Burtey, Stéphane 1969-...
Stephane Burtey researcher
VIAF ID: 204903843 ( Personal )
Permalink: http://viaf.org/viaf/204903843
Preferred Forms
4xx's: Alternate Name Forms (1)
Works
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22q11.2 microdeletion syndrome is a common cause of renal tract malformations |
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[About two cases of hypokaliemic periodic paralysis] |
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Activation of AhR and cardiovascular risks in hemodyalysis patient |
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Acute tubulointerstitial nephritis complicating Legionnaires' disease: a case report |
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Adhésion et activation des cellules sanguines par une membrane d'hémodialyse (AN-69ST) : conséquence sur l'expression de facteur tissulaire et la thrombogénecité de la membrane. |
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Alternative splicing events is not a key event for gene expression regulation in uremia |
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Analysis of published PKD1 gene sequence variants |
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Ancestrally-duplicated paraHOX gene clusters in humans |
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[Antiphospholipids antibodies and hemodialysis: a frequent association linked to arteriovenous fistula thrombosis] |
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ARAVU (AGE-RAGE et Vasculopathie Urémique) - Rôle de l'interaction AGE-RAGE dans un modèle de vieillissement vasculaire : la vasculopathie urémique. |
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Aryl Hydrocarbon Receptor Activation and Tissue Factor Induction by Fluid Shear Stress and Indoxyl Sulfate in Endothelial Cells |
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Ascorbic Acid and gene expression: another example of regulation of gene expression by small molecules? |
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Association between anti-C1q antibodies and glomerular tuft necrosis in lupus nephritis. |
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[Association of dermatopolymyositis and chronic lymphoid leukemia] |
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Atteintes neurovasculaires de l'insuffisance rénale : impact de l'insuffisance rénale sur la barrière hémato-encéphalique et la prédisposition aux accidents vasculaires cérébraux |
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The authors reply |
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Cardiovascular long-term follow-up after pediatric kidney transplantation. |
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The Case: Hypocalcemia, chronic renal failure and dysmorphism |
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Cellular, molecular and epigenetic mechanism implicated in complications of chronic kidney disease. |
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Cerebrovascular impairments in kidney diseases : impact of renal failure on the blood-brain barrier and stroke susceptibility. |
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Cloning and expression of the amphibian homologue of the human PKD1 gene. |
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Comparative safety and efficiency of five percutaneous kidney biopsy approaches of native kidneys: a multicenter study |
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[Cycloid psychoses] |
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Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans |
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Diagnostic performance of [(18)F]fluorodeoxyglucose positron emission tomography-computed tomography in cyst infection in patients with autosomal dominant polycystic kidney disease. |
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End stage renal disease control alternative splicing of PKD1. |
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Epitope Spreading of Autoantibody Response to PLA2R Associates with Poor Prognosis in Membranous Nephropathy. |
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Familial and syndromic lupus share the same phenotype as other early-onset forms of lupus |
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Female AhR Knockout Mice Develop a Minor Renal Insufficiency in an Adenine-Diet Model of Chronic Kidney Disease |
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Fractalkine expression induces endothelial progenitor cell lysis by natural killer cells |
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From physiopathology to treatment : design of autosomal dominant polycystic kidney disease's model. |
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From polycystins to centrosomes, a key enzyme : the calcium/calmodulin dependant kinase 2. |
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Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide French series comparing children and adults |
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Haemodialysis access via tissue-engineered vascular graft. |
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[Hashimoto's encephalopathy. A new case] |
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Hemodialysis vascular graft as a focus of persistent Q fever |
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Hepatitis E virus of subtype 3i in chronically infected kidney transplant recipients in southeastern France |
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Hypokalaemia and dysmorphia, is there a link? |
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Hyponatrémie en hospitalisation : facteurs favorisants, prise en charge et pronostic |
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Identification of molecular partners responding to the activation of Aryl hydrocarbon Receptor by uremic toxins. |
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Impact of a transitional consultation in kidney transplantation. |
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Impact of chronic kidney disease on myostatin accumulation and muscle regeneration : role of indoxyl sulfate. |
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Indole 3-acetic acid, indoxyl sulfate and paracresyl-sulfate do not influence anemia parameters in hemodialysis patients. |
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Indolic uremic solutes induce an endothelial procoagulant phenotype via the AHR pathway. |
