Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Ayesha Khurshid"'
Autor:
Muhammad Wasi Nayyar, Asad Mahmood, Jahanzeb Liaqat, Helen Mary Robert, Rafia Mahmood, Ayesha Khurshid
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 73, Iss 2 (2023)
Objective: To examine the clinical severity and infarct volume of acute ischemic stroke (AIS) compared to control subjects by comparing the mean platelet volume/platelet count (MPV/PC) ratio. Study Design: Cross-sectional (validation) study. Pl
Externí odkaz:
https://doaj.org/article/341129f1c21b47a6842519731a09c9c1
Autor:
Syed Owais Ali, Chaudhry Altaf Hussain, Hamid Saeed Malik, Rafia Mahmood, Ayesha Khurshid, Syeda Sarwat Fatima
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 71, Iss 2, Pp 646-50 (2021)
Objective: To determine the frequency of Ten-Eleven-Translocation-2 (TET2) gene mutation in Myeloproliferative Neoplasms (MPNs) and to generate a local data for evaluation of disease behavior in ten-eleven-translocation-2 positive and negative Patien
Externí odkaz:
https://doaj.org/article/c7d51ac6220d42e7bd84b5e651849042
Autor:
Saira Irum, Helen Mary Robert, Asad Mahmood, Rafia Mahmood, Ayesha Khurshid, Saleem Ahmed Khan
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 71, Iss SUPPL-1, Pp 28-31 (2021)
Objective: To determine the frequency of clinical features and cytogenetic abnormalities in patients of down syndrome and correlation of cytogenetic abnormalities with clinical features. Study Design: Cross sectional study. Place and Duration o
Externí odkaz:
https://doaj.org/article/8336c5f8ad23470cb5e56c95000e0e99
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 70, Iss 4, Pp 998-1002 (2020)
Objective: To determine pattern of different cytogenetic abnormalities found in patients of primary amenorrhea. Study Design: Cross sectional study. Place and Duration of Study: Chromosomal analysis was carried out on patients who were sent for
Externí odkaz:
https://doaj.org/article/444e6c7378484fa1a97f34f34805772d
Autor:
Sidra Barlas, Helen Mary Robert, Rafia Mahmood, Asad Mahmood, Ayesha Khurshid, Saleem Ahmed Khan
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 70, Iss 2, Pp 447-452 (2020)
Objective: To determine the frequency of NRAS and KRAS mutations in newly diagnosed acute myeloid leukemia patients and correlation with their clinicopathological parameters along with prognostic impact. Study Design: Cross-sectional study. Pla
Externí odkaz:
https://doaj.org/article/65062c8352474622aa56f06bac168cd4
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 70, Iss 1, Pp 22-26 (2020)
Objective: To determine the frequency and clinical features of inherited platelet function disorders diagnosed at Armed Forces Institute of Pathology. Study Design: Cross sectional study. Place and Duration of Study: Department of Haematology,
Externí odkaz:
https://doaj.org/article/e8d9694115eb4bea94cb57710fa53234
Autor:
Nabeela Khan, Chaudhry Altaf, Hamid Saeed Malik, Zunera Sajjad, Ayesha Khurshid, Muhammad Tahir Khadim
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 69, Iss 5, Pp 1010-1014 (2019)
Objective: To determine the diagnostic accuracy of Ret-He in detecting IDA, keep ingserum ferritin as goldstandard Study Design: Cross sectional study. Place and Duration of Study: Department of Haematology, AFIP Rawalpindi, from Jan to Jul 201
Externí odkaz:
https://doaj.org/article/84f63bc46de0419eb5b1119374074f31
Autor:
Saqib Hussain Korejo, Ch. Altaf Hussain, Tariq Ghafoor, Hamid Saeed Malik, Ayesha Khurshid, Rafia Mahmood
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 69, Iss 3, Pp 677-680 (2019)
Objective: To determine the frequency of hyperdiploidy in childhood acute lymphoblastic leukemia (ALL) and its association with remission status after induction therapy. Study Design: Observational study. Place and Duration of Study: Department
Externí odkaz:
https://doaj.org/article/2e51df00fde1429398b2238ea847cd99
Autor:
Dr Zunera Sajjad, Saleem Ahmed Khan, Hamid Saeed Malik, Chaudry Altaf, Nabeela Khan, Ayesha Khurshid
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 68, Iss 1, Pp 04-07 (2018)
Objective: To determine the frequency of prothrombin gene mutation in venous thromboembolism in our population. Study Design: Cross sectional study. Place and Duration of Study: Department of Haematology, Armed Forces Institute of Pathology Rawalp
Externí odkaz:
https://doaj.org/article/7a71ffb96f8e4537b10da7bf2606f4cf
Autor:
Khadija Iftikhar, Chaudhry Altaf, Rafia Mahmood, Ayesha Khurshid, Ali Ahmed, Saqib Hussain Korejo
Publikováno v:
Pakistan Journal of Medical Research, Vol 58, Iss 3 (2019)
Background: Glucose 6 phosphate dehydrogenase (G6PD) deficiency is an inherited enzymopathy that is associated with hemolytic anemia. Objective: To evaluate the diagnostic accuracy of G6PD biosensor analyzer used at study site for the quantitative me
Externí odkaz:
https://doaj.org/article/a7ad37f3db044b5185076050c2ae3442