Zobrazeno 1 - 10
of 1 239
pro vyhledávání: '"Glanzmann"'
Autor:
May AlMoshary
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 13, Iss 11, Pp 5395-5398 (2024)
Hemorrhagic cholecystitis is a rare and potentially life-threatening condition that requires immediate medical attention. If the gallbladder perforates, it can lead to even more severe complications. We present the case of a 27-year-old man with Glan
Externí odkaz:
https://doaj.org/article/76abd2275efe47e4ba6ebec2a291c991
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract Integrin αIIbβ3 is the predominant receptor for fibrinogen which mediates platelet aggregation, an important step in hemostasis and thrombosis. Several mutations have been reported in the genes encoding αIIb and β3 subunits among patient
Externí odkaz:
https://doaj.org/article/1c8366f51ae14188832fc7cf752632de
Autor:
Abdulrhman Ibrahim Alathaibi, Muhammad Matloob Alam, Mohammed Kamal, Mohamed Refai, Faisal Alosaimi, Omar Allehyani, Nojood Althubaity
Publikováno v:
Journal of Applied Hematology, Vol 15, Iss 3, Pp 246-249 (2024)
Congenital thrombocytopenias are a diverse range of diseases. Of them, Glanzmann thrombasthenia is an autosomal recessive platelet aggregation disorder due to defect in the alpha IIb/beta3 integrins, coded by the ITGA2B and ITGB3 genes. While most pa
Externí odkaz:
https://doaj.org/article/2fa1193e3b694e2d887fe1a1da4f6a4c
Autor:
Daiane Keller Cecconello, Fabiane Spagnol, Ana Paula Alegretti, Diogo André Pilger, Mariela Granero Farias
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S136-S142 (2024)
Introduction and Objective: Flow Cytometry (FC) is one of the techniques, which allows the identification and characterization of platelets. The detection of absent or reduced expression of the glycoproteins is the main objective of this technique. A
Externí odkaz:
https://doaj.org/article/ce61eaf3cffa4f62a8cd97c075121df1
Publikováno v:
Case Reports in Clinical Practice, Vol 9, Iss 2 (2024)
Glanzmann’s thrombasthenia (GT) is a rare genetic platelet disorder that leads to bleeding problems in affected individuals. We present a 28-year-old woman with GT who experienced a rare symptom of painless gross hematuria in the last month of preg
Externí odkaz:
https://doaj.org/article/ff2f2e36b7a04141987fe519589a9c12
Publikováno v:
Research and Practice in Thrombosis and Haemostasis, Vol 8, Iss 7, Pp 102586- (2024)
Background: Glanzmann thrombasthenia (GT) is a rare platelet function disorder that results in severe bleeding. We assessed clinical symptoms and psychological parameters to identify the unmet needs associated with GT. Objectives: Glanzmann’s 360 i
Externí odkaz:
https://doaj.org/article/be9d9c627f574974acdca4f6504061a2
Publikováno v:
Journal of Blood Medicine, Vol Volume 14, Pp 563-567 (2023)
Mouhammad J Alawad,1 Mohammad Abu-Tineh,2 Awni Alshurafa,2 Alaa Al-Taie,3 Anil Yousaf,2 Mohamed A Yassin2 1Department of Medical Education, Internal Medicine Residency Program, Hamad Medical Corporation, Doha, Qatar; 2Department of Medical Oncology,
Externí odkaz:
https://doaj.org/article/4280193b73e14731abb91dffe8ced289
Akademický článek
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Autor:
Doris Boeckelmann, Lara von Dobeneck, Hans Henkes, Hermann Eichler, Hannah Glonnegger, Barbara Zieger
Publikováno v:
Diseases, Vol 12, Iss 7, p 136 (2024)
Glanzmann Thrombasthenia (GT) is an inherited platelet disorder caused by defects in platelet integrin αIIbβ3 (GPIIb/IIIa), which is a platelet receptor essential for the binding of fibrinogen. This can lead to severe bleeding, especially after tra
Externí odkaz:
https://doaj.org/article/bd38395a7af84dae96fb6c84e0918e60
Autor:
Samaneh Rokhgireh, Abolfazl Mehdizadehkashi, Shahla Chaichian, Mohammad Faranoush, Fardis Salmanpour, Noosha Samieefar, Roya Derakhshan
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-8 (2023)
Abstract Background Glanzmann thrombasthenia (GT) is a rare bleeding disorder with a high prevalence in communities where consanguineous marriages are mainstream. Endometriosis is a chronic inflammatory disease, and its risk increases in women with m
Externí odkaz:
https://doaj.org/article/1218bfb923bd4ba19234a852c2450ca1