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aciduria
acoustic nerve, vestibular division of
acoustic neurinoma
acoustic neurinoma, bilateral
acquired immunodeficiency syndrome
adrenal mass
advances in neurology
adverse drug reaction
Alexanders disease
algorithm
Alzheimer's disease
Alzheimer's disease, early onset
Alzheimer's disease, familial
Alzheimer's disease, familial, late onset
Alzheimer's disease, pathogenesis
amniocentesis
amyloidosis
aneurysm
aneurysm, intracranial
aneurysm, intracranial, familial
anterior horn cell disease
antiviral agents
apolipoprotein E
APP
APP gene
areflexia
arrhythmia, cardiac
astrocytoma
ataxia
ataxia, cerebellar
ataxia, hereditary
atrial myxoma
audiogram
auditory evoked brainstem potentials
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
autonomic dysfunction
baclofen
basal ganglia, lesion of
basal ganglia, lesion, bilateral
blindness
brainstem, dysfunction
brainstem, lesion of
cafe au lait spots
CAG repeats
carcinoma
cardiomyopathy
CAT scan, abdomen
CAT scan, abnormal
cataracts
caudate nucleus, lesion of, bilateral
cavernous hemangioma
CD4 counts
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebral embolism
cerebral palsy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, young adult
children
chorea
chromosomal abnormality
chromosome 1
chromosome 14
chromosome 17
chromosome 21
chromosome 22
chromosome 4
chromosome 5
chromosome 6
chromosome 9
coagulopathy
congenital heart disease
congenital myopathy
constipation
contractures, joint
cranial nerve tumor
creatine phosphokinase(CPK)elevated
deafness
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, presenile
dentatorubral-pallidoluysian atrophy
developmental retardation
diet
differential diagnosis
DNA probes
dopa responsive dystonia
drug induced neurologic disorders
dysarthria
dyskinesia
dystonia
dystonia, children
Ehlers-Danlos syndrome
electromyogram
encephalitis, autoimmune
encephalopathy
endoscopy
enzyme, defect
ependymoma
Fabry's disease
facial weakness, bilateral
familial
fasciculation
fibromuscular dysplasia
fragile-X syndrome
Friedreich's ataxia
gadolinium
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glioma
GLUT1
GLUT1 deficiency syndrome
glutamate dehydrogenase deficiency
hamartoma
headache
hearing loss
hemoglobin abnormality, neurologic complications of
hereditary hemorrhagic telangiectasia(HHT)
high arched palate
highly active antiretroviral therapy
history of neurology
HLA
homocystinuria
human immunodeficiency virus type 1
huntingtin
Huntington's chorea
hydrocephalus
hydrocephalus, treatment of
hypertension
hypoglycorrhachia
hyporeflexia
hypotonia
hypotonia, infants
immune reconstitution inflammatory syndrome
inborn errors of metabolism
intellectual deficit
interferon
interferon beta 1-a
interferon beta 1-b
intracerebral hemorrhage
intracerebral hemorrhage, young adult
iris, abnormal
iron, brain
islet cell tumor
karyotyping
ketogenic diet
learning disability
learning disability, in children
Legius syndrome
lenticular nucleus, lesion of, bilateral
life expectancy
Lisch nodules
long bone lesion
lordosis
lumbar puncture
lymphoma
macrocephaly
macular degeneration
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, familial
meningioma
meningioma, familial
meningioma, multiple
mental retardation
merlin
microcephaly
migraine
migraine, hemiplegic
mimics
misdiagnosis
mitral valve prolapse
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
moyamoya
MRI
MRI, abnormal
MRI, muscle
MRI, paramagnetic effect
MRI, spine
multiple sclerosis
multiple sclerosis, clinical patterns
multiple sclerosis, diagnosis of
multiple sclerosis, pathogenesis
multiple sclerosis, treatment of
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, congenital
muscular dystrophy, Duchenne
myasthenia gravis
myasthenia gravis, familial incidence of
myasthenic syndrome
myoclonic jerks
myopathy
myotonia dystrophica
neck weakness
nemaline rod myopathy
neoplasm, peripheral nerve
neoplasm, primary of CNS
neoplasm, primary of CNS-children
neoplasm, primary of CNS-familial occurrence
nerve growth factor
neurocutaneous disease
neurofibroma
neurofibromatosis 1
neurofibromatosis 2
neurofibromatosis 2, presymptomatic
neurofibromin
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuromuscular disease, electrodiagnosis of
neuronal degeneration
neuropathology
neuropathy
neurotomy
next-generation sequencing
NF1 gene
nusinersen
nystagmus
ocular motility, disorders of
ophthalmoplegia
optic atrophy
optic glioma
palatal myoclonus
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
paroxysmal exertion-induced dyskinesia
patient information and support
pheochromocytoma
polycythemia, primary
practice guidelines
preclinical
precocious puberty
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
presenilin-1 gene
presenilin-2 gene
prognosis
progressive neurologic disorder
protein C deficiency
pruritus
pseudarthrosis
pseudoxanthoma elasticum
Purkinje cell
pyramidal tract dysfunction
recombinant DNA
repetitive nerve stimulation
respiratory failure
retinal degeneration
retinitis pigmentosa
review article
RFLPs
rigid spine syndrome
Riley-Day syndrome
root lesion, nerve
Rosenthal fiber encephalopathy
Rosenthal fibers
schwannoma
scoliosis
scoliosis, neurologic association with
screening
seizure
seizure, children
seizure, familial
seizure, neonatal
seizure, petit mal
sensory ganglia
sensory ganglia, abnormal
shunt procedure, ventricular
Shy-Drager syndrome
sickle cell disease
skin, lesions in neurologic disorders
skull x-ray, abnormal
skull x-ray, bony defect on
slit lamp examination
SMN1 gene
spasticity
speech disorder
spinal cord
spinal cord degeneration
spinal cord, lesion of
spinal cord, neoplasm
spinal cord, neoplasm, extramedullary intradural
spinal cord, neoplasm, intramedullary
spinal cord, neoplasm, neurofibroma
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 2
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 6
spinocerebellar ataxia type 7
spinocerebellar degeneration
spinopontine atrophy, dominant
SPRED1 mutation
steroid
striatal encephalitis
survival motor neuron gene
symmetric brain lesions
third ventricle
thrombocytopenia
tinnitus
tongue, fasciculations of
treatment of neurologic disorder
trinucleotide repeats
tuberous sclerosis
type 1 muscle fiber
ubiquilin 1
urinary catecholamines
ventriculostomy
ventriculostomy, endoscopic
Von Hippel Lindau
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
web sites
white freckles
Wood's light
workup
X-linked bulbospinal neuronopathy
Showing articles 300 to 350 of 2452 << Previous Next >>

