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advances in neurology
agenesis of corpus callosum
Aicardi's syndrome
Alzheimer's disease
amniocentesis
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amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
ANA
anti basal ganglia antibodies
anti MAG antibodies
antistreptolysin titer
antithyroid antibodies
aphasia
areflexia
arthrogryposis multiplex
asymptomatic
ataxia
ataxia, truncal
atidarsagene autotemcel
autism
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autoimmune disease
axonal spheroid
Babinski sign
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
bilateral periventricular nodular heterotopia
brain atrophy
brain biopsy
burst suppression pattern, electroencephalogram
CAT scan, abnormal
catatonia
central core disease
cerebellar degeneration
cerebral cortex
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
Charcot-Marie-Tooth
cherry red spot
cherry red spot-myoclonus syndrome
children
chorioretinitis
chromosomal abnormality
chromosome 5
Clinical Pathologic Conference(C.P.C.)
coloboma
confusion
confusional state, acute
congenital malformation
congenital malformation, non CNS
corpus callosum
cortical dysplasia, focal
cyst, porencephalic
deep gray nuclei
degenerative diseases of CNS
dentate nuclei
dentate nuclei, lesion of
developmental milestones
developmental milestones, loss of
developmental retardation
differential diagnosis
drooling
dropped head syndrome
dyskinesia
dysphagia
dystonia
efficacy
electroencephalogram
electroencephalogram, abnormalities of
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, focal
encephalitis, Rasmussen's
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, Hashimoto's
enzyme, defect
epidemiology of neurology
epilepsia partialis continua
eye movement, disorders of
Fabry's disease
facial asymmetry
falling
familial
Fazio-Londe's disease
fever
FLAMES
Friedreich's ataxia
gangliosidosis GM2
gaze palsy
gaze palsy, supranuclear
gene
gene therapy
genetic neurologic disorders
genetic screening
hallucination
headache
heavy metal intoxication
hemihypertrophy, congenital
hemiparesis
hemispherectomy
hepatomegaly
heterotopia
hexosaminidase-A
hexosaminidase-A and B
histopathology
Huntington's chorea
hyperreflexia
hypomelanosis of Ito
hypomyelination
hypopigmentation of skin
hypotonia
hypotonia, infants
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
infantile bilateral striatal necrosis
infantile neuronal degeneration
infantile spasm
insomnia
intellectual deficit
intellectual deterioration
iron, brain
Jewish
Kugelberg-Welander syndrome
lactic acidemia
Leigh's disease
lethargy
leukodystrophy
level of consciousness, decreased
lipid storage disorder of CNS
lysosomal storage disease
macrocephaly
malabsorption
malformation, CNS, congenital
megalencephaly
meningeal enhancement
mental retardation
mental status, abnormal
mesial temporal sclerosis
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
metachromatic leukodystrophy, late-infantile
microcephaly
micropthalmia
misdiagnosis
molecular genetics
monoclonal antibodies
mortality
motor neuron disease
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, cortical enhancement
MRI, diffusion weighted
MRI, eye of tiger sign
MRI, gradient-echo
MRI, hypointense signal foci on
MRI, negative
MRI, paramagnetic effect
muscle biopsy
muscle spasm
muscle wasting, diffuse
muscular dystrophy, Duchenne
mutism
myasthenia gravis
myoclonus
myoclonus, epilepsy
myotonia dystrophica
neoplasm, peripheral nerve
neoplasm, primary of CNS
neoplasm, primary of CNS-children
nerve conduction studies
nerve conduction studies, motor
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neurocutaneous disease
neurofibrillary degeneration
neurologic disease, diagnoses of
neurologic examination, focal
neuronal cell death
neuronal ceroid-lipofuscinosis
neuronal degeneration
neuronal migration disorder
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
night sweats
NMDA antagonists
nystagmus
nystagmus, rotary
opisthotonus
optic atrophy
optic nerve
optic nerve, lesion of
optic neuritis
PANK2 mutation
paraparesis, familial spastic
Parkinson disease
paroxysmal neurologic disorder
patient information and support
pediatric neurology
perineural invasion
personality change
pleocytosis of cerebrospinal fluid
pleocytosis of cerebrospinal fluid, neutrophilic
poison, mercury
poison, neurologic problems with
postural abnormality
prenatal diagnosis by amniocentesis
prognosis
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis, childhood
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
recurrent
respiratory tract infection
retinal degeneration
retropulsion
review article
rigidity
rituximab
safety
Sandhoff's disease
segmental demyelination
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seizure, adult onset
seizure, children
seizure, focal
seizure, intractable
seizure, intractable, treatment of
seizure, neonatal
seizure, prognosis in childhood
seizure, psychomotor-temporal lobe
seizure, surgical treatment of
seizure, treatment of
skin, biopsy
skin, lesions in neurologic disorders
SMN1 gene
sore throat
spasticity
speech disorder
speech disorder, childhood
speech, loss of
spinal cord
spinal cord degeneration
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar ataxia
startle reaction
status epilepticus
steroid therapy, CNS treatment and complications with
streptococcal infection
striatal encephalitis
striatonigral degeneration
striatonigral degeneration, infantile
striatum, lesion of
Sturge-Weber syndrome
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
survival motor neuron gene
symmetric brain lesions
Tay-Sachs disease
temporal lobe, status
thalamus, lesion of
thalamus, lesion of-bilateral
thyroiditis
titubation
tone, muscle, increased
treatment of neurologic disorder
tremor
tremor, intention
tricresylphosphate
trinucleotide repeats
tuberous sclerosis
ventricular enlargement
visual acuity, decreased
visual fields, constricted
visual loss
weakness
weakness, generalized
Werdnig-Hoffman disease
West disease
white matter disease
wide based gait
Showing articles 50 to 100 of 1434 << Previous Next >>

