Výsledky vyhledávání

Major arterial and venous thromboembolic complications in patients with COVID-19

Autor: N Lalor, A Raffaeli, F Bottini, J L Scapellato, N Banos, L Pezzati, D Intile, F Longo

Publikováno v: European Heart Journal. 42

Background Cardiovascular complications; myocardial infarction (MI), ischemic stroke, and pulmonary embolism (PE), represent an important source of adverse outcomes in COVID-19 disease. Objectives To evaluate the incidence of thromboembolic events, s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2ca2f2f2749cc88f6ab4f6f497e574d5
https://doi.org/10.1093/eurheartj/ehab724.1921

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Metabolic and Genetic Risk Factors for Migraine in Children

Autor: Maria Grazia Calevo, L Montaldi, Angelo Claudio Molinari, ME Celle, Edvige Veneselli, F Bottini, Giuseppe Minniti, Stefano Amato, D Di Pasquale, R Cerone

Publikováno v: Cephalalgia. 26:731-737

Migraine can induce ischaemic stroke, and is considered an independent risk factor for stroke in the young. To date, the nature of the link between migraine and stroke is essentially unknown. Forty-five children were studied. Homocysteine levels (fas

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c6ddd3c7b27d64cb2aac50e1cd2bb60
https://doi.org/10.1111/j.1468-2982.2006.01107.x

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Insight into molecular changes of the FIX protein in a series of Italian patients with haemophilia B

Autor: E. Della Valle, Maria Patrizia Bicocchi, M. Acquila, Camillo Rosano, Angelo Claudio Molinari, F. Bottini, Tiziana Lanza, Mirrela Pasino

Publikováno v: Haemophilia. 12:263-270

Summary. Deficiency or dysfunction of factor IX FIX leads to haemophilia B (HB), an X-linked, recessive, bleeding disorder. On a molecular basis, HB is due to a heterogeneous spectrum of mutations spread throughout the F9 gene. In several instances,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e9dafe2cff2ec5f838bac51aa2f55c6
https://doi.org/10.1111/j.1365-2516.2006.01275.x

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Germ-line origin of intron 1 inversion in two haemophilia A families

Autor: M. Acquila, Mirella Pasino, F. Bottini, Tiziana Lanza, Maria Patrizia Bicocchi, Cristina Santoro, Angelo Claudio Molinari

Publikováno v: Haemophilia. 9:717-720

Summary. Factor VIII gene inversion of intron 1 has recently been reported to be the mutation responsible for haemophilia A in about 5% of severe cases. In our series of patients, which is made up of 77 Italian cases negative for intron 22 inversion,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ab8c804a0804206a0907eeae811730f7
https://doi.org/10.1046/j.1351-8216.2003.00818.x

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Analysis of 18 novel mutations in the factor VIII gene

Autor: Maria Patrizia Bicocchi, Pier G. Mori, F. Bottini, Angelo Claudio Molinari, Maura Acquila, Camillo Rosano, Elio Boeri, Mirella Pasino, Tiziana Lanza

Publikováno v: British Journal of Haematology. 122:810-817

Summary. We describe 18 novel mutations, unreported in the Haemophilia A mutation Databases, that have been identified in a cohort of unrelated, Italian patients affected with haemophilia A (HA). Screening of the factor VIII gene (FVIII) was performe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f19e21dd48f8fa2c58bb8d019828e7cd
https://doi.org/10.1046/j.1365-2141.2003.04494.x

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