Výsledky vyhledávání - "Hugo Guglielmone"

Recurrent superficial venous thrombophlebitis because of mutations in the protein C and fibrinogen genes in a young Argentinian female

Autor: María A. Alvarez-Bollea, Luis A. Bastos, Gustavo Jarchum, Hugo Guglielmone

Publikováno v: Blood Coagulation & Fibrinolysis. 30:80-84

Hypodysfibrinogenemia and protein C deficiency are coagulopathies and in this report, we describe a young patient with both defects confirmed by molecular genetic tests. The patient was a 24-year-old woman referred for recurrent thrombophlebitis and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f13336dd05c17ac16ab922fcffe8c72
https://doi.org/10.1097/mbc.0000000000000790

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The old and the new in prekallikrein deficiency: historical context and a family from Argentina with PK deficiency due to a new mutation (Arg541Gln) in exon 14 associated with a common polymorphysm (Asn124Ser) in exon 5

Autor: Antonio, Girolami, Josè, Vidal, Marcela, Sabagh, Marcela, Salagh, Nora, Gervan, Maria, Parody, Edoardo, Peroni, Luisa, Sambado, Hugo, Guglielmone

Publikováno v: Seminars in thrombosis and hemostasis. 40(5)

Prekallikrein (PK) is one of the clotting factors involved in the contact phase of blood. PK has an important historical role as its deficiency state represents the second instance of a clotting defect without bleeding manifestations, the first one b

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdafaab0321c27b78f0c0c1f7d9e97bd
https://pubmed.ncbi.nlm.nih.gov/25075649

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Lack of evidence of neoantigen formation in different batches of a double-virus inactivated factor VIII concentrate manufactured in Argentina

Autor: Hugo, Guglielmone, Federico, Farias, Cristian, Moya, David, Navarro, María Susana, Vitali

Publikováno v: Blood transfusion = Trasfusione del sangue. 9(2)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4d2c7212ba4d5a679dd35530d10f283e
https://pubmed.ncbi.nlm.nih.gov/21084006

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Combined deficiency of factor V and factor VIII is due to mutations in either LMAN1 or MCFD2

Autor: Paula L. Bockenstedt, Arlette Ruiz-Saez, Randal J. Kaufman, Katharine A. Downes, Gustavo Jarchum, Marian Olpinski, Norma B. de Bosch, Flora Peyvandi, Beth McGee, Hugo Guglielmone, Salvador Minoldo, Bernard Chatelain, Wolfgang Sperl, Jennifer S. Yamaoka, William C. Nichols, Bin Zhang, David Ginsburg, Edward G. D. Tuddenham

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 FV and FVIII from the endoplasmic reticulum to the Golgi. In this

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af575f8969e1cbb96b657b468c169ee3
https://europepmc.org/articles/PMC1895703/

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Successful treatment with intravenous immunoglobulin (IVIg) in a patient with an acquired factor V inhibitor after liver transplantation

Autor: Gustavo Jarchum, Salvador Minoldo, Hugo Guglielmone

Publikováno v: Thrombosis and Haemostasis. 106:985-986

Successful treatment with intravenous immunoglobulin (IVIg) in a patient with an acquired factor V inhibitor after liver transplantation

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::916621888610e0b8a762c2664fef3c01
https://doi.org/10.1160/th11-05-0307

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Tissue Factor and Cancer Procoagulant as Predictors of Thrombosis or Progression in Cancer Patients

Autor: Marcelo Lavarda, Soledad Molnar, Hugo Guglielmone, Maria Laura Rizzi, Gustavo Jarchum, Salvador Minoldo

Publikováno v: Blood. 110:3136-3136

Background: Two procoagulant factors are associated with the tumor cell: tissue factor (TF) and cancer procoagulant (CP). The activation of the coagulation system can cause thrombosis and it has also been involved in the development of metastasis. Ai

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::dd58d2e2141eb594ab6b71a2bf999d7d
https://doi.org/10.1182/blood.v110.11.3136.3136

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Mutations in LMAN1 and MCFD2 May Account for All Cases of Combined Deficiency of Factor V and Factor VIII

Autor: Bin Zhang, Katherine Downes, Wolfgang Sperl, Marian Olpinski, Flora Peyvandi, William C. Nichols, Norma B. de Bosch, Paula L. Bockenstedt, Arlette Ruiz-Saez, Randal J. Kaufman, Bernard Chatelain, Beth McGee, David Ginsburg, Hugo Guglielmone

Publikováno v: Blood. 106:724-724

Factor V (FV) and factor VIII (FVIII) are two large plasma glycoproteins that function as essential cofactors for the proteolytic activation of prothrombin and factor X, respectively. Efficient biosynthesis of FV and FVIII requires LMAN1 and MCFD2, t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e3adf6589c6d82d550da679fb5fdcbda
https://doi.org/10.1182/blood.v106.11.724.724

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Akademický článek

Procoagulant factors in patients with cancer.

Autor: Molnar, Soledad¹ soledadmolnar@yahoo.com.ar, Guglielmone, Hugo¹, Lavarda, Marcelo¹, Rizzi, Maria Laura¹, Jarchum, Gustavo¹

Publikováno v: Hematology. Dec2007, Vol. 12 Issue 6, p555-559. 5p. 2 Charts, 2 Graphs.

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Akademický článek

Erratum.

Publikováno v: Seminars in Thrombosis & Hemostasis; 2014, Vol. 40 Issue 6, p712-712, 1p

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