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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
dysphagia
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
immunomodulation
immunosuppressive agents
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
monoclonal gammopathy
monoclonal gammopathy of uncertain significance
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, acquired
myopathy, amyloid
myopathy, centronuclear
myopathy, distal
myopathy, drug-induced
myopathy, glycogen storage
myopathy, mitochondrial
myopathy, scleromyxedema
myopia
myositis
myositis ossificans, progressive
myotonia congenita
myotonia dystrophica
nasal bridge, wide
neck, webbed
nemaline rod myopathy
nemaline rod myopathy, adult onset
neoplasm, primary of CNS
neuritis
neurologic complications of, systemic disease
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
old age, neurology of
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
stem cell transplantation
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
weight loss
wheelchair
whistle, inability to
winging of scapula
x-linked hydrocephalus
Zika virus infection
Showing articles 1250 to 1300 of 4285 << Previous Next >>

Stepwise Paralysis in a Patient with Adenocarcinoma of Lung
Neurol 86:e122-e127, Furlan, J.C.,et al, 2016

Clinicopathologic Conference, Cerebral Infarction from Internal Carotid Occlusion Related to Sickle Cell Arteriopathy
NEJM 374:1265-1275, Case 10-2016, 2016

Guillain-Barre Syndrome Outbreak Associated with Zika Virus Infection in French Polynesia: A Case-Control Study
Lancet 387:1531-1539,1486, Cao-Larmeau, V-M., et al, 2016

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

National Characteristics and Predictors of Neurology 30-day Readmissions
Neurol 86:669-675, Guterman, E.L.,et al, 2016

Pseudotumoral Presentation of Cerebral Amyloid Angiopathy-Related Inflammation
Neurol 86:912-919, Ronsin, S.,et al, 2016

Aneurysmal Subarachnoid and Spinal Hemorrhage Associated with Systemic Lupus Erythematosus
Stroke 47:e42-e45, Harriott, A.,et al, 2016

Missed Ischemic Stroke Diagnosis in the Emergency Department by Emergency Medicine and Neurology Services
Stroke 47:668-673, Arch, A.E.,et al, 2016

PCR Testing for the Diagnosis of Herpes Simplex Virus in Patients with Encephalitis or Meningitis
UpToDate, Dec, Caliendo, A.M., 2015

Cerebral Fat Embolism
Stroke 46:e251-e253, Mijalski, C.,et al, 2015

Practice Guideline: Idiopathic Normal Pressure Hydrocephalus: Response to Shunting and Predictors of Response
Neurol 85:2063-2071, Halperin, J.J.,et al, 2015

Bells Palsy: Aetiology, Clinical Features and Multidisciplinary Care
JNNP 86:1356-1361, Eviston, T.J.,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

Nigrosome 1 Detection at 3T MRI for the Diagnosis of Early-Stage Idiopathic Parkinson Disease: Assessment of DIagnostic Accuracy and Agreement on Imaging Asymmetry and Clinical Laterality
AJNR 36:2010-2016, Noh, Y.,et al, 2015

International Consensus Diagnostic Criteria for Neuromyelitis Optica Spectrum Disorders
Neurol 85:177-189, Wingerchuk, D.M.,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

Reversible Cerebral Vasoconstriction Syndrome, Part 1: Epidemiology, Pathogenesis, and Clinical Course
AJNR 36:1392-1399, Miller, T.R.,et al, 2015

CIDP Diagnostic Pitfalls and Perception of Treatment Benefit
Neurol 85:498-504, Allen, J.A. & Lewis, R.A., 2015

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

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

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

Inflammatory Cerebral Amyloid Angiopathy, Amyloid-B-Related Angiitis, and Primary Angiitis of the Central Nervous System
Stroke 46:e210-e213, Moussaddy, A.,et al, 2015

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

Non-Alzheimers Dementia 2 Lewy Body Dementias
Lancet 386:1683-1697, Walker, Z.,et al, 2015

Non-Alzheimers Dementia 3 Vascular Dementia
Lancet 386:1698-1706, OBrien, J.T. & Thomas, A., 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

Automated Differentiation between Epileptic and Nonepileptic Convulsive Seizures
Ann Neurol 77:348-351, Beniczky, S.,et al, 2015

Clinical Neurology: Why this Still Matters in the 21st Century
JNNP 86:229-233, Nicholl, D.J. & Appleton, J.P., 2015

Clinical Laboratory and Findings of 21 Patients with Radiation-Induced Myopathy
JNNP 86:152-158, Ghosh, P.S. & Milone M., 2015

Is it a Stroke?
BMJ 350:h56, Hankey, G.J. & Blacker, D.J., 2015

Multiple-System Atrophy
NEJM 372:249-263, Fanciulli, A. & Wenning, G.K., 2015

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

The Durability of Endovascular Coiling Versus Neurosurgical Clipping of Ruptured Cerebral Aneurysms: 18 Year Follow-Up of the UK Cohort of the International Subarachnoid Aneurysm Trial (ISAT)
Lancet 385:691-697,666, Molyneux, A.J.,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

A 35-Year-Old Man with 2 Episodes of Meningoencephalitis Associated with Flu-Like Illness
Neurol 84:e60-e64, Lewis, S.L., 2015

Kleine-Levin Syndrome in 120 Patients: Differential Diagnosis and Long Episodes
Ann Neurol 77:529-540, Lavault, S.,et al, 2015

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

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

Significant Period Between Presentation and Diagnosis in Basilar Artery Occlusion
Stroke 46:e79-e81, Organek, N.,et al, 2015

Brain Death Declaration
Neurol 84:1870-1879, Wahlster, S.,et al, 2015

Complications and Mortality in Hereditary Hemorrhagic Telangiectasia
Neurol 84:1886-1893, Donaldson, J.W.,et al, 2015

Burning Hands and Feet
Neurol 84:e146-e152, Chan, A.C. & Wilder-Smith, E., 2015

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

Prevalence of Amyloid PET Positivity in Dementia Syndromes
JAMA 313:1939-1949,1913, Ossenkoppele, R.,et al, 2015

Identifying and Managing Common Childhood Language and Speech Impairments
BMJ 350:h2318, Reilly, S.,et al, 2015

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

Two Uncommon Causes of Guillain-Barr� Syndrome: Hepatitis E and Japanese Encephalitis
Case Reports Neurol Med Art ID:759495, Bandyopadhyay, D.,et al, 2015

Clinical Outcomes after Neurogenic Stress Induced Cardiomyopathy in Aneurysmal Sub-Arachnoid Hemorrhage: A Prospective Cohort Study
Clin Neurol Neurosurg 128:4-9, Kilbourn, K.J.,et al, 2015

DWI Lesion Patterns in Cancer-Related Stroke-Specifying the Phenotype
Cerebrovasc Dis Extra 5:139-145, Schwarzbach, C.J.,et al, 2015



Showing articles 1250 to 1300 of 4285 << Previous Next >>