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Volume 15, Issue 2 (2022)

Review Articles

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The Phenomenon of Multidrug Resistance in Glioblastomas
Alexandr N. Chernov, Diana A. Alaverdian, Elvira S. Galimova, Alessandra Renieri, Elisa Frullanti, Ilaria Meloni, and Olga V. Shamova

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Hepatitis-Associated Aplastic Anemia
Alfadel Alshaibani, Carlo Dufour, Antonio Risitano, Regis de Latour, and Mahmoud Aljurf

Original Research Reports

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Mutation Profile in BCR-ABL1-Negative Myeloproliferative Neoplasms: A Single-Center Experience From India
Madhavi Maddali, Uday Prakash Kulkarni, Niveditha Ravindra, Arun Kumar Arunachalam, Arvind Venkatraman, Sharon Lionel, Marie Therese Manipadam, Anup J. Devasia, Anu Korula, N.A. Fouzia, Aby Abraham, Alok Srivastava, Biju George, Poonkuzhali Balasubramanian, and Vikram Mathews

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The Hispanic Paradox in Non-Small Cell Lung cancer
Rohit Kumar, Franklin Castillero, Shruti Bhandari, Sindhu Malapati, and Goetz Kloecker

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Spectrum of Myelodysplastic Syndrome in Patients Evaluated for Cytopenia(s). A Report from a Reference Centre in Saudi Arabia
Nour AlMozain, Ayman Mashi, Qasem Alneami, Amal Al-Omran, Nasir Bakshi, Tarek Owaidah, Salem Khalil, Haitham Khogeer, Shahrukh Hashmi, Suleimman Al-Sweedan, Thomas Morris, and Randa AlNounou

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The Risk and Prognosis of COVID-19 Infection in Cancer Patients: A Systematic Review and Meta-analysis
Ghada M. ElGohary, Shahrukh Hashmi, Jan Styczynski, Mohamed A. Kharfan-Dabaja, Rehab M. Alblooshi, Rafael de la Camara, Sherif Mohmed, Alfadel Alshaibani, Simone Cesaro, Nashwa Abd El-Aziz, Reem Almaghrabi, Usama Gergis, Navneet S. Majhail, Roy F. Chemaly, Mahmoud Aljurf, and Riad El Fakih

Brief Communication

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Clinicopathological Significance of Common Genetic Alterations in Patients With Acute Promyelocytic Leukemia
Sukanta Nath, Jina Bhattacharyya, Prem Chandra, Renu Saxena, Sudha Sazawal, and Kandarpa Kumar Saikia

Letters to the Editor

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Impact of the Major BCR-ABL1 Transcript Type on Clinical and Biological Parameters and Molecular Response in Patients With Chronic Myeloid Leukemia
Mourad Nachi, Ibtissem Kihel, Badra Entasoltane, Mohamed Brahimi, Nabil Yafour, Djaoued Guella, Amine Abed, and Mohamed A. Bekadja

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Familial Emberger Syndrome With Autoimmunity, Hyper-Immunoglobulin E and Lymphatic Impairment Caused by a Novel GATA2 Mutation
Moneerah AlGassim, Ahad F. Al Seraihi, AlFadel AlShaibani, Walter Conca, Saleem AlShehri, Moheieldin Moustafa Abouzied, Issam Hamadah, Saleh AlReshoodi, Majed Dasouki, and Farrukh Sheikh