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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 2050 to 2100 of 4195 << Previous Next >>

Is Measurement of D-Dimer Useful in the Diagnosis of Cerebral Venous Thrombosis?
Neurol 61:1057-1060, Lalive,P.H.,et al, 2003

Clinicopath Conf., Colchicine Myoneuropathy
NEJM 349:1656-1663, Case 33-2003, 2003

Spinal Dural Arteriovenous Fistulas: Clinical Features in 80 Patients
JNNP 74:1438-1440, Jellema,K.,et al, 2003

Identification of New Presenilin Gene Mutations in Early-Onset Familial Alzheimer Disease
Arch Neurol 60:1541-1544,1521, Tedde,A.,et al, 2003

Advances in Neuropathic Pain
Arch Neurol 60:1524-1534, Dworkin,R.H.,et al, 2003

Prolactinoma
NEJM 349:2035-2041, Schlechte,J.A., 2003

Diagnostic Approach in Patients with Symmetric Imaging Lesions of the Deep Gray Nuclei
The Neurologist 9:250-261, Finelli,P.F.&DiMario,Jr,F.J., 2003

A Prospective Randomized Comparison of Loop Recorders Versus Holter Monitors in Patients with Syncope or Presyncope
Am J Med 115;1-5,66, Sivakumaran,S.,et al, 2003

Hemisensory Syndrome is Associated with a Low Diagnostic Yield and a Nearly Uniform Benign Prognosis
JNNP 74:1113-1116, Toth,C., 2003

Neurovirological Methods and Their Applications
JNNP 74:1016-1022, Kennedy,P.G.E., 2003

Operational Definitions for the NINDS-AIREN Criteria for Vascular Dementia
Stroke 34:1907-1912, van Straaten,E.C.W.,et al, 2003

The Emergency Management of Headaches
The Neurologist 9:93-98, Green,M.W., 2003

Takayasu's Arteritis with Arteriographic Evidence of Intracranial Vessel Involvement
Neurol 60:1550-1551, Klos,K.,et al, 2003

T1 Hyperintensity in the Pulvinar: Key Imaging Feature for Diagnosis of Fabry Disease
AJNR 24:916-921, Takanashi,J.,et al, 2003

Antimyelin Antibodies as a Predictor of Clinically Definite Multiple Sclerosis After a First Demyelinating Event
NEJM 349:139-145,107, Berger,T.,et al, 2003

Mitochondrial Respiratory-Chain Diseases
NEJM 348:2656-2668, DiMauro,S. &Schon,E.A., 2003

Treating Post Lyme Disease
Neurol 60:1888-1889,1916,1923, Steiner,I., 2003

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

Challenging the Clinical Utility of the 14-3-3 Protein for the Diagnosis of Sporadic Creutzfeldt-Jakob Disease
Arch Neurol 60:813-816,803, Geschwind,M.D.,et al, 2003

Differentiation of Toxoplasmosis and Lymphoma in AIDS Patients by Using Apparent Diffusion Coefficients
AJNR 24:633-637,554, Camacho,D.L.A.,et al, 2003

Mass Lesions of the Brain in AIDS: The Dilemmas of Distinguishing Toxoplasmosis from Primary CNS Lymphoma
AJNR 24:554-555, Berger,J.R., 2003

Cerebral Angiographic Findings of Spontaneous Intracranial Hypotension
AJNR 24:707-708, Roll,J.D.,et al, 2003

Diagnostic Accuracy of Stroke Referrals from Primary Care, Emergency Room Physicians, and Ambulance Staff Using the Face Arm Speech Test
Stroke 34:71-76, Harbison,J.,et al, 2003

Does This Patient Have Parkinson Disease?
JAMA 289:347-353, Rao,G.,et al, 2003

Proton MR Spectroscopy in the Diagnostic Evaluation of Suspected Mitochondrial Disease
AJNR 24:33-41, Lin,D.D.M.,et al, 2003

Myotonic Dystrophy Type 2
Neurol 60:657-664, Day,J.W.,et al, 2003

Major Malformations in Offspring of Women with Epilepsy
Neurol 60:575-579, Kaaja,E.,et al, 2003

Vestibular Neuritis
NEJM 348:1027-1032, Baloh,R.W., 2003

Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases
Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003

Neuromyelitis Optica:What It Is and What It Might Be
Lancet 361:889-890, Weinshenker,B.G., 2003

Diffusion-Weighted Imaging Discriminates Progressive Supranuclear Palsy from PD, But Not From the Parkinson Variant of Multiple System Atrophy
Neurol 60:922-927, Seppi,K.,et al, 2003

The Accuracy of the Diagnosis of Paroxysmal Events in Children
Neurol 60:979-982, Stroink,H.,et al, 2003

Von Recklinghausen's Neurofibromatosis: Neurofibromatosis Type 1
Lancet 361:1552-1554, Reynolds,R.M., et al, 2003

Early or Late Appearance of "Dropped Head Syndrome" in Amyotropic Lateral Sclerosis
JNNP 74:683-686, Gourie-Devi,M.,et al, 2003

New T2 Lesions Enable an Earlier Diagnosis of Multiple Sclerosis in Clinically Isolated Syndromes
Ann Neurol 53:673-676, Dalton,C.M.,et al, 2003

West Nile Encephalitis
BMJ 326:865-869, Solomon,T.,et al, 2003

The Impact of Delays in Computed Tomography of the Brain on the Accuracy of Diagnosis and Subsequent Management in Patients with Minor Stroke
JNNP 74:77-81, Wardlaw,J.M.,et al, 2003

New Diagnostic Criteria for Multiple Sclerosis
Neurol 60:27-30,6, Tintore,M.,et al, 2003

The Morbidity of Guillain-Barre Syndrome Admitted to the Intensive Care Unit
Neurol 60:17-21, Henderson,R.D.,et al, 2003

Clinicopath Conf,Classic Polyarteritis Nodosa Associated with Hepatitis B Infection
NEJM 348:333-342, Case 3-2003, 2003

Primary Brain Tumours in Adults
Lancet 361:323-331, Behin,A.,et al, 2003

Investigation of Risk Factors in Children with Arterial Ischemic Stroke
Ann Neurol 53:167-173,149, Ganesan,V.,et al, 2003

The Neurobiology, Diagnosis, and Treatment of Narcolepsy
Ann Neurol 53:154-166, Scammell,T.E., 2003

Marchiafava-Bignami Disease: Longitudinal MR Imaging and MR Spectroscopy Study
AJNR 24:249-253, Gambini,A.,et al, 2003

Risk of Stroke Associated With Nonsteroidal Anti-Inflammatory Drugs
Stroke 34:379-386, Bak,S.,et al, 2003

Nonaspirin Nonsteroidal Anti-Inflammatory Drugs and Risk of Hospitalization for Intracerebral Hemorrhage
Stroke 34:387-391, Johnsen,S.P.,et al, 2003

Detection of Pathologic Prion Protein in the Olfactory Epithelium in Sporadic Creutzfeldt-Jakob Disease
NEJM 348:711-719,681, Zanusso,G.,et al, 2003

Clinicopath Conf., Chronic Inflammatory Demyelinating Polyneuropathy
NEJM 348:735-743, Case 6-2003, 2003

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

Rasmussen's Encephalitis
Neurol 60:422-425, Granata,T.,et al, 2003



Showing articles 2050 to 2100 of 4195 << Previous Next >>