Lista de obras - Gaetano Bergamaschi - Dominio Público Uruguay

A case of fever of unknown origin?

artículo científico publicado en 2015

A linkage between hereditary hyperferritinaemia not related to iron overload and autosomal dominant congenital cataract

scientific article published on 01 August 1995

A novel deletion of the l-ferritin iron-responsive element responsible for severe hereditary hyperferritinaemia-cataract syndrome

artículo científico publicado en 2002

A sensitive detection method for MPLW515L or MPLW515K mutation in chronic myeloproliferative disorders with locked nucleic acid-modified probes and real-time polymerase chain reaction.

artículo científico publicado en 2008

Abnormal regulation of HFE mRNA expression does not contribute to primary iron overload

scientific article published on 01 August 2000

Anaemia characterises patients with myelofibrosis harbouring Mpl mutation.

artículo científico publicado en 2007

Anemia in patients with Covid-19: pathogenesis and clinical significance

artículo científico publicado en 2021

Anemia of chronic disease and defective erythropoietin production in patients with celiac disease.

artículo científico publicado en 2008

Antigen profile and topographical distribution of marginal zone, monocytoid and epithelial-associated B-cells

scientific article published on 01 August 2005

Apoptosis: biological and clinical aspects.

artículo científico publicado en 1994

C-fms expression in B-cells and response to M-CSF

scientific article published on 01 August 1993

Cell Blood Count Alterations and Patterns of Anaemia in Autoimmune Atrophic Gastritis at Diagnosis: A Multicentre Study

scientific article published on 15 November 2019

Cell cycle distribution of cord blood-derived haematopoietic progenitor cells and their recruitment into the S-phase of the cell cycle

artículo científico publicado en 2000

Clonal nature of hematopoietic stem cell disorders

artículo científico publicado en 2004

Cord blood-derived hematopoietic progenitor cells: in vitro response to hematopoietic growth factors and their recruitment into the S-phase of the cell cycle

artículo científico publicado en 2000

Differential HFE allele expression in hemochromatosis heterozygotes

scientific article published on 01 April 2001

Effects of granulocyte-macrophage colony-stimulating factor and interleukin-3 on small cell lung cancer cells

artículo científico publicado en 1994

Effects of mitochondrial ferritin overexpression in normal and sideroblastic erythroid progenitors.

artículo científico publicado en 2013

Effects of recombinant human H-subunit and L-subunit ferritins on in vitro growth of human granulocyte—monocyte progenitors ⬇️

artículo científico publicado el 1 de marzo de 1988

Endothelial colony-forming cells from patients with chronic myeloproliferative disorders lack the disease-specific molecular clonality marker

scientific article published on 23 July 2009

Erythrophagocytosis increases the expression of erythroid potentiating activity mRNA in human monocyte-macrophages

scientific article published on 01 January 1993

Establishment and characterization of two cell lines derived from human glioblastoma multiforme

artículo científico publicado el 1 de mayo de 1992

Evaluation of erythroid marrow response to recombinant human erythropoietin in patients with cancer anaemia ⬇️

artículo científico publicado el 1 de noviembre de 1992

Evaluation of the bioactive and total transforming growth factor β1 levels in primary myelofibrosis.

artículo científico publicado en 2010

Expression of adhesion molecules and functional stimulation in human neutrophils: modulation by GM-CSF and role of the Bcr gene

artículo científico publicado en 1997

Familial-skewed X-chromosome inactivation as a predisposing factor for late-onset X-linked sideroblastic anemia in carrier females

artículo científico publicado en 2000

Ferroportin gene silencing induces iron retention and enhances ferritin synthesis in human macrophages

article

First episode of acute hemolysis due to G6PD deficiency in a middle-aged woman and transmission of the enzymatic defect through bone marrow transplant.

