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Differential
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abdominal cramps
acid maltase deficiency
acid maltase deficiency, adult
acral sensory symptoms
adrenoleukodystrophy
adrenomyeloneuropathy
agalsidase alfa
alpha glucosidase
aminoacidopathies
aminoacidurias
amniocentesis
angina pectoris
angiokeratoma
anhidrosis
anterior horn cell disease
anterior tibial muscle weakness
antiviral agents
Arnold Chiari malformation
arthropathy
arthropathy, neuropathic
arylsulfatase A
aspartate aminotransferase
aspiration
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
athetosis
atidarsagene autotemcel
attention deficit disorder with hyperactivity
attention span
autonomic dysfunction
axonal spheroid
Babinski sign
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar impression
behavioral disorder
blindness
blood dyscrasias, neurologic findings with
bone marrow biopsy
bone marrow transplantation
brain atrophy
brain biopsy
brain biopsy, complications of
brain biopsy, false negative
brain biopsy, indication
brainstem, infarction of
burning feet
burning feet, differential diagnosis of
burning hands
burning paresthesia
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataplexy
cataracts
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar infarction
cerebral cortical atrophy
cerebral ischemia
cerebrospinal fluid, gammaglobulin of
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, cryptogenic
cerebrovascular accident, familial occurrence
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, young adult
cerebrovascular disease
cerebrovascular disease, cardiovascular disease with
cherry red spot
cherry red spot-myoclonus syndrome
children
chorea
choreoathetosis
chromosomal abnormality
chronic graft versus host disease
Clinical Pathologic Conference(C.P.C.)
coagulopathy
cognition
complications
compression fracture
congestive heart failure
consanguinity
contractures, joint
cornea, abnormal
cornea, opacification in infancy-causes of
cornea, opacity of
corneal dystrophy
corpus callosum
corpus callosum, hypoplastic
corpus callosum, lesion of
creatine phosphokinase(CPK)elevated
creatinine, elevated
cry, abnormal
cultured skin fibroblasts
cystinosis
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, childhood
dementia, diagnostic evaluation of
developmental disability
developmental milestones, loss of
developmental retardation
diarrhea
differential diagnosis
difficulty going down stairs
diplopia
distal muscle weakness
drooling
dropped head syndrome
dysarthria
dysmorphic
dysostosis multiplex
dysphagia
dystonia
dystonia, face
dystonia, focal
dystonic lipidosis
echocardiogram
efficacy
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
enzyme treatment
enzyme, defect
episodic disorders
episodic neurologic deficits
exercise intolerance
exome sequencing
eye movement, disorders of
Fabry's disease
facial appearance, abnormal
falling
familial
Farber's disease
fever
foam cells
fracture, pathologic
Friedreich's ataxia
fucosidosis
gait disorder
galactosidase
gangliosidosis GM1
gangliosidosis GM2
gargoylism
Gaucher's disease
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
glucocerebrosidase
glycogen storage disease
glycoprotein
growth retardation
hand pain
head injury
hearing loss
heat intolerance
hemorrhagic diathesis
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
heralding manifestation
hexosaminidase-A
hexosaminidase-A and B
high arched feet
Hurler's syndrome
hydrocephalus
hyperreflexia
hypertonia
hypohidrosis
hypomyelination
hypotonia
hypotonia, infants
inattention
inborn errors of metabolism
inborn errors of metabolism, screening
inclusion bodies, intracytopasmic
incoordination
infection, recurrent
intellectual deficit
intellectual deterioration
intelligence quotient
intrathecal medication
Jakob-Creutzfeldt disease
jaundice
Jewish
klippel feil syndrome
Krabbe's disease
kyphoscoliosis, neurologic causes of
lactic acidemia
lead poisoning
learning disability, in children
Leigh's disease
leukocyte enzyme abnormality
leukodystrophy
Lewy body disease, diffuse
life expectancy
limb-girdle weakness
lipid storage disorder of CNS
liver disease
lymphadenopathy
lysosomal storage disease
lysosomes, abnoral
macrocephaly
Marinesco-Sjogren syndrome
megalencephaly
memory, impairment of
meningitis, chronic
mental retardation
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
metachromatic leukodystrophy, juvenile
metachromatic leukodystrophy, late-infantile
misdiagnosis
mitral valve prolapse
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, hypointense signal foci on
MRS
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, differential diagnosis of
muscle biopsy
muscle spasm
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy, Duchenne
myelopathy
myocardial infarction
myoclonus
myopathy
myopathy, vacuolar
N-acetyl-L-aspartic acid
neonatal screening, genetic neurologic disorders
neoplasm, primary of CNS
neuraminidase deficiency
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neurofibrillary degeneration
neurolipidosis IV
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic testing
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathic pain scale
neuropathology
neuropathy
neuropathy, demyelinating
neuropathy, painful
neuropathy, small-fiber
neuropathy, small-fiber, painful sensory
neurosis
next-generation sequencing
Niemann-Pick disease
ophthalmoplegia
optic atrophy
optokinetic nystagmus, abnormal
osteopetrosis
pain
pain, neuropathic
Parkinsonism syndrome
paroxysmal neurologic deficits
patient in waiting
pediatric neurology
peroxisomal disease
pes cavus
photophobia
polymerase chain reaction
polyneuropathy
Pompe's disease of glycogen storage
precipitating factors
preclinical
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
progressive neurologic disorder
proteinuria
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychomotor retardation
psychosis
quadriparesis
quadriplegia
rectal biopsy
remote effect of cancer on the nervous system
renal failure
respiratory failure
respiratory tract infection
retinal degeneration
retinopathy
retropulsion
review article
rigidity
safety
Salla disease
Sandhoff's disease
schizophrenia
scoliosis, neurologic association with
screening
sea-blue histiocytes
seizure
seizure, children
seizure, laughing as manifestation
sensorineural hearing loss
short stature
sick sinus syndrome
skin, biopsy
skin, lesions in neurologic disorders
slit lamp examination
small vessel disease
spasticity
speech, delayed development of
sphingomyelin
spinal cord, compression of
spinocerebellar degeneration
splenomegaly
startle reaction
stem cell transplantation
subdural hematoma
systemic illness
tandem gait, ataxic
Tay-Sachs disease
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
toe walking
tone, muscle, increased
tongue, enlarged
treatment of neurologic disorder
tremor
tremor, intention
tripping
urea-cycle enzymopathies
urinary sulfatidase excretion
urine test for metabolic disorders
vasculopathy
ventricular enlargement
vertebral-basilar insufficiency
vertigo
vision, failure of in childhood
visual acuity, decreased
visual fields, constricted
visual loss
visual loss, transient
Von Hippel Lindau
walking, delayed
walking, difficulty with
weakness
weakness, proximal
white matter disease
wide based gait
Showing articles 1300 to 1350 of 20238 << Previous Next >>

