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acyl CoA dehydrogenase deficiency
adrenoleukodystrophy
advances in neurology
alveolar hypoventilation
amniocentesis
anesthesia, general
arrhythmia, cardiac
aspiration
asymptomatic
ataxia
ataxia, hereditary
atrial fibrillation
atrial paralysis
atrioventricular block
autoimmune disease
baldness
cachexia
calf atrophy
calf hypertrophy
carcinoma
cardiomyopathy
cataracts
central nervous system, infection of
cerebral embolism
cerebral embolism, carotid origin
cerebrovascular accident
cerebrovascular accident, cardiac disease causing
cerebrovascular accident, young adult
children
chromosome 19
chromosome 3
Clinical Pathologic Conference(C.P.C.)
complications
confidentiality
congenital birth defects
congenital heart disease
contractures, joint
creatine phosphokinase(CPK)elevated
degenerative diseases of CNS
delay in diagnosis
descending paralysis
developmental retardation
diagnostic criteria
differential diagnosis
difficulty climbing stairs
distal muscle weakness
DNA probes
dropped head syndrome
dystrophin
echocardiogram
electrocardiogram, abnormal
electromyogram
Emery-Dreifuss muscular dystrophy
enzyme, defect
enzyme, muscle disease
ethics in neurology
facial appearance, abnormal
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
familial
family planning
fine motor function, impaired
foot drop
fragile-X syndrome
frontal balding
gait disorder
gait, waddling
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gowers maneuver
heart block
high arched palate
Huntington's chorea
hypercapnia
implantable cardioverter defibrillator
inborn errors of metabolism
inborn errors of metabolism, screening
learning disability
learning disability, in children
lid closure, weakness of
liver function enzymes
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve prolapse
molecular genetics
mortality
muscle atrophy, progressive
muscle biopsy
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, Duchenne, neonatal screening
muscular dystrophy, Duchenne, presymptomatic detection
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myoglobinuria
myopathy
myotonia
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
neck weakness
neonatal screening, genetic neurologic disorders
neoplasm, metastatic to CNS
neoplasm, primary intracranial
neoplasm, primary of CNS
nerve conduction studies
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neuronal migration disorder
neuropathy, hereditary peripheral
pacemaker, cardiac-transvenous
percussion induced muscle contraction
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proximal muscle atrophy
proximal myotonic myopathy
ptosis
review article
rhabdomyolysis
screening
shoulder-girdle wasting
slit lamp examination
speech disorder, childhood
speech, delayed development of
spinocerebellar ataxia
spinocerebellar degeneration
systemic illness
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
term infant
toe walking
treatment of neurologic disorder
trinucleotide repeats
tripping
ultrasonography
urine, dark
viral infection, CNS
weakness
weakness, progressive
weakness, proximal
wheelchair
whistle, inability to
winging of scapula
X-linked bulbospinal neuronopathy
x-linked hydrocephalus
x-linked mental retardation
Showing articles 500 to 550 of 1780 << Previous Next >>

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

Nusinersen Versus Sham Control in Infantile-Onset Spinal Muscular Atrophy
NEJM 377:1723-1732,1786, Finkel, R.S.,et al, 2017

Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
JAMA Neurol 74:737-740, Cohen, A.L.,et al, 2017

Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017

A 10-year-old boy with Bilateral Vision Loss
Neurol 88:e221-e224, Bulwa, Z.,et al, 2017

Buprenorphine for the Treatment of the Neonatal Abstinence Syndrome
NEJM 376:2341-2348, Kraft, W.K.,et al, 2017

Bipolar II Disorder as the Initial Presentation of CADASIL:An Underdiagnosed Manifestation
Neuropsych Dis Treat 13:2175-2179, Wang,J.,et al, 2017

Cerebellar Ataxia and Hearing Impairment
JAMA Neurol 74:243-244, Lin, C.Y. & Kuo, S.H., 2017

Clinicopathologic Conference, Vascular Malformations in Liver, Stomach, Esophagus, and Lungs that are Consistent with Hereditary Hemorrhagic Telangiectasia, Complicated
NEJM 376:972-980, Case 7-2017, 2017

Prehospital Emergency Care in Childhood Arterial Ischemic Stroke
Stroke 48:1095-1097, Stojanovski, B.,et al, 2017

Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
Neurol 88:1478-1479, Masson, R.,et al, 2017

Patient with Severe Moyamoya Disease Who Presents with Acute Cortical Blindness
Stroke 48:e126-e129, Sajja, A.,et al, 2017

A Child with Delayed Motor Milestones and Ptosis
Neurol 88:e158-e163, Ghosh, P.S., 2017

