Výsledky vyhledávání - "Antonio, Girolami"

Akademický článek

Peculiar, poorly known, rare congenital bleeding disorders presenting thrombotic events: an understudied chapter of molecular, blood coagulation defects

Autor: Antonio Girolami, Elisabetta Cosi, Silvia Ferrari, Claudia Santarossa, Bruno Girolami

Publikováno v: Journal of Biochemical and Clinical Genetics, Vol 3, Iss 2, Pp 84-93 (2020)

Very rare, peculiar congenital bleeding disorders are usually dealt with in clinics without giving much importance. We think that this practice is not correct since the disorders may often provide useful information about blood coagulation. In this r

Externí odkaz: https://doaj.org/article/4a6b4bdae63f43e886858ce64dff38c5

Zobrazit plný text záznamu

Akademický článek

Homozygous Prekallikrein Deficiency in the USA: Several Patients but Still Few Mutation Studies

Autor: Antonio Girolami MD, Silvia Ferrari PhD

Publikováno v: Clinical and Applied Thrombosis/Hemostasis, Vol 27 (2021)

Externí odkaz: https://doaj.org/article/984ad2db31414ccf9fa2208bfd267d29

Zobrazit plný text záznamu

Akademický článek

Worldwide distribution of prekallikrein (PK) deficiency: the defect seems mainly concentrated in West African countries and in the United States

Autor: Antonio Girolami, Silvia Ferrari

Publikováno v: Mediterranean Journal of Hematology and Infectious Diseases, Vol 13, Iss 1 (2021)

Externí odkaz: https://doaj.org/article/741852268c2c4d87855a4734f7920b90

Zobrazit plný text záznamu

Akademický článek

Prevalence of Cardiovascular Disorders in African-Americans With Congenital Prekallikrein Deficiency Versus Caucasians-Americans With the Same Defect

Autor: Antonio Girolami MD, Silvia Ferrari PhD, Bruno Girolami MD

Publikováno v: Clinical and Applied Thrombosis/Hemostasis, Vol 26 (2020)

Externí odkaz: https://doaj.org/article/b8c2567e474443b4a0e8e21cdb05cf8f

Zobrazit plný text záznamu

Akademický článek

Increased Prevalence of Reported Cases of Congenital Prekallikrein Deficiency Among African Americans as Compared With the General Population of the United States

Autor: Antonio Girolami MD, Silvia Ferrari PhD, Elisabetta Cosi MD, Bruno Girolami MD

Publikováno v: Clinical and Applied Thrombosis/Hemostasis, Vol 26 (2020)

Externí odkaz: https://doaj.org/article/118e2289eff14b568398a7b6c69c0244

Zobrazit plný text záznamu

Akademický článek

Spectrum of 5’UTR mutations in ANKRD26 gene in patients with inherited thrombocytopenia: c.-140C>G mutation is more frequent than expected

Autor: Silvia Ferrari, Anna Maria Lombardi, Maria Caterina Putti, Antonella Bertomoro, Irene Cortella, Isabella Barzon, Antonio Girolami, Fabrizio Fabris

Publikováno v: Platelets, Vol 28, Iss 6, Pp 621-624 (2017)

Externí odkaz: https://doaj.org/article/eb654c20e20d483da53fee3c1e8746d4

Zobrazit plný text záznamu

Plný text ve formátu HTML

Akademický článek

The Dysprothrombinemias due to Arg596 Mutations: A Conundrum With No Bleeding Tendency and Venous Thrombosis due to Antithrombin Resistance

Autor: Antonio Girolami MD, Silvia Ferrari PhD, Elisabetta Cosi MD, Maria Luigia Randi MD

Publikováno v: Clinical and Applied Thrombosis/Hemostasis, Vol 25 (2019)

Externí odkaz: https://doaj.org/article/b8b052f94e54486cbc6f6fa750b13897

Zobrazit plný text záznamu

Peculiar Congenital Factor VII Defect with the Proposita and Her Mother Showing the Same Compound Heterozygosity for Thr384Met and Arg413Gln

Autor: Diana García, Antonio Girolami, Mariano Paoletti, Silvia Ferrari

Publikováno v: Acta Haematologica. 144:100-104

Objective: To investigate a family with factor VII (FVII) deficiency from Argentina. Patients and Methods: The proposita is a 14-year-old girl who presented with a mild to moderate bleeding tendency. Menorrhagia is controlled with periodical administ

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ab0826ea9270bccae21768baf8ba94cf
https://doi.org/10.1159/000507071

Zobrazit plný text záznamu

Long-term safety outcomes of prekallikrein (Fletcher factor) deficiency: A systematic literature review of case reports

Autor: Moshe Y. Vardi, Catherine Rolland, Daniel J. Sexton, Jonathan A. Bernstein, Antonio Girolami

Publikováno v: Allergy and Asthma Proceedings. 41:10-18

Background: Hereditary prekallikrein (Fletcher factor) deficiency is a rare condition characterized by a prolonged activated partial thromboplastin time. Inhibitors of plasma kallikrein have recently been approved for prophylaxis of hereditary angioe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01948136e1294bf6afe0f28894f80ce9
https://doi.org/10.2500/aap.2020.41.190005

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání