Výsledky vyhledávání - "C. Borgna Pignatti"

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Triosephosphate isomerase deficiency: 2 new cases

Autor: P. De Stefano, G. Sirchia, Massimiliano Mariani, Alberto Zanella, G Morgese, C Borgna-Pignatti, M B Colombo

Publikováno v: Scandinavian Journal of Haematology. 34:417-424

2 new cases of triosephosphate isomerase (TPI) deficiency associated with severe haemolytic anaemia in 2 unrelated Italian families are described. Only 1 case was extensively investigated. TPI deficiency was detectable in erythrocytes, leucocytes, pl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f21e4fe6498cdf673cc91fdb51898b1
https://doi.org/10.1111/j.1600-0609.1985.tb00771.x

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Safety and efficacy of subcutaneous bolus injection of deferoxamine in adult patients with iron overload

Autor: M, Franchini, G, Gandini, M, de Gironcoli, A, Vassanelli, C, Borgna-Pignatti, G, Aprili

Publikováno v: Blood. 95:2776-2779

We compared 48-hour urinary iron excretion after a twice-daily subcutaneous bolus injection of deferoxamine and after 12 hours of subcutaneous continuous infusion of the drug in 27 patients with iron overload (mean age, 55.7 years). In most patients,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe100df80eab0777633f34c02bd1d5a3
https://doi.org/10.1182/blood.v95.9.2776.009k26_2776_2779

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Thromboembolic Events in Beta Thalassemia Major: An Italian Multicenter Study

Autor: C. Melevendi, F. Dore, Donatella Mattia, C. Borgna Pignatti, A Mangiagli, A. Di Palma, Vittorio Carnelli, G Pizzarelli, Maria Antonietta Romeo, Salvatore Musumeci, F. Di Gregorio, R. Longhi, Vincenzo Caruso

Publikováno v: Acta Haematologica. 99:76-79

Thromboembolic (TE) events have been frequently reported in β-thalassemic patients in association with known risk factors such as diabetes, complex cardiopulmonary abnormalities, hypothyroidism, liver function anomalies, and postsplenectomy thromboc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f23944e9964e66249bc2572c2346cc1d
https://doi.org/10.1159/000040814

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9 Clinical manifestations and therapy of transfusional haemosiderosis

Autor: C. Borgna-Pignatti, V. Gabutti

Publikováno v: Baillière's Clinical Haematology. 7:919-940

Summary Long-term blood transfusions lead to the accumulation of iron that in the absence of chelation therapy causes complications such as liver cirrhosis, growth failure, hypogonadism, hypothyroidism, hypoparathyroidism, diabetes and myocardiopathy

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d4386037c798529d8efe7c2a58f4c830
https://doi.org/10.1016/s0950-3536(05)80131-3

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Akademický článek

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Epidemiology and burden of rotavirus-associated hospitalizations in Ferrara, Italy

Autor: G, Gabutti, M, Marsella, C, Lazzara, E, Fiumana, A, Cavallaro, C, Borgna-Pignatti

Publikováno v: Journal of preventive medicine and hygiene. 48(1)

Objective of this study was to provide data on hospitalizations for rotavirus gastroenteritis (RVGE) in Ferrara, Italy. The study was conducted analyzing the hospital discharge forms of all children admitted to the Pediatric Department of the Univers

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::6e15c8c61302325b763e56ee695ea0c4
https://pubmed.ncbi.nlm.nih.gov/17506231

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Hereditary thrombocytopenia due to reduced platelet production--report on two families and mutational screening of the thrombopoietin receptor gene (c-mpl)

Autor: R, Tonelli, P, Strippoli, A, Grossi, A, Savoia, A, Iolascon, M, Savino, M S, Teriaca, V, Servedio, M, Morfini, L, Zelante, C, Borgna-Pignatti, P, Rosito, A, Pession, G, Paolucci, G P, Bagnara

Hereditary thrombocytopenias represent heterogeneous clinical and genetic syndromes. They include a consistent group of families which are considered as a separate clinical entity, characterized by autosomal dominant transmission, incomplete penetran

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::a8119dfc31b113a5681772931c5cf196
http://hdl.handle.net/11588/475699

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The haemochromatosis mutations do not modify the clinical picture of thalassaemia major in patients regularly transfused and chelated

Autor: C, Borgna-Pignatti, A, Solinas, C, Bombieri, R, Micciolo, M R, Gamberini, P, De Stefano, E, De Menis, P F, Pignatti

Publikováno v: British journal of haematology. 103(3)

Iron overload is the main cause of morbidity and mortality in patients with thalassaemia major. In order to establish if the presence of the mutations recently described in the haemochromatosis gene affects the severity of iron overload in thalassaem

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c6da7f679137bebb9f843aca89ab732e
https://pubmed.ncbi.nlm.nih.gov/9858237

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Subcutaneous bolus injection of deferoxamine in adult patients affected by onco-hematologic diseases and iron overload

Autor: C, Borgna-Pignatti, M, Franchini, G, Gandini, A, Vassanelli, M, De Gironcoli, G, Aprili

Publikováno v: Haematologica. 83(9)

Chelation therapy is often necessary for patients who undergo chronic transfusion therapy for myelodysplastic syndromes. In these patients, deferoxamine, the most widely used chelating agent, has been reported to be effective in reducing the iron bur

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9c2c2192887111e8aae52149003f795d
https://pubmed.ncbi.nlm.nih.gov/9825575

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