Lista de obras - Piero Farruggia - Dominio Público Uruguay

A 20-year long term experience of the Italian Diamond-Blackfan Anaemia Registry: RPS and RPL genes, different faces of the same disease?

artículo científico publicado en 2020

A retrospective study of paroxysmal nocturnal hemoglobinuria in pediatric and adolescent patients

artículo científico publicado en 2017

Abdomen/pelvis computed tomography in staging of pediatric Hodgkin Lymphoma: is it always necessary?

scientific article published on 03 August 2016

AluY-mediated germline deletion, duplication and somatic stem cell reversion in UBE2T defines a new subtype of Fanconi anemia.

artículo científico publicado en 2015

Are all cases of paediatric essential thrombocythaemia really myeloproliferative neoplasms? Analysis of a large cohort.

artículo científico publicado en 2015

Ataluren-driven Restoration of Shwachman-Bodian-Diamond Syndrome Protein Function in Shwachman-Diamond Syndrome Bone Marrow Cells

artículo científico publicado en 2017

Autoimmune neutropenia of childhood secondary to other autoimmune disorders: Data from the Italian neutropenia registry

artículo científico publicado en 2017

Autoimmune neutropenia of infancy: Data from the Italian neutropenia registry

artículo científico publicado en 2015

Bone marrow histology for the diagnosis of essential thrombocythemia in children: a multicenter Italian study.

artículo científico publicado en 2017

Castleman's disease in childhood: report of three cases and review of the literature

artículo científico publicado en 2011

Cerebral Stroke in a Teenage Girl with Paroxysmal Nocturnal Hemoglobinuria

artículo científico publicado en 2017

Clinical impact of miR-223 expression in pediatric T-Cell lymphoblastic lymphoma.

artículo científico publicado en 2017

Clinical manifestations and management of four children with Pearson syndrome

artículo científico publicado en 2011

Congenital and acquired neutropenia consensus guidelines on diagnosis from the Neutropenia Committee of the Marrow Failure Syndrome Group of the AIEOP (Associazione Italiana Emato-Oncologia Pediatrica).

artículo científico publicado en 2011

Congenital and acquired neutropenias consensus guidelines on therapy and follow-up in childhood from the Neutropenia Committee of the Marrow Failure Syndrome Group of the AIEOP (Associazione Italiana Emato-Oncologia Pediatrica).

artículo científico publicado en 2011

Congenital hepatic fibrosis: a very uncommon cause of pancytopenia in children

artículo científico publicado en 2005

Detection of prognostic factors in children and adolescents with Burkitt and Diffuse Large B-Cell Lymphoma treated with the AIEOP LNH-97 protocol

artículo científico publicado en 2016

Diagnosis and management of acquired aplastic anemia in childhood. Guidelines from the Marrow Failure Study Group of the Pediatric Haemato-Oncology Italian Association (AIEOP).

artículo científico publicado en 2015

Diagnosis and management of newly diagnosed childhood autoimmune haemolytic anaemia. Recommendations from the Red Cell Study Group of the Paediatric Haemato-Oncology Italian Association

artículo científico publicado en 2016

Diagnosis and management of primary autoimmune neutropenia in children: insights for clinicians.

artículo científico publicado en 2015

Diagnostic value of cell bound and circulating neutrophil antibody detection in pediatric neutropenia

artículo científico publicado en 2017

Effect of eradication of Helicobacter pylori in children with chronic immune thrombocytopenia: a prospective, controlled, multicenter study.

artículo científico publicado en 2010

Effectiveness of cyclosporine and mycophenolate mofetil in a child with refractory evans syndrome

artículo científico publicado en 2011

Efficacy of combined intravenous immunoglobulins and steroids in children with primary immune thrombocytopenia and persistent bleeding symptoms

artículo científico publicado en 2014

FIP1L1-PDGFRα-positive hypereosinophilic syndrome in childhood: a case report and review of literature.

artículo científico publicado en 2014

Fanconi anemia patients are more susceptible to infection with tumor virus SV40

artículo científico publicado en 2013

Fatigue perception in a cohort of children with chronic immune thrombocytopenia and their caregivers using the PedsQL MFS: Real-life multicenter experience of the Italian Association of Pediatric Hematology and Oncology (AIEOP)

artículo científico publicado en 2020

Focal nodular hyperplasia of the liver: an unusual association with diabetes mellitus in a child and review of literature

artículo científico publicado en 2010

HLA-G+3027 polymorphism is associated with tumor relapse in pediatric Hodgkin's lymphoma.

artículo científico publicado en 2017

Hepatopathy-thrombocytopenia syndrome (HTS) after actinomycin-D therapy: report of three cases and review of the literature

artículo científico publicado en 2011

Hodgkin lymphoma and nephrotic syndrome in childhood.

artículo científico publicado en 2010

Hypereosinophilic syndrome in childhood: clinical and molecular features of two cases.

artículo científico publicado en 2009

Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia.

