Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
acanthocytosis
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, medical precautions with
adducted thumb
advances in neurology
adverse drug reaction
agenesis of corpus callosum
alpha-fetoprotein
amniocentesis
anterior horn cell disease
anterior tibial muscle weakness
anticonvulsants
anticonvulsants, absorption
anticonvulsants, bioavailability
anticonvulsants, blood level determination of
anticonvulsants, compliance
anticonvulsants, subtherapeutic
anticonvulsants, teratogenicity of
anticonvulsants, untoward effects of
arbovirus
areflexia
arthralgia
ataxia, cerebellar
autoimmune disease
Bassen-Kornzweig syndrome
blindness
Brazil
breast feeding
calcification, intracranial
carcinoma
cardiomyopathy
caribbean
CAT scan
CAT scan, muscle
cataracts
Central America
central core disease
central nervous system, infection of
children
chromosomal abnormality
chromosome 5
clinodactyly
Cockayne's syndrome
complications
congenital birth defects
congenital deformities
congenital heart disease
congenital heart disease, CNS complications with
congenital malformation
congenital myopathy
congenital myopathy, inflammatory
consanguinity
contractures, joint
cornea, abnormal
counselling
creatine phosphokinase(CPK)elevated
cryptorchidism
deafmute
deafness
degenerative diseases of CNS
developmental abnormality of brain
developmental disability
developmental retardation
differential diagnosis
digits, abnormal
disability, neurological
drug induced neurologic disorders
dwarfism
dysmorphic
dystroglycanopathies
dystrophin
ear, abnormal
echocardiogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
Emery-Dreifuss muscular dystrophy
enzyme, induction
epidemic
epidemiology of neurology
exostosis
facial anomalies
facial appearance, abnormal
facial weakness, bilateral
facioscapulohumeral syndrome
familial
fasciculation
feeding disorder
fetus
fever
flavivirus
floppy infant
folic acid
foot drop
Friedreich's ataxia
gargoylism
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
glaucoma
Guillain Barre syndrome
hair, loss
Hallgren's syndrome
head circumference
headache
hearing loss
heart block
hemorrhagic diathesis
hepatosplenomegaly
histochemistry
histochemistry of muscle
human immunodeficiency virus type 1
Huntington's chorea
Hurler's syndrome
hydrocephalus
hydrocephalus, congenital
hydrocephalus, fetal
hydrocephalus, intrauterine
hyperkalemic periodic paralysis
hypertelorism
hypertrophic cardiomyopathy
hypokalemic periodic paralysis
hyporeflexia
hypotonia
hypotonia, infants
immunohistochemistry
inclusion body myositis
infection
intellectual deficit
intrauterine
intrauterine infection
intrauterine infection, viral
joint hypermobility
karyotyping
Kearns-Sayre syndrome
keratoconus
lamotrigine
Laurence-Moon-Bardet-Biedl syndrome
levonorgestrel
lid closure, weakness of
life expectancy
lissencephaly
lordosis
malformation, CNS, congenital
mental retardation
merosin
microcephaly
microdactyly
micrognathia
Miller-Dieker syndrome
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
mononeuritis multiplex
mortality
mosquito
motor neuron disease
MRI
MRI, abnormal
MRI, fetal
MRI, intrauterine
MRI, muscle
mucopolysaccharidoses
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle pain
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
muscular dystrophy, neurogenic hypothesis of
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myoglobinuria
myopathy
myopathy, centronuclear
myopathy, distal
myopathy, drug-induced
myopathy, mitochondrial
myopia
myositis
myositis ossificans, progressive
myotonia congenita
myotonia dystrophica
nasal bridge, wide
neck, webbed
nemaline rod myopathy
neoplasm, primary of CNS
neuritis
neurologic disease, diagnoses of
neuronal migration disorder
neuropathology
neuropathy
neuropathy, ataxic
neuropathy, painful
neuropathy, peripheral
Noonan Syndrome
nusinersen
obesity
obstetric neurologic injuries
ocular myopathy
oculopharyngeal muscular dystrophy
oral contraceptives
paraparesis
paraparesis, spastic
patient information and support
pectus excavatum
periodic paralysis
polydactyly
polyhydramnios
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polymyositis
polymyositis, infantile
polyneuropathy, chronic inflammatory demyelinating
practice guidelines
pregnancy, anticonvulsants during
pregnancy, neurologic complications in
prenatal
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
pseudoretinitis pigmentosa
psychiatric disorder
pulmonary stenosis
quality of life
rash
respirator
respiratory failure
retinitis pigmentosa
retinopathy
review article
rhabdomyolysis
schizophrenia
scoliosis
scoliosis, neurologic association with
screening
seizure
seizure, children
seizure, injury following
seizure, pregnancy
seizure, treatment of
seizure, treatment of, monotherapy
seizure, women
short stature
short thumb
skin, biopsy
skin, lesions in neurologic disorders
SMN1 gene
South America
Spielmeyer Vogt syndrome
spinal muscular atrophy
spinal muscular atrophy, classification
steroid
systemic illness
tongue, fasciculations of
trauma
treatment of neurologic disorder
trinucleotide repeats
tubular aggregates, muscle
ultrasonography
ultrasonography, head
ultrasonography, head, fetus-neonate
Usher's syndrome
valvulopathy
viral infection
viral infection, CNS
visual field defect
visual fields, constricted
visual impairment
vitamin K
vitamin supplementation
vomiting, recurrent
weakness
weakness, congenital
weakness, generalized
weakness, progressive
wheelchair
whistle, inability to
winging of scapula
x-linked hydrocephalus
Zika virus infection
Showing articles 1500 to 1550 of 4195 << Previous Next >>

