Search Results - "Buti, Elisa"
-
1
Urinary Biomarkers for Diagnosis and Prediction of Acute Kidney Allograft Rejection: A Systematic Review
Published in International journal of molecular sciences (19-09-2020)“…Noninvasive tools for diagnosis or prediction of acute kidney allograft rejection have been extensively investigated in recent years. Biochemical and molecular…”
Get full text
Journal Article -
2
Clinical and Genetic Characterization of Patients with Bartter and Gitelman Syndrome
Published in International journal of molecular sciences (18-05-2022)“…Bartter (BS) and Gitelman (GS) syndrome are autosomal recessive inherited tubulopathies, whose clinical diagnosis can be challenging, due to rarity and…”
Get full text
Journal Article -
3
3092 Case report: Renal cystic disease caused to heterozygous NEK8 variant in pediatric patient
Published in Nephrology, dialysis, transplantation (23-05-2024)“…Abstract Background and Aims Polycystic kidney diseases (PKDs) are the most prevalent inherited kidney disease [1]. They are caused by pathogenic variants in…”
Get full text
Journal Article -
4
Response to Third Dose of Vaccine Against SARS-CoV-2 in Adolescent and Young Adult Kidney Transplant Recipients
Published in Transplantation (01-08-2022)Get full text
Journal Article -
5
Renal Scintigraphy in the Follow-Up of Patients With Congenital Single Functioning Kidney: SA-PO621
Published in Journal of the American Society of Nephrology (01-11-2022)Get full text
Journal Article -
6
2814 Characterization of cardiological manifestations in patients with sodium-wasting tubulopathies
Published in Nephrology, dialysis, transplantation (23-05-2024)“…Abstract Background and Aims Bartter (BS) and Gitelman (GS) syndromes are rare tubulopathies caused by mutations affecting renal NaCl transporters, resulting…”
Get full text
Journal Article -
7
Response to Third Dose of Vaccine Against SARS-CoV-2 in Adolescent and Young Adult Kidney Transplant Recipients
Published in Transplantation (18-05-2022)Get full text
Journal Article -
8
1784 The potential impact of chronic subclinical hypervolemia on left ventricular hypertrophy in children on dialysis: a prospective longitudinal study
Published in Nephrology, dialysis, transplantation (23-05-2024)“…Abstract Background and Aims Hypervolemia poses a significant challenge in pediatric patients undergoing dialysis, potentially leading to severe complications…”
Get full text
Journal Article -
9
MO1024 CLOSTRIDIUM SEPTICUM INFECTION COMPLICATING HEMOLYTIC UREMIC SYNDROME: A CASE REPORT AND LITERATURE REVIEW
Published in Nephrology, dialysis, transplantation (29-05-2021)“…Abstract Background and Aims C.septicum is an anaerobic bacterium that resides in the gastrointestinal tract of herbivores. Its presence in human fecal flora…”
Get full text
Journal Article -
10
Defining diagnostic trajectories in patients with podocytopathies
Published in Clinical kidney journal (01-11-2022)“…Podocytopathies are glomerular disorders in which podocyte injury drives proteinuria and progressive kidney disease. They encompass a broad spectrum of…”
Get full text
Journal Article -
11
Lupus Nephritis Patterns and Response to Type I Interferon in Patients With DNASE1L3 Variants: Report of Three Cases
Published in American journal of kidney diseases (01-12-2024)“…DNASE1L3 is an extracellular nuclease that digests chromatin released from apoptotic cells. DNASE1L3 variants impair the enzyme function, enhance autoantibody…”
Get full text
Journal Article -
12
P1805UNEXPECTD COMPLEMENT GENES ABNORALITIES IN CHILDREN WITH SECONDARY HEMOLITIC UREMIC SYNDROME
Published in Nephrology, dialysis, transplantation (01-06-2020)“…Abstract Background and Aims Secondary hemolytic-uremic syndrome (HUS) is currently defined in the absence of genetic defects in complement genes (primary or…”
Get full text
Journal Article -
13
Plasma DNA Profile Associated with DNASE1L3 Gene Mutations: Clinical Observations, Relationships to Nuclease Substrate Preference, and In Vivo Correction
Published in American journal of human genetics (05-11-2020)“…Plasma DNA fragmentomics is an emerging area in cell-free DNA diagnostics and research. In murine models, it has been shown that the extracellular DNase,…”
Get full text
Journal Article -
14
Childhood-onset Erdheim-Chester disease in the molecular era: clinical phenotypes and long-term outcomes of 21 patients
Published in Blood (28-09-2023)“…[Display omitted] Erdheim-Chester disease (ECD) is a rare histiocytic disorder that can present as a localized infiltration of foamy histiocytes or a…”
Get full text
Journal Article -
15
Effect of antimetabolite regimen on cellular and humoral immune response to SARS-COV-2 vaccination in solid organ transplant recipients
Published in Immunology letters (01-08-2024)“…•Immunosuppressive treatment reduces both cellular and humoral immune response to SARS-CoV-2 mRNA vaccination.•Patients undergoing antimetabolites-including…”
Get full text
Journal Article -
16
P1813CLINICAL CHARACTERIZATION OF CONGENITAL SOLITARY FUNCTIONING KIDNEY IN CHILDREN
Published in Nephrology, dialysis, transplantation (01-06-2020)“…Abstract Background and Aims Congenital anomalies of the kidney and urinary tract (CAKUT) are the major cause of chronic kidney disease and end-stage kidney…”
Get full text
Journal Article -
17
FC040: Kidney Transplantation in Childhood-Onset ANCA-Associated Vasculitis: Outcomes in a Multicentre Cohort
Published in Nephrology, dialysis, transplantation (03-05-2022)“…Abstract BACKGROUND AND AIMS ANCA-associated vasculitis (AAV) is rare among children but leads to kidney failure (KF) in almost 30% of cases with renal…”
Get full text
Journal Article -
18
1,25 Dihydroxyvitamin D circulating levels, calcitriol administration, and incidence of acute rejection, CMV infection, and polyoma virus infection in renal transplant recipients
Published in Clinical transplantation (01-10-2016)“…Observation that 1,25‐Dihydroxyvitamin‐D3 has an immunomodulatory effect on innate and adaptive immunity raises the possible effect on clinical graft outcome…”
Get full text
Journal Article -
19
Lupus Nephritis Patterns and Response to Type I Interferon in Patients With DNASE1L3 Mutations: Report of Three Cases
Published in American journal of kidney diseases (24-07-2024)“…DNASE1L3 is an extracellular nuclease that digests chromatin released from apoptotic cells. DNASE1L3 mutations impair the enzyme function, enhance autoantibody…”
Get full text
Journal Article -
20