CADASIL: Treatment and Management Options.

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CADASIL: Treatment and Management Options. is …
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scholarly articleQ13442814

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P356DOI10.1007/S11940-017-0468-Z
P698PubMed publication ID28741120

P50authorCaterina MariottiQ67211429
Franco TaroniQ67510435
P2093author name stringAnna Bersano
Gloria Bedini
Eugenio Agostino Parati
Silvia Baratta
Joshua Oskam
P2860cites workCADASIL in central Italy: a retrospective clinical and genetic study in 229 patientsQ60469194
Angiographic complications in CADASILQ73164640
The phenotypic spectrum of CADASIL: clinical findings in 102 casesQ77568574
The natural history of CADASIL: a pooled analysis of previously published casesQ77835119
Diagnostic strategies in CADASILQ78415468
Motor cortex cholinergic dysfunction in CADASIL: a transcranial magnetic demonstrationQ80160482
Spectrum of mutations in biopsy-proven CADASIL: implications for diagnostic strategiesQ80357378
Co-aggregate formation of CADASIL-mutant NOTCH3: a single-particle analysisQ84235340
Memantine for dementiaQ22252980
Homocysteine-lowering interventions for preventing cardiovascular eventsQ24186605
Selective serotonin reuptake inhibitors (SSRIs) for stroke recoveryQ24202939
Memantine for dementiaQ24246560
The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patientsQ24629786
Notch signaling: cell fate control and signal integration in developmentQ27861061
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patientsQ28255796
Ergotamine in the acute treatment of migraine: a review and European consensusQ28378061
Notch signalingQ29618190
Notch3 is a major regulator of vascular tone in cerebral and tail resistance arteriesQ30486605
Cerebrovascular dysfunction and microcirculation rarefaction precede white matter lesions in a mouse genetic model of cerebral ischemic small vessel diseaseQ30492865
Cerebral hemorrhages in CADASIL: report of four cases and a brief reviewQ30620885
Effects of homocysteine lowering with B vitamins on cognitive aging: meta-analysis of 11 trials with cognitive data on 22,000 individualsQ30833390
CADASIL and CARASIL.Q30861866
Role of electron microscopy in the diagnosis of cadasil syndrome: a study of 32 patientsQ31120190
Case report: bipolar disorder as the first manifestation of CADASILQ31165840
The spectrum of Notch3 mutations in 28 Italian CADASIL familiesQ33214090
CadasilQ33470786
Pathogenic mutations associated with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy differently affect Jagged1 binding and Notch3 activity via the RBP/JK signaling PathwayQ33909665
Plasma homocysteine as a risk factor for dementia and Alzheimer's diseaseQ33957399
Cerebral microbleeds in CADASIL.Q34092506
Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosisQ34106491
Clinical spectrum of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathyQ34295928
Effects of short term atorvastatin treatment on cerebral hemodynamics in CADASIL.Q34631936
Oral triptans (serotonin 5-HT(1B/1D) agonists) in acute migraine treatment: a meta-analysis of 53 trialsQ34647375
Pericytes are involved in the pathogenesis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathyQ35757111
Recent progress on small vessel disease with cognitive impairmentQ35870878
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM intervalQ35882443
Acetazolamide for the prophylaxis of migraine in CADASIL: a preliminary experienceQ35973490
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: update on clinical, diagnostic, and management aspectsQ36288849
The NOTCH3 score: a pre-clinical CADASIL biomarker in a novel human genomic NOTCH3 transgenic mouse model with early progressive vascular NOTCH3 accumulationQ36417190
CADASIL mutations and shRNA silencing of NOTCH3 affect actin organization in cultured vascular smooth muscle cellsQ36459076
Genetics of ischaemic strokeQ36713912
Abnormal recruitment of extracellular matrix proteins by excess Notch3 ECD: a new pathomechanism in CADASILQ36904906
The comparisons of phenotype and genotype between CADASIL and CADASIL-like patients and population-specific evaluation of CADASIL scale in ChinaQ36922449
Investigation of the NOTCH3 and TNFSF7 genes on C19p13 as candidates for migraineQ36961494
Psychiatric disturbances in CADASIL: a brief reviewQ37126773
Congruence between NOTCH3 mutations and GOM in 131 CADASIL patientsQ37158175
Notch and vascular smooth muscle cell phenotype.Q37342396
Considerations on a mutation in the NOTCH3 gene sparing a cysteine residue: a rare polymorphism rather than a CADASIL variantQ37388350
CADASIL management or what to do when there is little one can do.Q37390715
Spontaneous intracerebral hemorrhage in CADASILQ37426546
Therapeutic strategies in migraine patients with mood and anxiety disorders: clinical evidenceQ37750571
Pathogenesis of CADASIL: transgenic and knock-out mice to probe function and dysfunction of the mutated gene, Notch3, in the cerebrovasculatureQ37802293
Is high homocysteine level a risk factor for cognitive decline in elderly? A systematic review, meta-analysis, and meta-regression.Q37894535
Rapid improvement of a complex migrainous episode with sodium valproate in a patient with CADASIL.Q37953847
Use of selective serotonin reuptake inhibitors and risk of stroke: a systematic review and meta-analysisQ38183266
Homocysteine and migraine. A narrative reviewQ38194756
Therapeutic modulation of Notch signalling--are we there yet?Q38208211