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 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

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

A 58-year-old man with Progressive Ptosis and Walking Difficulty
Neurol 89:e1-e5, Kuo, P.,et al, 2017

Clinicopathologic Conference, Advanced AIDS Complicated by HSV-1 Encephalopathy. Basal-Cell Carcinoma. Kaposis Sarcoma.
NEJM 376:2580-2589, Case 20-2017, 2017

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017

A Demure Teenager and Her Dystonic Foot
Neurol 89:e71-e75, Cullinane, P.W.,et al, 2017

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

Neuroimaging Changes in Menkes Disease, Part 1
AJNR 38:1850-1857, Manara, R.,et al, 2017

A 46-year-old man with Persistent Hiccups, Cognitive Dysfunction, and Imbalance
Neurol 89:e193-e196, Lamb, C.J.,et al, 2017

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

Ocrelizumab versus Interferon Beta-1a in Relapsing Multiple Sclerosis
NEJM 376:221-234,280, Hauser, S.L.,et al, 2017

Sudden-Onset Pulsatile Headache in a Previously Healthy Young Man
Neurol 88:e26-e29, Qin, C.,et al, 2017

A 35-year-old Woman with Hyperstartling Stiffness, and Accidental Falls
Neurol 88:e38-e41, Russo, S.P.,et al, 2017

