Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ch. Altaf Hussain"'
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
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 71, Iss 2, Pp 473-77 (2021)
Objective: To determine the frequency of trisomy 12 in B-Cell chronic lymphocytic leukaemia (CLL), to correlate its association with clinico-pathologic features and to determine the role of this cytogenetic defect to the prognosis. Study Design: Cros
Autor:
Ali Ahmed, Ch Altaf Hussain, Mohammad Abdul Naeem, Hamid Saeed Malik, Maria Khan, Saqib Hussain Korejo
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 71, Iss 2, Pp 579-83 (2021)
Objective: To determine the frequency of Del 13q14 in Chronic lymphocytic leukaemia, to compare its association with clinicpathologic features and to define the contribution of this abnormality to the prognosis. Study Design: Cross-sectional study. P
Autor:
Samrah Shahid, Parvez Ahmed, Maliha Saad, Saleem Ahmed Khan, Hamid Saeed Malik, Ayyub Muhammad Ayyub, Ch Altaf Hussain
Publikováno v:
Hematology & Transfusion International Journal. 6
Introduction: Nucleophosmin1 (NPM1) gene mutation is the most frequently occurring gene mutation in acute myeloid leukemia. This mutation is associated with good prognosis. AML patients should be screened for the NPM1 gene mutation to identify patien
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 71, Iss 2, Pp 473-77 (2021)
Objective: To determine the frequency of trisomy 12 in B-Cell chronic lymphocytic leukaemia (CLL), to correlate its association with clinico-pathologic features and to determine the role of this cytogenetic defect to the prognosis. Study Design: C
Externí odkaz:
https://doaj.org/article/15d87c8eb35b40779a713c232bdcc61f