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advances in neurology
alveolar hypoventilation
anesthesia, general
anxiety
arrhythmia, cardiac
arteriopathy
aspiration
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
baldness
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
brain atrophy
cachexia
CAT scan
CAT scan, abnormal
cataracts
cerebellar atrophy, primary
cerebellar degeneration
cerebellar vermis
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral infarction
cerebral infarction, subcortical
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, multiple
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease
choreoathetosis
chromosomal abnormality
chromosome 19
chromosome 3
cognition
complications
confidentiality
creatine phosphokinase(CPK)elevated
dementia
dementia, cerebrovascular disease causing
dementia, subcortical
depression
diplopia
distal muscle weakness
dystonia
electrocardiogram, abnormal
electromyogram
emotional lability
eye movement, disorders of
facial appearance, abnormal
facial weakness
facial weakness, bilateral
failure to thrive
familial
familial hemiplegic migraine
familial periodic ataxia
fever
gene
gene mutation
genetic counselling
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genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
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granular osmiphilic material
headache
heart block
hemiplegia
high arched palate
hypercapnia
hyperthermia
infantile bilateral striatal necrosis
intellectual deficit
lactic acidemia
lacunar infarction
leukoencephalopathy
malignant hyperpyrexia
mania
manic-depressive
metabolic acidosis
microangiopathy, brain
migraine
migraine with aura
migraine, hemiplegic
misdiagnosis
molecular genetics
MRI
MRI, abnormal
multiple sclerosis
muscle atrophy, progressive
muscle biopsy
muscle wasting, diffuse
muscle weakness
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
myoglobinuria
myotonia
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
neurologic disease, diagnoses of
neurologic evaluation
neuroophthalmology
Notch3 gene
nystagmus
nystagmus, gaze-paretic
optic atrophy
oscillopsia
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinson disease, dystonia with
Parkinson disease, L-dopa nonresponsive
Parkinson disease, rapid onset
Parkinsonism syndrome
paroxysmal neurologic deficits
percussion induced muscle contraction
pregnancy, neurologic complications in
prevention of neurologic disorders
prognosis
proximal myotonic myopathy
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychosis
psychotic behavior
ptosis
review article
rhabdomyolysis
rigidity
risk factors
seizure
skin, biopsy
slit lamp examination
striatum, lesion of
striatum, lesion of, bilateral
tachycardia
tachypnea
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
transient ischemic attack
transient neurologic deficit
treatment of neurologic disorder
trinucleotide repeats
vasculopathy
wheelchair
white matter disease
white matter disease, subcortical
Showing articles 100 to 150 of 1399 << Previous Next >>

A 36-Year-Old Man With Asymmetric Muscle Weakness
Neurol 99"1057-1061, Harada,Y.,et al, 2022

Spectrum of Neuroradiologic Findings Associated with Monogenic Interferonopathies
AJNR 43:2-10, Benjamin, P.,et al, 2022

Multiple Cranial Nerve Gadolinium Enhancement in Norrie Disease
Ann Neurol 91:158-159, Jokela, M.,et al, 2022

A 31-Year-Old Man with Sequential Vision Loss
Neurol 98:163-169, Fortes, B.,et al, 2022

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

Molecular and Neurological Features of MELAS Syndrome in Paediatric Patients: A Case Series and Review of the Literature
Mal Genet Genomic Med 10:e1955, Seed,L.M.,et al, 2022

Pseudotumor Cerebri Syndrome with COVID-19: A Case Series
J Neuro Ophthalmol 42:e545-e547, Mukharesh,L.,et al, 2022

Adult-Onset Niemann-Pick Disease Type C Masquerading As Spinocerebellar Ataxias
Mol Genet Genomic Med 10:e1906, Vo,M.L.,et al, 2022

Sturge-Weber Syndrome
www.UptoDate.com,Dec, Patterson,M.C., 2022

Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era
JAMA Neurol 79:405-413, Morton, S.U.,et al, 2022

Encephalopathies Associated with Severe COVID-19 Present Neurovascular Unit Alterations without Evidence for Strong Neuroinflammation
Neurol Neuroimmunol Neuroinflamm 8:e1029, Bernard-Valnet, R.,et al, 2021

Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
NEJM 385:1317-1325, Case 30-2021, 2021

COVID-19 Associated Myelitis Involving the Dorsal and Lateral White Matter Tracts
AJNR 42:1912-1917, Huang, H.Y.,et al, 2021

Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
Neurol 97:875-878, Dinov, D.,et al, 2021

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021

A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
Neurol 97:958-963, Davalos, L.,et al, 2021

"Disappearing Infarct" Is Late-Onset MELAS
Ann Neurol 90:1001-1002, Landis,T.M.,et al, 2021

ANA Investigates: Neurological Complications of Covid-19 Vaccines
Ann Neurol 89:856-857, Goss, A.L.,et al, 2021

Neurologic Involvement in Children and Adolescents Hospitalized in the United States for Covid-19 or Multisystem Inflammatory Syndrome
JAMA Neurol 78:536-547, LaRovere, K.L.,et al, 2021

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

Helping with Public Understand Adverse Events Associated with Covid-19 Vaccinations
JAMA Neurol 78:789-790, Kim, D.D.,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

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

Digital Health
Stroke 52:351-355, Silva, G.S. & Schwamm, L.H., 2021

A 6-Year-Old Boy with Muscle Twitching
Neurol 96:e301-e304, Lewis, H.S.,et al, 2021

Molecular Diagnostic Yield of Exome Sequencing in Patients with Cerebral Palsy
JAMA 325:467-475, Moreno-De-Luca, A.,et al, 2021

A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021

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

Pediatric Parainfectious Encephalitis Associated with COVID-19
Neurol 96:541-544, Gaughan, M.,et al, 2021

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

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

Bilateral Superior Ophthalmic Vein Thrombosis, Ischaemic Stroke, and Immune Thrombocytopenia After ChAdOx1 nCoV-19 Vaccination
Lancet 397:e11, Bayas, A.,et al, 2021

Changes in Stroke Hospital Care During the COVID-19 Pandemic
Stroke 52:3651-3660, Katsanos, A.H.,et al, 2021

Isolated Intracranial Hypertension Associated with COVID-19
Cephalagia 40:1452-1458, Tulius,M.,et al, 2020

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

A case of COVID-19-associated pharyngeal-cervical-brachial variant of Guillain-Barre syndrome
Neurol 95:978-983, Liberatore, G.,et al, 2020

Guillain-Barre Syndrome Associated with SARS-CoV-2
NEJM 382:2574-2576, Tuscano, G.,et al, 2020

Covd-19-Associated Myopathy Caused by Type 1 Interferonopathy
NEJM 383:2389-2390, Manzano, A.C.,et al, 2020

COVID-19-Associated PRES-like Encephalopathy with Perivascular Gadolinium Enhancement
AJNR 41:2206-2208, Conte, G.,et al, 2020

Hypointensity of the Basal Ganglia in Adults with Glucose Transporter Protein Type 1 Deficiency Syndrome: A Novel Magnetic Resonance Imaging Finding
Ann Neurol 87:10-11, Van Samkar, A.,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

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

COVID-19 is Catalyzing the Adoption of Teleneurology
Neurol 94:903-904, Klein, B.C. & Busis, N.A., 2020



Showing articles 100 to 150 of 1399 << Previous Next >>