Search Results - "Rovelli, Attilio"
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Lessons after the early management of the COVID-19 outbreak in a pediatric transplant and hemato-oncology center embedded within a COVID-19 dedicated hospital in Lombardia, Italy. Estote parati
Published in Bone marrow transplantation (Basingstoke) (01-10-2020)“…Italy is the second exposed country worldwide, after China, and Lombardia is the most affected region in Italy, with more than half of the national cases, with…”
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Lentiviral Hematopoietic Stem Cell Gene Therapy Benefits Metachromatic Leukodystrophy
Published in Science (American Association for the Advancement of Science) (23-08-2013)“…Metachromatic leukodystrophy (MLD) is an inherited lysosomal storage disease caused by arylsulfatase A (ARSA) deficiency. Patients with MLD exhibit progressive…”
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Open issues in Mucopolysaccharidosis type I-Hurler
Published in Orphanet journal of rare diseases (15-06-2017)“…Mucopolysaccharidosis I-Hurler (MPS I-H) is the most severe form of a metabolic genetic disease caused by mutations of IDUA gene encoding the lysosomal…”
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Enzyme replacement therapy and/or hematopoietic stem cell transplantation at diagnosis in patients with mucopolysaccharidosis type I: results of a European consensus procedure
Published in Orphanet journal of rare diseases (10-08-2011)“…Mucopolysaccharidosis type I (MPS I) is a lysosomal storage disorder that results in the accumulation of glycosaminoglycans causing progressive multi-organ…”
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Setting up and sustaining blood and marrow transplant services for children in middle-income economies: an experience-driven position paper on behalf of the EBMT PDWP
Published in Bone marrow transplantation (Basingstoke) (01-03-2021)“…Severe blood disorders and cancer are the leading cause of death and disability from noncommunicable diseases in the global pediatric population and a major…”
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Growth patterns in children with mucopolysaccharidosis type I-Hurler after hematopoietic stem cell transplantation: Comparison with untreated patients
Published in Molecular genetics and metabolism reports (01-09-2021)“…The impact of hematopoietic stem cell transplantation (HSCT) on growth in patients diagnosed with mucopolysaccharidosis I Hurler (MPS-IH) has been historically…”
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Risk for Secondary Thyroid Carcinoma After Hematopoietic Stem-Cell Transplantation: An EBMT Late Effects Working Party Study
Published in Journal of clinical oncology (10-06-2007)“…The effects of hematopoietic stem-cell transplantation (HSCT) on thyroid carcinogenesis needs to be determined in a large population. This study evaluates the…”
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Risk factors and severe outcome in thrombotic microangiopathy after allogeneic hematopoietic stem cell transplantation
Published in Transplantation (01-09-2006)“…Thrombotic microangiopathy (TMA) has been described as severe complication after hematopoietic stem cell transplantation (HSCT). The principal aim of this…”
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A new case report of severe mucopolysaccharidosis type VII: diagnosis, treatment with haematopoietic cell transplantation and prenatal diagnosis in a second pregnancy
Published in Italian journal of pediatrics (16-11-2018)“…A new patient with severe mucopolysaccharidosis (MPS) type VII is reported. Non-immune hydrops fetalis (NIHF) was diagnosed during pregnancy. At birth, he…”
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Germ‐Line TP53 Mutation in an Adolescent With CMML/Atypical CML and Familiar Cancer Predisposition
Published in HemaSphere (01-10-2020)“…Supplemental Digital Content is available in the text…”
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Combination Antifungal Therapy for Invasive Mold Infections Among Pediatric Patients with Hematological Malignancies: Data from A Real-Life Case-Series
Published in Pathogens & immunity (05-09-2019)“…Invasive mold infections in children with hematological malignancies are associated with high mortality rates. The use of combination antifungal therapy in…”
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Quality of life of Hurler syndrome patients after successful hematopoietic stem cell transplantation
Published in Blood advances (14-11-2017)“…Hurler syndrome (HS) is a lysosomal storage disease characterized by multisystem morbidity and death in early childhood. Hematopoietic stem cell…”
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Mesenchymal Stromal Cells Do Not Increase the Risk of Viral Reactivation Nor the Severity of Viral Events in Recipients of Allogeneic Stem Cell Transplantation
Published in Stem Cells International (01-01-2012)“…Mesenchymal stromal cells (MSC) are tested in clinical trials to treat graft versus host disease (GvHD) after stem cell transplantation (SCT). In vitro studies…”
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Childhood Cerebral X-Linked Adrenoleukodystrophy More Than 5 Years After Hematopoietic Cell Transplantation: The First Case From Serbia and Southeastern Europe
Published in Journal of child neurology (01-12-2010)“…We report the clinical course, brain magnetic resonance imaging (MRI), and proton magnetic resonance spectroscopy findings in a boy with childhood cerebral…”
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Extracorporeal Photochemotherapy for the Treatment of Chronic Graft-Versus-Host Disease: Trend for a Possible Cell Dose-Related Effect?
Published in Therapeutic apheresis and dialysis (01-04-2007)“…: Extracorporeal photochemotherapy (ECP) has been progressively introduced into the treatment of both acute and chronic graft‐versus‐host disease (cGvHD) over…”
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Autoimmune Hematological Diseases after Allogeneic Hematopoietic Stem Cell Transplantation in Children: An Italian Multicenter Experience
Published in Biology of blood and marrow transplantation (01-02-2014)“…Abstract Autoimmune hematological diseases (AHDs) may occur after allogeneic hematopoietic stem cell transplantation (HSCT), but reports on these complications…”
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Sleeping Beauty-engineered CAR T cells achieve antileukemic activity without severe toxicities
Published in The Journal of clinical investigation (01-11-2020)“…BACKGROUNDChimeric antigen receptor (CAR) T cell immunotherapy has resulted in complete remission (CR) and durable response in highly refractory patients…”
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Long-term outcome of Hurler syndrome patients after hematopoietic cell transplantation: an international multicenter study
Published in Blood (26-03-2015)“…Mucopolysaccharidosis type I–Hurler syndrome (MPS-IH) is a lysosomal storage disease characterized by multisystem morbidity and death in early childhood…”
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