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Differential
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aciduria
acoustic neurinoma
acoustic neurinoma, bilateral
acquired immunodeficiency syndrome
adrenoleukodystrophy
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
Alexanders disease
algorithm
alopecia
alpha-fetoprotein
Alzheimer's disease
Alzheimer's disease, diagnosis of
Alzheimer's disease, early onset
Alzheimer's disease, familial
amniocentesis
amyloid
amyloid angiopathy, cerebral
amyloid angiopathy, hereditary cystatin C
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, familial
anemia
anemia, hemolytic
anesthesia, general
anosmia
apolipoprotein E
APP gene
apraxia of eye movements
arteriopathy
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
attention deficit disorder with hyperactivity
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
autonomic dysfunction
Babinski sign
basal ganglia
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
benign familial neonatal convulsions
brachial neuritis
brachial plexus neuropathy
brachial plexus neuropathy, familial
brain biopsy
brainstem, lesion of
brainstem, neoplasms of
bulbar palsy, progressive
cafe au lait spots
calcification, intracranial
calcitonin gene-related peptide receptor blocker
cane
carcinoembryonic antigen
carcinoma
carcinoma of pancreas
CAT scan
CAT scan, abnormal
cataracts
caudate nucleus, atrophy
cavernous hemangioma
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellum, neoplasms of
cerebral atherosclerosis
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral infarction
cerebral infarction, subcortical
cerebral ischemia
cerebral palsy
cerebro hepato renal syndrome
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, young adult
Charcot-Marie-Tooth
children
chorea
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 11
chromosome 14
chromosome 17
chromosome 2
chromosome 22
chromosome 3
chromosome 7
chromosome 9
clindamycin
clonazepam
clubfoot as related to neurologic disease
Cockayne's syndrome
cognition
coma
compression neuropathy
compression neuropathy, recurrent
corpus callosum, lesion of
cost effectiveness
creatine phosphokinase(CPK)elevated
Creutzfeldt-Jakob disease, genetic
cryptococcal meningitis
cyst, neoplastic cerebellum
cytomegalovirus infection
degenerative diseases of CNS
dementia
dementia, familial
dementia, presenile
dementia, rapidly progressive
dementia, transmissible
dentate nuclei
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
developmental retardation
diabetes mellitus
diagnostic criteria
differential diagnosis
disability rating scale, neurological
DNA probes
dopa responsive dystonia
drooling
drug induced neurologic disorders
dysarthria
dysmorphic
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, children
dystonia, paroxysmal
dystrophin
ear, abnormal
electroencephalogram
electronystagmography
electroretinograph
encephalitis
encephalitis, autoimmune
encephalitis, focal
encephalitis, Rasmussen's
encephalitis, viral
enzyme, muscle disease
epidemiology of neurology
ethics in neurology
eye movement, disorders of
Fabry's disease
face, elongated
facial appearance, abnormal
familial
fasciculation
fatal familial insomnia
fragile-X syndrome
Friedreich's ataxia
fundus, abnormality of
gadolinium
gait disorder
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gerstmann-Straussler-Scheinker disease
GFAP gene
globus pallidus
globus pallidus, lesion of, bilateral
GLUT1 deficiency syndrome
gonadotropin-releasing hormone
growth retardation
gynecomastia
hair analysis
Hallervorden Spatz disease
hallucination
hamartoma
head circumference
headache
headache, positional
headache, recurrent
hearing loss
hemangioblastoma
hemiparesis
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
hepatosplenomegaly
Hispanics
HTRA1 gene
Hunter's syndrome
huntingtin
Huntington's chorea
Huntington's chorea, genetic counselling
Huntington's chorea, presymptomatic detection of
Huntington's disease, children
hyperactivity
hyperekplexia
hyperhidrosis
hyperkalemic periodic paralysis
hyperreflexia
hyperthermia
hypogonadism
hypotelorism
hypotonia
hypotonia, infants
imbalance
immunodeficiency
immunohistochemistry
immunoperoxidase staining
immunosuppression
in situ hybridization
inborn errors of metabolism
inclusion bodies, intracytopasmic
insomnia
intellectual deficit
intellectual deterioration
intracerebral hemorrhage
intracerebral hemorrhage, familial
intracerebral hemorrhage, young adult
iron, brain
Jakob-Creutzfeldt disease
joint hypermobility
Kallmann's syndrome
Kearns-Sayre syndrome
KRIT1 gene
Kugelberg-Welander syndrome
lacunar infarction
Laurence-Moon-Bardet-Biedl syndrome
