waddling
gangrene
gastrointestinal disease, neurologic complications
gaze palsy
gaze palsy, vertical
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glucose tolerance test, abnormal
Gowers maneuver
hand weakness
headache
headache, recurrent
hemiachromatopsia
hemiakathisia
hemianopia
hemianopia, homonymous
hemianopia, isolated homonymous
hemichorea
hemiplegia
hemochromatosis
hemochromatosis, primary
hepatic encephalopathy
hepatolenticular degeneration(Wilson's disease)
HMGcoA reductase inhibitors
hung reflex
hyperbaric oxygen
hypercoagulable state
hyperpigmentation of skin
hyperreflexia
hypersegmented polys
hypertrichosis
hypogonadism
hypopigmentation of skin
hypothermia
hypothyroidism
iatrogenic neurologic disorders
imbalance
incoordination
intellectual deterioration
jaundice
lactic dehydrogenase(LDH)
learning disability
learning disability, in children
lethargy
leukodystrophy
level of consciousness, decreased
limb ischemia
limb-girdle weakness
lipoma of CNS
lipoma of skin
liver function enzymes
Lorenzo's oil
Marcus Gunn pupil
memory, defect of recent
memory, impairment of
metabolic disorder, primary
methylmalonic acid, serum
midbrain, infarction of
migraine
migraine, children
migraine, equivalents
misdiagnosis
mood change
mortality
movement disorder
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, mass effect on
MRI, negative
MRI, spine
muscle biopsy
muscle pain
muscle stiffness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
muscular dystrophy, limb-girdle
muscular dystrophy, pattern of muscle involvement
myelopathy
myoedema
myoglobinuria
myopathy
myopathy, drug-induced
myopathy, necrotizing, autoimmune
myxedema, neurologic manifestations of
nausea and vomiting
nerve biopsy
neurocutaneous disease
neurofibromatosis 1
neuroleptic
neuroleptic malignant syndrome
neurologic complications
neurologic disease, diagnoses of
neurologic signs
neuropathy
neuropathy, sensory
neuropathy, toxic
neurotoxin
nocturia
nutritional deficiency
occipital lobe, infarction
occipital lobe, infarction, bilateral
ochronosis
optic atrophy
oral contraceptives, cerbrovascular disease and
oral contraceptives, neurologic complications with
osteoarthrosis
osteoporosis
pain, abdominal
palinopsia
papilledema
paraparesis
paraparesis, spastic
paresthesias
paresthesias, hands
Parkinsonism syndrome
peripheral blood smear, abnormal
peripheral pulse, absent
pernicious anemia
peroxisomal disease
personality change
phlebotomy
posterior cerebral artery
posterior cerebral artery embolism
posterior cerebral artery occlusion
posterior cerebral artery territory infarction
posterior cortical atrophy
postural abnormality
precipitating factors
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
prosopagnosia
protease inhibitor, HIV-1
proximal muscle atrophy
pruritus
pseudobulbar palsy
ptosis
pure sensory stroke
quadrantanopsia, superior
quadriparesis
radiation therapy, CNS treatment and complications with
reading
reading disorder, acquired
Red flags
renal failure
renal stones
respiratory failure
review article
rhabdomyolysis
rigidity
ritonavir
Romberg's sign
sarcoglycan
sarcoglycanopathy
sarcoidosis
sarcoidosis, CNS
sclerae, hyperpigmented
seizure
sensorineural hearing loss
serum alanine aminotransferase
sex reassignment surgery
silver toxicity
simultanagnosia
skin, biopsy
skin, cherry-red
skin, darkening of
skin, discoloration
skin, lesions in neurologic disorders
skin, pale
sleep apnea
speech disorder
speech disorder, childhood
speech, delayed development of
speech, slowed
spina bifida
splenium of corpus callosum
spondylolysis
statin therapy
steroid therapy, CNS treatment and complications with
stress, emotional
suicide
systemic illness
testicular atrophy
tethered spinal cord
thalamus, infarction of
toe walking
tongue, smooth
tongue, swelling
transgender
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, intention
trifluoperazine
tripping
Trousseau's syndrome
urinary frequency
urinary incontinence
urinary urgency
urine, dark
vasospasm
very long chain fatty acids
visual acuity, decreased, monocular
visual evoked response
visual field defect
visual loss
visual loss, slow-unilateral
visuospatial disturbance
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
white matter disease
winging of scapula
work loss
workup
Showing articles 500 to 550 of 1636 << Previous Next >>

Progressive Weakness with Respiratory Failure in a Patient with Sarcoidosis
Arch Neurol 69:534-537, Chaudhry,P.,et al, 2012

Clinical Reasoning: A Middle-Aged Woman with Progressive Symmetric Weakness and a CSF Pleocytosis
Neurol 78:e88-e92, Marks,D.,et al, 2012

Central Nervous System Involvement in Dengue
Neurol 78:736-742, Araujo,F.M.C.,et al, 2012

Inflammatory Myopathies with Anti-Ku Antibodies
Medicine 91:95-102, Rigolet,A.,et al, 2012

Cogan Syndrome An Analysis of Reported Neurological Manifestations
The Neurologist 18:55-63, Antonios,N. and Silliman,S., 2012

Clinicopathologic Conference,Necrotizing Noninflammatory Myopathy Consistent with Exposure to Statins
NEJM 36:944-954, Case 7-2012, 2012

Risk Factors for Spinal Cord Lesions in Dystonic Cerebral Palsy and Generalised Dystonia
JNNP 83:159-163, Guettard,E.,et al, 2012

