Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Muhammad Younus Jamal"'
Autor:
Muhammad Younus Jamal Siddiqi, Doris Boeckelmann, Arshi Naz, Ayisha Imran, Shariq Ahmed, Akbar Najmuddin, Barbara Zieger
Publikováno v:
Cells, Vol 12, Iss 2, p 213 (2023)
Glanzmann thrombasthenia (GT) is a rare autosomal recessive inherited platelet disorder occurring frequently in populations with high incidence of consanguineous marriages. GT is characterized by quantitative and/or qualitative defect of the platelet
Externí odkaz:
https://doaj.org/article/45cf6d9b300e4b5197f46185cf56deab
Autor:
Arshi Naz, Muhammad Younus Jamal, Samina Amanat, Ikram Din ujjan, Akber Najmuddin, Humayun Patel, Fazle Raziq, Nisar Ahmed, Ayisha Imran, Tahir Sultan Shamsi
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-7 (2017)
Abstract Background Autosomal recessive bleeding disorders (ARBDs) include deficiencies of clotting factors I, II, V, VII, X, XI, XIII, vitamin K dependent clotting factors, combined factor V & VIII, Von Willebrand Disease (vWD) type 3, Glanzmann’s
Externí odkaz:
https://doaj.org/article/d98164047c44450b892d10d2d7f3382d
Autor:
Siddiqi, Muhammad Younus Jamal1,2 (AUTHOR) younus.jamal@baqai.edu.pk, Boeckelmann, Doris3 (AUTHOR), Naz, Arshi1,4 (AUTHOR), Imran, Ayisha5 (AUTHOR), Ahmed, Shariq1 (AUTHOR), Najmuddin, Akbar6 (AUTHOR), Zieger, Barbara3 (AUTHOR)
Publikováno v:
Cells (2073-4409). Jan2023, Vol. 12 Issue 2, p213. 10p.
Autor:
Amanullah Bhutto, Tufail Hussain Tahir, Rukhsana Saboor, A Saboor Soomro, Muhammad Rizwan, Muhammad Younus Jamal Siddiqi
Publikováno v:
Pakistan Journal of Medical and Health Sciences. 16:867-869
Introduction: Testicular biopsy is an invasive diagnostic tool to evaluate spermatogenesis and has to be performed only following strict criteria. Objective: To compare open testicular biopsy and testicular fine needle aspiration (TEFNA) for spermato
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e445be82586dd004ddaf53e0a137453
https://doi.org/10.53350/pjmhs20221612867
https://doi.org/10.53350/pjmhs20221612867
Autor:
Ayisha Imran, Akber Najmuddin, Arshi Naz, Muhammad Younus Jamal, Samina Tufail Amanat, Nisar Ahmed, Fazle Raziq, Ikram Din Ujjan, Tahir Shamsi, Humayun Patel
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-7 (2017)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Autosomal recessive bleeding disorders (ARBDs) include deficiencies of clotting factors I, II, V, VII, X, XI, XIII, vitamin K dependent clotting factors, combined factor V & VIII, Von Willebrand Disease (vWD) type 3, Glanzmann’s thrombas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d7fab41a7e70323bff115bc2b8f9fa9