Zobrazeno 1 - 10
of 162
pro vyhledávání: '"AlSaheel A"'
Autor:
Mohammed Ayed Huneif, Ziyad Hamad Alhazmy, Anas M. Shoomi, Mohammed A. Alghofely, Humariya Heena, Aziza M. Mushiba, Abdulhamid Alsaheel
Publikováno v:
JCRPE, Vol 14, Iss 2, Pp 244-250 (2022)
Pseudohypoaldosteronism type 1 (PHA1) is an autosomal-recessive disorder characterized by defective regulation of body sodium (Na) levels. The abnormality results from mutations in the genes encoding subunits of the epithelial Na channel. Patients wi
Externí odkaz:
https://doaj.org/article/11fab897e5864f2bbed7ac3544d00bdd
Autor:
Osama Barakat, Muath Alsafrani, Hassan Alasmari, Faisal Alasmari, Abdullah Alzahrani, Reem Barakat, Wedad Alzahrani, Ali Alsaheel
Publikováno v:
The Journal of Medicine, Law & Public Health, Vol 3, Iss 1 (2023)
Background: Blood cultures (BCs) are frequently ordered during the course of investigation in emergency departments (EDs). However, there are few studies examining the clinical value of BCs and the prevalence of positive BCs in the adult ED. Methods
Externí odkaz:
https://doaj.org/article/985324ab98b24c89941092b389c16be3
Autor:
Abdulhameed Y Alsaheel, Sulaiman I Alayed, Yazzan M Alotaibi, Aseel A Alfahhad, Othman M Alothman, Hissah F Alnefaie
Publikováno v:
Journal of Family and Community Medicine, Vol 27, Iss 3, Pp 163-167 (2020)
BACKGROUND: Type 1 diabetes is the third most common chronic disease among teenagers. In Saudi Arabia, there is a gap of knowledge regarding hemoglobin A1C (HbA1c) concentration levels, and adherence to regular follow-up visits by patients. The aim o
Externí odkaz:
https://doaj.org/article/4063338b85e64d508581ad65ae208cfd
Autor:
Al-Hussaini A; Division of Pediatric Gastroenterology, Children's Specialized Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.; College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.; Prince Abdullah Bin Khaled Celiac Disease Research Chair, Department of Pediatrics, Faculty of Medicine, King Saud University, Riyadh, Saudi Arabia., Alsaheel A; Pediatric Endocrinology Department, King Fahad Medical City, Riyadh, Saudi Arabia., AlMalki M; Obesity, Endocrine, and Metabolism Center, Department of Endocrinology, King Fahad Medical City, Riyadh, Saudi Arabia., Troncone R; Translational Sciences & European Laboratory for the Investigation of Food-Induced Diseases, University Federico II, Naples, Italy., Alharthi H; UCLA immunogenetics Center, Department of Pathology and Laboratory Medicine, David Geffien School of Medicine at the University of California, Los Angeles, California, USA., Eltayeb-Elsheikh N; UCLA immunogenetics Center, Department of Pathology and Laboratory Medicine, David Geffien School of Medicine at the University of California, Los Angeles, California, USA., Alshammari G; Pediatric Endocrinology Department, King Fahad Medical City, Riyadh, Saudi Arabia., Allah SZ; Obesity, Endocrine, and Metabolism Center, Department of Endocrinology, King Fahad Medical City, Riyadh, Saudi Arabia., Aldossari G; UCLA immunogenetics Center, Department of Pathology and Laboratory Medicine, David Geffien School of Medicine at the University of California, Los Angeles, California, USA., AlRajhi N; Division of Pediatric Gastroenterology, Children's Specialized Hospital, King Fahad Medical City, Riyadh, Saudi Arabia., Abdulkareem F; Division of Pediatric Gastroenterology, Children's Specialized Hospital, King Fahad Medical City, Riyadh, Saudi Arabia., Alzahrani A; Division of Pediatric Gastroenterology, Children's Specialized Hospital, King Fahad Medical City, Riyadh, Saudi Arabia., AlNemer O; Pediatric Endocrinology Department, King Fahad Medical City, Riyadh, Saudi Arabia., AlMazrou L; Obesity, Endocrine, and Metabolism Center, Department of Endocrinology, King Fahad Medical City, Riyadh, Saudi Arabia., Bashir MS; Department of Biostatistics, Research Services Administration, Research Center at King Fahad Medical City, Riyadh, Saudi Arabia.
Publikováno v:
Journal of pediatric gastroenterology and nutrition [J Pediatr Gastroenterol Nutr] 2024 Oct 15. Date of Electronic Publication: 2024 Oct 15.
Autor:
Ahood Alazwari, Mali Abdollahian, Laleh Tafakori, Alice Johnstone, Rahma A. Alshumrani, Manal T. Alhelal, Abdulhameed Y. Alsaheel, Eman S. Almoosa, Aseel R. Alkhaldi
Publikováno v:
PLoS ONE, Vol 17, Iss 2 (2022)
The rising incidence of type 1 diabetes (T1D) among children is an increasing concern globally. A reliable estimate of the age at onset of T1D in children would facilitate intervention plans for medical practitioners to reduce the problems with delay
Externí odkaz:
https://doaj.org/article/c801bb99c63947d8a274e444a748bc81
Autor:
Alhasson, Haifa F., Alsaheel, Ghada M., Alsalamah, Alhatoon A., Alharbi, Noura S., Alhujilan, Joud M., Alharbi, Shuaa S.
Publikováno v:
International Journal of Information Technology; August 2024, Vol. 16 Issue: 6 p3633-3647, 15p
Autor:
Aqeel Alaqeel, Fahad Aljuraibah, Mohammed Alsuhaibani, Mohammed Huneif, Abdulhameed Alsaheel, Mohammad Al Dubayee, Abdulaziz Alsaedi, Ayman Bakkar, Ahmed Alnahari, Areej Taha, Khulood Alharbi, Yousef Alanazi, Samia Almadhi, Reem Al Khalifah
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
BackgroundOverburdened healthcare systems during the coronavirus disease (COVID-19) pandemic led to suboptimal chronic disease management, including that of pediatric type 1 diabetes mellitus (T1DM). The pandemic also caused delayed detection of new-
Externí odkaz:
https://doaj.org/article/0700730d42ca422a86b6f3e178c83bb7
Autor:
Alsaheel, Alaa, Alhassoun, Reem, Alrashed, Reema, Almatrafi, Noura, Almallouhi, Noura, Albahli, Saleh
Publikováno v:
Computers, Materials & Continua; 2023, Vol. 76 Issue 2, p2461-2482, 22p
Autor:
Alsaheel, Abdulhameed1 (AUTHOR), Alayed, Sulaiman2 (AUTHOR), Alotaibi, Yazzan2 (AUTHOR), Alfahhad, Aseel2 (AUTHOR), Alothman, Othman2 (AUTHOR), Alnefaie, Hissah3 (AUTHOR)
Publikováno v:
Journal of Family & Community Medicine. Sep-Dec2020, Vol. 27 Issue 3, p163-167. 5p.
Autor:
Anas M Shoomi, Abdulhamid AlSaheel, Mohammed Ayed Huneif, Ziyad Hamad AlHazmy, Mohammed A. AlGhofely, Humariya Heena, Aziza M Mushiba
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology. 14:244-250
Pseudohypoaldosteronism type 1 (PHA1) is an autosomal-recessive disorder characterized by defective regulation of body sodium levels. The abnormality results from mutations in the gene-encoding subunits of the epithelial sodium channel (ENaC). Patien