Gaetano Bergamaschi

Summary

Affiliation: University of Pavia
Country: Italy

Publications

  1. doi request reprint Serum hepcidin in inflammatory bowel diseases: biological and clinical significance
    Gaetano Bergamaschi
    Department of Internal Medicine, University of Pavia Medical School and Fondazione IRCCS Policlinico San Matteo, Pavia, Italy
    Inflamm Bowel Dis 19:2166-72. 2013
  2. pmc Prevalence and pathogenesis of anemia in inflammatory bowel disease. Influence of anti-tumor necrosis factor-alpha treatment
    Gaetano Bergamaschi
    Clinica, Medica I, Policlinico San Matteo, Piazzale Golgi, 27100 Pavia, Italy
    Haematologica 95:199-205. 2010
  3. doi request reprint Anemia of chronic disease and defective erythropoietin production in patients with celiac disease
    Gaetano Bergamaschi
    Department of Internal Medicine, University of Pavia Medical School and Fondazione IRCCS Policlinico San Matteo, Pavia, Italy
    Haematologica 93:1785-91. 2008
  4. ncbi request reprint Mutations on the von-Hippel-Lindau tumor suppressor gene
    Gaetano Bergamaschi
    Medicina Interna ed Oncologia Medica, Policlinico S Matteo, Pavia, Italy
    Haematologica 90:1. 2005
  5. ncbi request reprint Altered erythropoiesis in genetic hemochromatosisis
    Gaetano Bergamaschi
    Medicina Interna ed Oncologia Medica, Policlinico S Matteo, Pavia, Italy
    Haematologica 90:146. 2005
  6. ncbi request reprint Two novel mutations, L490R and V561X, in transferrin receptor 2 in Japanese patients with hemochromatosis
    Gaetano Bergamaschi
    Medicina Interna ed Oncologia Medica, Policlinico S Matteo, Pavia, Italy
    Haematologica 90:289A. 2005
  7. doi request reprint Increase in neuroendocrine cells in the duodenal mucosa of patients with refractory celiac disease
    Antonio Di Sabatino
    First Department of Medicine, Celiac Centre, St Matteo Hospital, University of Pavia, Pavia, Italy
    Am J Gastroenterol 109:258-69. 2014
  8. ncbi request reprint JAK2 V617F mutational status predicts progression to large splenomegaly and leukemic transformation in primary myelofibrosis
    Giovanni Barosi
    Unit of Clinical Epidemiology and Center for the Study of Myelofibrosis, Istituto di Ricovero e Cura a Carattere Scientifico IRCCS Policlinico S Matteo Foundation, Pavia, Italy
    Blood 110:4030-6. 2007
  9. ncbi request reprint Antigen profile and topographical distribution of marginal zone, monocytoid and epithelial-associated B-cells
    Gaetano Bergamaschi
    Medicina Interna ed Oncologia Medica IRCCS Policlinico S Matteo, 27100 Pavia, Italy
    Haematologica 90:1011B. 2005
  10. ncbi request reprint Absent phenotypic expression of X-linked sideroblastic anemia in one of 2 brothers with a novel ALAS2 mutation
    Mario Cazzola
    Department of Hematology, University of Pavia Medical School, Pavia, Italy
    Blood 100:4236-8. 2002