artículo científico publicado en 2004

Hereditary hyperferritinemia-cataract syndrome: relationship between phenotypes and specific mutations in the iron-responsive element of ferritin light-chain mRNA ⬇️

artículo científico publicado el 15 de julio de 1997

Histologic diagnosis and precocious treatment in a case of isolated promyelocytic sarcoma

artículo científico publicado en 1998

Idarubicin-containing regimen and G-CSF are capable of recruiting CD34+/DR- cells with high proliferative potential which sustain Ph-negative polyclonal hematopoiesis

artículo científico publicado en 1994

Increase in chromogranin A- and serotonin-positive cells in pouch mucosa of patients with ulcerative colitis undergoing proctocolectomy

scientific article published on 28 April 2018

Increase in neuroendocrine cells in the duodenal mucosa of patients with refractory celiac disease.

artículo científico publicado en 2014

Inhibition of c-ABL expression in hematopoietic progenitor cells using antisense oligodeoxynucleotides

scientific article published on 01 January 2000

Inhibitors of tyrosine phosphorylation induce apoptosis in human leukemic cell lines.

artículo científico publicado en 1993

Interferon-α protects Philadelphia-negative progenitors from exhaustion in chronic myeloid leukemia patients with cytogenetic response

artículo científico publicado en 2001

Intestinal expression of genes implicated in iron absorption and their regulation by hepcidin.

artículo científico publicado en 2016

JAK2 V617F mutation is a rare event in juvenile myelomonocytic leukemia

scientific article published on 07 December 2006

JAK2 V617F mutational status predicts progression to large splenomegaly and leukemic transformation in primary myelofibrosis.

artículo científico publicado en 2007

Juvenile genetic hemochromatosis is clinically and genetically distinct from the classical HLA-related disorder.

artículo científico publicado en 1998

MPL and JAK2 exon 12 mutations in patients with the Budd-Chiari syndrome or extrahepatic portal vein obstruction

artículo científico publicado en 2008

Molecular basis of new disorders of iron metabolism in man -editorial-

artículo científico publicado en 1999

Mutations on the von-Hippel-Lindau tumor suppressor gene

scientific article published on 01 January 2005

Myelodysplastic syndromes: mechanisms of transformation and neoplastic progression and their clinical implications ⬇️

artículo científico publicado el 1 de junio de 1991

Normal primitive haemopoietic progenitors are more frequent than their leukaemic counterpart in newly diagnosed patients with chronic myeloid leukaemia but rapidly decline with time

artículo científico publicado en 1999

Oligodeoxynucleotides antisense to c-abl specifically inhibit entry into S-phase of CD34+ hematopoietic cells and their differentiation to granulocyte-macrophage progenitors

scientific article published on 01 November 1995

Pathogenesis of chronic myelogenous leukemia.

artículo científico publicado en 1994

Pathogenesis, diagnosis and treatment of anaemia in immune-mediated gastrointestinal disorders

artículo científico publicado en 2018

Prevalence and pathogenesis of anemia in inflammatory bowel disease. Influence of anti-tumor necrosis factor-alpha treatment.

artículo científico publicado en 2009

Prevalence of anemia in inflammatory bowel diseases in european countries: a systematic review and individual patient data meta-analysis

artículo científico publicado en 2014

Renal function evaluation in liver cirrhosis: Preliminary report on the effect of the Royal Free Hospital Cirrhosis Glomerular Filtration Rate on the Model for End-Stage Liver Disease (MELD)

scientific article published on 16 December 2017

Restoration of normal polyclonal haemopoiesis in patients with chronic myeloid leukaemia autografted with Ph-negative peripheral stem cells

artículo científico publicado en 1994

Serum hepcidin in inflammatory bowel diseases: biological and clinical significance.

artículo científico publicado en 2013

Soluble transferrin receptor as a potential determinant of iron loading in congenital anaemias due to ineffective erythropoiesis

artículo científico publicado en 1999

Spleen endothelial cells from patients with myelofibrosis harbor the JAK2V617F mutation.

