Zobrazeno 1 - 10
of 777
pro vyhledávání: '"Watfa A"'
Autor:
Ahmed B. Idris, Watfa Al-Mamari, Taif Saud Al Humaidi, Kawther Abdullah Al Ma'ashri, Ahmed Alhabsi, Saquib Jalees, Ahlam Gaber, Muna Al-Jabri, M. Mazharul Islam, Amna Al-Futaisi
Publikováno v:
Global Public Health, Vol 19, Iss 1 (2024)
While telemedicine has shown promise for diagnosis and treatment, its integration into specialised clinics and mainstream healthcare is slow. A study at Sultan Qaboos University Hospital, Oman, investigated parental perceptions of virtual clinics and
Externí odkaz:
https://doaj.org/article/dbfd4cfda3e84e8ea880b9864b7ec8f8
Autor:
Marwa Al Busaidi, Feda E. Mohamed, Eiman Al-Ajmi, Nadia Al Hashmi, Khalid Al-Thihli, Amna Al Futaisi, Watfa Al Mamari, Fathiya Al-Murshedi, Fatma Al-Jasmi
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-10 (2023)
Abstract Background In metabolic stress, the cytosolic phosphoenolpyruvate carboxykinase (PEPCK-C) enzyme is involved in energy production through the gluconeogenesis pathway. PEPCK-C deficiency is a rare childhood-onset autosomal recessive metabolic
Externí odkaz:
https://doaj.org/article/4c46b9ee8ba94f4794bc083e28077f10
Autor:
Ghalia Al-Kasbi, Fathiya Al-Murshedi, Adila Al-Kindi, Nadia Al-Hashimi, Khalid Al-Thihli, Abeer Al-Saegh, Amna Al-Futaisi, Watfa Al-Mamari, Abdullah Al-Asmi, Zandre Bruwer, Khalsa Al-Kharusi, Samiya Al-Rashdi, Fahad Zadjali, Said Al-Yahyaee, Almundher Al-Maawali
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Abstract Global Developmental Delay/Intellectual disability (ID) is the term used to describe various disorders caused by abnormal brain development and characterized by impairments in cognition, communication, behavior, or motor skills. In the past
Externí odkaz:
https://doaj.org/article/97e903173bd84d2a861231bfdf46c280
Autor:
Praseetha Kizhakkedath, Watfa AlDhaheri, Ibrahim Baydoun, Mohammed Tabouni, Anne John, Taleb M. Almansoori, Saeed Al-Turki, Fatma Al-Jasmi, Hiba Alblooshi
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Birk–Landau–Perez syndrome (BILAPES) is an autosomal recessive cerebro-renal syndrome associated with genetic defects in the SLC30A9 gene, initially reported in 2017 in six individuals belonging to a large Bedouin kindred. The SLC30A9 gene encode
Externí odkaz:
https://doaj.org/article/3b607ce3803d4c6986d6c351815734d7
Autor:
Watfa Al-Mamari, Ahmed B. Idris, Samar Dakak, Muna Al-Shekaili, Zuwaina Al-Harthi, Asia M. Alnaamani, Fatma I. Alhinai, Saquib Jalees, Moza Al Hatmi, Mohamed A. El-Naggari, M. Mazharul Islam
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 19, Iss 4, Pp 305-309 (2019)
Objectives: This study aimed to provide an updated estimate of the prevalence of autism spectrum disorder (ASD) among Omani children. Methods: This retrospective descriptive study was conducted from December 2011 to December 2018. Data were retrieved
Externí odkaz:
https://doaj.org/article/36f3f3ef1c814583b7e117237129a95a
Autor:
Halima Al-Shehhi, Ahlam Gabr, Intisar Al-Haddabi, Raquel Tena, Anna Baquero, Watfa Al-Maamari, Almundher Al-Maawali
Publikováno v:
Oman Medical Journal, Vol 34, Iss 5, Pp 460-463 (2019)
Intellectual disability (ID) is the most common diagnosis noted among children with genetic disorders. It causes social and economic burden to families and communities. The genetic causes are not completely understood, and there is significant hetero
Externí odkaz:
https://doaj.org/article/4eb916e8b52f4c5cb77d88e3a4501082
Publikováno v:
Diabetes, Metabolic Syndrome and Obesity, Vol Volume 11, Pp 633-640 (2018)
Eisa Al-Balhan,1,* Hicham Khabbache,2,* Abdelhadi Laaziz,2 Ali Watfa,3 Abdelkader Mhamdi,4 Giovanni Del Puente,5 Nicola Luigi Bragazzi5–8 1Department of Educational Psychology, College of Education, Kuwait University, Kuwait City, Kuwait; 2Faculty
Externí odkaz:
https://doaj.org/article/975d42a7c1554b2e8ddfb41ea10bd9b9
Publikováno v:
Psychology Research and Behavior Management, Vol Volume 11, Pp 471-482 (2018)
Eisa M Al-Balhan,1 Hicham Khabbache,2 Ali Watfa,3 Tania Simona Re,4 Riccardo Zerbetto,5 Nicola Luigi Bragazzi4,6 1Department of Educational Psychology, College of Education, Kuwait University, Kuwait City, Kuwait; 2Faculty of Literature and Humanisti
Externí odkaz:
https://doaj.org/article/45c7b387fd844738abd1e9600e75f0ed
Autor:
Khabbache H, Jebbar A, Rania N, Doucet MC, Watfa AA, Candau J, Martini M, Siri A, Brigo F, Bragazzi NL
Publikováno v:
Psychology Research and Behavior Management, Vol Volume 10, Pp 103-108 (2017)
Hicham Khabbache,1 Abdelhak Jebbar,2,* Nadia Rania,3,* Marie-Chantal Doucet,4 Ali Assad Watfa,5 Joël Candau,6 Mariano Martini,7 Anna Siri,8,* Francesco Brigo,9,10,* Nicola Luigi Bragazzi1,2,4–8,11,* 1Faculty of Literature and Humanistic Studies, S
Externí odkaz:
https://doaj.org/article/d3eff67f6a054776a67ffd476de5901e
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 15, Iss 3, Pp 415-419 (2015)
The duplication of the short arm of chromosome 7 as de novo is extremely rare. The phenotype spectrum varies depending on the region of duplication. We report a case of de novo duplication of chromosomal region 7p21.1p22.2 in a three-year-old male ch
Externí odkaz:
https://doaj.org/article/4049e17e908d479f92540eebe3300e05