Zobrazeno 1 - 10
of 140
pro vyhledávání: '"Al-Tawari A"'
Autor:
Fahad A. Bashiri, Khaled Hundallah, Musaad Abukhaled, Mossaed Mohammed Alyahya, Amna Al Futaisi, Daniah Alshowaeir, Asmaa Al Tawari, Shaker Abdullah, Ata Ur Rehman Maaz, Eman Taryam AlShamsi, Walaa Alshuaibi, Faisal Alotaibi, Hesham Aldhalaan
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
Externí odkaz:
https://doaj.org/article/77f391486ba54cadb543f2938e8f9502
Autor:
Fahad A. Bashiri, Khaled Hundallah, Musaad Abukhaled, Mossaed Mohammed Alyahya, Amna Al Futaisi, Daniah Alshowaeir, Asmaa Al Tawari, Shaker Abdullah, Ata Ur Rehman Maaz, Eman Taryam AlShamsi, Walaa Alshuaibi, Faisal Alotaibi, Hesham Aldhalaan
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
Neurofibromatosis type 1 (NF1) is a complex multisystem genetic disorder that requires long-term, age-specific monitoring and multidisciplinary care. NF1 symptom burden can significantly affect the quality of life and impose a substantial economic bu
Externí odkaz:
https://doaj.org/article/83cb6bc2f4c9428a9ad72f362e838081
Autor:
Maryam Aburezq, Ahmad Alahmad, Rasha Alsafi, Asma Al-Tawari, Dina Ramadan, Magdy Shafik, Omar Abdelaty, Nawal Makhseed, Reem Elshafie, Mariam Ayed, Abrar Hayat, Fatima Dashti, Dana Marafi, Buthaina Albash, Laila Bastaki, Hind Alsharhan
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-13 (2023)
Abstract Background Biotin-thiamine-responsive basal ganglia disease (BTBGD) is a rare autosomal recessive neurometabolic disorder that is caused by biallelic pathogenic SLC19A3 variants and is characterized by subacute encephalopathy associated with
Externí odkaz:
https://doaj.org/article/24ae6e5fe6ee456cbc8b7a2bb5c1a858
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Publikováno v:
BMC Pediatrics, Vol 20, Iss 1, Pp 1-12 (2020)
Abstract Background Children and adolescents are becoming the most prolific users of smart technology (ST) devices due to the numerous advantages presented by these devices. However, the overuse of ST devices can have detrimental impacts on health. T
Externí odkaz:
https://doaj.org/article/00fbe6e5f194400090c9a5f1e2643c3b
Autor:
Fouad Alghamdi, Asmaa Al-Tawari, Hadil Alrohaif, Walaa Alshuaibi, Hicham Mansour, Annemieke Aartsma-Rus, André Mégarbané
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
The timely and accurate genetic diagnosis of Duchenne muscular dystrophy (DMD) enables prompt initiation of disease management and genetic counseling and optimal patient care. Despite the existence of best practice guidelines for the diagnosis of DMD
Externí odkaz:
https://doaj.org/article/2fa4eebc95d54d11a3a354a2155878dd
Autor:
Aburezq, Maryam, Alahmad, Ahmad, Alsafi, Rasha, Al-Tawari, Asma, Ramadan, Dina, Shafik, Magdy, Abdelaty, Omar, Makhseed, Nawal, Elshafie, Reem, Ayed, Mariam, Hayat, Abrar, Dashti, Fatima, Marafi, Dana, Albash, Buthaina, Bastaki, Laila, Alsharhan, Hind
Publikováno v:
Orphanet Journal of Rare Diseases; 9/5/2023, Vol. 18 Issue 1, p1-13, 13p
Autor:
Bashiri, Fahad A., Hundallah, Khaled, Abukhaled, Musaad, Alyahya, Mossaed Mohammed, Al Futaisi, Amna, Alshowaeir, Daniah, Al Tawari, Asmaa, Abdullah, Shaker, Maaz, Ata Ur Rehman, AlShamsi, Eman Taryam, Alshuaibi, Walaa, Alotaibi, Faisal, Aldhalaan, Hesham
Publikováno v:
Frontiers in Oncology; 2024, p1-2, 2p
Autor:
Haitham Elbashir, Waseem Fathalla, Vivek Mundada, Mehtab Iqbal, Asmaa A Al Tawari, Saleel Chandratre, Laila Bastaki, Ingy Romany, Omar Ismayl, Ahmad Abou Tayoun
Publikováno v:
Journal of neuromuscular diseases. 9(6)
Background: Duchenne muscular dystrophy (DMD) is a severe neuromuscular disorder which leads to progressive muscle degeneration and weakness. Most patients die from cardiac or respiratory failure. Gene transfer therapy offers a promising approach to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4eeff9250a45bcd5185f3f205f940330
https://pubmed.ncbi.nlm.nih.gov/36245386
https://pubmed.ncbi.nlm.nih.gov/36245386