MOG-IgG-Associated Encephalitis with FLAIR Hyperintensity Along the Brainstem Surface
Ann Neurol 96:460-462, Yin,J.,et al, 2024

Recurrent Rhombencephalitis Associatedwith Anti-GAD65 Antibody
Neurol 102:e208040, Alferes,A.R.,et al, 2024

Validation of the 2023 International Diagnostic Criteria for MOGAD in a Selected Cohort of Adults and Children
Neurol 103:e209321, Varley,J.A.,et al, 2024

Seizures When Exiting a Bath, A Rare Type of Reflex Epilepsy
Neurol 103:e210025, Pascarella,A.,et al, 2024

Cancer Frequency in MuSK Myasthenia Gravis and Histological Evidence of Paraneoplastic Etiology
Ann Neurol 96:1020-1025, Falso,S.,et al, 2024

A 65-Year-Old Woman with Isolated Macroglossia as the Initial Presentation of a Rare Disease
Neurol 103:e210070, Lara,C.,et al, 2024

Reversible Cerebral Atrophy and Substantia Nigra Changes after Vitamin B12 Treatment in Infantile Tremor Syndrome
Neurol 103:e210076, Singh,R.,et al, 2024

Slowly Expanding Lesions Differentiate Pediatric Multiple Sclerosis from Myelin Oligodendrocyte Glycoprotein Antibody Disease
Ann Neurol 96:1086-1091, Fadda,G.,et al, 2024

Overlapping Anti-NMDAR Encephalitis and Multiple Sclerosis: A Case Report and Literature Review
Front Immunol doi:10.3389/Fimmun.2023.1088801, Liu,P.,et al, 2023

Diagnosis of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease:International MOGAD Panel Proposed Criteria
Lancet Neurol doi.org110.1016/51474-4422(22)00431-8, Banwell,B.,et al, 2023

Glucose Hypermetabolism in the Basal Ganglia
Neurol 101:90-91, Kim,Y.E.,et al, 2023

An 82-Year-Old Woman with Subacute Ophthalmoparesis and Ataxia
Neurol 101:e570-e575, Rodrigo-Gisbert,M.,et al, 2023

Unpacking the CNS Manifestations of Epstein-Barr Virus:An Imaging Perspective
AJNR 44:1002-1008, Soni,N.,et al, 2023

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD):Clinical Features and Diagnosis
www.UptoDate.com, Sept, Flanagan,E.P. & Tillema,J-M, 2023

Tuberous Sclerosis Complex:Clinical Features
www.UptoDate.com, Dec, Randle,S., et al, 2023

Cerebral Cortical Encephalitis in Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease
Ann Neurol 93:297-302, Valencia-Sanchez,C., et al, 2023

Tumefactive Demyelination in MOG Ab-Associated Disease, Multiple Sclerosis, and AQP-4-IgG-Positive Neuromyelitis Optica Spectrum Disorder
Neurol 100:e1418-e1432, Cacciaguerra, L.,et al, 2023

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD): Clinical Features and Diagnosis
UptoDate.com, March, Flanagan,E.P. & Tillema,J-M, 2023

Neonatal Seizures
NEJM 388:1692-1700, Ropper.A.H., 2023

Cognitive and Clinical Characteristics of Patients with Limbic-Predominant Age-Related TDP-43 Encephalopathy
Neurol 100:e2027-e2035, Pagnotti,R.M.B.,et al, 2023

