Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Montaser M. Mohamed"'
Autor:
Montaser M. Mohamed, Mohamed A. Bakheet, Rofaida M. Magdy, Heba S. El‐Abd, Mohamad Hasan Alam‐Eldeen, Hany M. Abo‐Haded
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 10, Pp n/a-n/a (2021)
Abstract Background Maple syrup urine disease (MSUD) is an autosomal recessive inborn error of amino acid metabolism, with unique clinico‐radiological findings. This study aims to show the benefit of using the clinico‐radiological findings for ea
Externí odkaz:
https://doaj.org/article/e583ea460e0b4f1b93c1b076ff657494
Publikováno v:
The Egyptian Journal of Hospital Medicine. 90:1558-1569
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1cc7d0dfa3d003af165ab3c4a59ddf1
https://doi.org/10.21608/ejhm.2023.282507
https://doi.org/10.21608/ejhm.2023.282507
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