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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 150 to 200 of 2413 << Previous Next >>

CLOVES Syndrome
Neurol 96:e1487-e1488, Collins, M.,et al, 2021

Bilateral Temporal Pole Involvement in Adult-Onset X-Linked Adrenoleukodystrophy
JAMA Neurol 78:367-368, Liu, M.,et al, 2021

Brain and Skin Involvement in Erdheim-Chester Disease
Neurol 96:e1590-e1592, Budhram, A.,et al, 2021

An Unusual Cause of Sciatica in an Immunocompromised Patient
BMJ 372:n632, Kumar Singh, R., 2021

Alzheimers Disease
Lancet 397:1577-1590, Scheltens, P.,et al, 2021

Wilson Disease Presenting with Catatonia
Neurol 96:e2781-e2782, Patel, R.A. & Bailey, M., 2021

HIV Infection - Screening, Diagnosis, and Treatment
NEJM 384:2131-2143, Saag, M.S., 2021

Pembrolizumab-Induced Migrating Cortico-Subcortical Brain Lesions
Ann Neurol 89:1255-1256, Lambert, N.,et al, 2021

Encephalitis Induced by Immune Checkpoint Inhibitors
JAMA Neurol 78:864-873, Velasco, R.,et al, 2021

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021

Clinical and Genetic Features in Patients with Reflex Bathing Epilepsy
Neurol 97:e577-e586, Accogli, A.,et al, 2021

Clinicopathologic Conference, Acute human immunodeficiency virus type 1
NEJM 385:641-648, Case 24-2021, 2021

Genetics of Cluster Headache Takes a Leap
Ann Neurol 90:191-192, Palotie, A., 2021

Clinicopathologic Conference,Aceruloplasminemia, Hereditary
NEJM 383:1974-1983, Case 35-2020, 2020

Bilateral Ptosis, Dysphagia, and Progresive Weakness in a Patient of French-Canadian Background
Neurol 95:933-938, Paul,P.,et al, 2020

Clinicopathologic conference, Cryptococcal meningoencephalitis and advanced HIV infection
NEJM 383:2572-2580, Case 40-2020, 2020

Trends of Tuberculosis Case Detection, Mortality and Co-Infection with HIV in Ghana: A Retrospective Cohort Study
PLOSONE 15:e0234878, Osel, E.,et al, 2020

"Boule Du Biceps" in Dysferlinopathy
Neurol 94:83-84, El Sherif, R.,et al, 2020

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

Infection Risks Among Patients with Multiple Sclerosis Treated with Fingolimod, Natalizumab, Rituximab, and Injectable Therapies
JAMA Neurol 77:184-191, Luna, G.,et al, 2020

Randomized Placebo-Controlled Trial of Intravenous Immunoglobulin in Autoimmune LGI1/CASPR2 Epilepsy
Ann Neurol 87:313-323, Dubey, D.,et al, 2020

Randomized Placebo-Controlled Trial of Intravenous Immunoglobulin in Autoimmune LGI1/CASPR2 Epilepsy
Ann Neurol 87:313-323, Dubey, D.,et al, 2020

Myasthenia Gravis Following Dabrafenib and Trametinib for Metastatic Melanoma
Neurol 94:322-323, Zaloum, A.,et al, 2020

A 22-Year-Old Man with Progressive Bilateral Visual Loss
Neurol 94:625-630, Yang, S.L.,et al, 2020

A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
Neurol 94:e1213-e1218, Lima, J.E.E.,et al, 2020

A 42-year-old Woman with Progressive Cognitive Difficulties and Gait Imbalance
Neurol 94:e1219-e1226, Slama, M.C.C.,et al, 2020

Severe Neurological Toxicity of Immune Checkpoint Inhibitors: Growing Spectrum
Ann Neurol 87:659-669, Dubey, D.,et al, 2020

Clinicopathologic Conference, LGI1 autoimmune encephalitis
NEJM 382:1943-1950, Case 15-2020, 2020

A 25-year-old Woman with Recurrent Episodes of Collapse and Loss of Consciousness
Neurol 94:994-999, Wildman, J.,et al, 2020

A 53-year-old Woman with Lower Extremity Paresthesias
Neurol 94:1105-1108, Dehbashi, S.,et al, 2020

Severe Neurological Toxicity of Immune Checkpoint Inhibitors: Growing Spectrum
Ann Neurol 87:659-669, Dubey, D.,et al, 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

Association of Innovations in Radiotherapy and Systemic Treatments with Clinical Outcomes in Patients with Melanoma Brain Metastasis From 2007 to 2016
JAMA doi:10.1001/JAMANETWORKOPEN.2020.8204, Brastianos, H.C.,et al, 2020

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

Burning Pain in the Legs
NEJM 383:e18, Sacks, C.A., 2020

A 10-Year-Old Girl with Muscle Stiffness
Neurol 95:e773-e778, Prior, D.E. & Ghosh, P.S., 2020

Clinicopathologic Conference, HIV Type 2 Infection & Cerebral Toxoplasmosis
NEJM 383:859-866, Case 27-2020, 2020

Pediatric Leigh Syndrome
Ann Neurol 88:218-232, Alves, C.A.P.F.,et al, 2020

Spinal Xanthomatosis
Neurol 95:e1615-e1616, Valencia-Sanchez, C.,et al, 2020

Muscle Stiffness, Gait Instability, and Liver Cirrhosis in Wilsons Disease
Lancet 396:990, Kronlage, C.,et al, 2020

Bornavirus Encephalitis Shows a Characteristic Magnetic Resonance Phenotype in Humans
Ann Neurol 88:723-735, Finck, T.,et al, 2020

Sensory Ganglionopathy
NEJM 383:1657-1662, Amato, A.A. & Ropper, A.H., 2020

Recurrent Cerebral Ischemia During Pregnancies
Neurol 95:e2453-e2457, Bulwa, Z.,et al, 2020

Mycobacterium Haemophilum Infection
eMedicine.medscape.com 22144, Mazumder,S.A. & Chandrasekar,P.H., 2020

Neurodegeneration with Brain Iron Accumulation
AIAN 22:267-276, Batla, A. & Gaddipati, C., 2019

Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
Ther Adv Neurol Disord 12:1-15, Angelini, C.,et al, 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Clinical Characteristics and Treatment Outcomes for Patients Infected with Mycobacterium haemophilum
Emerg Inf Dis 25:1648-1652, Nookeu,P.,et al, 2019

Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
Neurol Sci 40:2251-2263, Donzuso,G.,et al, 2019



Showing articles 150 to 200 of 2413 << Previous Next >>