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acid maltase deficiency
acid maltase deficiency, adult
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
alpha glucosidase
alpha-synuclein
Alzheimer's disease
Alzheimer's disease, treatment of
anesthesia, general
anterior horn cell disease
arthritis
aspartate aminotransferase
asymptomatic
atidarsagene autotemcel
biologic markers
bone marrow transplantation
bradykinesia
calf hypertrophy
cardiomyopathy
carotid artery disease
cataracts
central nervous system, infection of
cerebrovascular accident
cerebrovascular disease
ceruloplasmin, serum
chelation therapy
children
choreoathetosis
chromosomal abnormality
cirrhosis
clinical trials
coenzyme Q10 deficiency
complications
congestive heart failure
copper
copper metabolism, abnormal
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
degenerative diseases of CNS
dementia, childhood
demyelinating disease
developmental retardation
diet
differential diagnosis
dysarthria
dyskinesia
dysphagia
dystonia
dystroglycanopathies
dystrophin
efficacy
Emery-Dreifuss muscular dystrophy
enzyme treatment
enzyme, defect
epidemiology of neurology
ethambutol
ethics in neurology
fatty acid, elevated plasma content
Gaucher's disease
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glioblastoma multiforme(astrocytoma Gr.III)
glutamic acid decarboxylase
glycogen storage disease
Gowers maneuver
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), screening for
hepatomegaly
history of neurology
Hurler's syndrome
hypogonadism
hypotonia
in situ hybridization
inborn errors of metabolism, screening
Kayser-Fleischer ring
Kearns-Sayre syndrome
L-dopa
Leber's hereditary optic neuropathy
Leigh's disease
Lesch-Nyhan syndrome
leukemia
leukocyte enzyme abnormality
leukodystrophy
Lewy body
life expectancy
lipid storage disorder of CNS
liver disease
liver transplantation
Lorenzo's oil
lysosomal storage disease
lysosomes, abnoral
MELAS syndrome
MERRF syndrome
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
metachromatic leukodystrophy, late-infantile
mimics
misdiagnosis
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mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
mortality
motor neuron disease
motor system
MRI
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mucopolysaccharidoses
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muscle weakness
muscular dystrophy
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muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
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muscular dystrophy, classification
muscular dystrophy, congenital
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muscular dystrophy, Duchenne, carrier
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muscular dystrophy, limb-girdle
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myoblast transfer
myopathy, mitochondrial
myopathy, quadriceps
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Parkinson disease, pathogenesis of
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
peroxisomal disease
polymerase chain reaction
Pompe's disease of glycogen storage
preclinical
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
progressive neurologic disorder
ProSavin
psychiatric problems in neurologic disorders
quality of life
respirator
respiratory failure
review article
rigidity
rippling muscle disease
safety
scoliosis
screening
seizure
sham surgery
sinemet
skin, darkening of
SMN1 gene
spinal muscular atrophy
spinal muscular atrophy, classification
stem cell transplantation
steroid
steroid therapy, CNS treatment and complications with
stimulation, deep brain
subarachnoid hemorrhage
subthalamic nucleus
survival motor neuron gene
synucleinopathy
systemic illness
testicular atrophy
toe walking
tongue, enlarged
treatment of neurologic disorder
tremor
viral infection
viral infection, CNS
weakness
weakness, progressive
weakness, proximal
web sites
Werdnig-Hoffman disease
white matter disease
Showing articles 250 to 300 of 1660 << Previous Next >>

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

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

Bionic Reconstruction to Restore Hand Function After Brachial Plexus Injury: A Case Series of Three Patients
Lancet 385:2183-2189, Aszmann, O.C.,et al, 2015

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

Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
JNNP 86:774-781, Van Egmond, M.E.,et al, 2015

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

Futile Interhospital Transfer for Endovascular Treatment in Acute Ischemic Stroke
Stroke 46:2156-2161, Fuentes, B.,et al, 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

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

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

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

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

Neuroimaging and Clinical Features in Type II (late-onset) Alexander Disease
Neurol 82:49-56, Graff-Radford, J.,et al, 2014

Cerebral Abnormalities in Adults with Ataxia-Telangiectasia
AJNR 35:119-123, Lin, D.D.M.,et al, 2014

Early Transfer of Patients with Stroke to Comprehensive Centers is Necessary
Stroke 45:3748-3749,3752, Sheth, K.N., 2014

Early Transfer of Patients with Stroke to Comprehensive Stroke Centers is not Necessary
Stroke 45:3750-3751,3752, Langhorne, P., 2014

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

Polycythemia Vera Presenting with Ischemic Strokes in Multiple Arterial Territories
Neurol 82:e168-e170, Billakota, S. & Husseini, N.E., 2014

Brugada Syndrome in Spinal and Bulbar Muscular Atrophy
Neurol 82:1813-1821, Araki, A.,et al, 2014

Familial Risk of Cerebral Palsy: Population Based Cohort Study
BMJ 349:g4294, g4514, Tollanes, M.C.,et al, 2014

Red Papules on the Tongue of a Patient with Hemiparesis
JAMA 312:741-742, Chiu, H.Y. & Lin, S.J., 2014

Somatic Mutations in Cerebral Cortical Malformations
NEJM 371:733-743, Jamuar, S.S.,et al, 2014

A 52-year-old Woman with Progressive Proximal Weakness
Neurol 83:e106-e109, Enduri, S.,et al, 2014

Clinicopathologic Conference, Severe Methylenetetrahydrofolate Reductase Deficiency
NEJM 371:847-858, Case 27-2014, 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

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

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



Showing articles 250 to 300 of 1660 << Previous Next >>