Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Margherita Scapin"'
Autor:
Silvia Vettore, Raffaella Scandellari, Stefano Moro, Anna Maria Lombardi, Margherita Scapin, Maria Luigia Randi, Fabrizio Fabris
Publikováno v:
Haematologica, Vol 93, Iss 11 (2008)
In Italy, a significant proportion of patients with autosomal dominant inheritance of macrothrombocytopenia have been recognized as having heterozygous Bernard-Soulier syndrome carrying the Bolzano-type defect. This condition prompted a systematic re
Externí odkaz:
https://doaj.org/article/a32f654ec43b47829185739e6266971a
Autor:
Margherita Scapin, Elena Duner, Fabiana Tezza, Maria Luigia Randi, Elisabetta Ruzzon, Fabrizio Fabris, Raffaella Scandellari
Publikováno v:
Aging Clinical and Experimental Research. 23:17-21
JAK2V617F mutation occurs in 90% of polycythemia vera (PV) and in 50% of essential thrombocythemia (ET) patients.253 consecutive patients affected by myeloproliferative disorders (MPD, 121 PV, 132 ET) were evaluated and stratified in 4 age groups: 18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76dfbc1cb2a7bdafda75790f20d8af78
https://doi.org/10.1007/bf03324948
https://doi.org/10.1007/bf03324948
Autor:
Fabrizio Fabris, Margherita Scapin, Fabiana Tezza, Pamela Scarparo, Maria Luigia Randi, Elena Duner, Raffaella Scandellari
Publikováno v:
Acta Haematologica. 123:140-145
Background: Philadelphia-negative myeloproliferative disorders (Ph-MPD) are common causes of unusual splanchnic or cerebral vein thrombosis, which is treated with unfractionated heparin (UFH) or low-molecular-weight heparin (LMWH). Heparin-induced th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb662957377abc55a044d3dd7e99ba83
https://doi.org/10.1159/000280466
https://doi.org/10.1159/000280466
Autor:
Fabrizio Fabris, Silvia Vettore, Margherita Scapin, Raffaella Scandellari, Maria Luigia Randi, Stefano Moro, Anna Maria Lombardi
Publikováno v:
Haematologica. 93:1743-1747
In Italy, a significant proportion of patients with autosomal dominant inheritance of macrothrombocytopenia have been recognized as having heterozygous Bernard-Soulier syndrome carrying the Bolzano-type defect. This condition prompted a systematic re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c5193cd8bc3b4a5b7e31d7bb02625c9
https://doi.org/10.3324/haematol.12830
https://doi.org/10.3324/haematol.12830
Autor:
Margherita Scapin, Andrea Garolla, Valentina Bosello, Carlo Foresta, Helena Sztajer, Fulvio Ursini, Leopold Flohé, Matilde Maiorino
Publikováno v:
Biology of Reproduction. 68:1134-1141
Phospholipid hydroperoxide glutathione peroxidase (PHGPx), the product of gpx-4, is the major selenoprotein in sperm and is considered essential for fertilization because of its multiple roles in spermatogenesis, such as hydroperoxide detoxification,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a6c226fd7c9d06d2645ff1dd7cab09f
https://doi.org/10.1095/biolreprod.102.007500
https://doi.org/10.1095/biolreprod.102.007500
Autor:
Renzo Deana, Arianna Donella-Deana, Fabrizio Fabris, Martina Frasson, Maria Luigia Randi, Elisa Magrin, Margherita Scapin, Anna Maria Brunati
Publikováno v:
Blood. 115(3)
Polycythemia vera (PV) and essential thrombocythemia (ET) are chronic myeloproliferative disorders characterized by an increased incidence of thrombo-hemorrhagic complications. The acquired somatic Janus kinase 2 (JAK2) V617F mutation is present in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b64908a6ad4ef40f9aa5be015b60b24e
https://pubmed.ncbi.nlm.nih.gov/19965650
https://pubmed.ncbi.nlm.nih.gov/19965650
Autor:
Luciana, Teofili, Tonia, Cenci, Maurizio, Martini, Sara, Capodimonti, Lorenza, Torti, Fiorina, Giona, Angela, Amendola, Maria Luigia, Randi, Maria Caterina, Putti, Margherita, Scapin, Giuseppe, Leone, Luigi Maria, Larocca
Publikováno v:
British journal of haematology. 145(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2470b02bd8d41c44e4acc014f488ec6c
https://pubmed.ncbi.nlm.nih.gov/19208099
https://pubmed.ncbi.nlm.nih.gov/19208099
Autor:
Tonia Cenci, Fiorina Giona, Giuseppe Leone, Luciana Teofili, Maria Caterina Putti, Maria Luigia Randi, Sara Capodimonti, Luigi Maria Larocca, Maurizio Martini, Margherita Scapin, Lorenza Torti, Angela Amendola
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::714c0085d0b8123dfaf85fc39d689178
http://hdl.handle.net/11573/414087
http://hdl.handle.net/11573/414087
Autor:
Antonio Piccoli, Margherita Scapin, Elisabetta Ruzzon, Fabrizio Fabris, Raffaella Scandellari, Maria Luigia Randi, Fabiana Tezza
Publikováno v:
Aging clinical and experimental research. 20(4)
Background and aims: A previous thrombotic event and advanced age are well-known risk factors for thrombosis in essential thrombocythemia (ET). In these patients, therefore, cytotoxic drugs are needed to reduce platelet count. In spite of this convin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad100151b7145aba2ee806718a4cb249
https://pubmed.ncbi.nlm.nih.gov/18852553
https://pubmed.ncbi.nlm.nih.gov/18852553
Autor:
Anna Maria Lombardi, Pamela Scarparo, Margherita Scapin, Elisabetta Bortoletto, Antonio Girolami, Liliana Santarossa
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 19(7)
A group of 29 patients with congenital factor XII (FXII) deficiency belonging to nine distinct families have been investigated. All were cases of true deficiency in the sense that there was no discrepancy between FXII activity and FXII antigen. From
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eaaaef10021c704ca4402df8e5de5338
https://pubmed.ncbi.nlm.nih.gov/18832903
https://pubmed.ncbi.nlm.nih.gov/18832903