leukemia
leukodystrophy
leukoencephalopathy
lymphoma
macrocephaly
macular degeneration
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, familial
malignant hyperpyrexia
manic-depressive
medulla oblongata
medulla oblongata, atrophy
medulla oblongata, lesion of
memory, impairment of
meningitis
meningitis, recurrent
meningitis, relapse
mental retardation
mental retardation, familial
metachromatic leukodystrophy
Mexican
Mexico
microcephaly
microhemorrhage, intracerebral
migraine
migraine, children
migraine, pathogenesis
migraine, prophylaxis
migraine, treatment of
mimics
misdiagnosis
molecular genetics
mongolism
monoclonal antibodies
mononeuropathy
mononeuropathy, recurrent
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, eye of tiger sign
MRI, gradient-echo
MRI, paramagnetic effect
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, susceptibility weighted
mucopolysaccharidoses
mucopolysacchariduria
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, familial
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle biopsy
muscle spasm
muscle stiffness
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, Duchenne, neonatal screening
muscular dystrophy, Duchenne, presymptomatic detection
muscular dystrophy, female occurrence of
muscular dystrophy, limb-girdle
myelin basic protein gene
myoclonus
myopathy
myopathy, mitochondrial
myopathy, proximal
myopia
myotonia
myotonia dystrophica
neonatal screening, genetic neurologic disorders
neoplasm, metastatic to CNS
neoplasm, posterior fossa
neoplasm, primary intracranial
neoplasm, primary of CNS
neurocutaneous disease
neurodegeneration with brain iron accumulation
neuroendocrinology
neurofibroma
neurofibromatosis 1
neurofibromatosis 2
neurofibromatosis 2, presymptomatic
neurologic disease
neurologic disease, diagnoses of
neuronal ceroid-lipofuscinosis
neuronal migration disorder
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, hereditary peripheral
neuropathy, peripheral
neurotomy
next-generation sequencing
night blindness
nonsteroidal anti-inflammatory drug
Notch3 gene
ocular motility, disorders of
oculopharyngeal muscular dystrophy
olfactory bulb
optic atrophy
optic glioma
optic nerve
optic neuropathy
pain
pain, flank
PANK2 mutation
paraparesis
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
Parkinsonism syndrome
paroxysmal dystonic choreoathetosis
paroxysmal neurologic deficits
pathology
patient information and support
periodic paralysis
peroxisomal disease
pheochromocytoma
pigmentary retinopathy
polycystic kidneys
polymerase chain reaction
polyneuropathy, familial
posterior fossa, lesion of
practice guidelines
prenatal diagnosis by amniocentesis
presenilin-1 gene
presenilin-2 gene
prevention of neurologic disorders
prion disease
progeria
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive spinal muscular atrophy
proximal myotonic myopathy
pseudobulbar palsy
pseudoxanthoma elasticum
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
radiation hypersensitivity
recombinant DNA
recurrent
refractive errors
Refsum's disease
renal cell carcinoma
renal cyst
retinal degeneration
retinal hemangioma
retinal lesion
retinal tumor
retinitis pigmentosa
retinopathy
review article
RFLPs
rigidity
risk factors
Rosenthal fibers
screening
seizure
seizure, children
seizure, familial
seizure, focal
seizure, intractable, treatment of
seizure, neonatal
sensorineural hearing loss
serotonin agonist
simian crease
skin, lesions in neurologic disorders
skull x-ray, abnormal
sleep pathology and physiology
small vessel disease
small vessel disease, cerebral
Southern immunoblot test
spastic ataxia
spasticity
spinal cord
spinal cord, lesion of
spinal cord, neoplasm
spinal muscular atrophy
spine, metastasis to
spinocerebellar ataxia
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar degeneration
spondylosis
spongy degeneration of brain
startle reaction
striatal encephalitis
stuporous
subarachnoid hemorrhage
synkinesis
tapetoretinal degeneration
telangiectases
testicular enlargement
thalamus, lesion of
tinnitus
tomaculous neuropathy
trauma
treatment of neurologic disorder
trigeminovascular system
trinucleotide repeats
triptans
Usher's syndrome
ventricular garlands
vibratory sensation, abnormal
viral infection
viral infection, CNS
visual field defect
visual loss
Von Hippel Lindau
Von Hippel Lindau, carrier
Von Hippel Lindau, screening protocol for
walking, difficulty with
Werdnig-Hoffman disease
Western immunoblot test
wheelchair
white matter disease
white matter disease, subcortical
workup
X-linked bulbospinal neuronopathy
x-linked mental retardation
X-linked neuropathy
Showing articles 350 to 400 of 1870 << Previous Next >>

