Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Tariq Masood Khan"'
Autor:
Tariq Masood Khan, Nadeem Ikram
Publikováno v:
Journal of Rawalpindi Medical College (2018)
Background: To find out the awareness about Crimean-Congo Hemorrhagic Fever (CCHF) among residents of Rawalpindi Methods: In this descriptive cross sectional survey, participants from general population of Rawalpindi were included. The sample size fo
Externí odkaz:
https://doaj.org/article/ef1c35d2660c4e3fb92f83f5711eddcd
Publikováno v:
Khyber Medical University Journal, Vol 16, Iss 3, Pp 207-12 (2024)
OBJECTIVE: To investigate the relationship between repeated blood transfusions and growth retardation in children with transfusion-dependent Thalassemia in Peshawar, Pakistan. METHODS: This cross-sectional study was conducted on transfusion-depende
Externí odkaz:
https://doaj.org/article/fb524762a4674af5867ca47bbfd25be8
Autor:
Zahid Ali, Mohammad Ismail, Inayat Ur Rehman, Gulab Fatima Rani, Muhammad Ali, Muhammad Tariq Masood Khan
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-10 (2023)
Abstract Regular blood transfusion is the mainstay of treatment in transfusion-dependent β-thalassemia (TDT); however, transfusions culminate in an array of serious complications. Therefore, a single-arm, non-randomized clinical trial was conducted
Externí odkaz:
https://doaj.org/article/55407d7374594136b42a927189762e3b
Publikováno v:
Khyber Medical University Journal, Vol 14, Iss 3, Pp 201-6 (2022)
OBJECTIVE: The current meta-analysis was carried out to identify the efficacy and safety of thalidomide in transfusion-dependent β-thalassemia (TDT) patients. METHODS: Six databases: PubMed, EMBASE, Scopus, Cochrane Library, EBSCOhost, and MEDLINE
Externí odkaz:
https://doaj.org/article/8d8be7e14662457ba49c267f0000f953
Autor:
Stephen F. Pastore, Tahir Muhammad, Ricardo Harripaul, Rebecca Lau, Muhammad Tariq Masood Khan, Muhammad Ismail Khan, Omar Islam, Changsoo Kang, Muhammad Ayub, Musharraf Jelani, John B. Vincent
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract In a multi-branch family from Pakistan, individuals presenting with palmoplantar keratoderma segregate in autosomal dominant fashion, and individuals with intellectual disability (ID) segregate in apparent autosomal recessive fashion. Initia
Externí odkaz:
https://doaj.org/article/2ba8a4534d8c463e94a9689d1d8a2244
Autor:
Abdul Rehman Khalil Shaikh, Ikram Ujjan, Muhammad Irfan, Arshi Naz, Tahir Shamsi, Muhammad Tariq Masood Khan, Muhammad Shakeel
Publikováno v:
PeerJ, Vol 9, p e10678 (2021)
Background The tet oncogene family member 2 (TET2) gene has been reported to be involved in DNA methylation and epigenetic regulation in acute myeloid leukemia (AML). Various studies have proven functional role of TET2 mutations in AML. We herein stu
Externí odkaz:
https://doaj.org/article/ce72e76b958d40339bb9e7b614a212f0
Autor:
Muhammad Idrees, Mohammad Waqas, Inayat U Rahman, Muhammad Ihtesham, Muhammad Tariq Masood Khan, Rashid Azeem
Publikováno v:
Journal of Medical Sciences. 30:216-221
Objective: This study was designed to investigate the effect of H. Pylori proteins JHP 0290 (FL) and JHP 0290 on host cell response. Materials and Methods: This study was conducted at Khyber Teaching Hospital (KTH), Peshawar from April 2021 to Septem
Publikováno v:
Journal of Medical Sciences. 30:3-8
Objective: To analyze the prevalence of CALR and JAK2 mutation co-occurrence in MF patients in KPK. Methods: This cross-sectional study included MF patients (n = 50) enrolled in the Hematology/Oncology department of Hayatabad Medical Complex (HMC), I
Autor:
Changsoo Kang, Muhammad Ayub, Musharraf Jelani, Tahir Muhammad, Omar Islam, Ricardo Harripaul, Muhammad Ismail Khan, Muhammad Tariq Masood Khan, John B. Vincent, Rebecca Lau, Stephen Pastore
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
In a multi-branch family from Pakistan, individuals presenting with palmoplantar keratoderma segregate in autosomal dominant fashion, and individuals with intellectual disability (ID) segregate in apparent autosomal recessive fashion. Initial attempt
Autor:
Asifullah Khan, Jamal Nasir, Musharraf Jelani, Hannah C. Dooley, Jumana Y. Al-Aama, Nirmal Vadgama, Hussein Sheikh Ali Mohamoud, Amin Jan, Andrea Gubas, Sharon A. Tooze, Fazal Rahim, Muhammad Ismail Khan, Muhammad Tariq Masood Khan, Changsoo Kang, Zahir Ali
Publikováno v:
Brain
Defects in autophagy are implicated in a growing number of diseases. Jelani et al. identify a mutation in WIPI2, a major autophagy gene, associated with a multisystemic global developmental disorder. Functional studies in cell lines derived from pati