Thalamic Astasia from Isolated Centromedian Thalamic Infarction
Neurol 78:146-147, Elwischger,K.,et al, 2012

Tai Chi and Postural Stability in Patients with Parkinsons Disease
NEJM 366:511-519, Li,F.,et al, 2012

Clincopathologic Conference,Graves Disease with Thyrotoxic Periodic Paralysis
NEJM 366:553-560, Case 4-2012, 2012

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

Solitary Sclerosis
Neurol 78:540-544, Schmalstieg,W.F.,et al, 2012

Cerebral Fat Embolism Syndrome in Sickle Cell Anaemia/�-Thalassemia: Importance of Susceptibility-weighted MRI
Clin Radiol 67:1023-1026, Mossa-Basha, M.,et al, 2012

Black Tongue Due to Adrenocortical Insufficiency
Arch Dis Child 97:1033, de Benedictis, F.M.,et al, 2012

Addisons Disease
Contemp Clin Dent 3:484-486, Sarkar, S.B.,et al, 2012

Rapidly Progressive Corticobasal Degeneration Syndrome
Case Rep Neurol 3:185-190, Herrero Valverde, A.,et al, 2011

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

Motor Vehicle Accidents, Suicides, and Assaults in Epilepsy: A Population-Based Study
Neurol 76:801-806, 770, Kwon,C.,et al, 2011

Recognizing Guillain-Barr� Syndrome in Preschool Children
Neurol 76:807-810, Roodbol,J.,et al, 2011

Blind, Breathless, and Paralysed from Benign Malaria
Lancet 377:438, Flower,B.,et al, 2011

Clinicopathologic Conference, Sjogrens syndrome with dorsal-root ganglionitis
NEJM 364:1856-1865, Case 14-2011, 2011

Random skin biopsy and bone marrow biopsy for diagnosis of intravascular large B cell lymphoma
Ann Hematol 90:417-421, Matsue, K.,et al, 2011

Post-acute care and secondary prevention after ischaemic stroke
BMJ 342:d2083, McArthur, K.S.,et al, 2011

Late onset autism and anti-NMDA-receptor encephalitis
Lancet 378:98;378, Creten, C.,et al, 2011

Treatment of Severe Neurological Deficits with IgG Depletion through Immunoadsorption in Patients with Escherichia coli O104:H4-Associated Haemolytic Uraemic Syndrome: A Prospective Trial
Lancet 378:1166-1173,1120, Greinacher, A.,et al, 2011

Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
UpToDate, Feb, Shovlin, C., 2011

A Strange Case of Waitress Headache
Lancet 378:1824, Libera, D.D.,et al, 2011

Computerized Visual Field Defects in Posterior Cortical Atrophy
Neurol 77:2119-2122, Pelak, V.S.,et al, 2011

Exercise-Associated Numbness and Tingling in the Legs
Arch Neurol 68:1599-1602, Sharp, L.,et al, 2011

Clinicopathologic Conference, Thymoma with Paraneoplastic Myasthenia Gravis, Polymyositis and Myocarditis, and Brain Stem Encephalitis
NEJM 365:2413-2422, Case 39-2011, 2011

In-flight Seizures and Fatal Air Embolism
Arch Neurol 68:661-664, Arnaiz, J.,et al, 2011

Myoglobinuria and Muscle Pain are Common in Patients With Limb-Girdle Muscular Dystrophy 21
Neurol 76:194-195, Mathews,K.D.,et al, 2011

Prediction of Respiratory Insufficiency in Guillain-Barr� Syndrome
Arch Neurol 67:781-787, Walgaard,C.,et al, 2010

Clincopath Conference, Endogenous Endophthalmitis Due to Aspergillus Niger
NEJM 363:1749-1758, Case 33-2010, 2010

Comparative Analysis of Therapeutic Options Used for Myasthenia Gravis
Ann Neurol 68:797-805, Mandawat,A.,et al, 2010

Delirious Deficiency
Lancet 376:1362, Olsen,R.Q &Regis,J.T., 2010

A Meta-Regression of the Long-Term Effects of Deep Brain Stimulation on Balance and Gait in PD
Neurol 75:1292-1299, St. George,R.J.,et al, 2010

New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
JNNP 81:946-953, Klinge,L.,et al, 2010

Sensory Ganglionopathy Due to Gluten Sensitivity
Neurol 75:1003-1008, Hadjivassiliou,M.,et al, 2010

Copper Deficiency as a Treatable Cause of Poor Balance
BMJ 340:864-866, Khaleeli,Z., et al, 2010

Clinicopath Conf., Progressive Multifocal Leukoencephalopathy
NEJM 362:1431-1437, Case 11-2010, 2010

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

Transverse Myelitis
NEJM 363:564-572, Frohman,E.M. &Wingerchuk,D.M., 2010

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

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

Polyneuritis Cranialis Caused by Varicella Zoster Virus in the Absence of Rash
Neurol 74:85-86, Murata,K.,et al, 2010

Subclinical Hypothyroidism Presenting with Gait Abnormality
The Neurologist 16:115-116, Edvardsson,B. &Persson,S., 2010

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

Clinicopath Conf, Intravascular Large-B-Cell Lympoma
NEJM 362:1129-1138, Case 9-2010, 2010

Sjogren Syndrome: Neurologic Complications
www.Medlink.com,Jan, Roman,G.C., 2010



Showing articles 500 to 550 of 1636 << Previous Next >>