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

Treatment of Neuromyelitis Optica with Mycophenolate Mofetil
Arch Neurol 66:1128-1133, Jacob,A.,et al, 2009

Progressive Multifocal Leukoencephalopathy After Natalizumab Monotherapy
NEJM 361:1081-1087, Linda,H.,et al, 2009

Treatment of Progressive Multifocal Leukoencephalopathy Associated with Natalizumab
NEJM 361:1075-1080, Wenning,W.,et al, 2009

Reemergence of PML in Natalizumab-Treated Patients--New Cases, Same Concerns
NEJM 361:1041-1043, Major,E., 2009

Combined Corticosteroid and Antiviral Treatment for Bell Palsy: A Systematic Review and Meta-analysis
JAMA 302:985-993, 1003, Almeida,J.,et al, 2009

High-Dose Cytarabine Plus High-Dose Methotrexate Versus High-Dose Methotrexate Alone in Patients with Primary CNS Lymphoma: A Randomised Phase 2 Trial
Lancet 374:1512-1520, 1477, Ferreri,A.,et al, 2009

N-Methyl-D-Aspartate Receptor Antibodies in Pediatric Dyskinetic Encephalitis Lethargica
Ann Neurol 66:704-709, Dale,R.,et al, 2009

Multifocal Paraneoplastic Cortical Encephalitis Associated With Myasthenia Gravis and Thymoma
Arch Neurol 66:1407-1409, Hammoud,K.,et al, 2009

CNS Complications of Radiotherapy and Chemotherapy
Lancet 374:1639-1651, Soussain,C.,et al, 2009

Best Practice Recommendations for the Selection and Management of Patients with Multiple Sclerosis Receiving Natalizumab Therapy
Mutliple Sclerosis 15:S26-S36, Coyle,P.K.,et al, 2009

Brain Lesions Are Most Often Reversible in Acute Thrombotic Thrombocytopenic Purpura
Neurol 73:66-70, Burrus,T.M.,et al, 2009

Frequency, Characteristics, and Risk Factors for Amiodarone Neurotoxicity
Arch Neurol 66:865-869, Orr,C.F. &Ahlskog,E., 2009

Neurological Consequences of Atrioesophageal Fistula After Radiofrequency Ablation in Atrial Fibrillation
Arch Neurol 66:884-887, St�llberger,C.,et al, 2009

Parkinsonism in HIV-Infected Patients on Highly Active Antiretroviral Therapy
Neurol 73:401-403, Tisch,S. &Brew,B., 2009

Diagnosis and New Treatments in Muscular Dystrophies
JNNP 80:706-714, Manzur,A.Y. &Muntoni,F., 2009

Treating Childhood Acute Lymphoblastic Leukemia Without Cranial Irradiation
NEJM 360:2730-2741, Pui,C.-H.,et al, 2009

