Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Mansour A Qurashi"'
Autor:
Mohammed Y Hasosah, Alaa I Iskandarani, Ayman I Shawli, Ashraf F Alsahafi, Ghassan A Sukkar, Mansour A Qurashi
Publikováno v:
The Saudi Journal of Gastroenterology, Vol 23, Iss 3, Pp 206-208 (2017)
Neuroblastoma amplified sequence (NBAS) gene mutation or infantile liver failure syndrome type 2 (ILFS type 2) is an extremely rare disease characterized by episodic liver failure precipitated by intercurrent febrile illness, and liver function recov
Externí odkaz:
https://doaj.org/article/ff1599e0b74f41c48236a5b34da86483
Autor:
Mansour Al Qurashi MD, Hanan Al-Najjar MD, Syed Sameer Aga PhD, Hadeel Mohammad MD, Ahmed Mustafa MD, Mohammed Al Hindi MD, Abrar Ahmed MD, Mohammad Al Harbi MD, Mohammad Hasosah MD, Ashraf Alsahaf MD, Mona Aldabbagh MD, Sara Abed MD
Publikováno v:
Global Pediatric Health, Vol 11 (2024)
Objectives. Post exposure prophylaxis (PEP) with the hepatitis B vaccine (HBVac) in combination with HBV immunoglobulins (HBIG) significantly minimizes the odds of vertical transmission of HBV to newborn infants. In this retrospective study, we aimed
Externí odkaz:
https://doaj.org/article/eed1a49529a94b4c987a5a4b674ea596
Autor:
Mansour Al Qurashi, Hadeel Mohammad, Syed Sameer Aga, Ahmed Mustafa, Jubara Alallah, Mohammed Al Hindi, Mohammed Al Harbi, Mohammed Hasosah
Publikováno v:
Pediatric Reports, Vol 16, Iss 3, Pp 551-557 (2024)
Zinc (Zn) is a vital trace element that plays a pivotal role in protein synthesis, cellular growth, and differentiation and is involved as a cofactor of metalloenzymes, performing a wide variety of metabolic, immune, and synthesis roles. Zn is requir
Externí odkaz:
https://doaj.org/article/7bf13385817d4d18be56564083789baf
Autor:
Mansour Al Qurashi, Abdulaziz Al-Khotani, Farzeen Mohtisham, Eman AlRaddadi, Heba AlShaikh, Alqassem Y. Hakami, Syed Sameer Aga
Publikováno v:
Case Reports in Pediatrics, Vol 2024 (2024)
Ischemic limb lesions occasionally occur in neonates admitted to neonatal intensive care units. Known risk factors include the placement of arterial catheters, arterial punctures to obtain blood samples, and the use of vasoactive/vasopressor medicati
Externí odkaz:
https://doaj.org/article/e072ab30944542958f6a59b43416ab45
Autor:
Lina Raffa MD, PhD, Aliaa Alamri MD, Amal Alosaimi MD, Sara Alessa MD, Suzan AlHarbi MD, Sara AlNowaiser, Huda Ahmedhussein MD, Hashem Almarzouki MD, Mansour Al Qurashi MD
Publikováno v:
Global Pediatric Health, Vol 10 (2023)
Background. The Jeddah retinopathy of prematurity (JED-ROP) algorithm, which is more specific to the population in Saudi Arabia, was established to decrease the number of infants screened without missing type 1 ROP cases. Methods. The data reviewed w
Externí odkaz:
https://doaj.org/article/2e02c3abe610436ead1226a2ba9d1374
Autor:
Mohammed Bhader, Mohammed Al-Hindi, Abdullah Ghaddaf, Anas Alamoudi, Amal Abualola, Renad Kalantan, Norah AlKhulifi, Ibrahim Halawani, Mansour Al-Qurashi
Publikováno v:
Children, Vol 10, Iss 12, p 1935 (2023)
The noninvasive neurally adjusted ventilatory assist (NIV-NAVA) is a newly developed noninvasive ventilation technique with promising clinical and ventilatory outcomes for preterm infants. This systematic review and meta-analysis aimed to investigate
Externí odkaz:
https://doaj.org/article/be7e59ccdb524244b5e94eed6f803cec
Autor:
Duaa Alammari, Hanan Al-Kadri, Mansour Al-Qurashi, Majid Alshamrani, Fayssal Farahat, Aiman Altamimi, Anmar Najjar
Publikováno v:
Eastern Mediterranean Health Journal.
Background: COVID-19 vaccine acceptance and uptake are major public health challenges in Saudi Arabia. Aims: To vaccinate all affiliates of King Saud Bin Abdulaziz University for Health Sciences (KSAU-HS) within a limited time period using evidence-b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::815f9c57c77d1e0eaa5f41e2d394fb55
https://doi.org/10.26719/emhj.23.034
https://doi.org/10.26719/emhj.23.034
Autor:
Syed Sameer Aga, Mujeeb Zafar Banday, Saniya Nissar, Mansour Al Qurashi, Abdullah A. Awadh, Alqassem Y. Hakami, A. Malli
Publikováno v:
Genetic Polymorphism and Disease ISBN: 9781003246244
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b36bdb7ed18fea0a7e6191d1fdae5776
https://doi.org/10.1201/9781003246244-7
https://doi.org/10.1201/9781003246244-7
Autor:
Mansour Al Qurashi, Ahmed Mustafa, Syed Sameer Aga, Abrar Ahmad, Abdellatif El-Farra, Aiman Shawli, Mohammed Al Hindi, Mohammed Hasosah
Publikováno v:
BMC Medical Genomics. 15
Background Of the many types of mitochondrial diseases, mutations affecting BCS1L gene are regarded as chief cause of the defective mitochondrial complex-III, affecting normal mitochondrial functioning, and leading to wide variety of phenotypes. Case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d2e96c6f6079f238e80128a7d10e182
https://doi.org/10.1186/s12920-022-01210-2
https://doi.org/10.1186/s12920-022-01210-2
Autor:
Mansour Al Qurashi, Shima Alahmadi, Ahmed Mustafa, Syed Sameer Aga, Mohammed Al Hindi, Abrar Ahmed, Hadeel Mohammad, Rasha ElSharabasy, Sara Abed, Iman AlThubaiti, Nabila Alrashdi
Publikováno v:
Clinical Pediatrics. :000992282311635
Inborn errors of metabolism (IEMs) are inherited biochemical/metabolic disorders that are commonly present in the immediate neonatal period. The aim of this retrospective study was to determine the incidence and distribution of IEMs in newborn infant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::558d74a8e6af539f35c9c70b356477ee
https://doi.org/10.1177/00099228231163511
https://doi.org/10.1177/00099228231163511