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acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acquired immunodeficiency syndrome, congenital
acquired immunodeficiency syndrome, infants and children
acromicria
advances in neurology
Aicardi-Goutieres syndrome
Alexanders disease
anemia
aneurysm
aneurysm, asymptomatic
aneurysm, intracranial
anorexia
apraxia of eye movements
aqueduct of Sylvius, stenosis
arm swing, reduced
arthritis
aspartocyclase
aspiration
aspirin
ataxia
ataxia, truncal
ataxic gait
attention span
autoimmune epilepsy
B 12 deficiency
B 12 deficiency, infants
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
biologic markers
blindness
blood transfusion
bone marrow biopsy
bradykinesia
brain atrophy
brain biopsy
breast feeding
Brown-Vialetto-Van Laere syndrome
cachexia
calcification, gyral
calcification, intracranial
Canavan's disease
CAT scan
CAT scan, abnormal
cataplexy
cerebellar lesion
cerebral cortical atrophy
cerebral palsy
cerebral vasculature
cerebral venous infarction
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
cerebrovascular disease
cherry red spot
cherry red spot-myoclonus syndrome
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 3
Clinical Pathologic Conference(C.P.C.)
cold hands sign
complications
consanguinity
contractures, joint
controversies in neurology
corpus callosum, atrophy of
corpus callosum, thinning
cough
cranial nerve enhancement
cranial nerve enlargement
cranial neuropathy
cranial neuropathy, multiple
crawl regression
cry, abnormal
crying
cultured skin fibroblasts
cyst
cyst, parenchymal
D-dimer
decision analysis
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, childhood
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
developmental milestones
developmental milestones, loss of
developmental retardation
diagnostic criteria
differential diagnosis
difficulty climbing stairs
diplopia
dopa responsive dystonia
drooling
dropped head syndrome
dysarthria
dysmetria
dysphagia
dysphonia
dystonia
dystonia, children
electroencephalogram, abnormalities of
encephalitis
encephalitis, autoimmune
encephalopathy
encephalopathy, neonatal
encephalopathy, progressive
endoscopic surgery
endoscopy
enzyme, defect
epileptic encephalopathy
episodic disorders
evoked potentials
eye movement, disorders of
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
FARS2 deficiency
feeding disorder
fever
fine motor function, impaired
finger tapping
foam cells
fontanel, bulging
frontal bossing
fundus, abnormality of
gait disorder
galactorrhea
gangliosidosis GM2
Gaucher's disease
gaze palsy
gaze palsy, supranuclear
gender
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
glaucoma
globoid cells
glucocerebrosidase
glutamic acid decarboxylase, antibody
granular osmiphilic material
growth retardation
Hallervorden Spatz disease
hand deformity
hands, fisted
head circumference
head lag
headache
hearing loss
hepatic failure
hepatitis
hepatomegaly
hepatosplenomegaly
hexosaminidase-A
human immunodeficiency virus type 1
human immunodeficiency virus type 1, infants and children
hydrocephalus
hydrocephalus, complications with
hydrocephalus, etiology
hydrocephalus, fetal
hydrocephalus, non-communicating(obstructive)
hydrocephalus, treatment of
hyperhomocysteinemia
hyperpigmentation of skin
hyperreflexia
hypertonia
hypomyelination
hyporeflexia
hypothermia
hypotonia
hypotonia, infants
immunomodulation
inattention
inborn errors of metabolism
incoordination
infant, evaluation of
infantile tremor syndrome
intellectual deficit
intellectual deterioration
interferon alpha
intracranial pressure, increased
introverted
iron, brain
irritability
jaundice
Jewish
Krabbe's disease
lactic acidemia
L-dopa
Leigh's disease
lethargy
leukocyte enzyme abnormality
leukocytosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
life expectancy
lipid storage disorder of CNS
liver disease
liver function enzymes
lymphadenopathy
lymphadenopathy, axillary
lymphadenopathy, paraaortic
lysosomal storage disease
macrocephaly
malformation, vascular
masked facies
meconium staining
memory, impairment of
meningeal enhancement
meningitis, CSF cell count-normal
mental retardation
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
metachromatic leukodystrophy, late-infantile
microcephaly
midbrain, lesion of
misdiagnosis
mitochondrial disease
monoclonal antibodies
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, angiography
MRI, contrast enhanced
MRI, diffusion weighted
MRI, hypointense signal foci on
MRI, paramagnetic effect
MRS
mucopolysaccharidoses
muscle biopsy
muscle spasm
myasthenia gravis
myasthenia gravis, infantile and juvenile
myelination of nervous system
myoclonus
myoclonus, epilepsy
nasal speech
nausea and vomiting
neck trauma
nerve conduction studies
neuroaxonal dystrophy
neurocutaneous disease
neurofibrillary degeneration
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic examination
neurologic signs
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
Niemann-Pick disease
nystagmus
nystagmus, rotary
ophthalmoplegia
opisthotonus
opportunistic infection
opportunistic infection, CNS
optic atrophy
optic chiasm, enlarged
optic nerve
optic nerve, enlarged
pain
PANK2 mutation
papilledema
paraparesis, familial spastic
paraparesis, spastic
PAS positive material in the brain
pediatric neurology
pleocytosis of cerebrospinal fluid
port wine nevus
postural abnormality
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
prolactin, elevated
psychological testing
psychomotor retardation
psychosis
ptosis
pulmonary infiltrates
pyramidal tract
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
rash
rectal biopsy
renal tubular acidosis
retinal degeneration
retinitis pigmentosa
retropulsion
Rett's syndrome
reversible neurologic disorder
review article
riboflavin transporter deficiency
rigidity
rituximab
Rosenthal fibers
running
scoliosis
scoliosis, neurologic association with
screening
sedimentation rate, elevated
seizure
seizure, children
seizure, drug resistance
seizure, intractable
serositis
short stature
shunt procedure, ventricular
shunt procedure, ventricular-complications of
skin, lesions in neurologic disorders
slurred speech
somnolence
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
speech, loss of
splenomegaly
spongy degeneration of brain
spontaneous remission
startle reaction
status epilepticus
stereotyped behavior
stiff joints
strabismus
striatonigral degeneration
striatonigral degeneration, infantile
strokelike episodes
Sturge-Weber syndrome
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
substantia nigra
suck, poor
symmetric brain lesions
systemic illness
systemic juvenile idiopathic arthritis
Tay-Sachs disease
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytosis
titubation
toe walking
tone, muscle, increased
toxoplasmosis, CNS
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, intention
trichopoliodystrophy
tuberous sclerosis
tumor necrosis factor
tyrosine hydroxylase deficiency
vasculopathy
vegetarianism
ventricular enlargement
ventriculostomy
ventriculostomy, endoscopic
visual acuity, decreased
visual evoked response
visual field defect
visual fields, constricted
visual impairment
visual loss
vitamin deficiency
vomiting, episodic
vomiting, recurrent
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
Werdnig-Hoffman disease
West disease
wheelchair
white hair
white matter disease
wide based gait
workup
wrist drop
x-linked hydrocephalus
Showing articles 350 to 400 of 2279 << Previous Next >>

Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 988, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 996, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Lipogranulomatosis (Farber Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 960, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, The Phenylketonuria
Adams & Victors Principles of Neurology, Chp 37, pg 968, Ropper, A.H.,et al, 2014

Sturge-Weber Syndrome
UptoDate , Nov, Bodensteiner, J.B., 2014

Herpes Simplex Virus Encephalitis:Clinical Manifestations,Diagnosis and Outcome in 106 Adult Patients
J Clin Virol 60:112-118, Sili,U.,et al, 2014

Neurosyphilis Orofacial Dyskinesia: The Candy Sign
MovDisord 28:246-247, Martinelli, P.,et al, 2013

Febrile Infection-Related Epilepsy Syndrome: A Study of 12 Patients
Seizure 22:553-559, Caraballo, R.H.,et al, 2013

Meningoencephalitis from Borrelia Miyamotoi in an Immunocompromised Patient
NEJM 368:240-245, Gugliotta, J.L.,et al, 2013

Sturge-Weber Syndrome
MedLink Neurology, July, Comi, A.M., 2013

Anemia and Risk of Dementia in Older Adults
Neurol 81:528-533, Hong, C.H.,et al, 2013

Frontotemporal Dementia
BMJ 347:f4827, Warren, J.D.,et al, 2013

A 35-Year-Old Woman with Acute Seizures and Behavior Change
Neurol 81:e55-e59, Rejeski, J.J.,et al, 2013

Clinical Presentation of Chronic Traumatic Encephalopathy
Neurol 81:1122-1129, Stern, R.A.,et al, 2013

Clinicopathologic Conference, Acute Infectious Mononucleosis due to Epstein-Barr Virus Infection, Complicated by Acute Otitis Media and Postinfectious Cerebellitis
NEJM 369:1253-1261, Case 30-2013, 2013

Is There a Link Between Open-Angle Glaucoma and Dementia?: The Three-City-Alienor Cohort
Ann Neurol 74:171-179, Helmer, C.,et al, 2013

Mystery Case: A Young Boy with Myoclonic Jerks
Neurol 81:e130-e134, Musleh, C.,et al, 2013

Central Nervous System Involvement in Whipple Disease
Medicine 92:324-330, Compain, C.,et al, 2013

Cognitive Delay in a 7-year-old Girl
Neurol 81: e148-e150, Cachia, D. & Stine, C., 2013

