Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Andrea Rovati"'
Autor:
Edoardo Troncone, Alessandro Fugazza, Andrea Rovati, Paola Spaggiari, Andrea Anderloni, Silvia Carrara, Alessandro Repici
Publikováno v:
Journal of gastrointestinal and liver diseases : JGLD. 27(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5eddfa458388eeaeb680c0cd235bda74
https://pubmed.ncbi.nlm.nih.gov/30240462
https://pubmed.ncbi.nlm.nih.gov/30240462
Publikováno v:
Blood. 91:2139-2145
Serum erythropoietin (sEpo) concentration is primarily related to the rate of renal production and, under the stimulus of hypoxia, increases exponentially as hemoglobin (Hb) decreases. Additional factors, however, appear to influence sEpo, and in thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41c056408965feb5912565aa46626566
https://doi.org/10.1182/blood.v91.6.2139.2139_2139_2145
https://doi.org/10.1182/blood.v91.6.2139.2139_2139_2145
Autor:
Andrea Cairo, Flora Peyvandi, R. Palla, Mariagabriella Mariani, Silvia Maria Trisolini, Dario Consonni, Luca A. Lotta, Andrea Rovati
Publikováno v:
Thrombosis research. 128(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dc632c08a0c461a53774bf9d23b3a4f
https://pubmed.ncbi.nlm.nih.gov/21872296
https://pubmed.ncbi.nlm.nih.gov/21872296
Autor:
Andrea Rovati, Giovanni Claudiani, Gaetano Bergamaschi, Paola Cerani, Angioletta Iannone, Mario Cazzola
Publikováno v:
Blood. 92:2979-2981
To the Editor: Genetic hemochromatosis (GH) is a common HLA-linked recessive disorder characterized by progressive parenchymal iron loading and the appearance of clinical manifestations in the fifth decade of life, predominantly in males. HFE has bee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a5d1ebd56e6ac6dd1c35758072ca256
https://doi.org/10.1182/blood.v92.8.2979
https://doi.org/10.1182/blood.v92.8.2979
Publikováno v:
Blood. 91:360-362
To the Editor: In a recent article in BLOOD, Sergeyeva et al[1][1] describe a secondary form of congenital polycythemia that appears to be particularly frequent in Chuvasia, a region in the central part of European Russia. This erythrocytosis is tran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::887be1b7bdc218aff692eb1671131543
https://doi.org/10.1182/blood.v91.1.360b
https://doi.org/10.1182/blood.v91.1.360b
Autor:
Dario Consonni, Luca A. Lotta, Carla Valsecchi, Giuseppe Bettoni, Roberta Palla, Andrea Rovati, Michele Pizzuti, Flora Peyvandi, Gloria Casoli, Dino Fa Motti
Publikováno v:
Blood. 116:2532-2532
Abstract 2532 Background: Thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening disease characterized by acute episodes of thrombocytopenia and microangiopathic hemolytic anemia due to disseminated microvascular thrombosis. Up to 40%
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32f9e1e961934c4623e7afcf54a89fd2
https://doi.org/10.1182/blood.v116.21.2532.2532
https://doi.org/10.1182/blood.v116.21.2532.2532
Autor:
Andrea Rovati, Mariagabriella Mariani, Silvia Maria Trisolini, Roberta Palla, Andrea Cairo, Luca A. Lotta, Flora Peyvandi
Publikováno v:
Blood. 114:3521-3521
Abstract 3521 Poster Board III-458 Thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening disease characterized by thrombocytopenia, microangiopathic haemolytic anemia and widespread microvascular thrombosis, resulting in multiorgan is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec772197697c2c5099d8e7cb521c8b7c
https://doi.org/10.1182/blood.v114.22.3521.3521
https://doi.org/10.1182/blood.v114.22.3521.3521