Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Iqraa Ansar"'
Autor:
Maimoona Khan, Abdullah Jamal, Faiz Anwer, Ahsan Wahab, Hassaan Imtiaz, Muhammad Khawar Sana, Ali Younas Khan, Jack Khouri, Abdul Rafae, Muzammil M. Khan, Abdur Jamil, Hamid Ehsan, Iqraa Ansar, Taimoor Jaffar Ali
Publikováno v:
OncoTargets and therapy
Carfilzomib (CFZ) is a proteasome inhibitor currently approved for the treatment of relapsed and refractory multiple myeloma (RRMM). Multiple trials are ongoing to evaluate its efficacy and safety in newly diagnosed multiple myeloma (NDMM). The use o
Autor:
Hamza Hashmi, Amrat Ehsan, Adeel Masood, Abdul Rafae, Arooj Umar, Muhammad Khawar Sana, Hamid Ehsan, Iqraa Ansar, Karun Neupane, Ahsan Wahab
Publikováno v:
Clinical lymphoma, myelomaleukemia. 22(5)
With recent advances in novel chemotherapeutic agents and increasing use of autologous hematopoietic stem cell transplant, there has been a significant improvement in outcomes for patients with AL Amyloidosis. Daratumumab, with its excellent safety a
Autor:
Mobeen Zaka Haider, Muhammad Muaaz Aslam, Laila Hashim, Iqraa Ansar, Ayesha Sarwar, Muhammad Salman Faisal, Moazzam Shahzad, Tehniat Faraz Ahmed, Zahoor Ahmed, Sundas Ali, Faiz Anwer
Publikováno v:
Expert review of hematology. 14(12)
Oncolytic viruses are genetically engineered viruses that target myeloma-affected cells by detecting specific cell surface receptors (CD46, CD138), causing cell death by activating the signaling pathway to induce apoptosis or by immune-mediated cellu
Autor:
Ali Jaan, Ahsan Wahab, Sundas Ali, Ahmad Muneeb, Hamid Ehsan, Raheel Iftikhar, Muhammad Salman Faisal, Muhammad Ammar Shafqat, Muhammad Khawar Sana, Farhan Khalid, Iqraa Ansar, Faiz Anwer
Publikováno v:
Blood. 136:23-25
Introduction: β-thalassemia major (TM) is one of the most prevalent inherited hemoglobinopathies in Pakistan. It has one of the highest prevalence of transfusion-dependent TM patients globally, with an estimated greater than 100,000 active cases. Ea
Report of a Fatal Case of Hemophagocytic Lymphohistiocytosis Syndrome and a Review of the Literature
Publikováno v:
Cureus
Hemophagocytic lymphohistiocytosis (HLH) is a rare condition in children, with a high mortality rate of 41.99%. Often, due to the atypical presentation of HLH, the syndrome is difficult to diagnose. We report a case of an atypical presentation of HLH
Autor:
Iqraa Ansar, Faizan Shaukat, Ghazan Askar, Awaiz Ahmed, Hamza Khan, Muhammad Usman Shabbir, Abdullah Zaki, Muhammad Imran Sohail
Publikováno v:
Cureus
Hydatid disease is a parasitic infestation by Echinococcus granulosus, which involves the liver and lungs primarily. The authors report a case of disseminated hydatid disease involving multiple organs simultaneously in a 7-year-old child from Kabul,
Autor:
Muhammad Salman Faisal, Hassaan Imtiaz, Faiz Anwer, Muhammad Aadil Rahman, Anum Javaid, Iqraa Ansar, Sadia Ansar, Karun Neupane, Hafiz Muhammad Haroon Afzal, Ahsan Wahab, Kanza Noor Butt, Hamid Ehsan, Ali Younas Khan, Muhammad Yasir Anwar
Publikováno v:
Blood. 136:46-47
Background: Amyloidosis is characterized by the deposition of misfolded lambda or kappa light chain (AL) proteins in tissue. It commonly affects the heart, which correlates with poor prognosis. Disease-modifying therapies aim to suppress the producti
Autor:
Faiz Anwer, Iqraa Ansar, Muhammad Aslam Khan, Yazan Samhouri, John Lister, Lynna Alnimer, Ali Younas Khan, Muhammad S. Anil, Urwat Til Vusqa, Salman Fazal, Muhammad Yasir Anwar, Taha Sheikh
Publikováno v:
Blood. 136:25-26
Introduction The ability of the neoplastic cells to escape from immune surveillance has been considered as a hallmark of cancer. The upregulation of programmed death-1 (PD-1) and programmed death ligand-1/2 (PDL-1) axis is a major immune escape pathw