Results 121 to 130 of about 8,252,758 (233)
Identification of Copy Number Variants as a Suspected Cause of Cerebral Small Vessel Disease
Whole‐exome sequencing of 111 patients with suspected familial cerebral small vessel disease (CSVD) identified novel copy number variants in four patients across NOTCH3, LMNB1, and COL4A2, using bioinformatic and molecular techniques. These validated CNVs suggest structural variation is an underrecognized potential causal contributor to monogenic CSVD ...
Solomon K. Guyler +5 more
wiley +1 more source
Olaparib‐associated cutaneous vasculitis in a patient with breast cancer
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Marcial Álvarez‐Salafranca +3 more
wiley +1 more source
ABSTRACT Eosinophilia, defined as an absolute eosinophil count (AEC) of ≥ 0.5 × 109/L, is a frequently encountered finding with a vast spectrum of potential underlying etiologies. Hypereosinophilia (HE) is defined as AEC > 1.5 × 109/L and may become life‐threatening when eosinophil‐induced organ damage occurs, defining the hypereosinophilic syndrome ...
Stijn Wigerinck, Peter Vandenberghe
wiley +1 more source
A case of small vessel vasculitis
Anti-neutrophil cytoplasmic antibodies (ANCA) associated vasculitis is the most common primary systemic small-vessel vasculitis occurring in adults. Although the etiology is not always known, the incidence of vasculitis is increasing, with a variability ...
Madhulika Mahashabde, Harshad Patil
core +1 more source
Rapid induction of remission in large vessel vasculitis by IL-6 blockade
OBJECTIVE: To evaluate the effect of IL-6 blockade using tocilizumab in inducing remission of arterial large vessel vasculitides (LVV). METHODS: Five consecutive patients with giant-cell arteritis (GCA) and two with Takayasu’s arteritis ...
MN Seitz +5 more
doaj +1 more source
To assess the clinical value of 18F‐fluorodeoxyglucose (FDG) positron emission tomography (PET) in a prospective cohort of patients with large vessel vasculitis (LVV) and comparator subjects.
P. Grayson +10 more
semanticscholar +1 more source
Objective To characterize the clinical features, treatment, and outcomes of a large, international cohort of childhood‐onset Takayasu arteritis (cTAK). Methods Patients with a diagnosis of cTAK were identified in A Registry of Childhood Vasculitis and divided into subcohorts by era‐of diagnosis: pre‐biologic (PB; 1986–2006), early biologic (EB; 2007 ...
James Bistolarides +29 more
wiley +1 more source
Factors relacionats amb el manteniment de la inflamació i l'oclusió vascular. Implicacions en l'evolució dels pacients amb arteritis de cèl·lules gegants. [PDF]
[cat] L'arteritis de cèl·lules gegants (ACG) és una vasculitis sistèmica de caràcter granulomatós que afecta vasos de calibre mitjà i gran. Per aprofundir en els mecanismes que intervenen en el desenvolupament de la hiperplasia intimal i la inflamació en
Lozano Garcia, Ester
core +2 more sources
Introduction: Primary Sjögren's syndrome (PSS) is a systemic autoimmune disease that mainly affects exocrine glands. Little is known about PSS associated cervical and intracranial cerebral large-vessel vasculitis outside of individual case reports ...
Juehua Zhu +8 more
doaj +1 more source
Tubulointerstitial Nephritis With Uveitis Syndrome: A Case Report and Review of Literature
ABSTRACT TINU syndrome should be considered in any child presenting with unexplained renal dysfunction and uveitis. Early recognition and a multidisciplinary approach involving nephrology and ophthalmology are essential to prevent irreversible renal and ocular damage.
Abdulelah Alshaiban
wiley +1 more source