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

Use of MRI in the Diagnosis of Fetal Brain Abnormalities in Utero (MERIDIAN): A Multicentre, Prospective Cohort Study
Lancet: 389:538-546,483, Griffiths, P.D.,et al, 2017

Clinicopathologic Conference, Posterior Cortical Atrophy with Frontotemporal Lobe Dementia with Gene Mutation
JAMA Neurol 74:114-118, , 2017

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

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

Chikungunya Virus-Associated Encephalitis
Neurol 86:94-102, Gerardin, P.,et al, 2016

Zika Virus Associated with Microcephaly
NEJM 374: DOI:10.1056/NEJMoa1600651, Mlakar, J.,et al, 2016

A 62-Year-Old Woman with Bizarre Behavior and Recurrent Episodes of Behavioral Arrest
Neurol 86:e62-e65, Briglia, H.,et al, 2016

Minimally Invasive Surgery for Intracerebral and Intraventricular Hemorrhage
Stroke 47:1399-1406, Fiorella, D.,et al, 2016

Thiamine Deficiency Presenting as Intraventricular Hemorrhage
Stroke 47:e95-e97, Al-Bayati, A.R.,et al, 2016

Performance of Bedside Stroke Recognition Tools in Discrimination Childhood Stroke from Mimics
Neurol 86:2154-2161, Mackay, M.T.,et al, 2016

Mills Syndrome
Neurol 87:e54, Porto, F.H.G.,et al, 2016

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

Physician-Assisted Death
Neurol 87:1152-1160, Abrahao, A.,et al, 2016

Congenital Zika Virus Syndrome in Brazil: A Case Series of the first 1501 livebirths with complete investigation
Lancet 388:891-897, Franca, G.V.A.,et al, 2016

Zika Virus: An Emergent Neuropathological Agent
Ann Neurol 80:479-489, White, M.K.,et al, 2016

Candida Infections of the Central Nervous System
UptoDate Jan, Kauffman, C.A., 2016

Listeria infections in Neonates
Neoreviews 17:e515-e520, McKinney, J.S., 2016

Moyamoya Disease Presenting with Subarachnoid Hemorrhage: Clinical Features and Neuroimaging of a Case Series
Brit J Neurosurg 29:804-810, Wan, M.,et al, 2015

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

A Case of Hirayama Disease Presenting with Polymyoclonus
Neurol 85:e156, Ong, J.J.Y.,et al, 2015

Complex Regional Pain Syndrome
Neurol 84:89-96, Birklein, F.,et al, 2015

Community Based Case-Control Study of Childhood Stroke Risk Associated with Congenital Heart Disease
Stroke 46:336-340, Fox, C.K.,et al, 2015

Acute Ischemic Stroke in Pediatric Patients
Stroke 46:e32-e33, Mittal, S.O.,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

Two Cases of Congenital Myasthenic Syndrome with Vocal Cord Paralysis
Neurol 84:1281-1282, Al-Shahoumi, R.,et al, 2015

Owls Eye Sign
Neurol 84:1500, Kumar, S.,et al, 2015

Clinicopathologic Conference, Primitive Neuroectodermal Tumor of CNS, with Involvement of Thalamus, Medial Cerebral Cortex, Brainstem, Cerebellum and Subarachnoid Space
NEJM 372:1550-1562, Case 12-2015, 2015

Clinicopathologic Conference, CAT Scratch Disease (Encephalopathy Associated with Bartonella Henselae)
NEJM 372:2050-2058, Case 16-2015, 2015

Guidelines for the Management of Spontaneous Intracerebral Hemorrhage
Stroke 46:2032-2060, Hemphill, J.C.,et al, 2015

Radiation Necrosis in Pediatric Patients with Brain Tumors Treated with Proton Radiotherapy
AJNR 36:1572-1578, Kralik, S.F.,et al, 2015

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

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

Responsibilities of Health Care PRofessionals in Counseling and Educating Patients with Incurable Neurological Diseases Regarding "Stem Cell Tourism"
JAMA Neurol 72:1342-1345, Bowman, M.,et al, 2015

Cavernous Sinus Thrombosis in Children
Stroke 46:2657-2660, Press, C.A.,et al, 2015

Recurrent Stroke in Childhood Cancer Survivors
Neurol 85:1056-1064, Fullerton, H.J.,et al, 2015

Predominant Intraventricular Hemorrhage From a Ruptured Posterior Communicating Artery Aneurysm
Neurohosp 4:164, Nakagawa, K. & Lee, S.B, 2014



Showing articles 500 to 550 of 1780 << Previous Next >>