A 49-Year-Old Man with Contractures, Weakness, and Cardiac Arrhythmia
Neurol 72:2036-2043, Kissel,J.T.,et al, 2009

Cyclophosphamide Therapy in Pediatric Multiple Sclerosis
Neurol 72:2076-2082,2064, Makhani,N.,et al, 2009

Lyme Neuroborreliosis: Manifestations of a Rapidly Emerging Zoonosis
AJNR 30:1079-1087, Hildenbrand,P.,et al, 2009

Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
Neurol 73:430-437, Verhagen,M.M.M.,et al, 2009

Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
Ann Neurol 66:11-18,1, Florance,N.R.,et al, 2009

A 75-Year-Old Woman with Progressive Right-Hand Tremor and Inability to Use Her Right Side
Neurol 73:1399-1405, Kertesz,A.,et al, 2009

Interventions in the Management of Serum Lipids for Preventing Stroke Recurrence
Stroke 40:e622-e623, Manktelow,B. &Potter,J., 2009

Primary Central Nervous System Lymphoma in a Patient Treated with Natalizumab
Ann Neurol 66:403-406, 261, 262, Schweikert,A.,et al, 2009

Intravascular Lymphoma Masquerading as Multiembolic Stroke Developing After Coronary Artery By-Pass Surgery
The Neurologist 15:98-101, Sumer,M.,et al, 2009

Results of the Stroke Prevention by Aggressive Reduction in Cholesterol Levels (SPARCL) Trial by Stroke Subtypes
Stroke 40:1405-1409, Amarenco,P.,et al, 2009

PML-IRIS in Patients with HIV Infection: Clinical Manifestations and Treatment with Steroids
Neurol 72:1458-1464,1454, Tan,K.,et al, 2009

Prescribe Prednisolone Alone for Bells Palsy Diagnosed Within 72 Hours of Symptom Onset
BMJ 338:410-411, Madhok,V.,et al, 2009

Opportunistic Infections and Other Risks with Newer Multiple Sclerosis Therapies
Ann Neurol 65:367-377, Berger,J.R. &Houff,S., 2009

Fast-In, Fast-Out
Lancet 373:1398, Hefele,B.,et al, 2009

Human Natural Autoantibodies in the Treatment of Neurologic Disease
Neurol 72:1269-1276, Rodriguez,M.,et al, 2009

Diagnostic Value of N-methyl-D-aspartate Receptor Antibodies in Women with New-Onset Epilepsy
Arch Neurol 66:458-464, Niehusmann,P.,et al, 2009

Clinicopath Conf, Acute HIV-1 Infection
NEJM 360:1540-1548, Case 11-2009, 2009

Tularemic Meningitis in the United States
Arch Neurol 66:523-527, Hofinger,D.M.,et al, 2009

Community-Acquired Bacterial Meningitis in Elderly Patients: Experience over 30 Years
Medicine 88:115-119, Cabellos,C.,et al, 2009

Diagnosis and New Treatment in Muscle Channelopathies
JNNP 80:360-365, Meola,G.,et al, 2009

The Neurologic Manifestations of Systemic Lupus Erythematosus
The Neurologist 15:115-121, Greenberg,B.M., 2009

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

Statin Therapy After First Stroke Reduces 10-Year Stroke Recurrence and Improves Survival
Neurol 72:1816-1822, Milionis,H.J.,et al, 2009

Clinicopath Conf, Neuro-Behcets Disease
NEJM 360:2341-2351, Case 17-2009, 2009

Persistent Fainting After Implantation of a "Curative" Pacemaker
NEJM 360:88-89, Kasim,S.,et al, 2009

Relapse Management in Multiple Sclerosis
The Neurologist 15:1-5, Thrower,B.W., 2009

Treatment of CNS Sarcoidosis with Infliximab and Mycophenolate Mofetil
Neurol 72:337-340, Morovan,M. &Segal,B.M., 2009

Assessment of Potential Drug Interactions in Patients with Epilepsy: Impact of Age and Sex
Neurol 72:419-425, Gidal,B.E.,et al, 2009

Rapidly Progressive Neurodegenerative Dementias
Arch Neurol 66:201-207, Josephs,K.A.,et al, 2009

Brown-S�quard Syndrome After Herpes Zoster
Neurol 72:670-671, Young-Barbee,C.,et al, 2009

Clinicopath Conf, Neurosarcoidosis
NEJM 360:802-809, Case 6-2009, 2009

Neurologic Immune Reconstitution Inflammatory Syndrome in HIV/AIDS: Outcome and Epidemiology
Neurol 72:835-841, McCombe,J.A.,et al, 2009

Neurosarcoidosis: A Study of 30 New Cases
JNNP 80:297-304, Joseph,F.G. &Scolding,N.J., 2009



Showing articles 1300 to 1350 of 20238 << Previous Next >>