Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Nagham N. Hindi"'
Publikováno v:
Journal of Personalized Medicine, Vol 11, Iss 9, p 877 (2021)
The exponential expansion of genomic data coupled with the lack of appropriate clinical categorization of the variants is posing a major challenge to conventional medications for many common and rare diseases. To narrow this gap and achieve the goals
Externí odkaz:
https://doaj.org/article/4a6651c846ee4118a8b82314ca87a5f0
Publikováno v:
Journal of Personalized Medicine
Journal of Personalized Medicine, Vol 11, Iss 877, p 877 (2021)
Journal of Personalized Medicine, Vol 11, Iss 877, p 877 (2021)
The exponential expansion of genomic data coupled with the lack of appropriate clinical categorization of the variants is posing a major challenge to conventional medications for many common and rare diseases. To narrow this gap and achieve the goals
Autor:
Mohammad Saleh, Nagham N Hindi
Publikováno v:
Naunyn-Schmiedeberg's Archives of Pharmacology. 391:953-963
Neutropenia is a hematologic disorder commonly reported in patients with chronic hepatitis C viral (HCV) infection. The objective of the present analysis is to describe the change in neutrophil count resulting from peglated interferon alpha 2-a (PEG-
Autor:
Mohammad Saleh, Nagham N Hindi
Publikováno v:
Clinical and Experimental Pharmacology and Physiology. 45:636-642
Neutropenia is a haematologic disorder commonly reported in patients with chronic hepatitis C virus (HCV) infection treated with pegylated interferon alfa-2a (PEG-IFN α-2a). The objective of the present project is to identify patient characteristics
Autor:
Elsakrmy N; Division of Biological and Biomedical Sciences, College of Health and Life Sciences, Hamad Bin Khalifa University, Education City, Qatar Foundation, P.O.Box: 34110, Doha, Qatar; Division of Genomics and Precision Medicine, College of Health and Life Sciences, Hamad Bin Khalifa University, Education City, Qatar Foundation, P.O.Box: 34110, Doha, Qatar., Aouida M; Division of Biological and Biomedical Sciences, College of Health and Life Sciences, Hamad Bin Khalifa University, Education City, Qatar Foundation, P.O.Box: 34110, Doha, Qatar., Hindi N; Division of Biological and Biomedical Sciences, College of Health and Life Sciences, Hamad Bin Khalifa University, Education City, Qatar Foundation, P.O.Box: 34110, Doha, Qatar., Moovarkumudalvan B; Division of Biological and Biomedical Sciences, College of Health and Life Sciences, Hamad Bin Khalifa University, Education City, Qatar Foundation, P.O.Box: 34110, Doha, Qatar; Division of Genomics and Precision Medicine, College of Health and Life Sciences, Hamad Bin Khalifa University, Education City, Qatar Foundation, P.O.Box: 34110, Doha, Qatar., Mohanty A; Division of Biological and Biomedical Sciences, College of Health and Life Sciences, Hamad Bin Khalifa University, Education City, Qatar Foundation, P.O.Box: 34110, Doha, Qatar; Division of Genomics and Precision Medicine, College of Health and Life Sciences, Hamad Bin Khalifa University, Education City, Qatar Foundation, P.O.Box: 34110, Doha, Qatar., Ali R; Division of Biological and Biomedical Sciences, College of Health and Life Sciences, Hamad Bin Khalifa University, Education City, Qatar Foundation, P.O.Box: 34110, Doha, Qatar., Ramotar D; Division of Biological and Biomedical Sciences, College of Health and Life Sciences, Hamad Bin Khalifa University, Education City, Qatar Foundation, P.O.Box: 34110, Doha, Qatar. Electronic address: dramotar@hbku.edu.qa.
Publikováno v:
DNA repair [DNA Repair (Amst)] 2022 Sep; Vol. 117, pp. 103359. Date of Electronic Publication: 2022 Jun 26.