Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Rabia Wali"'
Autor:
Zunaira Shaukat, Rabia Wali, Saadiya Javed Khan, Summiya Nizamuddin, Romena Qazi, Kainat Memon, Najma Shaheen
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 72, Iss 5 (2022)
Objective: To study organisms causing bacteremia and their outcome in cancer children with febrile neutropenia (FN) admitted at our centre. Study Design: Retrospective longitudinal study. Place and duration of study: Department of Pediatric Oncolo
Externí odkaz:
https://doaj.org/article/8993e5e11340459b850861a2a7a18312
Publikováno v:
Journal of Global Oncology, Vol 5, Pp 1-6 (2019)
PURPOSE: Hodgkin lymphoma is the most common cancer in children, adolescents, and young adults. Overall survival is approximately 80% to 90%. A subset of these patients has refractory disease or experience disease relapse. Conventional salvage therap
Externí odkaz:
https://doaj.org/article/514a0aa0447e48138386c3781b8baa39
Autor:
Najma Shaheen, Kainat Memon, Romena Qazi, Summiya Nizamuddin, Saadiya Javed Khan, Rabia Wali, Zunaira Shaukat
Publikováno v:
Pakistan Armed Forces Medical Journal. 72:1544-49
Objective: To study organisms causing bacteremia and their outcome in cancer children with febrile neutropenia (FN) admitted at our centre. Study Design: Retrospective longitudinal study. Place and duration of study: Department of Pediatric Oncology,
Autor:
Rabia Wali, Yasmeen Iqbal
Publikováno v:
Global Social Sciences Review. :100-107
The aim of the study was to analyze the relationship of the kinematical factors with the ball velocity of the drag flick performance of the national elite players in field hockey. To attain this purpose, 64 drag flicks of sixteen players were recorde
Publikováno v:
Humanities & Social Sciences Reviews. 9:549-555
Purpose of the study: This study aims to investigate the relationship of sports participation with achievement, motivation, and innovation traits among university students. Methodology. A sample of 325 students was approached at the University of Lah
Autor:
Naureen Mushtaq, Fatima Mustansir, Khurram Minhas, Sadia Usman, Bilal Mazhar Qureshi, Fatima Mubarak, Ehsan Bari, Syed Ather Enam, Altaf Ali Laghari, Gohar Javed, Shahzad Shamim, Aneela Darbar, Ahmed Nadeem Abbasi, Salman Kirmani, Shahazadi Resham, Afia Bilal, Syed Ahmer Hamid, Nida Zia, Najma Shaheen, Rabia Wali, Tariq Ghafoor, Uzma Imam, Ata Ur Rehman Maaz, Sara Khan, Normand Laperriere, Francois Desbrandes, Peter Dirks, James Drake, Annie Huang, Uri Tabori, Cynthia Hawkins, Ute Bartels, Vijay Ramaswamy, Eric Bouffet
Publikováno v:
Pediatric bloodcancerREFERENCES. 69(9)
Low- and middle-income countries sustain the majority of pediatric cancer burden, with significantly poorer survival rates compared to high-income countries. Collaboration between institutions in low- and middle-income countries and high-income count
Autor:
Rabia Wali, Zunaira Shaukat
Publikováno v:
Cureus
Constitutional mismatch repair deficiency (CMMRD) is an autosomal recessive disorder caused by biallelic mutations in DNA mismatch repair genes 1. These patients have clinical stigmata of neurofibromatosis 1 (NF-1) with childhood onset of hematologic
Autor:
Aamna Hassan, Humayun Bashir, Rabia Wali, Asma Mahreen, Maimoona Siddique, Saima Riaz, M. Khalid Nawaz
Publikováno v:
European Journal of Nuclear Medicine and Molecular Imaging. 44:1198-1206
Objective To evaluate whether positron emission tomography/computed tomography using fluorine-18 fluoro-deoxyglucose (18F-FDG PET-CT) predicts bone marrow involvement (BMI) in pediatric Hodgkin’s lymphoma (pHL) with sufficient accuracy to supplant
Autor:
Bianca, Tesi, Samuel C C, Chiang, Dalia, El-Ghoneimy, Ayad Ahmed, Hussein, Cecilia, Langenskiöld, Rabia, Wali, Zehra, Fadoo, João Pinho, Silva, Ramón, Lecumberri, Sule, Unal, Magnus, Nordenskjöld, Yenan T, Bryceson, Jan-Inge, Henter, Marie, Meeths
Publikováno v:
Pediatric bloodcancer. 62(12)
Perforin, encoded by PRF1, is a pore-forming protein crucial for lymphocyte cytotoxicity. Biallelic PRF1 nonsense mutations invariably result in early-onset hemophagocytic lymphohistiocytosis (HLH), termed familial HLH type 2 (FHL2). In contrast, bia
Publikováno v:
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP. 22(7)
Fanconi anaemia (FA) is an autosomal recessive inherited disorder with progressive bone marrow failure, associated congenital malformation and solid and haematological malignancies. Acute myeloid leukemia is the commonest haematological malignancy fo