Collaborators

Detail Information

Publications19

  1. doi request reprint Serum hepcidin in inflammatory bowel diseases: biological and clinical significance
    Gaetano Bergamaschi
    Department of Internal Medicine, University of Pavia Medical School and Fondazione IRCCS Policlinico San Matteo, Pavia, Italy
    Inflamm Bowel Dis 19:2166-72. 2013
    ..Hepcidin, a peptide produced by hepatocytes, regulates body iron homeostasis. Inflammation increases serum hepcidin, and its determination can be useful in the differential diagnosis of anemias during inflammatory diseases...
  2. pmc Prevalence and pathogenesis of anemia in inflammatory bowel disease. Influence of anti-tumor necrosis factor-alpha treatment
    Gaetano Bergamaschi
    Clinica, Medica I, Policlinico San Matteo, Piazzale Golgi, 27100 Pavia, Italy
    Haematologica 95:199-205. 2010
    ..We investigated the prevalence and pathogenesis of anemia in patients with inflammatory bowel disease...
  3. doi request reprint Anemia of chronic disease and defective erythropoietin production in patients with celiac disease
    Gaetano Bergamaschi
    Department of Internal Medicine, University of Pavia Medical School and Fondazione IRCCS Policlinico San Matteo, Pavia, Italy
    Haematologica 93:1785-91. 2008
    ..Although celiac disease is a chronic condition characterized by an intense inflammatory response of the intestinal mucosa, scant data are available about the prevalence of anemia of chronic disease in celiac disease...
  4. ncbi request reprint Mutations on the von-Hippel-Lindau tumor suppressor gene
    Gaetano Bergamaschi
    Medicina Interna ed Oncologia Medica, Policlinico S Matteo, Pavia, Italy
    Haematologica 90:1. 2005
  5. ncbi request reprint Altered erythropoiesis in genetic hemochromatosisis
    Gaetano Bergamaschi
    Medicina Interna ed Oncologia Medica, Policlinico S Matteo, Pavia, Italy
    Haematologica 90:146. 2005
  6. ncbi request reprint Two novel mutations, L490R and V561X, in transferrin receptor 2 in Japanese patients with hemochromatosis
    Gaetano Bergamaschi
    Medicina Interna ed Oncologia Medica, Policlinico S Matteo, Pavia, Italy
    Haematologica 90:289A. 2005
  7. doi request reprint Increase in neuroendocrine cells in the duodenal mucosa of patients with refractory celiac disease
    Antonio Di Sabatino
    First Department of Medicine, Celiac Centre, St Matteo Hospital, University of Pavia, Pavia, Italy
    Am J Gastroenterol 109:258-69. 2014
    ..Several immune-mediated gastrointestinal disorders, including celiac disease (CD), are associated with neuroendocrine cell hyperplasia. However, neuroendocrine cells have never been explored in refractory CD (RCD)...
  8. ncbi request reprint JAK2 V617F mutational status predicts progression to large splenomegaly and leukemic transformation in primary myelofibrosis
    Giovanni Barosi
    Unit of Clinical Epidemiology and Center for the Study of Myelofibrosis, Istituto di Ricovero e Cura a Carattere Scientifico IRCCS Policlinico S Matteo Foundation, Pavia, Italy
    Blood 110:4030-6. 2007
    ..We conclude that JAK2 V617F genotype should be considered in any future risk stratification of patients with PMF...
  9. ncbi request reprint Antigen profile and topographical distribution of marginal zone, monocytoid and epithelial-associated B-cells
    Gaetano Bergamaschi
    Medicina Interna ed Oncologia Medica IRCCS Policlinico S Matteo, 27100 Pavia, Italy
    Haematologica 90:1011B. 2005
  10. ncbi request reprint Absent phenotypic expression of X-linked sideroblastic anemia in one of 2 brothers with a novel ALAS2 mutation
    Mario Cazzola
    Department of Hematology, University of Pavia Medical School, Pavia, Italy
    Blood 100:4236-8. 2002
    ..This observation is relevant to genetic counseling, emphasizing the importance of gene-based diagnosis...
  11. ncbi request reprint Effects of the R216Q mutation of GATA-1 on erythropoiesis and megakaryocytopoiesis
    Carlo L Balduini
    Clinica Medica III, IRCCS Policlinico, San Matteo University, piazzale Golgi 27100 Pavia, Italy
    Thromb Haemost 91:129-40. 2004
    ....
  12. ncbi request reprint First episode of acute hemolysis due to G6PD deficiency in a middle-aged woman and transmission of the enzymatic defect through bone marrow transplant
    Ester Orlandi
    Division of Hematology, IRCCS Policlinico San Matteo, 27100 Pavia, Italy
    Haematologica 89:ECR04. 2004
  13. ncbi request reprint TP53 codon 72 polymorphism in patients with chronic myeloid leukemia
    Gaetano Bergamaschi
    Haematologica 89:868-9. 2004
    ..We found that allele A1 was more frequent in patients with chronic myeloid leukemia (CML) than in controls, and among CML patients who had no cytogenetic response than among responders...
  14. ncbi request reprint Mitochondrial ferritin expression in erythroid cells from patients with sideroblastic anemia
    Mario Cazzola
    Department of Hematology, University of Pavia Medical School and Istituto di Ricovero e Cura a Carattere Scientifico IRCCS Policlinico S Matteo, Pavia, Italy
    Blood 101:1996-2000. 2003
    ..These findings suggest that most of the iron deposited in perinuclear mitochondria of ring sideroblasts is present in the form of MtF and that this latter might be a specific marker of sideroblastic anemia...
  15. pmc 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
    Alessandro Pancrazzi
    UF di Ematologia, University of Florence, Viale Morgagni 85, 50134 Florence, Italy
    J Mol Diagn 10:435-41. 2008
    ..It can also provide a quantitative estimate of mutant allele burden that might be useful for both patient prognosis and monitoring response to therapy...
  16. ncbi request reprint Anaemia characterises patients with myelofibrosis harbouring Mpl mutation
    Paola Guglielmelli
    Department of Haematology, University of Florence, Florence, Italy
    Br J Haematol 137:244-7. 2007
    ..121 g/l; P = 0.002) and were more likely to require regular transfusional support (P = 0.012). These data indicate that MPL mutation in myelofibrosis characterises patients with more severe anaemic phenotype...
  17. ncbi request reprint The expression of CXCR4 is down-regulated on the CD34+ cells of patients with myelofibrosis with myeloid metaplasia
    Vittorio Rosti
    Transplant Research Area, IRCCS Policlinico S Matteo, Viale Golgi 19, 27100 Pavia, Italy
    Blood Cells Mol Dis 38:280-6. 2007
    ..We studied the expression of the chemokine receptor CXCR4 on circulating CD34+ cells of patients with myelofibrosis with myeloid metaplasia (MMM), and examined its relationship to the severity of disease...
  18. ncbi request reprint Role of the JAK2 mutation in the diagnosis of chronic myeloproliferative disorders in splanchnic vein thrombosis
    Massimo Primignani
    Gastroenterology Unit and Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, Department of Medicine and Medical Specialties, University of Milan and IRCCS Maggiore Hospital, Mangiagalli and Regina Elena Foundation, Milan, Italy
    Hepatology 44:1528-34. 2006
    ..In conclusion, CMPD is the major cause of primary EHPVO or BCS. JAK2 V617F is a very reliable and noninvasive molecular marker for CMPD and should be used as a first test for diagnosis...
  19. ncbi request reprint A novel deletion of the L-ferritin iron-responsive element responsible for severe hereditary hyperferritinaemia-cataract syndrome
    Mario Cazzola
    Division of Haematology, University of Pavia Medical School, IRCCS Policlinico S Matteo, 27100 Pavia, Italy
    Br J Haematol 116:667-70. 2002
    ..A double-gradient denaturing gradient gel electrophoresis (DG-DGGE) method easily detected the above deletion...