Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Angham Al Mutair"'
Autor:
Amir Babiker, Ghadeer L. Aljahdali, Mohammed K. Alsaeed, Abdulrahman F. Almunif, Mohamud S. Mohamud, Angham Al Mutair, Fahad Al Juraibah, Ibrahim Al Alwan
Publikováno v:
Oman Medical Journal, Vol 37, Iss 1, Pp e341-e341 (2022)
Objectives: Diabetic ketoacidosis (DKA) is a life-threatening complication and a leading cause of hospitalization in patients with type 1 diabetes mellitus (T1DM). We aimed to assess the risk factors of admissions of children with DKA in a specialize
Externí odkaz:
https://doaj.org/article/cd4f93daa1e04d14b7144399dd489e7d
Autor:
Jan M. Wit, Asma Deeb, Bassam Bin-Abbas, Angham Al Mutair, Ekaterina Koledova, Martin O. Savage
Publikováno v:
JCRPE, Vol 11, Iss 4, Pp 329-340 (2019)
It is over sixty years since the first administration of human growth hormone (GH) to children with GH deficiency, and over thirty years since recombinant human GH has been available for treatment of GH deficiency and a wider range of non-GH deficien
Externí odkaz:
https://doaj.org/article/38ea6126a9ff45e78a6acf95cd09edd9
Autor:
Fadia AlBuhairan, Waleed Tamimi, Hani Tamim, Angham Al Mutair, Naila Felimban, Yasmin Altwaijri, Mohamed Shoukri, Ibrahim Al Alwan
Publikováno v:
Annals of Saudi Medicine, Vol 32, Iss 4, Pp 408-411 (2012)
BACKGROUND AND OBJECTIVES: Increasing numbers of children with chronic health conditions are now surviving into adolescence and adulthood because of advancing health care. These chronic health conditions are generally known to impact a child's growth
Externí odkaz:
https://doaj.org/article/ec321b958738448ca07ed4c0ff7e6ef0
Autor:
Hanan Al Azkawi, Angham Al Mutair
Publikováno v:
Case Reports in Pediatrics, Vol 2012 (2012)
Hypocalcemia is a rare but reversible cause of dilated cardiomyopathy with limited cases being reported in the literature. Vitamin D deficiency is the main cause of hypocalcemia in almost all reported cases. We report a newborn presented with hypocal
Externí odkaz:
https://doaj.org/article/a30eba0cd7f44605b2c550ce0ef0134e
Publikováno v:
Journal of Biochemical and Clinical Genetics, Vol 2, Iss 2, Pp 151-155 (2019)
Background: Maple syrup urine disease (MSUD) is a rare autosomal recessive metabolically inherited disorder, caused by an abnormal function of the branched-chain α-keto acid dehydrogenase complex in the mitochondria. Case Presentation: The proband w
Externí odkaz:
https://doaj.org/article/7257afbeeeb84e1781e6a32255ae09b6
Publikováno v:
Hormone Research in Paediatrics.
Introduction: Sensenbrenner syndrome; cranioectodermal dysplasia; (OMIM #218330) is a rare genetic condition inherited as autosomal recessive with less than 70 reported cases worldwide. It results in multiorgan abnormalities along with ectodermal str
Publikováno v:
International Journal of Innovative Research in Medical Science. 6:212-218
Objectives: This study aims to assess the experience of the full Distance Learning approach among nursing students during COVID-19 Outbreak at KSAU-HS in the three regions (Riyadh, Jeddah, and Al-Ahsa). The study covers the following objectives; meas
Autor:
Fahad Al Juraibah, Mohammed Al Dubayee, Khalid Al Noaim, Amir Babiker, Ibrahim Al Alwan, Angham Al Mutair, Mohsen Al Atawi
Publikováno v:
European Journal of Medical Case Reports. :91-94
Autor:
Amir Babiker, Abdulrahman Almunif, Fahad Al Juraibah, Mohamud S. Mohamud, Angham Al Mutair, Ibrahim Al Alwan, Ghadeer L Aljahdali, Mohammed Alsaeed
Publikováno v:
Oman medical journal. 37(1)
Objectives: Diabetic ketoacidosis (DKA) is a life-threatening complication and a leading cause of hospitalization in patients with type 1 diabetes mellitus (T1DM). We aimed to assess the risk factors of admissions of children with DKA in a specialize
Publikováno v:
Journal of the Endocrine Society
Introduction: Monogenic diabetes results from a mutation in single gene, predominantly inherited and typically affects the young. DNAJC3 acts in attenuating endoplasmic reticulum stress and is found in abundance in pancreatic tissue. Clinical Case: W