Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Kawthar Abdulrhim Bokari"'
Autor:
Haifa Asseri, Kawthar Abdulrhim Bokari, Ayman A. Bakkar, Kamel T. Abidi, Maram Alotaibi, Naglaa M. Kamal
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 11, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Backgroundd Sjogren–Larsson syndrome (SLS) is a rare autosomal recessive disorder, characterized by a triad of spastic tetraplegia or diplegia, congenital ichthyosis, and intellectual disability. Methods We report a seven‐years‐old female born
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54859d0af5b48dfe00b9b84a3b2c7a57
https://doaj.org/article/6a62e44c07444112946fabe035096b28
https://doaj.org/article/6a62e44c07444112946fabe035096b28
Autor:
K. Maazoun, Kawthar Abdulrhim Bokari, Naglaa M. Kamal, Imed Krichen, Rasha A, Mostafa Yl Khalif, Murad Kitar, Ubaidullah Khan, Haifa Assiri
Publikováno v:
Clinical Medicine Insights. Pediatrics
Clinical Medicine Insights: Pediatrics, Vol 15 (2021)
Clinical Medicine Insights: Pediatrics, Vol 15 (2021)
Background: Splenic cysts are one of the relatively rare conditions in pediatric surgery practice. Primary non-parasitic splenic cysts are even more scarce. Case presentation: A 13-years-old female patient presented with chronic left hypochondrial pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de3e5ab5f33ce8a8c951fe2fa8404f7b
https://doi.org/10.1177/11795565211021597
https://doi.org/10.1177/11795565211021597