Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Mohamed Mansy"'
Autor:
Mohamed Abdelmalak Abokandil, Saber Waheeb, Wessam Zaghloul, Manal Abdelgawad, Mona Abdelhady, Mohamed Mansy, Mostafa Kotb
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-5 (2024)
Abstract Background Progressive familial intrahepatic cholestasis is an autosomal recessive genetic disorder that manifests primarily with jaundice and pruritus and can progresses from persistent cholestasis to cirrhosis and late childhood liver fail
Externí odkaz:
https://doaj.org/article/2e15d55f344e426f8a2be85c6f75fc31
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-6 (2024)
Abstract Background Ganglioneuromatosis is a rare type of benign neurogenic tumor that usually affects the sites of the major sympathetic ganglia in the retroperitoneum and the posterior mediastinum. Affection of the gastrointestinal tract is rare, a
Externí odkaz:
https://doaj.org/article/6c4bbdc307ab454b93dd1afcdb97f220
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 102, Iss , Pp 102773- (2024)
Background: Ureteral atresia is a rare disease that is usually associated with a non-functioning dysplastic kidney. The condition may be unilateral or bilateral, short, or long, and may involve any part of the ureter. Case description: A 4-year-old b
Externí odkaz:
https://doaj.org/article/6bb9d75a199e4038b38ae483f5616efc
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 101, Iss , Pp 102763- (2024)
Background: Double appendix, also known as vermiform appendix duplex, is a rare congenital anomaly. It is estimated to occur in 1 in 25,000 people with fewer than hundred cases reported worldwide. Case description: A 10-year-old boy presented to our
Externí odkaz:
https://doaj.org/article/a9c0d88935214d14a7eac226be722207
Autor:
Hussein Sabit, Areej Kassab, Donia Alaa, Shaza Mohamed, Shaimaa Abdel-Ghany, Mohamed Mansy, Osama A. Said, Mona A. Khalifa, Halah Hafiz, Asmaa M. Abushady
Publikováno v:
Current Issues in Molecular Biology, Vol 45, Iss 5, Pp 4080-4099 (2023)
The pathophysiology of several psychiatric diseases may entail disturbances in the hypothalamic–pituitary–adrenal (HPA) axis and metabolic pathways. Variations in how these effects present themselves may be connected to individual variances in cl
Externí odkaz:
https://doaj.org/article/84099f71caa04f099178e319f339db5c
Publikováno v:
Case Reports in Gastroenterology, Vol 15, Iss 1, Pp 431-435 (2021)
Congenital lumbar hernias are uncommonly seen in the pediatric age group, with only about 60 cases reported in the literature. It is usually accompanied by a multitude of congenital anomalies involving different organ systems of the body. For instanc
Externí odkaz:
https://doaj.org/article/4276c56266e249749c5c2e75afd434ec
Publikováno v:
BMC Pediatrics, Vol 20, Iss 1, Pp 1-4 (2020)
Abstract Background Hemiscrotal agenesis (HSA) is an exceedingly rare congenital anomaly in scrotal development. It is characterized by unilateral absence of scrotal skin with intact midline raphe. In the English literature, only seven patients were
Externí odkaz:
https://doaj.org/article/af1fb8a6f674419e994aad857d6b297a
Autor:
Hussein Sabit, Mohamed Abdel-Hakeem, Tahsin Shoala, Shaimaa Abdel-Ghany, Mokhtar Mamdouh Abdel-Latif, Jawaher Almulhim, Mohamed Mansy
Publikováno v:
Pharmaceutics, Vol 14, Iss 8, p 1566 (2022)
Nanomedicines have gained popularity due to their potential therapeutic applications, especially cancer treatment. Targeted nanoparticles can deliver drugs directly to cancer cells and enable prolonged drug release, reducing off-target toxicity and i
Externí odkaz:
https://doaj.org/article/14624690b5d94535b0e9b0a8608e0c0e
Publikováno v:
F1000Research, Vol 9 (2020)
Background: This study was conducted to evaluate the role of exogenous epidermal growth factor (EGF) injection on the Ki-67 immuno-expression in submandibular salivary gland tissue of rats receiving doxorubicin (DXR). Methods: A total of 21 two-month
Externí odkaz:
https://doaj.org/article/a823891de8a24d8e9b7c23c6adfee9d6
Publikováno v:
ALEXMED ePosters. 4:15-16