Intrauterine Exposure to Carbamazepine and Specific Congenital Malformations: Systematic Review and Case-Control Study
BMJ 341:c6581, 1229, Jentik,J.,et al, 2010

Neuromyelitis Optica in France: A Multicenter Study of 125 Patients
Neurol 74:736-742, Collongues,N.,et al, 2010

Tourettes Syndrome
NEJM 363:2332-2338, Kurlan,R., 2010

JC Virus Infection of the Brain
AJNR 31:1564-1576, Bag,A.K.,et al, 2010

Profound Deafness in Childhood
NEJM 363:1438-1450, Kral,A.,et al, 2010

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

How Much Would Performing Diffusion-Weighted Imaging for All Transient Ischemic Attacks Increase MRI Utilization?
Stroke 41:2218-2222, Adeoye,O.,et al, 2010

Childhood Posterior Circulation Arterial Ischemic Stroke
Stroke 41:2201-2209, Mackay,M.T.,et al, 2010

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

The Case Against Confirmatory Tests for Determining Brain Death in Adults
Neurol 75:77-83, Wijdicks,E.F.M., 2010

Paramedic Diagnosis of Stroke: Examining Long-Term Use of the Melbourne Ambulance Stroke Screen (MASS) in the Field
Stroke 41:1363-1366, Bray,J.E., et al, 2010

Agreement Regarding Diagnosis of Transient Ischemic Attach Fairly Low Among Stroke-Trained Neurologists
Stroke 41:1367-1370, Castle,J., et al, 2010

Valproic Acid Monotherapy in Pregnancy and Major Congenital Malformations
NEJM 362:2185-2193, Jentink,J., et al, 2010

Does This Patient Have a Hemorrhagic Stroke? Clinical Findings Distinguishing Hemorrhagic Stroke From Ischemic Stroke
JAMA 303:2280-2286, Runchey,S. &McGee,S., 2010

Prevalence and Predictors of Paroxysmal Atrial Fibrillation on Holter Monitor in Patients With Stroke or Transient Ischemic Attack
Stroke 41:2596-2600, Alhadramy,O.,et al, 2010

Pain in Guillain-Barre Syndrome: A Long-Term Follow-Up Study
Neurol 75:1439-1447, Ruts,L.,et al, 2010

Diagnostic Role of Target Lesion on Diffusion-WEighted Imaging, A Case of Cerebral Aspergillosis and Review of the Literature
Neurologist 16:364-367, Finelli,P.F.,et al, 2010

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

Challenge of the Unknown: A Systematic Review of Acute Encephalitis in Non-Outbreak Situations
Neurol 75:924-932, Granerod,J. et al, 2010

Guidelines for the Management of Spontaneous Intracerebral Hemorrhage
Stroke 41:2108-2129, Morgenstern,L.B.,et al, 2010

Hypertrophic Nerves Producing Myelopathy in Fulminant CIDP
Neurol 75:750, Staff,N.P.,et al, 2010

