Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Hanan Al Azkawi"'
Autor:
Ibrahim Al Alwan, Hanan Al Azkawi, Motasim Badri, Hani Tamim, Mohammed Al Dubayee, Waleed Tamimi
Publikováno v:
Annals of Saudi Medicine, Vol 33, Iss 6, Pp 579-583 (2013)
BACKGROUND AND OBJECTIVES: To determine factors associated with pubertal gynecomastia. DESIGN AND SETTINGS: A cross-sectional study among healthy male school children and adolescents in Riyadh, Saudi Arabia. METHODS: Subjects were selected from diver
Externí odkaz:
https://doaj.org/article/540e802d8a5f4440b9428786e24453bd
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
Autor:
Hanan AL Azkawi, Ibrahim AlAlwan
Publikováno v:
Case Reports in Medicine, Vol 2010 (2010)
There are no adequate data that evaluate the safety and effectiveness of lowering triglyceride levels in very young children. The authors report a family with two male siblings, 7 and 4 years old, affected by familial hyperchylomicronemia. The oldest
Externí odkaz:
https://doaj.org/article/f2cc3606e22d454bb2570e4f7ea45c7e
Autor:
Manal Al-Kindi, Hanan Al-Azkawi, Aisha Al-Sinani, Waad-Allah S. Mula-Abed, Nahid Nahavandi, Ghariba Al-Kusaibi
Publikováno v:
Oman Medical Journal, Vol 30, Iss 2, Pp 129-134 (2015)
This is the first case report in Oman and the Gulf region of a 17-β-hydroxysteroid dehydrogenase type 3 (17-β-HSD3) deficiency with a novel mutation in the HSD17B3 gene that has not been previously described in the medical literature. An Omani chil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fea277ebea5d010e1e47df96d733cbb5
http://www.omjournal.org/fultext_PDF.aspx?DetailsID=632&type=fultext
http://www.omjournal.org/fultext_PDF.aspx?DetailsID=632&type=fultext
Autor:
Hanan Al Azkawi, Ibrahim Al Alwan, Motasim Badri, Waleed Tamimi, Mohammed Al Dubayee, Hani Tamim
Publikováno v:
Annals of Saudi Medicine, Vol 33, Iss 6, Pp 579-583 (2013)
BACKGROUND AND OBJECTIVES: To determine factors associated with pubertal gynecomastia. DESIGN AND SETTINGS: A cross-sectional study among healthy male school children and adolescents in Riyadh, Saudi Arabia. METHODS: Subjects were selected from diver
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2208e475522ede79046d56a298585dab
https://www.annsaudimed.net/doi/full/10.5144/0256-4947.2013.579
https://www.annsaudimed.net/doi/full/10.5144/0256-4947.2013.579
Autor:
Angham Al Mutair, Hanan Al Azkawi
Publikováno v:
Case Reports in Pediatrics
Case Reports in Pediatrics, Vol 2012 (2012)
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::6387e31117c7b3bee5dc023e7d5f2420
https://doi.org/10.1155/2012/945437
https://doi.org/10.1155/2012/945437
Autor:
Ibrahim AlAlwan, Hanan Al Azkawi
Publikováno v:
Case Reports in Medicine, Vol 2010 (2010)
Case Reports in Medicine
Case Reports in Medicine
There are no adequate data that evaluate the safety and effectiveness of lowering triglyceride levels in very young children. The authors report a family with two male siblings, 7 and 4 years old, affected by familial hyperchylomicronemia. The oldest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b23f2907f2e862b0308739f3ca004cc0
https://doi.org/10.1155/2010/807434
https://doi.org/10.1155/2010/807434
Autor:
Aisha Al-Sinani, Waad-Allah S. Mula-Abed, Manal Al-Kindi, Ghariba Al-Kusaibi, Hanan Al-Azkawi, Nahid Nahavandi
Publikováno v:
Oman Medical Journal, Vol 30, Iss 2, Pp 129-134 (2015)
This is the first case report in Oman and the Gulf region of a 17-β-hydroxysteroid dehydrogenase type 3 (17-β-HSD3) deficiency with a novel mutation in the HSD17B3 gene that has not been previously described in the medical literature. An Omani chil
Externí odkaz:
https://doaj.org/article/f07c8beda5124afab0c8d868a88e2fa0