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De la physiopathologie à la thérapeutique : développement de modèles de la polykystose rénale autosomique dominante |
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La maladie cardiovasculaire dans une cohorte de patients transplantés rénaux à l'age pédiatrique, médiane de suivi : 12 années |
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Mean platelet volume and arteriovenous fistula dysfunction in a prospecti cohort of chronic hemodyalisis patients. |
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Mécanismes cellulaires, moléculaires et épigénétiques impliqués dans les complications de l'insuffisance rénale chronique |
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[Mechanisms of rupture of indwelling central venous catheters. 2 cases] |
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Membranoproliferative glomerulonephritis and mixed cryoglobulinemia after hepatitis C virus infection secondary to glomerular NS3 viral antigen deposits. |
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Meta-Analysis of Potent P2Y12-ADP Receptor Antagonist Therapy Compared to Clopidogrel Therapy in Acute Coronary Syndrome Patients with Chronic Kidney Disease |
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Modular transcriptional repertoire analyses identify a blood neutrophil signature as a candidate biomarker for lupus nephritis. |
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Modular transcriptional repertoire analyses of adults with systemic lupus erythematosus reveal distinct type I and type II interferon signatures |
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Mutation screening of the PKD1 transcript by RT-PCR. |
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Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1. |
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N-acetylcysteine inhibits endothelial tissue factor upregulation by the uremic toxin indoxyl sulfate. |
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New approach to non-invasive monitoring of alcohol by perspiration using MOX multi-sensors. |
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New diagnostic and prognostic marker in membranous nephropathy. |
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Nouveaux marqueurs diagnostiques et pronostiques dans la glomérulonéphrite extra-membraneuse : suivi des anticorps anti-PLA2R1 chez le greffé rénal : caractérisation des épitopes reconnus par les anticorps anti-PLA2R1 : identification d'une nouvelle cible antigénique |
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Plasma Xanthine Oxidase Activity Is Predictive of Cardiovascular Disease in Patients with Chronic Kidney Disease, Independently of Uric Acid Levels |
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Prise en charge du myélome multiple : expérience dans le Service de Néphrologie du CHU de Marseille, période 2000-2008 |
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Quality of vitamin K-antagonist treatment in chronic hemodialiysis. |
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Remission of C3 glomerulopathy with rituximab as only immunosuppressive therapy. |
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Renal amyloidosis : Experience in the nephrology department of the University Hospital of Marseille : Period 2000-2011. |
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Renal failure associated with colonoscopy-what is the link? |
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Risk factors for severity of COVID-19 in chronic dialysis patients from a multicentre French cohort |
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Rôle de l'Aryl Hydrocarbon Receptor dans la thrombose durant la maladie rénale chronique |
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The role of calprotectin in vascular calcification associated with chronic kidney disease. |
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Role of the uremic toxins and the transcription factor AhR in the regulation of liver transporters expression in chronic kidney disease. |
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Screening for mutations in PKD1 and PKD2 with High Resolution Melt. |
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Serum levels of miR-126 and miR-223 and outcomes in chronic kidney disease patients |
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Serum microRNAs are altered in various stages of chronic kidney disease: a preliminary study |
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The stromal vascular fraction from adipose tissue in urology : therapeutic properties and model for evaluating the vasculocompetence of the renal transplant. |
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Sudden Onset Nephrotic-Range Proteinuria |
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Survival of patients with ANCA-associated vasculitis on chronic dialysis: data from the French REIN registry from 2002 to 2011. |
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[Sweet's syndrome and aseptic abscess of the spleen] |
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Thrombotic microangiopathy associated with Gemcitabine use: presentation and outcome in a national French retrospective cohort |
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Thymic disease associated with nephrotic syndrome: a new case with membranous nephropathy and literature review |
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Towards Addressing the Body Electrolyte Environment via Sweat Analysis:Pilocarpine Iontophoresis Supports Assessment of Plasma Potassium Concentration. |
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Les toxines urémiques provoquent un phénotype procoagulant de l'endothelium par la voie du facteur de transcription AHR |
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Transcriptome analysis of a rat PKD model: Importance of genes involved in extracellular matrix metabolism |
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Trends in Survival and Renal Recovery in Patients with Multiple Myeloma or Light-Chain Amyloidosis on Chronic Dialysis. |
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An unusual renal colic: a tribute to Joseph Hyrtl (1810-1894) and Max Brödel (1870-1941) |
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Vancomycin-induced Henoch-Schönlein purpura: a case report. |
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