Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Radwa, Gamal"'
Publikováno v:
Egyptian Liver Journal, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract Tetrahydrobiopterin deficiency in newborns with atypical hyperphenylalaninemia requires rapid and accurate diagnosis and the ability to distinguish it from the classical type to prevent early irreversible neurological damage. The study aimed
Externí odkaz:
https://doaj.org/article/3cf44746b57e452ca673395eedb7f82b
Autor:
Heba Elsedfy, Radwa Gamal
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 24, Iss 1, Pp 1-7 (2023)
Abstract Background A case of thyroid hormone deficiency which presented at birth. Thyroid hormones are essential for brain development and normal cognitive function. Common symptoms of congenital hypothyroidism (CH) include constipation, decreased a
Externí odkaz:
https://doaj.org/article/130eb3059b6c45f5ae6ac55149b278a4
Publikováno v:
Geo Journal of Tourism and Geosites, Vol 46, Iss 1, Pp 148-155 (2023)
This study aims to fill the salient gap in the area of museums' atmospheric elements by examining their effect on the Egyptian visitors’ behavioral outcomes and the resulting effect on their intention to revisit the museum. An online questionnaire
Externí odkaz:
https://doaj.org/article/feb024cba3d34e76ab6d9a9217f1f9e9
Akademický článek
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Publikováno v:
Maǧallaẗ Al-Turāṯ wa Al-Taṣmīm, Vol 2, Iss 9, Pp 78-96 (2022)
The research presents a historical overview of the digital revolution for the development that libraries have gone through to reach digital libraries, the reasons for its inception, and it presents the interactive digital trend and its impact on the
Externí odkaz:
https://doaj.org/article/9cb715b6b5e9446789db69a1ef4c9ad0
Publikováno v:
The Egyptian Journal of Hospital Medicine. 90:904-913
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f93ac8a5efac2ecf938f267b169081b0
https://doi.org/10.21608/ejhm.2023.279962
https://doi.org/10.21608/ejhm.2023.279962
Autor:
Rabah M. Shawky, Radwa Gamal
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 19, Iss 4, Pp 429-432 (2018)
We report a 3 month old female, third in order of birth of non consanguineous Egyptian parents with the typical features of Cantu syndrome including coarse features, low frontal hairline, hairy forehead, broad flat nasal bridge, anteverted nares, lon
Externí odkaz:
https://doaj.org/article/b4f16a7946b94d17bdcf39c4149da159
Autor:
Solaf M. Elsayed, Radwa Gamal
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 18, Iss 4, Pp 393-396 (2017)
The publisher regrets that this article has been temporarily removed. A replacement will appear as soon as possible in which the reason for the removal of the article will be specified, or the article will be reinstated.The full Elsevier Policy on Ar
Externí odkaz:
https://doaj.org/article/5a8bbfacdb81460db42808d4ac85aff6
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 18, Iss 4, Pp 397-401 (2017)
We report a 4 month old male, 4th in order of birth of healthy consanguineous Egyptian parents with typical characteristics of microcephalic osteodysplastic primordial dwarfism most probably belongs to type I (MOPD I). The patient had intrauterine gr
Externí odkaz:
https://doaj.org/article/fedca39b873f4cf7bf488d12555ae2d7
Autor:
Solaf M. Elsayed, Nagia Fahmy, Radwa Gamal, Mohamed Wafik, Dina Zamzam, Mai Fahmy, Mahmoud Suelam
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 18, Iss 3, Pp 295-298 (2017)
Neurofibromatosis type I (NF1) is an autosomal dominant disorder with involvement of both the cutaneous and nervous systems. Patients are susceptible to neurological complication in the form of tumors of the brain and spinal cord. Multiple sclerosis
Externí odkaz:
https://doaj.org/article/33271d4bfa5d4959aa1fc1d8878f2f09