Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Minoo Ahmadinejad"'
Publikováno v:
Iranian Journal of Pathology, Vol 16, Iss 3, Pp 332-336 (2021)
Hereditary deficiency of plasma prekallikrein (PPK) is a rare autosomal recessive disease. The affected patients are often asymptomatic and diagnosed incidentally during preoperative investigations or during hospitalization by isolated prolongation o
Externí odkaz:
https://doaj.org/article/db8bdb3229924e69a2d94fa11ea8faed
Publikováno v:
International Journal of Hematology-Oncology and Stem Cell Research, Vol 15, Iss 4 (2021)
Background: Heparin-induced thrombocytopenia (HIT) is a serious adverse drug reaction. HIT diagnosis needs an algorithmic approach including clinical evaluation and laboratory tests (screening and confirmatory). Few studies have been conducted on HIT
Externí odkaz:
https://doaj.org/article/73564a046af1453d9287a12ca004ac5f
Autor:
Maria Teresa Pagliari, Ulrich Budde, Luciano Baronciani, Peyman Eshghi, Minoo Ahmadinejad, Zahra Badiee, Mohammad-Reza Baghaipour, Olga Benítez Hidalgo, Eugenia Biguzzi, Imre Bodó, Giancarlo Castaman, Jenny Goudemand, Mehran Karimi, Bijan Keikhaei, Riitta Lassila, Frank W.G. Leebeek, Maria Fernanda Lopez Fernandez, Renato Marino, Johannes Oldenburg, Ian Peake, Cristina Santoro, Reinhard Schneppenheim, Andreas Tiede, Gholamreza Toogeh, Alberto Tosetto, Marc Trossaert, Hamideh Yadegari, Eva M.K. Zetterberg, Pier Mannuccio Mannucci, Augusto B. Federici, Jeroen Eikenboom, Flora Peyvandi
Publikováno v:
Journal of Thrombosis and Haemostasis, 21(4), 787-799. Wiley-Blackwell Publishing Ltd
Background: Type 3 von Willebrand disease (VWD) is the most severe form of this disease owing to the almost complete deficiency of von Willebrand factor (VWF). Replacement therapy with plasma-derived products containing VWF or recombinant VWF rarely
Autor:
Hassan Abolghasemi, MD, Yunes Panahi, PhD, Minoo. Ahmadinejad, MD, Gholamreza Toogeh, MD, Mehran Karimi, MD, Aziz Eghbali, MD, Nargess Bigom Mirbehbahani, MD, Bighan Keikhaei Dehdezi, MD, Zahra Badiee, MD, Hamid Hoorfar, MD, Peyman Eshghi, MD, Nader Maghsoudi, PhD, Amirhossein Sahebkar, PhD, Mohammad Gholami- Fesharaki, PhD
Publikováno v:
Journal of Pharmacopuncture, Vol 21, Iss 2, Pp 76-81 (2018)
Objective: This study compared the safety and efficacy of Safacto® versus xyntha® in patients with severe hemophilia A. Methods: Thirty-three male patients with severe hemophilia A were randomly divided into two groups. Seventeen patients received
Externí odkaz:
https://doaj.org/article/31d83db47fbb4d37a53316706c5fa101
Autor:
Mahdi Zahedpanah, Azita Azarkeivan, Minoo Ahmadinejad, Mohamad R Tabatabaiee, Bashir Hajibeigi, Mahtab Maghsudlu
Publikováno v:
Journal of Applied Hematology, Vol 9, Iss 4, Pp 126-130 (2018)
BACKGROUND: Platelet dysfunction may be one of the pathophysiologic complications in beta-thalassemia patients. However, the results obtained from the platelet aggregation vary in different types of β-thalassemia and among patients. OBJECTIVE: We ev
Externí odkaz:
https://doaj.org/article/f62498d851c448e28f38ff2e9034be3f
Publikováno v:
Transfusion Medicine. 31:494-498
BACKGROUND Fresh frozen plasma (FFP) is used to treat coagulation disorders. Even though the activity of labile coagulation factors gradually decreases once thawed, it can be used up to 24 h after thawing, if stored properly. In this study, the level
Autor:
Nafiseh Nasri Nasrabadi, Nasser Mohammadpour Dounighi, Minoo Ahmadinejad, Hadi Rabiei, Maryam Tabarzad, Mojtaba Najafi, Hossein Vatanpour
Publikováno v:
Iranian Journal of Pharmaceutical Research. 21
Background: The venom of Echis carinatus contains both procoagulant and anticoagulant components that can either promote or block the blood coagulation cascade, and some of these components affect platelet function in different ways. Objectives: The
Publikováno v:
Tehran University Medical Journal, Vol 71, Iss 7, Pp 480-484 (2013)
Background: It is rare to find squamous metaplasia in the thyroid gland. Its existence is usually seen in association with a pathological lesion such as mucoepidermoid carcinoma, squamous cell carcinoma and diffuse sclerosing variant of papillary thy
Externí odkaz:
https://doaj.org/article/ca72d922b803450d822e38ee8bab421c
Autor:
Katayoun Karimi, Mohammad Reza Managhchi, Ali Arabkhazaeli, Gholamreza Toogeh, Sanaz Homayoun, Fatemeh Vosough, Minoo Ahmadinejad
Publikováno v:
Blood Coagulation & Fibrinolysis. 31:530-535
Diagnosis of hemophilia A is generally based on the measurement of plasma factor VIII activity (FVIII:C) using the one-stage assay (OSA) or the two-stage chromogenic substrate assay (CSA). The results of these methods show considerable discrepancy in
Autor:
Maria Teresa Pagliari, Frits R. Rosendaal, Minoo Ahmadinejad, Zahra Badiee, Mohammad‐Reza Baghaipour, Luciano Baronciani, Olga Benítez Hidalgo, Imre Bodó, Ulrich Budde, Giancarlo Castaman, Peyman Eshghi, Jenny Goudemand, Mehran Karimi, Bijan Keikhaei, Riitta Lassila, Frank W.G. Leebeek, Maria Fernanda Lopez Fernandez, Pier Mannuccio Mannucci, Renato Marino, Johannes Oldenburg, Ian Peake, Cristina Santoro, Reinhard Schneppenheim, Andreas Tiede, Gholamreza Toogeh, Alberto Tosetto, Marc Trossaert, Hamideh Yadegari, Eva M.K. Zetterberg, Flora Peyvandi, Augusto B. Federici, Jeroen Eikenboom
Publikováno v:
Journal of Thrombosis and Haemostasis, 20(5), 1106-1114. WILEY
Journal of Thrombosis and Haemostasis, 20(5), 1106-1114. Wiley-Blackwell Publishing Ltd
Journal of Thrombosis and Haemostasis, 20(5), 1106-1114. Wiley-Blackwell Publishing Ltd
Background\ud \ud Type 3 von Willebrand disease (VWD) is a severe bleeding disorder caused by the virtually complete absence of von Willebrand factor (VWF). Pathophysiological mechanisms of VWD like defective synthesis, secretion, and clearance of VW
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46d842656b347c2e973e2fd7704d87b9
https://hdl.handle.net/1887/3307282
https://hdl.handle.net/1887/3307282