Interpretation of NOTCH3 mutations in the diagnosis of CADASIL.Q38213076
Effects of sapropterin on endothelium-dependent vasodilation in patients with CADASIL: a randomized controlled trialQ38424269
Successful Use of Intravenous Tissue Plasminogen Activator as Treatment for a Patient with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy: A Case Report and Review of Literature.Q38726318
CADASIL: Imaging Characteristics and Clinical CorrelationQ38945618
Results of a multicenter, double-blind, randomized, parallel-group, placebo-controlled, single-dose study comparing the fixed combination of acetaminophen, acetylsalicylic acid, and caffeine with ibuprofen for acute treatment of patients with severeQ39208535
Therapeutic NOTCH3 cysteine correction in CADASIL using exon skipping: in vitro proof of concept.Q39970746
Donepezil in patients with subcortical vascular cognitive impairment: a randomised double-blind trial in CADASIL.Q40120849
Predictors of Clinical Worsening in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy: Prospective Cohort StudyQ40310544
Brain volume changes in CADASIL: a serial MRI study in pure subcortical ischemic vascular diseaseQ40323159
Diffusion magnetic resonance histograms as a surrogate marker and predictor of disease progression in CADASIL: a two-year follow-up studyQ40375032
Notch3 is required for arterial identity and maturation of vascular smooth muscle cellsQ40408474
Long-term prognosis and causes of death in CADASIL: a retrospective study in 411 patientsQ40483321
A two-year clinical follow-up study in 80 CADASIL subjects: progression patterns and implications for clinical trialsQ40508931
Differential lesion patterns in CADASIL and sporadic subcortical arteriosclerotic encephalopathy: MR imaging study with statistical parametric group comparison.Q40729011
Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementiaQ41611079
Reduced cerebrovascular CO(2) reactivity in CADASIL: A transcranial Doppler sonography studyQ42497899
Cholinergic neuronal deficits in CADASIL.Q42504530
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: from stroke to vessel wall physiologyQ43071273
Acetazolamide improves cerebral hemodynamics in CADASIL.Q43130867
Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3-negative patientsQ43206146
Recommendations for the predictive genetic test in Huntington's diseaseQ43453202
Hyperhomocysteinemia in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).Q43836523
Cerebral hemodynamics and white matter hyperintensities in CADASIL.Q44456707
Clinical spectrum of CADASIL and the effect of cardiovascular risk factors on phenotype: study in 200 consecutively recruited individualsQ44523405
Homocysteine is a risk factor for cerebral small vessel disease, acting via endothelial dysfunctionQ44649021
Positron emission tomography examination of cerebral blood flow and glucose metabolism in young CADASIL patientsQ44797133
Parkinsonism is a late, not rare, feature of CADASIL: a study on Italian patients carrying the R1006C mutationQ44872355
The influence of genetic and cardiovascular risk factors on the CADASIL phenotypeQ44960188
Homocysteine and stroke: evidence on a causal link from mendelian randomisationQ45225758
Cognitive impairment and cerebral hypoperfusion in a CADASIL patient improved during administration of lomerizine.Q45975872
Effect of B-vitamins on stroke risk among individuals with vascular disease who are not on antiplatelets: A meta-analysisQ46344721
Galantamine therapy in dementia associated with CADASILQ46358259
Does donepezil improve executive function in patients with CADASIL?Q46736693
Characterization of Notch3-deficient mice: normal embryonic development and absence of genetic interactions with a Notch1 mutationQ47408089
CADASIL mimicking multiple sclerosis: The importance of clinical and MRI red flags.Q47970947
Hereditary multi-infarct dementia. Morphological and clinical studies of a new diseaseQ48271434
Cysteine-sparing CADASIL mutations in NOTCH3 show proaggregatory properties in vitroQ48368188
Blood pressure and haemoglobin A1c are associated with microhaemorrhage in CADASIL: a two-centre cohort studyQ48470173
Systemic blood pressure profile in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathyQ48699356
Clinical Pregenetic Screening for Stroke Monogenic Diseases: Results From Lombardia GENS RegistryQ48704656
Cognition in CADASIL.Q48810511
MRI hyperintensities of the temporal lobe and external capsule in patients with CADASIL.Q48955726
Cerebral hemodynamics in CADASIL before and after acetazolamide challenge assessed with MRI bolus trackingQ49057398
CADASIL presenting as schizophreniform organic psychosis.Q51038579
Low blood pressure and the risk of dementia in very old individuals.Q51944569
Intracerebral hemorrhages in CADASIL.Q53583841
Blood pressure and dementia in persons 75+ years old: 3-year follow-up results from the Kungsholmen Project.Q53758300
Notch3 ectodomain is a major component of granular osmiophilic material (GOM) in CADASILQ57187397
Impaired vasoreactivity in mildly disabled CADASIL patientsQ60445604
P433issue9
P304page(s)31
P577publication date2017-09-01
P1433published inCurrent treatment options in neurologyQ26842298
P1476titleCADASIL: Treatment and Management Options
P478volume19

Reverse relations

cites work (P2860)
Q90015682A Patient with Combined CADASIL and MTHFR Homozygosity
Q90620516Periventricular Hyperintensities Mimicking Multiple Sclerosis

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