Salvador Minoldo
Overview
Explore the profile of Salvador Minoldo including associated specialties, affiliations and a list of published articles.
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Articles
4
Citations
49
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0
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Recent Articles
1.
Identification and characterization of novel mutations implicated in congenital fibrinogen disorders
Smith N, Bornikova L, Noetzli L, Guglielmone H, Minoldo S, Backos D, et al.
Res Pract Thromb Haemost
. 2018 Oct;
2(4):800-811.
PMID: 30349899
Introduction: Fibrinogen is a complex molecule comprised of two sets of Aα, Bβ, and γ chains. Fibrinogen deficiencies can lead to the development of bleeding or thromboembolic events. The objective...
2.
Girolami A, Minoldo S, Ferrari S, Colussi D, Lombardi A, Guglielmone H
Cardiovasc Hematol Disord Drug Targets
. 2017 Sep;
17(2):136-141.
PMID: 28891452
Objective: The aim was to report a new family with congenital FX deficiency. Patients And Methods: The proposita is a 41 year old female with a moderate bleeding tendency (easy...
3.
Guglielmone H, Minoldo S, Jarchum G, Daga D, Bocco J
Thromb Res
. 2007 Jul;
121(3):429-30.
PMID: 17604827
No abstract available.
4.
Zhang B, McGee B, Yamaoka J, Guglielmone H, Downes K, Minoldo S, et al.
Blood
. 2005 Nov;
107(5):1903-7.
PMID: 16304051
Mutations in LMAN1 (ERGIC-53) or MCFD2 cause combined deficiency of factor V and factor VIII (F5F8D). LMAN1 and MCFD2 form a protein complex that functions as a cargo receptor ferrying...