artículo científico publicado en 2017

Identification of point mutations and large intragenic deletions in Fanconi anemia using next-generation sequencing technology

artículo científico publicado en 2015

Idiopathic neutropenia of infancy: Data from the Italian Neutropenia Registry

scientific article published on 18 December 2018

Immune neutropenias of infancy and childhood

artículo científico publicado en 2015

Infectious complications in children with severe congenital, autoimmune or idiopathic neutropenia: a retrospective study from the Italian Neutropenia Registry.

artículo científico publicado en 2013

Kinetics of Circulating Plasma Cell-Free DNA in Paediatric Classical Hodgkin Lymphoma

artículo científico publicado en 2016

Lethal sepsis and malignant transformation in severe congenital neutropenia: report from the Italian Neutropenia Registry

scientific article published on 25 January 2015

Long-term follow-up analysis after rituximab therapy in children with refractory symptomatic ITP: identification of factors predictive of a sustained response

artículo científico publicado en 2008

Long-term results of the AIEOP MH'96 childhood Hodgkin's lymphoma trial and focus on significance of response to chemotherapy and its implication in low risk patients to avoid radiotherapy.

artículo científico publicado en 2018

MPL W515L mutation in pediatric essential thrombocythemia.

artículo científico publicado en 2013

Management of chronic childhood immune thrombocytopenic purpura: AIEOP consensus guidelines

artículo científico publicado en 2009

Mesenchymal stromal cells from Shwachman-Diamond syndrome patients fail to recreate a bone marrow niche in vivo and exhibit impaired angiogenesis

artículo científico publicado en 2018

Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology

Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology.

artículo científico publicado en 2014

Mycophenolate mofetil for the treatment of children with immune thrombocytopenia and Evans syndrome. A retrospective data review from the Italian association of paediatric haematology/oncology.

artículo científico publicado en 2016

Pearson syndrome.

artículo científico publicado en 2018

Plasma cell-free DNA in paediatric lymphomas.

artículo científico publicado en 2013

Poikiloderma with neutropenia: a case report and review of the literature

artículo científico

Postchemotherapy PET evaluation correlates with patient outcome in paediatric Hodgkin's disease.

artículo científico publicado en 2011

Recombinant erythropoietin vs. blood transfusion care in infants with hereditary spherocytosis: a retrospective cohort study of A.I.E.O.P. patients (Associazione Italiana Emato-Oncologia Pediatrica).

artículo científico publicado en 2017

Reversible posterior leukoencephalopathy syndrome: report of 2 simultaneous cases in children.

artículo científico publicado en 2006

Ribosomal RNA analysis in the diagnosis of Diamond-Blackfan Anaemia.

artículo científico publicado en 2016

Somatic, hematologic phenotype, long-term outcome, and effect of hematopoietic stem cell transplantation. An analysis of 97 Fanconi anemia patients from the Italian national database on behalf of the Marrow Failure Study Group of the AIEOP (Italian A

article

Split chimerism may be enough to cure Evans syndrome

scientific article published on 19 June 2006

Synovial sarcoma of the neck in a child: a multidisciplinary approach

artículo científico publicado en 2008

The prognostic value of biological markers in paediatric Hodgkin lymphoma

artículo científico publicado en 2015

Treatment of human papillomavirus infection with interferon alpha and ribavirin in a patient with acquired aplastic anemia

artículo científico publicado en 2014

Vocal cord palsy after vincristine treatment in a child and the inefficacy of glutamic acid in the prevention of relapse: a case report.

artículo científico publicado en 2012

p38 Mitogen-activated protein kinase inhibition enhances in vitro erythropoiesis of Fanconi anemia, complementation group A-deficient bone marrow cells.

artículo científico publicado en 2014

Lista de obras de Piero Farruggia

A 20-year long term experience of the Italian Diamond-Blackfan Anaemia Registry: RPS and RPL genes, different faces of the same disease?

A retrospective study of paroxysmal nocturnal hemoglobinuria in pediatric and adolescent patients

Abdomen/pelvis computed tomography in staging of pediatric Hodgkin Lymphoma: is it always necessary?

AluY-mediated germline deletion, duplication and somatic stem cell reversion in UBE2T defines a new subtype of Fanconi anemia.

Are all cases of paediatric essential thrombocythaemia really myeloproliferative neoplasms? Analysis of a large cohort.

Ataluren-driven Restoration of Shwachman-Bodian-Diamond Syndrome Protein Function in Shwachman-Diamond Syndrome Bone Marrow Cells

Autoimmune neutropenia of childhood secondary to other autoimmune disorders: Data from the Italian neutropenia registry

Autoimmune neutropenia of infancy: Data from the Italian neutropenia registry

Bone marrow histology for the diagnosis of essential thrombocythemia in children: a multicenter Italian study.

Castleman's disease in childhood: report of three cases and review of the literature

Cerebral Stroke in a Teenage Girl with Paroxysmal Nocturnal Hemoglobinuria

Clinical impact of miR-223 expression in pediatric T-Cell lymphoblastic lymphoma.

Clinical manifestations and management of four children with Pearson syndrome

Congenital and acquired neutropenia consensus guidelines on diagnosis from the Neutropenia Committee of the Marrow Failure Syndrome Group of the AIEOP (Associazione Italiana Emato-Oncologia Pediatrica).

