Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Tehmina nafees sonia Khan"'
Autor:
Tehmina Nafees Sonia Khan, Samina Naz Mukry, Shahtaj Masood, Lubna Meraj, Bikha Ram Devrajani, Javed Akram, Naveena Fatima, Sidra Maqsood, Ayesha Mahesar, Roomana Siddiqui, Sadia Ishaque, Muhammad Bilal Afzal, Sanam Mukhtar, Sara Ahmed, Arshi Naz, Tahir Sultan Shamsi
Publikováno v:
BMC Infectious Diseases, Vol 21, Iss 1, Pp 1-10 (2021)
Abstract Background Convalescent plasma(CP) was utilized as potential therapy during COVID-19 pandemic in Pakistan. The study aimed at appraisal of CP transfusion safety and usefulness in COVID pneumonia. Methods Single arm, MEURI study design of non
Externí odkaz:
https://doaj.org/article/54ba2fa0edb94ec5ab71b12a5efd6ac1
Autor:
Tehmina Nafees Sonia Khan, Tariq Masood, Zara tul ain Bashir, Tasneem Farzana, Abdul Sattar, Tahir Shamsi
Publikováno v:
Liaquat Medical Research Journal, Vol 4, Iss 2 (2022)
This study was aimed to compare hemostatic, fibrinolytic and thrombotic parameters in pre and post induction chemotherapy in acute myeloid leukemia (AML) and acute lymphoid leukemia (ALL). A total of 110 diagnosed acute leukemia patients and 40 norma
Externí odkaz:
https://doaj.org/article/08359d3de837402f9890e08023421570
Autor:
Nimra Javed, Shazia Yasin, Javeria Fatima, Tehmina Nafees Sonia Khan, Tooba Fateen, Nazish Saqlain, Saima Farhan
Publikováno v:
Liaquat Medical Research Journal, Vol 4, Iss 2 (2022)
Diabetes Mellitus (DM) is the most frequently occurring metabolic disorder, caused by inadequacy in secretion of insulin or malfunction leading to chronic hyperglycemia. Well-established corroborations have been reported in the literature suggesting
Externí odkaz:
https://doaj.org/article/99e4f02b29444d6c915aa25479617af7
Autor:
Samina Naz Mukry, Javed Akram, Sidra Maqsood, Arshi Naz, Muhammad Bilal Afzal, Sadia Ishaque, Roomana Siddiqui, Bikha Ram Devrajani, Tahir Shamsi, Naveena Fatima, Shahtaj Masood, Ayesha Mahesar, Sara Ahmed, Sanam Mukhtar, Lubna Meraj, Tehmina nafees sonia Khan
Publikováno v:
BMC Infectious Diseases, Vol 21, Iss 1, Pp 1-10 (2021)
BMC Infectious Diseases
BMC Infectious Diseases
Background Convalescent plasma(CP) was utilized as potential therapy during COVID-19 pandemic in Pakistan. The study aimed at appraisal of CP transfusion safety and usefulness in COVID pneumonia. Methods Single arm, MEURI study design of non-randomiz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2c3863759a10d726bce6e8ce16cdfad
https://doaj.org/article/54ba2fa0edb94ec5ab71b12a5efd6ac1
https://doaj.org/article/54ba2fa0edb94ec5ab71b12a5efd6ac1
Autor:
Shariq Ahmed, Anne Goodeve, Tahir Sultan Shamsi, Ikram Din Ujjan, Tehmina nafees sonia Khan, Arijit Biswas, Nazish Saqlain, Arshi Naz, Johannes Oldenburg, Nisar Ahmed
Publikováno v:
Thrombosis Journal
Thrombosis Journal, Vol 15, Iss 1, Pp 1-8 (2017)
Thrombosis Journal, Vol 15, Iss 1, Pp 1-8 (2017)
Background Congenital afibrinogenemia (OMIM #202400) is a rare coagulation disorder that was first described in 1920. It is transmitted as an autosomal recessive trait that is characterized by absent levels of fibrinogen (factor I) in plasma. Consang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54990efc8f751d0e0b0a4b5295ba0138
https://eprints.whiterose.ac.uk/126102/3/s12959-017-0143-3.pdf
https://eprints.whiterose.ac.uk/126102/3/s12959-017-0143-3.pdf
Autor:
Akbar Najmuddin, Tehmina nafees sonia Khan, Arshi Naz, Ayisha Imran, Tahir Shamsi, Yonus Jamal, Shariq Ahmed
Publikováno v:
Blood. 126:4658-4658
Background: Glanzmann thrombasthenia (GT) is most common inherited platelet functional defect. It is an autosomal recessive disorder, characterized by a bleeding diathesis. Incidence is increased in locations where consanguineous marriages are common
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ebd5da5614ed86a3ae0c9ea92bc7c37
https://doi.org/10.1182/blood.v126.23.4658.4658
https://doi.org/10.1182/blood.v126.23.4658.4658
Autor:
Shariq Ahmed, Anne Goodeve, Tahir Shamsi, Arjit Biswas, Nisar Ahmed, Johannes Oldenburg, Tehmina nafees sonia Khan, Arshi Naz
Publikováno v:
Blood. 126:4664-4664
Background: Congenital afibrinogenemia (OMIM #202400) is a rare coagulation disorder which was first described in 1920. It is transmitted as an autosomal recessive trait characterized by absent levels of fibrinogen (factor I) in plasma. Consanguinity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92c70edcc62b4c03e29dc558e856c525
https://doi.org/10.1182/blood.v126.23.4664.4664
https://doi.org/10.1182/blood.v126.23.4664.4664
Autor:
Shahla Tariq, Arshi Naz, Nazish Saqlain, Noman A Malik, Tehmina nafees sonia Khan, Tahir Shamsi
Publikováno v:
Blood. 126:4667-4667
Background: Congenital afibrinogenemia is inherited as an autosomal recessive trait and consanguinity is common among affected families. Phenotypic expression of this particular factor deficiency is still not unanimously established in research liter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::094f049a0f012431f7f6ad8a8b4b0f12
https://doi.org/10.1182/blood.v126.23.4667.4667
https://doi.org/10.1182/blood.v126.23.4667.4667