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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 400 to 450 of 1870 << Previous Next >>

A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
Ann Neurol 77:1-7, Scripko, P.,et al, 2015

Encephalitis of Unclear Origin Diagnosed by Brain Biopsy
JAMA Neurol 72:66-72, Gelfand, J.M.,et al, 2015

The Tablet Device in Hospital Neurology and in Neurology Graduate Medical Education: A Preliminary Study
Neurohosp 5:15-21, George, P.,et al, 2015

Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
NEJM 372:1151-1162, Miller, B.L.,et al, 2015

Beyond Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: An IOM Report on Redefining an Illness
JAMA 313:1101-1102, Clayton, E.W., 2015

Short Stature, Imperforate Anus, and Polydactyly
Neurol 84:e117, Dumitrascu, O.,et al, 2015

A Case of Refractory Nocturnal Seizures
Neurol 84:e134-e136, Pavlakis, P.P. & Douglass, L.M., 2015

Rapid Assessment and Treatment of Transient Ischemic Attacks and Minor Stroke in Canadian Emergency Departments
Stroke 46:2987-2990, Kamal, N.,et al, 2015

Non-Alzheimers Dementia 1 Frontotemporal Dementia
Lancet 386:1672-1682, Bang, Jee.,et al, 2015

Paroxysmal Kinesigenic Dyskinesia
Neurol 85:1546-1553, Huang, X.J.,et al, 2015

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Creutzfeldt-Jakob Disease (Subacute Spongiform Encephalopathy)
Adams & Victors Principles of Neurology, Chp 33, pg 769, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Gertsmann-Straussler Schneinker Syndrome
Adams & Victors Principles of Neurology, Chp 33, pg 773, Ropper, A.H.,et al, 2014

Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Pseudotumor Cerebri
Adams & Victors Principles of Neurology, Chp 30, pg 628, Ropper, A.H.,et al, 2014

Intracranial Neoplasms and Paraneoplastic Disorders, Oligodendroglioma
Adams & Victors Principles of Neurology, Chp 31, pg 654, Ropper, A.H.,et al, 2014

Intracranial Neoplasms and Paraneoplastic Disorders, Meningioma
Adams & Victors Principles of Neurology, Chp 31, pg 656, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Pyridoxine Dependent Seizures
Adams & Victors Principles of Neurology, Chp 37, pg 951, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Galactosemia
Adams & Victors Principles of Neurology, Chp 37, pg 951, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Tay Sachs Disease
Adams & Victors Principles of Neurology, Chp 37, pg 957, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Infantile Gaucher Disease
Adams & Victors Principles of Neurology, Chp 37, pg 958, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Infantile Niemann-Pick Disease
Adams & Victors Principles of Neurology, Chp 37, pg 958, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Globoid Cell Leukodystrophy (Krabbe Disease, Galactocerebrosidase)
Adams & Victors Principles of Neurology, Chp 37, pg 959, 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, Metachromatic Leukodystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 971, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Neuroaxonal Dystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 972, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Hepatolenticular Degeneration (Wilson Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 982, Ropper, A.H.,et al, 2014

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, Fabry Disease
Adams & Victors Principles of Neurology, Chp 37, pg 991, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Alzheimer Disease
Adams & Victors Principles of Neurology, Chp 39, pg 1063, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Familial Dementia with Spastic Paraparesis
Adams & Victors Principles of Neurology, Chp 39, pg 1081, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Parkinson Disease
Adams & Victors Principles of Neurology, Chp 39, pg 1082, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Friedreich Ataxia
Adams & Victors Principles of Neurology, Chp 39, pg 1102, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Cerebellar Degeneration
Adams & Victors Principles of Neurology, Chp 39, pg 1105, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Olivopontocerebellar Atrophy
Adams & Victors Principles of Neurology, Chp 39, pg 1106, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Machado-Joseph-Azorean Disease
Adams & Victors Principles of Neurology, Chp 39, pg 1107, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1109, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Werdnig-Hoffman Disease, Spinal Muscular Atrophy
Adams & Victors Principles of Neurology, Chp 39, pg 1116, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Kugelberg-Welander Syndrome SMAIII
Adams & Victors Principles of Neurology, Chp 39, pg 1118, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Kennedy Syndrome (X-Linked Bulbospinal Muscular Atrophy)
Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Hereditary Spastic Paraplagia
Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014

Cerebral Venous Thrombosis
Stroke 45:e16-e18, Gulati, D.,et al, 2014

Chronic and Slowly Progressive Weakness of the Legs and Hands
BMJ 348:g459, Nightingale, H.,et al, 2014

Bannayan-Riley-Ruvalcaba Syndrome: MRI Neuroimaging Features in a Series of 7 Patients
AJNR 35:402-406, Bhargava, R.,et al, 2014

Neuronal Intranuclear Inclusion Disease Cases with Leukoencephalopathy Diagnosed via Skin Biopsy
JNNP 85:354-356, Sone, J.,et al, 2014

Neuroimaging in Intracerebral Hemorrhage
Stroke 45:903-908, Macellari, F.,et al, 2014

Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
NEJM 370:911-920, Zhou, Q.,et al, 2014

Autism
Lancet 383:896-910, Lai, M.C.,et al, 2014

Long-Term Safety and Tolerability of ProSavin, a Lentiviral Vector-Based Gene Therapy for Parkinsons Disease: A Dose Escalation, Open-Label, Phase 1/2 Trial
Lancet 383:1138-1146,1107, Palfi, S.,et al, 2014

Griscelli Syndrome and CNS Lymphohistiocytosis
Neurol 82:e122-e123, Saini, A.G.,et al, 2014

Parkinson Disease Subtypes
JAMA 71:499-504, Thenganatt, M. & Jankovic, J., 2014

ICU-Acquired Weakness and Recovery from Critical Illness
NEJM 370:1626-1635, Kress, J.P. & Hall, J.B., 2014



Showing articles 400 to 450 of 1870 << Previous Next >>