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acanthocytosis
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, medical precautions with
adducted thumb
advances in neurology
adverse drug reaction
agenesis of corpus callosum
alpha-fetoprotein
amniocentesis
anterior horn cell disease
anterior tibial muscle weakness
anticonvulsants
anticonvulsants, absorption
anticonvulsants, bioavailability
anticonvulsants, blood level determination of
anticonvulsants, compliance
anticonvulsants, subtherapeutic
anticonvulsants, teratogenicity of
anticonvulsants, untoward effects of
arbovirus
areflexia
arthralgia
ataxia, cerebellar
autoimmune disease
Bassen-Kornzweig syndrome
blindness
Brazil
breast feeding
calcification, intracranial
carcinoma
cardiomyopathy
caribbean
CAT scan
CAT scan, muscle
cataracts
Central America
central core disease
central nervous system, infection of
children
chromosomal abnormality
chromosome 5
clinodactyly
Cockayne's syndrome
complications
congenital birth defects
congenital deformities
congenital heart disease
congenital heart disease, CNS complications with
congenital malformation
congenital myopathy
congenital myopathy, inflammatory
consanguinity
contractures, joint
cornea, abnormal
counselling
creatine phosphokinase(CPK)elevated
cryptorchidism
deafmute
deafness
degenerative diseases of CNS
developmental abnormality of brain
developmental disability
developmental retardation
differential diagnosis
digits, abnormal
disability, neurological
drug induced neurologic disorders
dwarfism
dysmorphic
dystroglycanopathies
dystrophin
ear, abnormal
echocardiogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
Emery-Dreifuss muscular dystrophy
enzyme, induction
epidemic
epidemiology of neurology
exostosis
facial anomalies
facial appearance, abnormal
facial weakness, bilateral
facioscapulohumeral syndrome
familial
fasciculation
feeding disorder
fetus
fever
flavivirus
floppy infant
folic acid
foot drop
Friedreich's ataxia
gargoylism
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
glaucoma
Guillain Barre syndrome
hair, loss
Hallgren's syndrome
head circumference
headache
hearing loss
heart block
hemorrhagic diathesis
hepatosplenomegaly
histochemistry
histochemistry of muscle
human immunodeficiency virus type 1
Huntington's chorea
Hurler's syndrome
hydrocephalus
hydrocephalus, congenital
hydrocephalus, fetal
hydrocephalus, intrauterine
hyperkalemic periodic paralysis
hypertelorism
hypertrophic cardiomyopathy
hypokalemic periodic paralysis
hyporeflexia
hypotonia
hypotonia, infants
immunohistochemistry
inclusion body myositis
infection
intellectual deficit
intrauterine
intrauterine infection
intrauterine infection, viral
joint hypermobility
karyotyping
Kearns-Sayre syndrome
keratoconus
lamotrigine
Laurence-Moon-Bardet-Biedl syndrome
levonorgestrel
lid closure, weakness of
life expectancy
lissencephaly
lordosis
malformation, CNS, congenital
mental retardation
merosin
microcephaly
microdactyly
micrognathia
Miller-Dieker syndrome
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
mononeuritis multiplex
mortality
mosquito
motor neuron disease
MRI
MRI, abnormal
MRI, fetal
MRI, intrauterine
MRI, muscle
mucopolysaccharidoses
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle pain
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
muscular dystrophy, neurogenic hypothesis of
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myoglobinuria
myopathy
myopathy, centronuclear
myopathy, distal
myopathy, drug-induced
myopathy, mitochondrial
myopia
myositis
myositis ossificans, progressive
myotonia congenita
myotonia dystrophica
nasal bridge, wide
neck, webbed
nemaline rod myopathy
neoplasm, primary of CNS
neuritis
neurologic disease, diagnoses of
neuronal migration disorder
neuropathology
neuropathy
neuropathy, ataxic
neuropathy, painful
neuropathy, peripheral
Noonan Syndrome
nusinersen
obesity
obstetric neurologic injuries
ocular myopathy
oculopharyngeal muscular dystrophy
oral contraceptives
paraparesis
paraparesis, spastic
patient information and support
pectus excavatum
periodic paralysis
polydactyly
polyhydramnios
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polymyositis
polymyositis, infantile
polyneuropathy, chronic inflammatory demyelinating
practice guidelines
pregnancy, anticonvulsants during
pregnancy, neurologic complications in
prenatal
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
pseudoretinitis pigmentosa
psychiatric disorder
pulmonary stenosis
quality of life
rash
respirator
respiratory failure
retinitis pigmentosa
retinopathy
review article
rhabdomyolysis
schizophrenia
scoliosis
scoliosis, neurologic association with
screening
seizure
seizure, children
seizure, injury following
seizure, pregnancy
seizure, treatment of
seizure, treatment of, monotherapy
seizure, women
short stature
short thumb
skin, biopsy
skin, lesions in neurologic disorders
SMN1 gene
South America
Spielmeyer Vogt syndrome
spinal muscular atrophy
spinal muscular atrophy, classification
steroid
systemic illness
tongue, fasciculations of
trauma
treatment of neurologic disorder
trinucleotide repeats
tubular aggregates, muscle
ultrasonography
ultrasonography, head
ultrasonography, head, fetus-neonate
Usher's syndrome
valvulopathy
viral infection
viral infection, CNS
visual field defect
visual fields, constricted
visual impairment
vitamin K
vitamin supplementation
vomiting, recurrent
weakness
weakness, congenital
weakness, generalized
weakness, progressive
wheelchair
whistle, inability to
winging of scapula
x-linked hydrocephalus
Zika virus infection
Showing articles 1050 to 1100 of 4195 << Previous Next >>

