Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Elsayed, Abdelkreem"'
Autor:
Abdelrahim A. Sadek, Mohammed A. Aladawy, Tarek M. M. Mansour, Khulood M. Sayed, Rin Khang, Elsayed Abdelkreem
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-9 (2024)
Abstract Background Neurofibromatosis type 1 (NF1) is a multisystem genetic disorder that commonly involves skin, nerves, and skeletal system with increased neoplastic predisposition. This disease has been rarely associated with multiple congenital a
Externí odkaz:
https://doaj.org/article/cdc4a47f5e204d5f9f061b5eaa8c6688
Publikováno v:
Journal of the Egyptian Public Health Association, Vol 96, Iss 1, Pp 1-10 (2021)
Abstract Background Coronavirus disease 2019 (COVID-19) and related isolation measures have substantial adverse economic, social, and psychological consequences and expose children to increased risk of violence. The present study aimed to investigate
Externí odkaz:
https://doaj.org/article/4d98eb6a520140ec93d691ebb78ec6bd
Autor:
Yasuhiko Ago, Hideo Sugie, Tokiko Fukuda, Hiroki Otsuka, Hideo Sasai, Mina Nakama, Elsayed Abdelkreem, Toshiyuki Fukao
Publikováno v:
JIMD Reports, Vol 48, Iss 1, Pp 15-18 (2019)
Abstract We describe the case of a 4‐year‐old boy who suffered from frequent ketotic hypoglycemia (KH) but did not have hepatomegaly or elevated liver enzyme levels. However, the patient was found to have a rare variant in the PHKA2 gene. To dete
Externí odkaz:
https://doaj.org/article/12f8ec4428a547d897c7fdbd0e46676c
Autor:
Elsayed Abdelkreem, Hager A. Mohamed, Abdelrahim A. Sadek, Abdelhady R. Abdel-Gawad, Amr A. Othman
Publikováno v:
The Egyptian Journal of Hospital Medicine. 90:1494-1500
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffbfc2a7c5c848e5a89fabe9a4cff9cf
https://doi.org/10.21608/ejhm.2023.282376
https://doi.org/10.21608/ejhm.2023.282376
Autor:
Elsayed Abdelkreem, Hanna Alobaidy, Yuka Aoyama, Shaimaa Mahmoud, Mohamed Abd El Aal, Toshiyuki Fukao
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 18, Iss 2, Pp 199-203 (2017)
Beta-ketothiolase (mitochondrial acetoacetyl-CoA thiolase, T2) deficiency is an autosomal recessive disorder characterized by impaired metabolism of ketones and isoleucine. In this study, we report on the first two siblings with T2 deficiency from Li
Externí odkaz:
https://doaj.org/article/4dce69d884134504a90fe0fa28b0e54a
Autor:
Eman M. Fahmy, Elsayed Abdelkreem, Osama E. Mohamed, Mostafa M. Abosdera, Abdelrahim A. Sadek
Publikováno v:
The Egyptian Journal of Hospital Medicine. 88:3069-3077
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::375d9e999bfc07ff83eb86fac8f4c171
https://doi.org/10.21608/ejhm.2022.244542
https://doi.org/10.21608/ejhm.2022.244542
Autor:
Mohammed Abd Elsameea, Mohammed Abd-Elkader, Eman M. Fahmy, Elsayed Abdelkreem, Mostafa A. ElTaher
Publikováno v:
Journal of Pediatric Infectious Diseases. 17:148-154
Objective Our objective was to investigate the relative frequency and pattern of inborn errors of immunity (IEIs) among Egyptian children with recurrent acute otitis media (rAOM). Methods This was a cross-sectional study that included children from t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c21faca05b1d3e5a304a7626efde7b2
https://doi.org/10.1055/s-0042-1748761
https://doi.org/10.1055/s-0042-1748761
Publikováno v:
Indian Journal of Pediatrics. 88:771-777
To investigate the effectiveness of nebulized magnesium sulfate in treating persistent pulmonary hypertension of newborn (PPHN). Twenty-eight mechanically ventilated term neonates with severe PPHN were randomized into two groups: NebMag group (n = 14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61cad0a9a53010b93c70c5b60854eda3
https://doi.org/10.1007/s12098-020-03643-y
https://doi.org/10.1007/s12098-020-03643-y
Autor:
Mostafa El-Taher, Mohammed Abd Elsameea, Mohammed Abd-Elkader, Eman Fahmy, Elsayed Abdelkreem
Publikováno v:
Abstract- und Posterband - 93. Jahresversammlung der Deutschen Gesellschaft für HNO-Heilkunde, Kopf- und Hals-Chirurgie e.V., Bonn Interface - Fokus Mensch im Zeitalter der technisierten Medizin.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4e69a7735887ac9cf5bb8a25d62d266
https://doi.org/10.1055/s-0042-1746940
https://doi.org/10.1055/s-0042-1746940
Autor:
Abdelrahim A. Sadek, Mohammed A. Aladawy, Tarek M. M. Mansour, Mohamed F. Ibrahim, Montaser M. Mohamed, Eman F. Gad, Amr A. Othman, Hosny A. Ahmed, Abdin K. Kasim, Wael M. Wagdy, Mohamed H. T. Hasan, Elsayed Abdelkreem
Publikováno v:
Journal of child neurology. 37(5)
Megalencephalic leukoencephalopathy with subcortical cysts (MLC) is a rare genetic form of cerebral white matter disease whose clinicoradiologic correlation has not been completely understood. In this study, we investigated the association between cl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14f8b153af7bed1b8b6a0e297ea654b2
https://pubmed.ncbi.nlm.nih.gov/35322718
https://pubmed.ncbi.nlm.nih.gov/35322718