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acetazolamide
alcohol
alternating hemiplegia
alternating hemiplegia of childhood
alternating rapid movement
aminoacidopathies
aminoacidurias
antibodies to voltage-gated calcium channels
areflexia
arthralgia
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, truncal
ataxic gait
ATP1A3 gene
calcium channel dysfunction
CAT scan
CAT scan, abnormal
cataracts
central core disease
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellar vermis
cerebral cortical atrophy
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
channelopathy
Charcot-Marie-Tooth
children
chloride channel dysfunction
chorea
chromosomal abnormality
chromosome 19
ciguatera poisoning
Clinical Pathologic Conference(C.P.C.)
cogwheel rigidty
coma
coma, episodic
conjunctivitis
cryopyrin-associated periodic syndrome
deep gray nuclei
degenerative diseases of CNS
dementia
dentate nuclei, lesion of
developmental retardation
diagnostic criteria
differential diagnosis
diplopia
down-beat nystagmus
down-beat nystagmus, primary position of gaze
dysarthria
dystonia
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
encephalopathy
episodic disorders
episodic neurologic deficits
exercise
exercise intolerance
exome sequencing
eye movement, disorders of
familial
familial hemiplegic migraine
familial periodic ataxia
fever
fever, recurrent
fingerprint bodies
Friedreich's ataxia
frontal bossing
gait disorder
gene
gene mutation
genetic neurologic disorders
genetic testing
globus pallidus, lesion of, bilateral
granular osmiphilic material
head circumference
headache
hearing loss
hypertrophic intracranial pachymeningitis
hypokalemic periodic paralysis
hypotonia
imbalance
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incoordination
intellectual deficit
lactic acidemia
leukodystrophy
leukoencephalopathy
lysosomal storage disease
malignant hyperpyrexia
maple syrup urine disease
memory, impairment of
meningitis, aseptic
meningitis, carcinomatous
metabolic acidosis
metabolic disorder, primary
microcephaly
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
migraine, hemiplegic
molecular genetics
motor neuron disease
movement disorder
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, diffusion weighted
muscle weakness
myasthenic syndrome
myoclonus
myoclonus, epilepsy
myokymia
myotonia
myotonia congenita
nausea and vomiting
negative
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neurologic testing
neuromyotonia
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathy
neuropathy, hereditary peripheral
nystagmus
nystagmus, gaze-paretic
nystagmus, hereditary
nystagmus, monocular
nystagmus, periodic
nystagmus, vertical
optic atrophy
optic atrophy, bilateral
oscillopsia
paralysis
paramyotonia congenita
Parkinson disease, dystonia with
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
periodic paralysis
peroxisomal disease
pleocytosis of cerebrospinal fluid
pons, lesion of
potassium channel antibodies
potassium channel dysfunction
precipitating factors
pregnancy, neurologic complications in
primary episodic ataxia
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rash
recurrent
red eye
respiratory tract infection
review article
seizure
sensorineural hearing loss
short stature
skin, lesions in neurologic disorders
skull bone, thickening
slurred speech
sodium channel dysfunction
spinocerebellar ataxia
spinocerebellar ataxia type 6
spinocerebellar degeneration
status epilepticus
storage disease of CNS
stress, emotional
strokelike episodes
stuttering
symmetric brain lesions
tinnitus
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, intention
trinucleotide repeats
urea-cycle enzymopathies
vertigo
vertigo, episodic
vertigo, treatment of
vitamin E deficiency
walking, difficulty with
weakness
wheelchair
white matter disease
Showing articles 350 to 400 of 3240 << Previous Next >>

A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
Neurol 104:e213729, Shen,D.,et al, 2025

Upadacitinib - An Up-and-Comer for Treatment of Giant-Cell Arteritis
NEJM 392:2062-2064, Koster,M.J. & Warrington,K.J., 2025

RNF213 Polymorphisms in Intracranial Artery Dissection
Genes doi.org/10.3390/genesis 15060725, Zedde,M.,et al, 2024

Safety and Efficacy of Staged, Bilateral Focused Ultrasound Thalamotomy in Essential Tremor, An Open-Label Clinical Trial
JAMA Neurol 81:939-946, Kaplitt,M.G.,et al, 2024

Genome Sequencing in the NICU and PICU is Here to Stay
Neurol 104:e210267, Hoffman,E.P. and Kesari,A., 2024

Middle Meningeal Artery Embolisation for Nonacute Subdural Hematoma
NEJM 391:1901-1912, Ni,J.L.W.,et al, 2024

Adjunctive Middle Meningeal Artery Embolization for Subdural Hematoma
NEJM 391:1890-1900, Davies,J.M.,et al, 2024

Clinicopathologic Conference, Myasthenia Gravis
NEJM 391:1441-1450, Case 32-2024, 2024

Powassan Virus Encephalitis: A Tertiary Center Experience
Clin Inf Dis 78:80-89, Mendoza,M.A.,et al, 2024

A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
Neurol 103:e209796, Bouchart,J.,et al, 2024

Neuroleptic Malignant Syndrome
NEJM 391:1130-1138, Wijdicks,E.F.M. & Ropper,A.H., 2024

A 22-Year-Old Woman with Episodic Weakness and Jaundice
Neurol 103:e210018, Rathinasbapathi,M.,et al, 2024

Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
Neurol 103:e209844, Dhawan,A.,et al, 2024

Primary Central Nervous System Vasculitis
NEJM 391:1028-1037, Salvarani,C.,et al, 2024

Pomalidomide for Epistaxis in Hereditary Hemorrhagic Telangiectasia
NEJM 391:1015-1027, Al-Samkari,H.,et al, 2024

Vitamin B12 Deficiency:NICE Guideline Summary
BMJ 385:q1019, q1262, Sands,T.,et al, 2024

Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
JAMA Neurol 81:762-770, Lee,S-U.,et al, 2024

Clinicopathologic Conference, Paraneoplastic Encephalomyelitis Due to Small-Cell Lung Carcinoma and Concurrent Cerebral Amyloid Angiopathy
NEJM< 391357-369, Case 23-2024, 2024

Hyperventilation-Induced Alternating Hemiplegia with Concomitant Hemispheric EEG Slowing in a 7-Year-Old Girl with Headache
Neurol 103:e209759, Proietti,J.,et al, 2024

Vestibular Drop Attacks Diagnosed with Valuable Insights from CCTV
Lancet 404:787-788, Joffily,L.,et al, 2024

Distinguishing Transient Cerebral Ischemia From Other Brief Neurologic Events
Neurol 102:e208024, Warach,S. & Schellinger, P.D., 2024

A 51-Year-Old Woman with Abnormal Corups Callosum Signal
JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 2024

Treatment and Outcomes of Cervical Artery Dissection in Adults:A Scientific Statement From the American Heart Association
Stroke 55:e91-e106, YaghikS.,et al, 2024

Cavernous Maliformations of the Central Nervous System
NEJM 390:1022-1028, Smith,E.R., 2024

Posttransplant Anti-GABAA Receptor Antibody-Associated Autoimmune Encephalitis
Neurol 102:e209245, Togni,C.L.,et al, 2024

Anti-NMDA Receptor Encephalitis Presenting with Cerebellitis in a Pediatric Patient
Neurol 102:e209259, Moehlman,M. & Kornbluh,A.B., 2024

Diffusely Enhancing Lesions on MRI in DPPX Antibody-Associated Encephalitis
JAMA Neurol 8:418-419, Liu,M.,et al, 2024

Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
Neurol 102:e209385, Nishida,K.,, 2024

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
JAMA Neurol 81:1-82, Chu,X.C.,et al, 2024

Clinicopathological Conference, Glutamic Acid Decarborylase 65 Autoantibody-Associated Stiff-Person Syndrome
NEJM 390:1712-1719, Case 14-2024, 2024

HaNDL Syndrome The Innocent Lymphocytic Pleocytosis
Neurologist 29:163-165, Keskin,K.G.,et al, 2024

Clinicopatholigic Conference, Rheumatoid Arthritis with Vasculitis Causing A Confluent Mononeuritis Multiplex
NEJM 390:1312-1322, Case 11-2024, 2024

Treatment Modalities and Outcomes in Brainstem Cavernous Malformations: A Large Multicenter Observational Cohort Study
Stroke 55:1151-1160, Lu,J.,et al, 2024

Vascular Malformations of the Central Nervous System
www.UptoDate.Com, March, Singer,R.J.,et al, 2024

Clinicopathologic Conference, Thyrotoxic Periodic Paralysis Associated with Graves Disease
NEJM 390:1514-1522, Case 13-2024, 2024

Primary Brain Tumours in Adults
Lancet 402:1564-1579, van den Bent,M.,et al, 2023

Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
Neurol 101:e1884-e1892, van der Veen,S.,et al, 2023

Trial of Botulinum Toxin for Isolated or Essential Head Tremor
NEJM 389:1753-1765, Marques,A.,et al, 2023

Shrimp Sign in Ataxic Cerebellar Progressive Multifocal Leukoencephalopathy
Neurol 101:918-919, Varela,F.J.,et al, 2023

Pachymeningitis and Aortitis as the Initial Presentation of Granulomatosis with Polyangiitis
Neurol 101:979-980, Li,X.,et al, 2023

Hereditary Hemorrhagic Telangiectasia, Clinical Presentations, and Management
Stroke 54:e512-e515, Silveira,L.,et al, 2023

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

A 67-YEar-Old Man with Multiple Intracranial Lesions
Neurol 101:e845-e851, Ngo,A.,et al, 2023

Idiopathic Orbital Inflammation and Tolosa-Hunt Syndrome with Intracranial Extension
Neurol 101:371-374, Yu,S. & Chen,T., 2023

Wernekinck Commissure Syndrome
Radiopaedia doi.org/10.53347/rlD-85274, Aug, Deng,F.,et al, 2023

A 62-Year-Old Woman with Transient Vision Loss
Neurol 101:e1097-e1103, Silva,L.M.T.,et al, 2023

Neurologic Complications of Babesiosis, United States, 2011-2021
Emerg Inf Dis 29:1127-1135, Locke,S.,et al, 2023

Clinicopathologic Conference, Noncirrhotic hyperammonemia after Roux-en-Y Gastric Bypass
NEJM 389:1221-1230, Case 30-2023, 2023

A 17-Year-Old Girl with Progressive Cognitive Impairment
Neurol 101:e1466-e1472, Zhao,B.,et al, 2023



Showing articles 350 to 400 of 3240 << Previous Next >>