Cerebral Mitochondrial Microangiopathy Leads to Leukoencephalopathy in Mitochondrial Neurogastrointestinal Encephalopathy
AJNR 39:427-434, Gramegna, L.L.,et al, 2018

Value of the Central Vein Sign at 3T to Differentiate MS from Seropositive NMOSD
Neurol 90:e1183-e1190, Cortese, R.,et al, 2018

A 42-year-old man with unilateral leg weakness
Neurol 90:e1085-e1090, Schneider, R.,et al, 2018

Neonatal Abstinence Syndrome
JAMA 319:1362-1374, Wachman, E.,et al, 2018

Practice Guide Update Summary: Mild Cognitive Impairment
Neurol 90:126-135, Petersen, R.C.,et al, 2018

Diagnosis of Cerebral Amyloid Angiopathy
Stroke 49:491-497, Greenberg, S.M.,et al, 2018

Optic Nerve Head Edema Among Patients Presenting to the Emergency Department
Neurol 90:e373-e379, Sachdeva, V.,et al, 2018

Persistent Postural-Perceptual Dizziness (PPPD): A Common, Characteristic and Treatable Cause of Chronic Dizziness
Pract Neurol 18:5-13, Popkirov, S.,et al, 2018

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Maternal Use of antiepileptic Agents During Pregnancy and Major Congenital Malformations in Children
JAMA 318:1700-1701, Bromley, R.L.,et al, 2017

Clinicopathologic Conference, Paroxysmal Nocturnal Hemoglobinuria
NEJM 377:2581-2590, Case 40-2017, 2017

Guillain-Barre Syndrome following tuberculosis: A rare association
J Neurosci Rural Pract 8:296-299, Lakhotia, A.N.,et al, 2017

The Future of the Neurologic Examination
JAMA Neurol 74:1291-1292, Aminoff, M.J., 2017

Long-Term Benefit of Enzyme Replacement Therapy in Pompe Disease
Neurol 89:2365-2373, Kuperus, E.,et al, 2017

Population-based Study of Ischemic Stroke Risk after Trauma in Children and Young Adults
Neurol 89:2310-2316, Fox, C.K.,et al, 2017

Paraneoplastic and Autoimmune Encephalitis
UptoDate July, Dalmau, J.,et al, 2017

A Comparative Study of CIDP in a Cohort of HIV-Infected and HIV-Uninfected Patients
Neurol Neuroimmunol Neuroinflamm 4:e315, Moodley, K.,et al, 2017