Clinical and Neuroimaging Features in Gorlin-Goltz Syndrome
Neurol 88:e52-e54, da paz Oliveira, G.,et al, 2017

Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
JAMA Neurol 74:245-246, Lopez Chiriboga, A.S.,et al, 2017

Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
JAMA Neurol 74:238-241, Dubey, D.,et al, 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

Clinicopathologic Conference Cryptococcal Meningitis in a Patient with Chronic HIV Infection
NEJM 376:1065-1071, Case 8-2017, 2017

A 13-year-old boy with Chronic Ataxia and Developmental Delay
Neurol 88:e116-e121, Libdeh, 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

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

Man with Recurrent Paralysis and Cerebral White Matter Lesions
JAMA Neurol 74:599-600, Xiao, F., 2017

Human Immunodeficiency Virus Presenting as Progressive Multifocal Leukoencephalopathy Restricted to the Posterior Fossa
JAMA Neurol 74:597-598, Schubert, R.D. & Richie, M.B., 2017

A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
Neurol 88:e185-e189, Vazquez do Campo, R.,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

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

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

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

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

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

Disseminated Aspergillosis in an HIV-positive Cannabis user taking steroid treatment
Lancet Infect Dis 17:882, Salam, A.P. & Pozniak, A.L., 2017

Cerebral Venous Sinus Thrombosis in Homocystinuria: Dietary Intervention in Conjunction with Anticoagulation
Sage Open Med Case Reports 5:1-4, Yap, S.,et al, 2017

CNS Cryptococcosis in HIV
eMedicine.com Nov 2017, Gliksman, F.J. & Singh, N.N., 2017

Adult-Onset Niemann-Pick Disease Type C: Rapid Treatment Initiation Advised but Early Diagnosis Remains Difficult
Front Neurol doi.10.3398/jneur.2017.00108, Piroth,T.,et al, 2017

Cognitive Impairment Profile in adult Patients with Neimnn Pick Type C Disease
Orphanet J Rare Dis 12:166, Heitz, C., et al, 2017

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017

Anal Carcinoma
NCCN.org April 2017 V2.2017, , 2017

Holmes Tremor
Neurol 86:931-938, Raina, G.B.,et al, 2016

Neurological, Respiratory, Musculoskeletal, Cardiac and Ocular Side-Effects of Anti-PD-1 Therapy
Eur J Cancer 60:210-225, Zimmer, L.,et al, 2016

Immune-related adverse events with immune checkpoint blockade: a comprehensive review
Eur J Cancer 54:139-148, Michot, JM,.,et al, 2016

Acute Demyelinating Polyneuropathy Caused by Nivolumab in a Man with Metastatic Non-Small Cell Lung Cancer
J Gerontol Geriatr Res 5:3, Sabeeh-Ur-Rehman, B. & Bhaumik, S., 2016

Performance Testing of PCR Assay in Blood Samples for the Diagnosis of Toxoplasmic Encephalitis in AIDS Patients from the French Departments of America and Genetic Diversity of Toxoplasma Gondii: A Prospective and Multicentric Study
PLoS Negl Trop Dis 10:e0004790, Ajzenberg, D.,et al, 2016

Safety and Diagnostic Value of Brain Biopsy in HIV Patients: A Case Series and Meta-Analysis of 1209 Patients
JNNP 87:722-733, Lee, A.M.,et al, 2016

Syphilitic Optic Neuropathy: Re-Emerging Cases Over a 2-Year Period
Neuro-Ophthalmol 40:69-73, Apinyawasisuk, S.,et al, 2016

Neuroradiologic Patterns and Novel Imaging Findings in Aicardi-Goutieres Syndrome
Neurol 86:28-35, La Piana, R.,et al, 2016

Faciobrachial Dystonic Seizures
Neurol 86:e60-e61, Schmerler, D.A.,et al, 2016

Leukodystrophy and Progressive Myoclonic Epilepsy Disclosing DRPLA
Neurol 86:e58-e59, Sgobbi de Souza, P.V.,et al, 2016



Showing articles 300 to 350 of 2452 << Previous Next >>