Cerebral Amyloid Angiopathy
UpToDate: May 2010, Greenberg,S.M.,et al, 2010

Successful Management of Natalizumab-Associated Progressive Multifocal Leukoencephalopathy and Immune Reconstitution Syndrome in a Patient With Multiple Sclerosis
Arch Neurol 67:1391-1394, Schr�der,A.,et al, 2010

Brain Biopsy in Children With Primary Small-Vessel Central Nervous System Vasculitis
Ann Neurol 68:602-610, 573, Elbers,J.,et al, 2010

Rett Syndrome: Revised Diagnostic Criteria and Nomenclature
Ann Neurol 68:944-950, Neul,J.L.,et al, 2010

Dysexecutive Syndrome: Diagnostic Criteria and Validation Study
Ann Neurol 68:855-864, Godefroy,O.,et al, 2010

Early Intracerebral Hematoma Expansion after Aneurysmal Rupture
Stroke 41:2592-2595, Van Asch, C.J.J.,et al, 2010

Chronic Inflammatory Demyelinating Polyneuropathy: Etiology, Clinical Features, and Diagnosis
UpToDate, Sept, Lewis, R., 2010

AIDS - Related Lymphomas: Primary CNS Lymphoma
UpToDate, April, Doweiko, J.P., 2010

Pulmonary AVMs, including hereditary hemorrhagic telangiectasia: Diagnosis and Treatment
UpTo Date, August, Gossage, J.R., 2010

Longitudinally Extensive Myelopathy in Caucasians: A West Australian Study of 26 Cases from the Perth Demyelinating Diseases Database
JNNP 81:209-212, Qiu,W.,et al, 2010

MRI Criteria for MS in Patients with Clinically Isolated Syndromes
Neurol 74:427-434, Montalban,X.,et al, 2010

Diagnosis and Management of the Antiphospholipid Syndrome
BMJ 340:1125-1132, Cohen,D., et al, 2010

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

Open Biopsy in Patients With Acute Progressive Neurologic Decline and Absence of Mass Lesion
Neurol 75:419-424, Schuette,A.J., et al, 2010

Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
Neurol 75:316-323,298, Paradas,C., et al, 2010

Clinicopath Conf, Inflamatory Cerebral Amyloid Angiopathy,
NEJM 363:373-381, Case 22-2010, 2010

Natalizumab Treatment in a Patient With Chronic Inflammatory Demyelinating Polyneuropathy
Arch Neurol 67:881-883, Wolf,C., et al, 2010

Optimal Screening Strategy for Familial Intracranial Aneurysms: A Cost-Effectiveness Analysis
Neurol 74:1671-1679, Bor,A.S.E., et al, 2010

How Neurologists Think A Cognitive Psychology: Perspective on Missed Diagnoses
Ann Neurol 67:425-433, Vickrey,B.G., et al, 2010

Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
Brain 133:655-670, Leen,W.G., et al, 2010

Leptomeningeal Metastases in the MRI Era
Neurol 74:1449-1454, Clarke,J.L., et al, 2010

A Comparison of MRI Criteria for Diagnosing Pediatric ADEM and MS
Neurol 74:1412-1415, 1404, Ketelslegers,I.A., et al, 2010

Screening for Intracranial Aneurysms in Patients with Bicuspid Aortic Valve
Neurol 74:1430-1433, Schievink,W.I., et al, 2010

Prevalence of Superficial Siderosis in Patients with Cerebral Amyloid Angiopathy
Neurol 74:1346-1350, Linn,J., et al, 2010

Can Electronic Clinical Documentation Help Prevent Diagnostic Errors?
NEJM 362:1066-1069, Schiff,G.D. &Bates,D.W., 2010

Untangling the Web - Patients, Doctors, and the Internet
NEJM 362:1063-1066, Hartzband,P. &Groopman,J., 2010

Negative CT Angiography Findings in Patients with Spontaneous Subarachnoid Hemorrhage: When is Digital Subtraction Angiography Still Needed?
AJNR 31:695-705, Agid,R., et al, 2010

Is the Diagnosis at Hand?
The Lancet 375:1134, Holmes,M.V., et al, 2010

Whole-Genome Sequencing in a Patient with Charcot-Marie-Tooth Neuropathy
NEJM 362:1181-1191, Lupski,J.R., et al, 2010



Showing articles 1500 to 1550 of 4195 << Previous Next >>