artículo científico publicado en 2012

Subcutaneous erythropoietin for treatment of refractory anemia in hematologic disorders. Results of a phase I/II clinical trial ⬇️

artículo científico publicado el 1 de enero de 1992

Successful pregnancy following gonadotropin therapy in a young female with juvenile idiopathic hemochromatosis and secondary hypogonadotropic hypogonadism ⬇️

artículo científico publicado el 1 de julio de 1995

TP53 codon 72 polymorphism in patients with chronic myeloid leukemia

artículo científico publicado en 2004

The dysmetabolic iron overload syndrome is clinically and genetically distinct from HFE-related genetic hemochromatosis

scientific article published on 01 February 1999

Two novel mutations, L490R and V561X, in transferrin receptor 2 in Japanese patients with hemochromatosis.

artículo científico publicado en 2005

X-linked Wiskott-Aldrich syndrome in a girl

scientific article published on 01 June 1998

c-abl function in normal and chronic myelogenous leukemia hematopoiesis: in vitro studies with antisense oligomers

artículo científico publicado el 1 de enero de 1992

Lista de obras de Gaetano Bergamaschi

A case of fever of unknown origin?

A linkage between hereditary hyperferritinaemia not related to iron overload and autosomal dominant congenital cataract

A novel deletion of the l-ferritin iron-responsive element responsible for severe hereditary hyperferritinaemia-cataract syndrome

A sensitive detection method for MPLW515L or MPLW515K mutation in chronic myeloproliferative disorders with locked nucleic acid-modified probes and real-time polymerase chain reaction.

Abnormal regulation of HFE mRNA expression does not contribute to primary iron overload

Anaemia characterises patients with myelofibrosis harbouring Mpl mutation.

Anemia in patients with Covid-19: pathogenesis and clinical significance

Anemia of chronic disease and defective erythropoietin production in patients with celiac disease.

Antigen profile and topographical distribution of marginal zone, monocytoid and epithelial-associated B-cells

Apoptosis: biological and clinical aspects.

C-fms expression in B-cells and response to M-CSF

Cell Blood Count Alterations and Patterns of Anaemia in Autoimmune Atrophic Gastritis at Diagnosis: A Multicentre Study

Cell cycle distribution of cord blood-derived haematopoietic progenitor cells and their recruitment into the S-phase of the cell cycle

Clonal nature of hematopoietic stem cell disorders

Cord blood-derived hematopoietic progenitor cells: in vitro response to hematopoietic growth factors and their recruitment into the S-phase of the cell cycle

Differential HFE allele expression in hemochromatosis heterozygotes

Effects of granulocyte-macrophage colony-stimulating factor and interleukin-3 on small cell lung cancer cells

Effects of mitochondrial ferritin overexpression in normal and sideroblastic erythroid progenitors.

Effects of recombinant human H-subunit and L-subunit ferritins on in vitro growth of human granulocyte—monocyte progenitors ⬇️

Endothelial colony-forming cells from patients with chronic myeloproliferative disorders lack the disease-specific molecular clonality marker

Erythrophagocytosis increases the expression of erythroid potentiating activity mRNA in human monocyte-macrophages

Establishment and characterization of two cell lines derived from human glioblastoma multiforme

Evaluation of erythroid marrow response to recombinant human erythropoietin in patients with cancer anaemia ⬇️

Evaluation of the bioactive and total transforming growth factor β1 levels in primary myelofibrosis.

Expression of adhesion molecules and functional stimulation in human neutrophils: modulation by GM-CSF and role of the Bcr gene

Familial-skewed X-chromosome inactivation as a predisposing factor for late-onset X-linked sideroblastic anemia in carrier females

Ferroportin gene silencing induces iron retention and enhances ferritin synthesis in human macrophages

First episode of acute hemolysis due to G6PD deficiency in a middle-aged woman and transmission of the enzymatic defect through bone marrow transplant.

