Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Mohammed, Al Balwi"'
Autor:
Ahmad Alfares, Majid Alfadhel, Ahmed Mujamammi, Batoul Alotaibi, Sarah Albahkali, Mohammed Al Balwi, Hicham Benabdelkamel, Afshan Masood, Rizwan Ali, Amani Almuaysib, Saeed Al Mahri, Sameer Mohammad, Ibrahim O. Alanazi, Assim Alfadda, Saleh AlGhamdi, Bahauddeen M. Alrfaei
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 7 (2020)
Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) is a coenzyme encoded by ACADVL that converts very-long-chain fatty acids into energy. This process is disrupted by c.65C > A; p.Ser22∗ mutation. To clarify mechanisms by which this mutation lea
Externí odkaz:
https://doaj.org/article/228c8a37491a44cfa334be6ea544ec44
Autor:
Khadega A. Abuelgasim, Hinna Rehan, Maha Alsubaie, Nasser Al Atwi, Mohammed Al Balwi, Saeed Alshieban, Areej Almughairi
Publikováno v:
Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-8 (2018)
Abstract Background Chronic lymphocytic leukemia and chronic myeloid leukemia are the most common types of adult leukemia. However, it is rare for the same patient to suffer from both. Richter’s transformation to diffuse large B-cell lymphoma is fr
Externí odkaz:
https://doaj.org/article/3162c12880904690b5fdca4312338259
Autor:
Wala Al Balwi, Maha Al Turki, Ziad A. Memish, Hana M. A. Fakhoury, Mohammed Al Balwi, Ali H. Hajeer
Publikováno v:
Journal of Epidemiology and Global Health. 12:548-551
The objective of this study was to investigate the effect of age and BMI on the risk of death in patients with coronavirus disease 2019 (COVID-19). A cohort of 206 Saudi COVID-19 patients was included in this study. Data on age, BMI, hospitalization,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bac3ad06890c3b3946016c465bbdd6d0
https://doi.org/10.1007/s44197-022-00075-z
https://doi.org/10.1007/s44197-022-00075-z
Autor:
Amna Malik, Ahmed Bait Amer, Mohammed Salama, Bander Haddad, Muhammad T. Alrifai, Mohammed Al Balwi, William Davies, Wafaa Eyaid
Publikováno v:
Journal of Medical Case Reports, Vol 11, Iss 1, Pp 1-6 (2017)
Abstract Background X-linked ichthyosis is a dermatological condition caused by deficiency for the enzyme steroid sulfatase. Previously, X-linked ichthyosis/steroid sulfatase deficiency has been associated with developmental and neurological phenotyp
Externí odkaz:
https://doaj.org/article/2fb81e0eed51422fa2d33caf76845b64
Autor:
Yaseen Arabi, Dunia Jawdat, Abderrezak Bouchama, Hani Tamim, Waleed Tamimi, Mohammed Al-Balwi, Hasan M Al-Dorzi, Musharaf Sadat, Lara Afesh, Mashan L Abdullah, Walid Mashaqbeh, Maram Sakhija, Mohamed A Hussein, Adila ElObeid, Abdulaziz Al-Dawood
Publikováno v:
PLoS ONE, Vol 14, Iss 1, p e0209669 (2019)
BackgroundDuring critical illness in humans, the effects of caloric restriction on the inflammatory response are not well understood. The aim of this study is to examine the associations of caloric restriction, inflammatory response profiles and outc
Externí odkaz:
https://doaj.org/article/16a3fce9f5e249ecad3ab6a0d418be07
Autor:
Omalkhair Abulkhair, Mohammed Al Balwi, Ola Makram, Lamia Alsubaie, Medhat Faris, Hussam Shehata, Ahmed Hashim, Banu Arun, Ahmed Saadeddin, Ezzeldin Ibrahim
Publikováno v:
Journal of Global Oncology, Vol 4 (2018)
Purpose: Over the past three decades, the incidence rate of breast cancer (BC) among Arab women has continually increased. However, data on the prevalence of BRCA1/2 mutations are scarce. Although the population in Saudi Arabia is at large homogeneou
Externí odkaz:
https://doaj.org/article/57e7d38210594c53aee612afb1da7234
Publikováno v:
Annals of Saudi Medicine, Vol 33, Iss 4, Pp 382-386 (2013)
BACKGROUND AND OBJECTIVES: Mucolipidosis II (MLII) is characterized by severe global developmental delay, coarse facial features, skeletal deformities, and other systemic involvement. It is caused by a deficiency in N-acetylglucosamine-1 phosphotrans
Externí odkaz:
https://doaj.org/article/47bb2d4ef15d44a48a256158515e46af
Autor:
Victor Krajka, Arndt Rolfs, Joanne Trinh, Rami Abou Jamra, Kristian Tveten, Geir J. Braathen, Rabea Affan, Mohammed Al Balwi, Frauke Hinrichs, Øystein L. Holla, Marija Dulovic-Mahlow, Maximilian E. R. Weiss, Nataliya Di Donato, Shivendra Kishore, Skadi Beblo, Martin Werber, Krishna Kumar Kandaswamy, Elisa Rahikkala, Katja Lohmann, Nouriya Al-Sannaa, Øyvind L. Busk, Gabriela Oprea, Hauke Baumann, Nir Navot, Anne-Karin Kahlert, Melissa Vos
Publikováno v:
The American Journal of Human Genetics. 105:213-220
De novo variants represent a significant cause of neurodevelopmental delay and intellectual disability. A genetic basis can be identified in only half of individuals who have neurodevelopmental disorders (NDDs); this indicates that additional causes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4a1c3003604ddf1836c9655987c0557
https://doi.org/10.1016/j.ajhg.2019.05.005
https://doi.org/10.1016/j.ajhg.2019.05.005
Autor:
Mohamed Boudjelal, Musaad A. Alshammari, Hajar Al Zahrani, Lolwah Al Riyees, Mohammed Al Balwi, Hassan Al Nikhli, Tlili Barhoumi, Rizwan Ali, Alshaimaa Alhallaj, Abdul Latif Khan, Yasser A. Alshawakir, Omar Baz, Abdullah H. Alanazi, Abdullah Mashhour
Publikováno v:
Cells
Volume 10
Issue 6
Cells, Vol 10, Iss 1303, p 1303 (2021)
Volume 10
Issue 6
Cells, Vol 10, Iss 1303, p 1303 (2021)
In vitro studies of a disease are key to any in vivo investigation in understanding the disease and developing new therapy regimens. Immortalized cancer cell lines are the best and easiest model for studying cancer in vitro. Here, we report the estab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84dea1c3707824bc981b87e4cb4ba83d
Autor:
Mohammed Al-Balwi, Abdulrahman Al Muitiri, Fuad Al Mutairi, Abdulrahman Alswaid, Taghrid Aloraini, Majid Alfadhel, Ahmed Alfares, Anar Alfarsi, Wafaa Eyaid, Ali Alothaim, Lamia Alsubaie, Rashed Alniwaider, Aqila Asinan
Background: Whole exome sequencing (WES) is widely used as a first-tier diagnostic test. The diagnostic yield for WES is estimated at approximately 50%, leaving the requesting clinician with 50% ambiguous or negative results in cases where the diseas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61bdf942daa117463f7b95053d0ae082
https://doi.org/10.21203/rs.3.rs-147916/v1
https://doi.org/10.21203/rs.3.rs-147916/v1