Subarachnoid Hemorrhage
NEJM 377:257-266, Lawton, M.T. & Vates, G.E., 2017

A 15-month-old boy with Progressive Lethargy and Spasticity
Neurol 89:e135-e139, Zhang, R.,et al, 2017

Neurologic Complications Associated with the Zika Virus in Brazilian Adults
JAMA Neurol 74:1190-1198,1164, Ferreira da Silva, I.R.,et al, 2017

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

A 50-year-old Woman with SLE and a Tumefactive Lesion
Neurol 89:e140-e145, Choi, J.H.,et al, 2017

Recrudescence of Deficits After Stroke
JAMA Neurol 74:1048-1055, Topcuoglu, M.A.,et al, 2017

Endovascular Therapies for Acute Ischemic Stroke in Children
Stroke 48:2026-2030, Huang, M.I.,et al, 2017

Diagnosis and Management of Dementia with Lewy Bodies
Neurol 89:88-100, McKeith, I.G.,et al, 2017

A New Potential Biomarker for Dementia with Lewy Bodies
Neurol 89:318-326, Donadio, V.,et al, 2017

Lumbar Puncture Test in Normal Pressure Hydrocephalus: Does the Volume of CSF Removed Affect the Response to Tap?
AJNR 38:1456-1460, Thakur, S.K., et al, 2017

Nonmicrocephalic Infarcts with Congenital Zika Syndrome Suspected Only after Neuroimaging Evaluation Compared with Those with Microcephaly at Birth and Postnatally: How Large is the Zika Virus "Iceberg"?
AJNR 38:1427-1434, Aragao, M.F.V.V.,et al, 2017

Migraine
NEJM 377:553-561, Charles, A., 2017

Cerebral Amyloid Angiopathy-Related Inflammation Presenting with Isolated Leptomeningitis
Neurol 89:e66-e67, Kang, P.,et al, 2017

Introduction of a Dedicated Emergency Department MR Imaging Scanner at the Barrow Neurological Institute
AJNR 38:1480-1485, Buller, M. & Karis, JP, 2017

Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
AJNR 38:1467-1474, Bond, K.M.,et al, 2017

Overview of IgG4-related Disease
UptoDate, July, Moutsopoulos,H.,et al, 2017

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

Pregabalin Use Early in Pregnancy and the Risk of Major Congenital Malformations
Neurol 88:2020-2025, Patorno, E.,et al, 2017

"Phacing" a New Cause of Carotid Artery Dissection
Neurologist 22:54-56, Kulyk, C.,et al, 2017

Primary Angiitis of the Central Nervous System
Stroke 48:1248-1255, Boulouis, G.,et al, 2017

Pregnancy, Hormonal Treatments for Infertility, Contraception, and Menopause in Women After Ischemic Stroke
Stroke 48:501-506, Caso, V.,et al, 2017

Autopsy Validation of ���I-FP-CIT Dopaminergic Neuroimaging for the Diagnosis of DLB
Neurol 88:276-283, Thomas, A.J.,et al, 2017

Diagnostic Challenges and Clinical Characteristics of Hepatitis E Virus-Associated Guillain-Barre Syndrome
JAMA Neurol 74:26-33, Stevens, O.,et al, 2017

Clinical Decision-Making in Functional and Hyperkinetic Movement Disorders
Neurol 88:118-123,114, van der Salm, S.M.A.,et al, 2017

Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
Neurologist 22:1-13, Kalman, B., 2017

Investigations in GABA? Receptor Antibody-Associated Encephalitis
Neurol 88:1012-1020,1010, Spatola, M.,et al, 2017

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

Diagnosis of Multiple Sclerosis: Progress and Challenges
Lancet 389:1336-1346, Brownlee, W.J.,et al, 2017

Neurological Autoantibody Prevalence in Epilepsy on Unknown Etiology
JAMA Neurol 74:397-402,384, Dubey, D.,et al, 2017

ED Misdiagnosis of Cerebrovascular Events in the Era of Modern Neuroimaging
Neurol 88:1468-1477, Tarnutzer, A.A.,et al, 2017

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

Cervical Artery Dissection in Patients = 60
Neurol 88:1313-1320, Traenka, C.,et al, 2017

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



Showing articles 1050 to 1100 of 4195 << Previous Next >>