Should We Test for IgG Antibodies Against MOG in Both Serum and CSF in Patients with Suspected MOGAD?
Neurol 100:497-498, Kim,H.J. & Palace, J., 2023

Autoimmune Encephalitis Misdiagnosis in Adults
JAMA Neurol 80:30-39, Flanagan,E.P.,et al, 2023

A 67-Year-Old Woman with Progressive Tingling Sensations and Imlalance
Neurol 100:151-157, Horta,L.F.B.,et al, 2023

Differentiating Multiple Sclerosis from AQP4-Neuromyelitis Optica Spectrum Disorder and MOG-Antibody Disease with Imaging
Neurol 100:e308-e323, Cortesa,R.,et al, 2023

Occult Breast Cancer with Anti-Ri Antibody Positivity and Pontine Hot Cross Bun Sign
JAMA Neurol 80:207-208, Liu,Y.,et al, 2023

Brain Calcification in a Young Woman With Seizures, Explore the Rare Differentials
Neurol 100:397-398, Menon,B.,et al, 2023

A Dizzy Architect
Neurol 98:543-549, Scutelnic, A.,et al, 2022

A 48-Year-Old Woman Presenting with Vertigo, Ptosis, and Red Eyes
Neurol 98:678-683, Kim, K.T.,et al, 2022

Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
Lancet 400:1144, Sabino de Oliveira, D.,et al, 2022

Dura Mater Thickening and Enhancement in Anti-NMDAR Encephalitis
Neurol 99:628-629, Xia, C. & Chen, H.S., 2022

Clinical Manifestations and Diagnosis of Listeria Monocytogenes Infection
UptoDate Aug, Gelfand, M.S.,et al, 2022

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
Neurol 99:997-1003, Chaity,D.K.,et al, 2022

Updates on Sturge-Weber Syndrome
Stroke 53:3769-3779, Yeom,S.E.&Comi,A.M., 2022

Atypical Unilateral Cortical Ribboning in Anti-NMDA Receptor Encephalitis
Neurol 99:1062-1063, Chen,A.Y.,et al, 2022

A 56-Year-Old Man with Unusual Presentation of Subacute Encephalopathy and Seizure
Neurol 98:e95-e102, Wang, T.,et al, 2022

Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
NEJM 386:173-180, Case 1-2022, 2022

A 67-Year-Old Woman with Progressive Diplopia, Vertigo, and Ataxia
Neurol 98:e669-e674, Sakoda, M.,et al, 2022

Glial Fibrillary Acidic Protein Autoimmunity
Neurol 98:e653-e668, Gravier-Dumonceau, A.,et al, 2022

A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
Neurol 98:851-853, Meng, D.,et al, 2022

Rituximab Therapy in the Treatment of Juvenile Myasthenia Gravis
Neurol 98:e2368-e2376, Molimard, A.,et al, 2022

A 77-Year-Old Man with Involuntary Movements, Sleep Changes, Falls, Bulbar Symptoms, and Cognitive Complaints
Neurol 99:26-30, Cao, T.Q.,et al, 2022

Case Report of Lambl Excrescences in a Pediatric Patient with Multifocal Strokes
Neurol 99:73-76, Robertson, D.M.,et al, 2022

Epidemiology, Survival, and Clinical Characteristics of Inclusion Body Myositis
Ann Neurol 92:201-212, Lindgren, U.,et al, 2022

Neuromyelitis Optica Spectrum Disorder
NEJM 387:631-639, Wingerchuk, D.M. & Lucchinetti, C.F., 2022

Neuroimaging Findings in Parechovirus Encephalitis: A Case Series of Pediatric Patients
Pediatr Neurol 130:41-45, Tierradentro-Garcia, L.O.,et al, 2022

Miller Fisher Syndrome and Acute Motor and Sensory Axonal Neuropathy (AMSAN) Variant Guillain-Barre Overlap Syndrome (MFS/AMSAN-GBS) After Upper Respiratory Tract Infection (URTI)
Acta Sci Clin Case Reports 3:19-24, Chau,T.C. & Muhamad,N.A.N., 2022

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

CNS Demyelinating Attacks Requiring Ventilatory Support With Myelin Oligodendrocyte Glycoprotein or Aquaporin-4 Antibodies
Neurol 97:e1351-e1358, Zhao-Fleming,H.H.,et al, 2021

Limitations of a Commercial Assay as Diagnostic Test of Autoimmune Encephalitis
Front Immunol 12:691536, Ruiz-Garcia,R.,et al, 2021



Showing articles 50 to 100 of 1434 << Previous Next >>