Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ali M. Alsuheel"'
Autor:
Mohammad A. Alqahtani, Ayed A. Shati, Minjing Zou, Ali M. Alsuheel, Abdullah A. Alhayani, Saleh M. Al-Qahtani, Hessa M. Gilban, Brain F. Meyer, Yufei Shi
Publikováno v:
International Journal of Endocrinology, Vol 2015 (2015)
Congenital adrenal hyperplasia (CAH) due to steroid 11β-hydroxylase deficiency is the second most common form of CAH, resulting from a mutation in the CYP11B1 gene. Steroid 11β-hydroxylase deficiency results in excessive mineralcorticoids and andro
Externí odkaz:
https://doaj.org/article/f6789759e2874903a43b3c8cf939d15c
Autor:
Abdelwahid Saeed Ali, Saleh M. Al-Qahtani, Harish C. Chandramoorthy, Ahmed Musa Al-Hakami, Ali M. Alsuheel, Ayed A. Shati
Publikováno v:
Saudi Journal of Medicine and Medical Sciences
Saudi Journal of Medicine and Medical Sciences, Vol 7, Iss 2, Pp 80-85 (2019)
Saudi Journal of Medicine & Medical Sciences
Saudi Journal of Medicine and Medical Sciences, Vol 7, Iss 2, Pp 80-85 (2019)
Saudi Journal of Medicine & Medical Sciences
Background: Human metapneumovirus (hMPV) is a Paramyxovirus known to cause acute respiratory tract infections in children and young adults. To date, there is no study from the Aseer region of Saudi Arabia determining the proportion and severity of hM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2732bdc6d90f4a2a468aa3512879a54d
Autor:
Hessa M. Jelban, Ali M. Alsuheel, Abdelwahid Saeed Ali, Ayed A. Shati, Ahmed M. Al-Hakami, Mohammad A. Al Qahtani, Abdulrahim R. Hakami
Publikováno v:
Journal of Taibah University Medical Sciences. 11:388-394
Objectives This study is aimed at determining the seroprevalence and possible infectivity factors of human cytomegalovirus (HCMV) in children affected by type 1 diabetes mellitus (T1DM) in the Aseer Region of KSA. Methods A total of 205 children diag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ec183a2f45f3cf4f0115aed871f3060
https://doi.org/10.1016/j.jtumed.2016.01.001
https://doi.org/10.1016/j.jtumed.2016.01.001
Publikováno v:
International Journal of Medicine and Medical Sciences. 6:59-62
Diarrhea present initially at early neonatal period is rare and is generally caused by congenital malabsorptive disorders. Congenital glucose-galactose malabsorption (CGGM) is a rare autosomal recessive disorder present as a protracted diarrhea in ea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5661bc09db450de6f4383dcaa7cae5af
https://doi.org/10.5897/ijmms2013.1008
https://doi.org/10.5897/ijmms2013.1008
Autor:
Saleh M. Al-Qahtani, Ayed A. Shati, Ali S Alshehri, Fach Arzt Ahmad Neklawi, Muhammad Rafique, Ali M. Alsuheel
Publikováno v:
Bangladesh Journal of Otorhinolaryngology. 19:36-40
Aim of Study: To determine effectiveness of myringotomy and grommet insertion (MGI) for patients with otitis media with effusion (OME), who failed medical treatment. Methods: A retrospective study was done on 86 patients who underwent MGI for OME bet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68b41dec5fb7d9e408d934cc4d9dac4c
https://doi.org/10.3329/bjo.v19i1.14861
https://doi.org/10.3329/bjo.v19i1.14861
Autor:
Osama Mohammed Saed Abdul-Wahab, Ayed A. Shati, Ahmed M. Al-Hakami, Ashish Kumar, Fateha Benahmed, Ali M. Alsuheel
Publikováno v:
American Journal of Immunology. 9:1-8
Mycoplasma pneumoniae is one of four most common species of organisms that are responsible for most clinically significant infections in humans. It is a frequent cause of acute respiratory infections in both children and adults. The organism can caus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e894298878a736bf9f0a23e791d03277
https://doi.org/10.3844/ajisp.2013.1.8
https://doi.org/10.3844/ajisp.2013.1.8
Autor:
Ayed A. Shati, Muhammad Rafique, Fach Arzt, Ali Maeed, Ahmad Neklawi, Ali M. Alsuheel, S Al-Shehri, Saleh M. Al-Qahtani
Publikováno v:
Bahrain Medical Bulletin. 35:14-16
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0cec24806c9637150a972758f46f73a5
https://doi.org/10.12816/0000509
https://doi.org/10.12816/0000509
Autor:
Faiqa Imtiaz, Ali M. Alsuheel, Mohammed Banemai, Hadeel Al-Manea, Hamad Al-Zaidan, Buthainah Albash, Mohammed Al-Owain, Rabab Allam
Publikováno v:
European journal of pediatrics. 173(5)
Glycogen storage disease type IX (GSD IX) is a common form of glycogenosis due to mutations in PHKA1, PHKA2, or PHKB and PHKG2 genes resulting in the deficiency of phosphorylase kinase. The first two genes are X-linked while the latter two follow an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed316fb2a032fb3c7edf1456c2a9246b
https://pubmed.ncbi.nlm.nih.gov/24326380
https://pubmed.ncbi.nlm.nih.gov/24326380