MR Neurography for the Diagnosis of Hypertrophic Neuropathies
Neurol 89:e201, Sgobbi de Souza, P.V.,et al, 2017

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
NEJM 377:1713-1722,1786, Mendell, J.R.,et al, 2017

CGRP - The Next Frontier for Migraine
NEJM 377:2190-2191, Hershey, A.D., 2017

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017

Pacemakers in MRI for the Neuroradiologist
AJNR 38:2222-2230, Korutz, A.W.,et al, 2017

A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
Ann Neurol 79:507-519, Vodopivec, I.,et al, 2016

Cryptogenic Stroke
NEJM 374:2065-2074, Saver, J.L., 2016

Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease
JAMA Neurol 73:668-674, Martikainen, M.H.,et al, 2016

Imaging, Intervention, and Workflow in Acute Ischemic Stroke: The Calgary Approach
AJNR 37:978-984, Zerna, C.,et al, 2016

Safety and Diagnostic Value of Brain Biopsy in HIV patients: a Case Series and Meta-Analysis of 1209 Patients
JNNP 87:722-733, Lee, A.M.,et al, 2016

A Young Man with Progressive Vision and Hearing Loss
JAMA Neurol 73:880-883, Kung, N.H.,et al, 2016

Choreoathetosis, Dystonia, and Myoclonus in 3 Siblings with Autosomal Recessive Spinocerebellar Ataxia Type 16
JAMA Neurol 73:888-890, Kawarai, T.,et al, 2016

The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification
Neurol 87:e56-e57, Saini, A.G.,et al, 2016

Neuromyelitis Optica Spectrum Disorders
UpToDate, May, Glisson,C.C., 2016

Evolutionary Pressures on the Electronic Health Record
JAMA 316:923-924, Zulman, D.M.,et al, 2016

Neurological Management of Von Hippel-Lindau Disease
Neurologist 21:73-78, Hodgson, T.S.,et al, 2016

Long-Term Preclinical Magnetic Resonance Imaging Alterations in Sporadic Creutzfeldt-Jakob Disease
Ann Neurol 80:629-632, Zanusso, G.,et al, 2016

Facial Grimacing and Sensorineural Hearing Loss in a Woman with Cirrhosis of the Liver
Neurol 87:e239, Sgobbi de Souza, P.V.,et al, 2016

A 30-year-old Man with Progressive Weakness and Atrophy
Neurol 87:e227-e230, Quinn, C.,et al, 2016

Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
NEJM 375:1879-1890, Case 34-2016, 2016

Neuroradiologic Patterns and Novel Imaging Findings in Aicardi-Goutieres Syndrome
Neurol 86:28-35, La Piana, R.,et al, 2016

Leukodystrophy and Progressive Myoclonic Epilepsy Disclosing DRPLA
Neurol 86:e58-e59, Sgobbi de Souza, P.V.,et al, 2016

