Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Abid Sohail Taj"'
Autor:
Muhammad Tariq Masood Khan, Arshi Naz, Abid Sohail Taj, Tahir Sultan Shamsi, Muahmmad Tariq Hamayun Khan, Nazish Farooq, Jawad Ahmed
Publikováno v:
Khyber Medical University Journal, Vol 9, Iss 1, Pp 19-23 (2017)
OBJECTIVES: To determine the frequency of misdiagnosis among documented factor IX (FI) deficient (hemophilia B) patients of Khyber Pakhtunkhwa (KP) province of Pakistan and to discern role of different diagnostic tests employed in this regard. MET
Externí odkaz:
https://doaj.org/article/84a60d8b0f5f4299b96ac9cb7ffa2cbf
Publikováno v:
Scholars Journal of Applied Medical Sciences. 10:1425-1430
Aim And Objectives: AML is the most common acute leukemia affecting adults, its incidence increases with increasing age; the study aims to find out the clinical and haematological parameters of adult AML patients and the frequency of AML FAB subtype
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b32fca58c1af335fbecc63320ffa7eea
https://doi.org/10.36347/sjams.2022.v10i09.002
https://doi.org/10.36347/sjams.2022.v10i09.002
Publikováno v:
Iranian Journal of Pediatric Hematology & Oncology.
Background: This study aimed to assess the frequency determination of c.1115_1118delTTGG and c.3788_3790delTCT Fanconi's anemia A gene (FANCA) gene mutation in the North of Khyber Pakhtunkhwa (KPK) Pakistan Fanconi’s Anemia Population. Materials an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0824609103603ec885545a3f32d68682
https://doi.org/10.18502/ijpho.v12i3.10059
https://doi.org/10.18502/ijpho.v12i3.10059
Autor:
Zafar Iqbal, Aamer Aleem, Mudassar Iqbal, Mubashar Iqbal Naqvi, Ammara Gill, Abid Sohail Taj, Abdul Qayyum, Najeeb ur-Rehman, Ahmad Mukhtar Khalid, Ijaz Hussain Shah, Muhammad Khalid, Riazul Haq, Mahwish Khan, Shahid Mahmood Baig, Abid Jamil, Muhammad Naeem Abbas, Muhammad Absar, Amer Mahmood, Mahmood Rasool, Tanveer Akhtar
Publikováno v:
PLoS ONE, Vol 8, Iss 2, p e55717 (2013)
BACKGROUND: BCR-ABL kinase domain mutations are infrequently detected in newly diagnosed chronic-phase chronic myeloid leukemia (CML) patients. Recent studies indicate the presence of pre-existing BCR-ABL mutations in a higher percentage of CML patie
Externí odkaz:
https://doaj.org/article/006171ec52514c238b8255891fec978c
Publikováno v:
Hemophilia-Recent Advances
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bb87d80ab8b241215ea2f9b51ef0471
https://doi.org/10.5772/intechopen.81429
https://doi.org/10.5772/intechopen.81429
Autor:
Ayisha Imran, Nisar Ahmed, Abid Sohail Taj, Muhammad Tariq Hamayun Khan, Tahir Shamsi, Nazish Farooq, Shariq Ahmed, Jawad Ahmed, Arshi Naz, Muhammad Tariq Masood Khan
This study aimed to (1) identify F9 genetic alterations in patients with hemophilia B (HB) of Pakistani origin and (2) determine the genotype–phenotype relationships in these patients. Diagnosed cases of HB were identified through registries at des
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c1a9f97db75ed4d9ae9fa20dafeec5b
https://europepmc.org/articles/PMC6714882/
https://europepmc.org/articles/PMC6714882/
Publikováno v:
Pakistan Journal of Medical Sciences
Objectives 1: To assess the diagnostic utility of three polymorphisms (DdeI, XmnI and TaqI) and direct sequencing in haemophilia B (HB) carrier detection in Pakistani families. 2: To compare phenotypes of HB carriers with those of healthy females. Me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f366a5e2caf5ec3a43738c04ffd91bb9
https://doi.org/10.12669/pjms.333.12496
https://doi.org/10.12669/pjms.333.12496
Autor:
Daniel L. Polla, Attia Razzaq, Asbjørn Holmgren, Sheikh Riazuddin, Vincent Zoete, Mureed Hussain, Periklis Makrythanasis, Abid Sohail Taj, Saima Riazuddin, Michel Guipponi, Muhammad Ansar, Sylviane Hanquinet, Jawad Ahmed, Muhammad T. Sarwar, Jamshed Khan, Federico Santoni, Stylianos E. Antonarakis, Justyna Iwaszkiewicz, Sohail A. Paracha, Muhammad Zaman Khan Assir, Naila Batool, Eirik Frengen, Arjan P.M. de Brouwer, Hans van Bokhoven, Zafar Iqbal, Doriana Misceo
Publikováno v:
Genetics in Medicine, 20, 7, pp. 778-784
Genetics in Medicine, Vol. 20, No 7 (2018) pp. 778-784
Genetics in Medicine, 20, 778-784
Genetics in Medicine, Vol. 20, No 7 (2018) pp. 778-784
Genetics in Medicine, 20, 778-784
PurposeTo elucidate the novel molecular cause in two unrelated consanguineous families with autosomal recessive intellectual disability.MethodsA combination of homozygosity mapping and exome sequencing was used to locate the plausible genetic defect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e136c2e3f1bb68eab70da5c3daea4f95
https://pubmed.ncbi.nlm.nih.gov/28837161
https://pubmed.ncbi.nlm.nih.gov/28837161
Publikováno v:
Blood. 134:4816-4816
Background Thalassemia is one of the most common genetic blood disorders worldwide. The carrier rate of β thalassemia in Pakistan is found to be around 5-7%, rendering it a major health concern. Approximately 5000 children are diagnosed with thalass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f0a14a4eef608d8563b15285cdfcb28
https://doi.org/10.1182/blood-2019-130049
https://doi.org/10.1182/blood-2019-130049
Autor:
Mudassar Iqbal, Jamil Amjad Hashmi, Noreen Sabir, Muhammad Farooq Sabar, Zafar Iqbal, Muhammad Irfan, Afia Muhammad Akram, Tashfin Awan, Mehmood Hussain Qazi, Sajjad Karim, Muhammad Khalid, Muhammad Hassan Siddiqi, Tanveer Akhtar, Aamer Aleem, Ijaz H Shah, Muhammad Absar, Abdullah Alanazi, Akhtar Hussain, Masood A. Shammas, Mahmood Rasool, Ammara T Gill, Ahmad Mukhtar Khalid, Abid Sohail Taj, Aamir Mahmood, Anjum Saeed, Abid Jameel
Publikováno v:
Molecular diagnosistherapy. 19(5)
BACKGROUND: Fusion oncogenes (FOs) resulting from chromosomal abnormalities have an important role in leukemogenesis in pediatric B cell acute lymphoblastic leukemia (ALL). The most common FOs are BCR-ABL, MLL-AF4, ETV6-RUNX1, and TCF3-PBX1, all of w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3faf2720c7e19a4645c173d74024d945
https://pubmed.ncbi.nlm.nih.gov/26266519
https://pubmed.ncbi.nlm.nih.gov/26266519