12 results match your criteria: "San Bartolo Hospital[Affiliation]"
Graefes Arch Clin Exp Ophthalmol
November 2023
Eye Clinic, ASST Spedali Civili Di Bescia, Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia Medical School, Piazzale Spedali Civili, 1, 25125, Brescia, Italy.
Purpose: To provide a comprehensive review of the incidence, risk factors, and management of early complications after deep anterior lamellar keratoplasty (DALK), Descemet stripping automated keratoplasty (DSAEK), and Descemet membrane endothelial keratoplasty (DMEK).
Methods: A literature review of complications, that can occur from the time of the transplant up to 1 month after the transplant procedure, was conducted. Case reports and case series were included in the review.
JAMA Netw Open
September 2022
Ann & Robert Lurie Children's Hospital of Chicago, Northwestern University, Chicago, Illinois.
Importance: Increasing evidence indicates that acute kidney injury (AKI) occurs frequently in children and young adults and is associated with poor short-term and long-term outcomes. Guidance is required to focus efforts related to expansion of pediatric AKI knowledge.
Objective: To develop expert-driven pediatric specific recommendations on needed AKI research, education, practice, and advocacy.
Am J Ophthalmol
September 2022
St. Paul's Eye Unit, Royal Liverpool University Hospital (S.B.K., V.R.), Liverpool, UK; Department of Eye and Vision Science, Institute of Ageing and Chronic Disease, University of Liverpool (S.B.K., V.R.), Liverpool, UK; Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, Ophthalmology Clinic, University of Brescia (V.R.), Brescia, Italy; Instituto Universitario Fernandez-Vega, Universidad de Oviedo, and Fundacion de Investigacion on Oftalmologica (V.R.), Oviedo, Asturias, Spain. Electronic address:
Purpose: To evaluate factors affecting the outcomes of preloaded Descemet membrane endothelial keratoplasty (pl-DMEK) with endothelium-inward.
Design: Retrospective clinical case series and a comparative tissue preparation study.
Methods: Participants: Fifty-five donor tissues for ex vivo study and 147 eyes of 147 patients indicated with Fuchs endothelial dystrophy or pseudophakic bullous keratopathy with or without cataract.
Histopathology
January 2021
Department of Pathology, Boston Children's Hospital, Boston, MA, USA.
Aims: Primary intracranial sarcoma, DICER1-mutant is a recently described central nervous system tumour with specific genomic and DNA-methylation profiles. Although some of its histological features (focal spindle-cell morphology, intracytoplasmic eosinophilic granules, and focal heterologous differentiation) are common across most reported cases, the presence of significant histological variability and the lack of differentiation pose diagnostic challenges. We aim to further define the immunoprofile of this tumor.
View Article and Find Full Text PDFActa Neurochir (Wien)
January 2020
Department of Neuroscience and Neurosurgery, San Bartolo Hospital, Vicenza, Italy.
Int J Gynaecol Obstet
February 2020
Department of Obstetrics and Gynecology, San Bartolo Hospital, Vicenza, Italy.
Background: The FIGO Working Group (FWG) in Pelvic Floor Medicine and Reconstructive Surgery (2012-2015) established a consensus among international opinion leaders in evaluating current evidence and providing practice recommendations.
Objectives: To provide an update of the previous clinical opinion report on conservative and surgical treatment of posterior compartment prolapse.
Search Strategy: Search of evidence was performed using Pubmed, Embase, and Cochrane Library databases up to August 2018.
Clin Cancer Res
October 2014
Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Purpose: Activated signal transducer and activator of transcription 3 (STAT3) regulates tumor growth, invasion, cell proliferation, angiogenesis, immune response, and survival. Data regarding expression of phosphorylated (activated) STAT3 in diffuse large B-cell lymphoma (DLBCL) and the impact of phosphorylated STAT3 (pSTAT3) on prognosis are limited.
Experimental Design: We evaluated expression of pSTAT3 in de novo DLBCL using immunohistochemistry, gene expression profiling (GEP), and gene set enrichment analysis (GSEA).
Haemophilia
May 2014
Department of Cell Therapy and Hematology, Hemophilia and Thrombosis Center, San Bartolo Hospital, Vicenza, Italy.
The deficiency or abnormal function of von Willebrand factor (VWF) causes von Willebrand disease (VWD), the most frequent inherited bleeding disorder. The laboratory diagnosis of VWD can be difficult as the disease is heterogeneous and an array of assays is required to describe the phenotype. Basic classification of quantitative (type 1 and 3) and qualitative (type 2) VWD variants requires determination of VWF antigenic (VWF:Ag) levels and assaying of VWF ristocetin cofactor (VWF:RCo) activity, determining the capacity of VWF to interact with the platelet GPIb-receptor.
View Article and Find Full Text PDFClin Cancer Res
May 2014
Authors' Affiliations: Departments of Hematopathology and Biostatistics and Bioinformatics, The University of Texas MD Anderson Cancer Center; The Methodist Hospital, Houston, Texas; Memorial Sloan-Kettering Cancer Center; Weill Medical College of Cornell University; Columbia University Medical Center and New York Presbyterian Hospital, New York, New York; University of North Carolina School of Medicine, Chapel Hill, North Carolina; Cleveland Clinic, Cleveland, Ohio; University of California San Francisco School of Medicine, San Francisco, California; Gundersen Lutheran Health System, La Crosse, Wisconsin; Feinberg School of Medicine, Northwestern University, Chicago, Illinois; San Bartolo Hospital, Vicenza; San Raffaele H. Scientific Institute, Milan, Italy; University Hospital, Basel, Switzerland; Hospital Universitario Marques de Valdecilla, Santander, Spain; Aalborg University Hospital, Aalborg; Odense University Hospital, Odense, Denmark; Medical School of Taizhou University, Taizhou, Zhejiang; University of Hong Kong Li Ka Shing Faculty of Medicine, Hong Kong, China; Radboud University Nijmegen Medical Centre, Nijmegen, the Netherlands; and Asan Medical Center, Ulsan University College of Medicine, Seoul, Korea.
Purpose: Epstein-Barr virus-positive (EBV(+)) diffuse large B-cell lymphoma (DLBCL) of the elderly is a variant of DLBCL with worse outcome that occurs most often in East-Asian countries and is uncommon in the Western hemisphere. We studied the largest cohort of EBV(+) DLBCL, independent of age, treated with rituximab combined with CHOP (R-CHOP) in developed Western countries.
Experimental Design: A large cohort (n = 732) of patients with DLBCL treated with R-CHOP chemotherapy is included from the multicenter consortium.
AIDS Care
February 2004
Department of Infectious Diseases, San Bartolo Hospital, Vincenza, Italy.
Haematologica
March 2002
Department of Cellular Therapy and Hematology, Division of Hematology, San Bartolo Hospital, Vicenza, Italy.
Background And Objectives: CD56 antigen expression has been reported in several hematologic malignancies. In acute myeloid leukemia (AML)M2 with t(8;21) and acute promyelocytic leukemia (APL) it has been found to be consistently associated with an unfavorable prognosis, whereas in other AML subtypes its role remains uncertain. We investigated CD56 expression in a cohort of AML patients in order to assess its frequency and prognostic relevance.
View Article and Find Full Text PDFHaematologica
August 1994
Department of Hematology, San Bartolo Hospital, Vicenza, Italy.
Background: High dose intravenous immunoglobulin (h.d. Ig) is increasingly used in several hematological diseases.
View Article and Find Full Text PDF