Hereditary hyperferritinemia-cataract syndrome: relationship between phenotypes and specific mutations in the iron-responsive element of ferritin light-chain mRNA ⬇️

Histologic diagnosis and precocious treatment in a case of isolated promyelocytic sarcoma

Idarubicin-containing regimen and G-CSF are capable of recruiting CD34+/DR- cells with high proliferative potential which sustain Ph-negative polyclonal hematopoiesis

Increase in chromogranin A- and serotonin-positive cells in pouch mucosa of patients with ulcerative colitis undergoing proctocolectomy

Increase in neuroendocrine cells in the duodenal mucosa of patients with refractory celiac disease.

Inhibition of c-ABL expression in hematopoietic progenitor cells using antisense oligodeoxynucleotides

Inhibitors of tyrosine phosphorylation induce apoptosis in human leukemic cell lines.

Interferon-α protects Philadelphia-negative progenitors from exhaustion in chronic myeloid leukemia patients with cytogenetic response

Intestinal expression of genes implicated in iron absorption and their regulation by hepcidin.

JAK2 V617F mutation is a rare event in juvenile myelomonocytic leukemia

JAK2 V617F mutational status predicts progression to large splenomegaly and leukemic transformation in primary myelofibrosis.

Juvenile genetic hemochromatosis is clinically and genetically distinct from the classical HLA-related disorder.

MPL and JAK2 exon 12 mutations in patients with the Budd-Chiari syndrome or extrahepatic portal vein obstruction

Molecular basis of new disorders of iron metabolism in man -editorial-

Mutations on the von-Hippel-Lindau tumor suppressor gene

Myelodysplastic syndromes: mechanisms of transformation and neoplastic progression and their clinical implications ⬇️

Normal primitive haemopoietic progenitors are more frequent than their leukaemic counterpart in newly diagnosed patients with chronic myeloid leukaemia but rapidly decline with time

Oligodeoxynucleotides antisense to c-abl specifically inhibit entry into S-phase of CD34+ hematopoietic cells and their differentiation to granulocyte-macrophage progenitors

Pathogenesis of chronic myelogenous leukemia.

Pathogenesis, diagnosis and treatment of anaemia in immune-mediated gastrointestinal disorders

Prevalence and pathogenesis of anemia in inflammatory bowel disease. Influence of anti-tumor necrosis factor-alpha treatment.

Prevalence of anemia in inflammatory bowel diseases in european countries: a systematic review and individual patient data meta-analysis

Renal function evaluation in liver cirrhosis: Preliminary report on the effect of the Royal Free Hospital Cirrhosis Glomerular Filtration Rate on the Model for End-Stage Liver Disease (MELD)

Restoration of normal polyclonal haemopoiesis in patients with chronic myeloid leukaemia autografted with Ph-negative peripheral stem cells

Serum hepcidin in inflammatory bowel diseases: biological and clinical significance.

Soluble transferrin receptor as a potential determinant of iron loading in congenital anaemias due to ineffective erythropoiesis

Spleen endothelial cells from patients with myelofibrosis harbor the JAK2V617F mutation.

Subcutaneous erythropoietin for treatment of refractory anemia in hematologic disorders. Results of a phase I/II clinical trial ⬇️

Successful pregnancy following gonadotropin therapy in a young female with juvenile idiopathic hemochromatosis and secondary hypogonadotropic hypogonadism ⬇️

TP53 codon 72 polymorphism in patients with chronic myeloid leukemia

The dysmetabolic iron overload syndrome is clinically and genetically distinct from HFE-related genetic hemochromatosis

Two novel mutations, L490R and V561X, in transferrin receptor 2 in Japanese patients with hemochromatosis.

X-linked Wiskott-Aldrich syndrome in a girl

c-abl function in normal and chronic myelogenous leukemia hematopoiesis: in vitro studies with antisense oligomers