Results 81 to 90 of about 3,107 (209)

Use of recombinant factor VIIa for bleeding in children with Glanzmann thrombasthenia.

, 2003
Glanzmann thrombasthenia is a very rare inherited platelet function disorder in which bleeding may be extremely difficult to stop. Recombinant factor VIIa is one of the alternative treatments for bleeding.
Caglar, K, Cetinkaya, A, Gurgey, A, Aytac, ŞEVKİYE SELİN, Gumruk, FATMA   +4 more
core   +1 more source

Correlation of Platelet Receptor Expression in Glanzmann Thrombasthenia with Clinical Presentation and Haematological Parameters

Pakistan Armed Forces Medical Journal
Objective: To correlate platelet receptor expression with clinico-haematological parameters in patients of Glanzmann Thrombasthenia. Study Design: Cross-sectional study.
Ahmad Cheema, Manzar Bozdar, Hamid Saeed Malik, Muhammad Hussain, Rafia Mahmood, Aysha Khan, Ayesha Khurshid, Syeda Samia Shafaat   +7 more
doaj   +1 more source

Diagnostic tool for Glanzmann\u27s thrombasthenia clinicopathologic spectrum [PDF]

, 2008
Objective: To platelet aggregometry and describe the clinical spectrum of Glanzmann\u27s thrombasthenia diagnosed by platelet aggregometry.Study design: A case-series.Place and duration of study: This study was carried out at the clinical laboratories at
Adil, Salman, Rahman, Yasmeen, Shaikh, Mohammad Usman, Moiz, Bushra, Ali, Natasha Bahadur, Rizvi, Bushra   +5 more
core  

Glanzmann\u27s thrombasthenia: report of a case and review of the literature.

, 2010
Glanzmann\u27s thrombasthenia is a rare congenital bleeding disorder. Patients usually present with mucocutaneous bleeding and excessive bleeding associated with trauma and/or surgery.
Bromberg, Michael, Hurford, Matthew T, Sebastiano, Christopher, MD, Breen, Karen   +3 more
core   +1 more source

Endometriosis and Glanzmann's thrombasthenia

, 2016
Glanzmanns thrombasthenia (GT) is a rare bleeding syndrome characterized by deficiency or defect of platelet aggregation complex. The pathogenesis of endometriosis is controversial but the strongest evidence leans towards retrograde menstruation.
MANGANARO, Lucia, Resta, S, TICINO, ADELE, PIACENTI, ILARIA, ANASTASI, Emanuela, BENEDETTI PANICI, PIERLUIGI, IMPERIALE, LUDOVICA, PORPORA, Maria Grazia   +7 more
core  

Oral management of Glanzmann's thrombasthenia. A case report

, 1975
The oral management of a patient with Glanzmann's thrombasthenia has been described. Although evidence of detrimental effects produced by electrosurgery has been previously well documented, the benefits achieved in this case showed any such damage to be ...
Brown, G., Nixon, K. C., David W. Keys, Graham Brown, Kenneth C. Nixon, Keys, D. W.   +5 more
core   +1 more source

Clinico-Demographic Trends in Inherited Bleeding Disorders: Insights from Dhaka Medical College

Haematology Journal of Bangladesh
Background: The blood coagulation system is very delicately balanced; is maintained in a fluid state in the vasculature and rapidly clots to seal an injury.
Nahid Sultana, Md. Adnan Hasan Masud, Salma Afrose, Tasneem Ara, Mohammad Ali, Akhil Ranjan Biswas, Md. Manirul Islam, Mohit Kumer Pramanik, Romena Alam, Hasnain Imtiaz   +9 more
doaj   +1 more source

Glanzmann's thrombasthenia.

Indian pediatrics, 1992
During January 1981 to June 1991, 20 patients from 16 unrelated families were detected to have Glanzmann's thrombasthenia (GT). Twelve families (75%) had history of consanguinity, with 6 first cousins and 3 uncle-niece marriages; of these 7 were Muslims, 6 Hindus and 3 Christians. There were 12 girls and 8 boys; the mean age at diagnosis was 7.05 +/- 6.
M B, Agarwal, U M, Agarwal, C, Viswanathan, A A, Bhave, V, Billa   +4 more
openaire   +1 more source

Glanzmann’s Thrombasthenia Diagnosed following Knee Arthroscopy

Case Reports in Orthopedics, 2015
A 41-year-old man with an unremarkable medical history presented with a painful knee after a sports injury. He was diagnosed with a medial meniscal tear.
John E. Zvijac, Sharhabil S. Ammus, Fernando Aran, Gary M. Kiebzak   +3 more
doaj   +1 more source

Spontaneous hemarthrosis in combined Glanzmann thrombasthenia and type 2N von Willebrand disease.

, 2014
Glanzmann thrombasthenia is a rare autosomal recessive inherited bleeding disorder characterized by the lack of platelet aggregation, caused by deficiencies and/or abnormalities of platelet GPIIb-IIIa receptor.
PONTARA, ELENA, DAIDONE, VIVIANA, ZANONATO, ELISA, PELOSO CATTINI, MARIA GRAZIA, BARBON, GIOVANNI, CASONATO, SANDRA, GRESELE, PAOLO, GIROLAMI, ANTONIO   +7 more
core   +1 more source