Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Tariq Ghafoo"'
Genetic analysis of osteopetrosis in Pakistani families identifies novel and known sequence variants
Autor:
Chunyu Liu, Muhammad Ajmal, Zaineb Akram, Tariq Ghafoor, Muhammad Farhan, Sobia Shafique, Sughra Wahid, Shahar Bano, Jianqiu Xiao, Humayoon Shafique Satti, Feng Zhang, Tahir Naeem Khan
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-9 (2021)
Abstract Osteopetrosis is a genetically heterogenous, fatal bone disorder characterized by increased bone density. Globally, various genetic causes are reported for osteopetrosis with all forms of inheritance patterns. A precise molecular diagnosis i
Externí odkaz:
https://doaj.org/article/2bf5b2c415524ca4aafc8083fa1e385f
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 72, Iss 5 (2022)
Objective: To study the clinical profile and induction outcome in children diagnosed with T-cell acute lymphoblastic leukaemia and lymphoblastic lymphoma. Study Design: Cross-sectional study. Place and Duration of Study: Paediatric Oncology Uni
Externí odkaz:
https://doaj.org/article/9f412ab794f3413eb0dfe68d01ae8077
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 71, Iss 2, Pp 469-72 (2021)
Objective: To find out the rate of remission of Pre-B Acute Lymphoblastic Leukaemia in children at the end of induction treatment with United Kingdom Acute Lymphoblastic Leukaemia (UKALL) 2011 chemotherapy protocol. Study Design: Prospective obser
Externí odkaz:
https://doaj.org/article/6017fa56f59f4f739266757055a01153
Autor:
Tariq Azam Khattak, Muhammad Farhan, Tariq Ghafoor, Tariq Mahmood Satti, Qamar Un Nisa Chaudhry, Mehreen Ali Khan
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 71, Iss 1, Pp 190-195 (2021)
Objective: To determine the treatment outcome of Hematopoietic stem cell transplantation in Fanconi Anemia. Study Design: Case series. Place and Duration of Study: Armed Forces Bone Marrow Transplant Center, Rawalpindi, from Jan 2001 to Jun 2018. Met
Externí odkaz:
https://doaj.org/article/9deb7db96e0c4bbab0f6126f1f8f1d0c
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 70, Iss 1, Pp 195-200 (2020)
Objective: To assess the relationship of hypocalcemia with prematurity and low birth weight. Study Design: Prospective observational study Place and Duration of Study: Study was conducted in Pak Emirates Military Hospital Pakistan, from Jan 201
Externí odkaz:
https://doaj.org/article/9aacc4ca9591446aaf803ca526088835
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:
Tariq Ghafoor, Farrah Bashir
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 69, Iss 1, Pp 217-220 (2019)
Chronic granulomatous disease (CGD) is a rare primary immunodeficiency disorder of phagocytes, characterized by repeated bacterial and fungal infections. We present a boy suffering from recurrent infections since infancy who was treated with various
Externí odkaz:
https://doaj.org/article/771d19490f8a4404a6bae68bf96828c0
Autor:
Raheel Iftikhar, Qamar un Nisa Chaudhry, Tariq Mehmood Satti, Syed Kamran Mahmood, Tariq Ghafoor, Ghassan Umair Shamshad, Nighat Shahbaz, Mehreen Ali Khan, Tariq Azam Khattak, Jahanzeb Rehman, Muhammad Farhan, Saima Humayun, Humera Haq, Syeda Ammaara Anwaar Naqvi, Faiz Anwer, Humayoon Shafique Satti, Parvez Ahmed
Publikováno v:
Clinical Hematology International, Vol 2, Iss 2 (2020)
Allogeneic stem cell transplant for high-risk aplastic anemia (AA) yields inferior results using conventional cyclophosphamide (CY)-based conditioning. The use of fludarabine (Flu)-based regimens has resulted in improved outcomes in high-risk patient
Externí odkaz:
https://doaj.org/article/d351dd7dd74c441297ae6d732ecfb695
Publikováno v:
Case Reports in Oncological Medicine, Vol 2020 (2020)
Inflammatory myofibroblastic tumor (IMT) is a rare entity of neoplastic origin. It usually occurs in children and adolescents and most commonly involves pulmonary and gastrointestinal sites. Here, the authors present two cases; one is the nine months
Externí odkaz:
https://doaj.org/article/cce8a24705604aaf838ba7a68551c2a0
Autor:
Raheel iftikhar, Qamar Un nisa Chaudhry, Tariq Mehmood Satti, Syed Kamran Mahmood, Tariq Ghafoor
Publikováno v:
Clinical Case Reports, Vol 7, Iss 7, Pp 1442-1444 (2019)
Key Clinical Message Post‐transplant lymphoproliferative disorders are rare but potentially life‐threatening complication of HSCT. Although not frequently reported but PTLD can occur as a late post‐transplant complication in HSCT recipients. A
Externí odkaz:
https://doaj.org/article/a592a9b8556a4e92be824b7a1bac52d1