MRI Findings of Biotin-Responsive Basal Ganglia Disease Before and After Treatment
Neurol 86:e71-e72, Saeedan, M.B. & Dogar, M.A., 2016

A Neonate with Micrognathia and Hypotonia
Neurol 86:e80-e84, Vawter-Lee, M.M.,et al, 2016

Hydrocephalus in Children
Lancet 387:788-799, Kahle, K.T.,et al, 2016

Computer-Assisted Diagnostic Checklist in Clinical Neurology
Neurologist 21:23-27, Finelli,P.F. and McCabe, A.L., 2016

Zika Virus as a Cause of Neurologic Disorders
NEJM 374:1506-1509, Broutet, N.,et al, 2016

Safety and Diagnostic Value of Brain Biopsy in HIV Patients: A Case Series and Meta-Analysis of 1209 Patients
JNNP 87:722-733, Lee, A.M.,et al, 2016

Wilson Disease
Yamada Textbook of Gastroenterology Chp 102, Metabolic Diseases of Liver, 6th Ed, Sunderam, S.S., & Sokol, R.J., 2016

The Effectiveness of Electronic Differential Diagnoses (DDX) Generators: A Systematic Review and Meta-Analysis
PLoS ONE 11:e0148991, Riches, N.,et al, 2016

Myasthenia Gravis
NEJM 375:2570-2581, Gilhus, N.E.,et al, 2016

Neonatal Abstinence Syndrome
NEJM 375:2468-2479, McQueen, K. & Murphy-Oikonen, J., 2016

A Woman with Intellectual Disability, Amenorrhoea, Seizures, and Balance Problems
JAMA Neurol 73:1494-1495, Hughes, A.J.C.,et al, 2016

SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
Eur J Hum Genet 24:1016-1021, Choquet,K.,et al, 2016

Primary CNS T-Cell Lymphomas: A Clinical, Morphologic, Immonophenotypic and Molecular Analysis
Am J Surg Pathol 39:1719-1729, Menon, M.P.,et al, 2015

Treatment of Brain Metastases
J Clin Oncol 33:3475-3484, Lin, X. & DeAngelis, L.M., 2015

Spinal Cord Ischemia: Practical Imaging Tips, Pearls, and Pitfalls
AJNR 36:825-830, Vargas, M.I.,et al, 2015

Stroke Prevention in Atrial Fibrillation
JAMA 313:1950-1962, Lip, G.Y.H. & Lane, D.A., 2015

Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use
Neurol 84:e165-e169, Whitlock, J.B.,et al, 2015

Care and Outcomes of Patients with In-Hospital Stroke
JAMA Neurol 72:749-755,746, Saltman, A.P.,et al, 2015

A 28-year-old Woman with Lower Extremity Spasticity and Microcytic Anemia
Neurol 85:e11-e14, Bonda, C.,et al, 2015

Screening with MRI for Accurate and Rapid Stroke Treatment
Neurol 84:2438-2444, 2394, Shah, S.,et al, 2015

A 51-year-old Woman with Weakness and Stiff Neck
Neurol 85:e32-e36, Kassardjian, C.D. & Milone, M., 2015

Characyeristic features and progression of abnormalities on MRI for CARASIL
Neurol 85:459-463, Sekine, Y., etal, 2015

A 27-Year Old Man with Rapidly Progressive Coma
Neurol 85:e74-e78, Wong,J.M.,et al, 2015

Recognizing Autoimmune-Mediated Encephalitis in the Differential Diagnosis of Limbic Disorders
AJNR 36:2196-2205, da Rocha, A.J.,et al, 2015

Molybdenum Cofactor Deficiency
Neurol 85:e175-e178, Nagappa, M.,et al, 2015

Epilepsy in Adults with Mitochondrial Disease: A Cohort Study
Ann Neurol 78:949-957, Whittaker, R.G.,et al, 2015

DARS-Associated Leukoencephalopathy can Mimic a Steroid-Responsive Neuroinflammatory Disorder
Neurol 84:226-230,218, Wolf, N.I.,et al, 2015



Showing articles 350 to 400 of 1870 << Previous Next >>