Congenital and acquired neutropenias consensus guidelines on therapy and follow-up in childhood from the Neutropenia Committee of the Marrow Failure Syndrome Group of the AIEOP (Associazione Italiana Emato-Oncologia Pediatrica).

Congenital hepatic fibrosis: a very uncommon cause of pancytopenia in children

Detection of prognostic factors in children and adolescents with Burkitt and Diffuse Large B-Cell Lymphoma treated with the AIEOP LNH-97 protocol

Diagnosis and management of acquired aplastic anemia in childhood. Guidelines from the Marrow Failure Study Group of the Pediatric Haemato-Oncology Italian Association (AIEOP).

Diagnosis and management of newly diagnosed childhood autoimmune haemolytic anaemia. Recommendations from the Red Cell Study Group of the Paediatric Haemato-Oncology Italian Association

Diagnosis and management of primary autoimmune neutropenia in children: insights for clinicians.

Diagnostic value of cell bound and circulating neutrophil antibody detection in pediatric neutropenia

Effect of eradication of Helicobacter pylori in children with chronic immune thrombocytopenia: a prospective, controlled, multicenter study.

Effectiveness of cyclosporine and mycophenolate mofetil in a child with refractory evans syndrome

Efficacy of combined intravenous immunoglobulins and steroids in children with primary immune thrombocytopenia and persistent bleeding symptoms

FIP1L1-PDGFRα-positive hypereosinophilic syndrome in childhood: a case report and review of literature.

Fanconi anemia patients are more susceptible to infection with tumor virus SV40

Fatigue perception in a cohort of children with chronic immune thrombocytopenia and their caregivers using the PedsQL MFS: Real-life multicenter experience of the Italian Association of Pediatric Hematology and Oncology (AIEOP)

Focal nodular hyperplasia of the liver: an unusual association with diabetes mellitus in a child and review of literature

HLA-G+3027 polymorphism is associated with tumor relapse in pediatric Hodgkin's lymphoma.

Hepatopathy-thrombocytopenia syndrome (HTS) after actinomycin-D therapy: report of three cases and review of the literature

Hodgkin lymphoma and nephrotic syndrome in childhood.

Hypereosinophilic syndrome in childhood: clinical and molecular features of two cases.

Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia.

Identification of point mutations and large intragenic deletions in Fanconi anemia using next-generation sequencing technology

Idiopathic neutropenia of infancy: Data from the Italian Neutropenia Registry

Immune neutropenias of infancy and childhood

Infectious complications in children with severe congenital, autoimmune or idiopathic neutropenia: a retrospective study from the Italian Neutropenia Registry.

Kinetics of Circulating Plasma Cell-Free DNA in Paediatric Classical Hodgkin Lymphoma

Lethal sepsis and malignant transformation in severe congenital neutropenia: report from the Italian Neutropenia Registry

Long-term follow-up analysis after rituximab therapy in children with refractory symptomatic ITP: identification of factors predictive of a sustained response

Long-term results of the AIEOP MH'96 childhood Hodgkin's lymphoma trial and focus on significance of response to chemotherapy and its implication in low risk patients to avoid radiotherapy.

MPL W515L mutation in pediatric essential thrombocythemia.

Management of chronic childhood immune thrombocytopenic purpura: AIEOP consensus guidelines

Mesenchymal stromal cells from Shwachman-Diamond syndrome patients fail to recreate a bone marrow niche in vivo and exhibit impaired angiogenesis

Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology

Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology.

Mycophenolate mofetil for the treatment of children with immune thrombocytopenia and Evans syndrome. A retrospective data review from the Italian association of paediatric haematology/oncology.

Pearson syndrome.

Plasma cell-free DNA in paediatric lymphomas.

Poikiloderma with neutropenia: a case report and review of the literature

Postchemotherapy PET evaluation correlates with patient outcome in paediatric Hodgkin's disease.

Recombinant erythropoietin vs. blood transfusion care in infants with hereditary spherocytosis: a retrospective cohort study of A.I.E.O.P. patients (Associazione Italiana Emato-Oncologia Pediatrica).

Reversible posterior leukoencephalopathy syndrome: report of 2 simultaneous cases in children.

Ribosomal RNA analysis in the diagnosis of Diamond-Blackfan Anaemia.

Somatic, hematologic phenotype, long-term outcome, and effect of hematopoietic stem cell transplantation. An analysis of 97 Fanconi anemia patients from the Italian national database on behalf of the Marrow Failure Study Group of the AIEOP (Italian A

Split chimerism may be enough to cure Evans syndrome

Synovial sarcoma of the neck in a child: a multidisciplinary approach

The prognostic value of biological markers in paediatric Hodgkin lymphoma

Treatment of human papillomavirus infection with interferon alpha and ribavirin in a patient with acquired aplastic anemia

Vocal cord palsy after vincristine treatment in a child and the inefficacy of glutamic acid in the prevention of relapse: a case report.

p38 Mitogen-activated protein kinase inhibition enhances in vitro erythropoiesis of Fanconi anemia, complementation group A-deficient bone marrow cells.