Zobrazeno 1 - 10
of 225
pro vyhledávání: '"AlBakheet A"'
Autor:
Hashim AlSalman, Hassan alsayegh, Nada Elmukhtar, Ahmad AlZahrani, Salman AlBakheet, Qasem AlAlwan, Ahmed Almuslim, Haniyya AlRehaily, Mohammed Al Salman
Publikováno v:
Radiology Case Reports, Vol 19, Iss 4, Pp 1333-1339 (2024)
Dendritic fibromyxolipoma (DFML) is a benign, very rare, and slow-growing soft tissue tumor commonly involving the muscular fascia of the foot, calf, shoulders, back, or head and neck muscles. Many authors consider dendritic fibromyxolipoma a variant
Externí odkaz:
https://doaj.org/article/0bb93fda45684c729aec9ca33f24810d
Autor:
Aqilah M. Alsaleh, Eid Albalawi, Abdulelah Algosaibi, Salman S. Albakheet, Surbhi Bhatia Khan
Publikováno v:
Diagnostics, Vol 14, Iss 12, p 1213 (2024)
Deep learning has attained state-of-the-art results in general image segmentation problems; however, it requires a substantial number of annotated images to achieve the desired outcomes. In the medical field, the availability of annotated images is o
Externí odkaz:
https://doaj.org/article/c472b99613b1439e8666644805b9cf81
Akademický článek
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Autor:
Hanan AlQudairy, Hesham AlDhalaan, Sarah AlRuways, Nouf AlMutairi, Maha AlNakiyah, Reema AlGhofaili, Albandary AlBakheet, Adeeb Alomrani, Omar A. Alharbi, Ehab Tous, Moeen AlSayed, Hamad AlZaidan, Maha M. AlRasheed, Ali AlOdaib, Namik Kaya
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2023)
BackgroundSLC13A5 (solute carrier family 13, member 5) encodes sodium/citrate cotransporter, which mainly localizes in cellular plasma membranes in the frontal cortex, retina, and liver. Pathogenic variants of the gene cause an autosomal recessive sy
Externí odkaz:
https://doaj.org/article/f56bc988f5994c58ab1d7a633c6c517e
Autor:
Albandary AlBakheet, Hanan AlQudairy, Joud Alkhalifah, Sheikhah Almoaily, Namik Kaya, Zuhair Rahbeeni
Publikováno v:
Frontiers in Genetics, Vol 13 (2023)
Background: Hypoxanthine-guanine phosphoribosyltransferase (HPRT1) deficiency is an inborn error of purine metabolism responsible for Lesch–Nyhan syndrome (LNS). The disease is inherited in an X-linked recessive manner and predominantly affects mal
Externí odkaz:
https://doaj.org/article/4e2c80f6c8d7492fb746d1f236332d6e
Autor:
Mazhor Aldosary, Shahad Baselm, Maha Abdulrahim, Rawan Almass, Maysoon Alsagob, Zainab AlMasseri, Rozeena Huma, Laila AlQuait, Tarfa Al‐Shidi, Eman Al‐Obeid, Albandary AlBakheet, Basma Alahideb, Lujane Alahaidib, Alya Qari, Robert W. Taylor, Dilek Colak, Moeenaldeen D. AlSayed, Namik Kaya
Publikováno v:
JIMD Reports, Vol 60, Iss 1, Pp 75-87 (2021)
Abstract SLC25A42 is the main transporter of coenzyme A (CoA) into mitochondria. To date, 15 individuals have been reported to have one of two bi‐allelic homozygous missense variants in the SLC25A42 as the cause of mitochondrial encephalomyopathy,
Externí odkaz:
https://doaj.org/article/48917f01742c4d66a01fabd9bebcdbd0
Autor:
Mostafa Ahmed Alwabari, Ali Malik Alquraini, Ali Saeed Albakheet, Reham Saad Alsaljah, Huda Alkuhl, Javed Ashraf, Abdel Raouf Alotaibi, Syed Akhtar Hussain Bokhari
Publikováno v:
Saudi Journal of Oral Sciences, Vol 8, Iss 1, Pp 14-21 (2021)
Introduction: Diet of an individual plays a remarkable role in maintaining health. Urbanization has had a great impact on the food habits of the society with the balance shifting to sweetened and refined food consumption. Dietary habits also has rema
Externí odkaz:
https://doaj.org/article/076e27a41c9c448293093e7b496c9680
Autor:
Albakheet, Salman S., Lee, Young Han, Hahn, Seok, Song, Ho-Taek, Suh, Jin-Suck, Kaushik, Sivaram
Publikováno v:
In Magnetic Resonance Imaging October 2020 72:19-24
Autor:
Albakheet, AlBandary, Almuallami, Duaa, Almass, Rawan, Qari, Alya, Kenana, Rosan, AlQudairy, Hanan, Huma, Rozeena, Binomar, Hadeel, Wakil, Salma Majid, Alowain, Mohammad, Colak, Dilek, Kaya, Namik, AlSayed, Moeenaldeen D.
Publikováno v:
Clinical Dysmorphology; Apr2024, Vol. 33 Issue 2, p55-62, 8p
Autor:
Altassan, Ruqaiah, AlQudairy, Hanan, AlJebreen, Sarah, AlMuhaizea, Mohammed, Al‐Hindi, Hindi, Pena‐Guerra, Karla A., Ghebeh, Hazem, Almzroua, Amer, Albakheet, Albandary, AlDosary, Mazhor, Colak, Dilek, Arold, Stefan T., Kaya, Namik
Publikováno v:
American Journal of Medical Genetics. Part A; Apr2024, Vol. 194 Issue 4, p1-5, 5p