Early Child Development and Exposure to Antiepileptic Drugs Prenatally and Through Breastfeeding
JAMA Neurol 70:1367-1374, Veiby, G.,et al, 2013

An Expanded Role for Neuroimaging in the Evaluation of Memory Impairment
AJNR 34:2075-2082, Desikan, R.S.,et al, 2013

New Insights into the Dementia Epidemic
NEJM 369:2275-2277, Larson, E.B.et al, 2013

Teleneurology Applications
Neurol 80:670-676, Wechsler, L.,et al, 2013

Disability in Multiple Sclerosis
Neurol 80:1018-1024, Kister, I.,et al, 2013

PET Imaging for Alzheimer Disease: Are Its Benefits Worth the Cost?
JAMA 309:1099-1100, Mitka, M., 2013

Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
Neurol 80:e162-e165, Pressman, P.,et al, 2013

Limbic Encephalitis as the Presenting Feature of Sj�gren Syndrome
Neurol Clin Pract 3:165-167, Finelli, P. & Inoa, V., 2013

Clinicopathologic Conferences, Celiac Disease, Addisons Disease, and Major Depression Disorder
NEJM 368:2015-2024, Case 16-2013, 2013

Ataxia, Dementia, and Hypogonadotropism Caused by Disordered Ubiquitination
NEJM 368:1992-2003, Margolin, D.,et al, 2013

Sturge-Weber Syndrome and Port-Wine Stains Caused by Somatic Mutation in GNAQ
NEJM 368:1971-1979, Shirley, M.,et al, 2013

Should Patients with Dementia who Wander be Electronically Tagged? Yes
BMJ 346:f3603, McShane, R., 2013

Clinicopathologic Conference, Blind and Confused, Neuromyelitis Optica Spectrum Disorder
JAMA Neurol 70:932-936, Sharma, V.,et al, 2013

Clinical Spectrum of CNS Aquaporin-4 Autoimmunity
Neurol 78:1179-1185, Kim, S.,et al, 2013

Subacute Sclerosing Panencephalitis
www.MedLink.com, February, Auwaeter,P.G.&Johnson,R.T., 2013

Criteria for the Diagnosis of Corticobasal Degeneration
Neurol 80:496-503, Armstrong, M.J.,et al, 2013

Functional Impairment in Progressive Supranuclear Palsy
Neurol 80:380-384, Duff, K.,et al, 2013

Severe Carotid Stenosis and Impaired Cerebral Hemodynamics can Influence Cognitive Deterioration
Neurol 80:2145-2150, Balestrini, S.,et al, 2013

Cortical Pathology in Multiple Sclerosis Patients with Epilepsy: A 3 Year Longitudinal Study
JNNP 83:49-54, Calabrese, M.,et al, 2012

Expanding the Clinical, Radiological and Neuropathological Phenotype of Chronic Lymphocytic Inflammation with Pontine Perivascular Enhancement Responsive to Steroids (CLIPPERS)
JNNP 83:15-22, Simon, N.G.,et al, 2012

Autoimmune Epilepsy
Arch Neurol 69:582-593,565, Quek, A.M.L.,et al, 2012

Development of a Suspicion Index to Aid Diagnosis of Niemann-Pick Disease Type C
Neurol 78:1560-1567,1546, Wijburg, F.A.,et al, 2012

Hashimoto Encephalopathy
Neurol 78:e134, Afshari, M.,et al, 2012

Clinical Reasoning: Encephalopathy in a 10-year-old boy
Neurol 79:e12-e18, Rodan, L. & Tein, I., 2012

Immunotherapy-Responsive Chorea as the Presenting Feature of LGI1-Antibody Encephalitis
Neurol 79:195-196, Tofaris,G.K.,et al, 2012

Anti-Glutamic Acid Decarboxylase Limbic Encephalitis Without Epilepsy Evolving Into Dementia with Cerebellar Ataxia
Arch Neurol 69:1064-1066, Mirabelli-Badenier, M.,et al, 2012

Range of Genetic Mutations Associated with Severe Non-Syndromic Sporadic Intellectual Disability: An Exome Sequencing Study
Lancet 380:1674-1682, Rauch, A.,et al, 2012

Diagnostic Exome, Sequencing in Persons with Severe Intellectual Disability
NEJM 367:1921-1929, Ligt, J.,et al, 2012

Evidence-based Guideline: Diagnostic accuracy of CSF 14-3-3 Protein in Sporadic Creutzfeldt-Jakob Disease
Neurol 79:1499-1506, Muayqil, T.,et al, 2012

Placebo-Controlled Phase 3 Study of Oral BG-12 for Relapsing Multiple Sclerosis
NEJM 367:1098-1106,1149, Gold, R.,et al, 2012

The Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale
Stroke 43:2871-2876, Pescini, F.,et al, 2012



Showing articles 350 to 400 of 2279 << Previous Next >>