Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Hend, Abd El Baky"'
Autor:
Magd A. Kotb, Hend Abd El Baky, Shaimaa Sayed, Mohammed Al Komy, Marwa Onsy, Aya Aly, Andrew Tamer, Esraa Mohamed
Publikováno v:
Pediatric Sciences Journal, Vol 3, Iss 1, Pp 67-71 (2023)
Autosomal recessive polycystic kidney disease (ARPKD) is a rare genetic disorder that presents as an isolated polycystic renal disease in childhood, or associated with congenital hepatic fibrosis and/or Caroli disease. The spectrum of complications o
Externí odkaz:
https://doaj.org/article/7d4aaa361cc14993bb54e97bc4b3df2b
Autor:
Magd A. Kotb, Mohamed ELGharib, Hesham Abd ElKader, Magda El-Monayeri, Ahmed El-Hennawy, Sherif Kaddah, Hend Abd El Baky, Nazira A. Abdalla, Radwa A. Shamma, Iman Ali Abdel Aziz
Publikováno v:
Pediatric Sciences Journal, Vol 2, Iss 1, Pp 89-98 (2022)
Background: Venous ischemia in a closed compartment results in congestion, impeded blood supply, cell death and a cascade of events that involves immune system to remove cellular debris. Aim of the Work: To report our experience with chronic hepatic
Externí odkaz:
https://doaj.org/article/a9ee2c26310e492084d78213f05d2621
Autor:
Magd A. Kotb, Mona Hamdy, Khaled Eid, Mona Aziz, Mai Abd El Salam, Hend Abd El Baky, Nabil Lotfi, Niveen Salama
Publikováno v:
Pediatric Sciences Journal, Vol 1, Iss 2, Pp 98-106 (2021)
Background: Children with β-thalassemia major differ regarding age at presentation, transfusion requirements and unpredictable timing, rate and severity of hemolytic crisis. The blood transfusions are associated with iron overload. Glutathione S tra
Externí odkaz:
https://doaj.org/article/acd5c11354cc417596e2ae33f816a157
Autor:
Magd A. Kotb, Dalia S. Mosallam, Heba Amin Ragab, Hend Abd El Baky, Ahmed El Hatw, Alaa F. Hamza, Hesham Abd El Kader, Gamal El Tagy, Haytham Esmat, Sherif Shehata, Nahla I. Sabry
Publikováno v:
Pediatric Sciences Journal, Vol 1, Iss 1, Pp 34-40 (2021)
Background: Chylous ascites (CA) is accumulation of lipid rich lymph in peritoneal cavity. CA is rare among children. In pediatric age, causes of CA varies according to the age group, leading primary causes include congenital malformation of lymphati
Externí odkaz:
https://doaj.org/article/d94c3b2d900a4ac4af7fc3eeea7d4eb0
Publikováno v:
Case Reports in Rheumatology, Vol 2020 (2020)
Osteoid osteoma (OO) is a benign bone tumor that usually presents between 10 and 35 years of age. The metaphysis and diaphysis of the femur and tibia are the typical locations. The diagnosis is usually straightforward when images reveal a radiolucent
Externí odkaz:
https://doaj.org/article/d111fa181641403387468faf740188b5
Autor:
Nabil Lotfi, Mona Hamdy, Mai Abd El Salam, Magd A. Kotb, Niveen Salama, Hend Abd El Baky, Mona Aziz, Khaled Eid
Publikováno v:
Pediatric Sciences Journal. 1:98-106
Background: Children with β-thalassemia major differ regarding age at presentation, transfusion requirements and unpredictable timing, rate and severity of hemolytic crisis. The blood transfusions are associated with iron overload. Glutathione S tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7affc4536644f1370e1a75764261499
https://doi.org/10.21608/cupsj.2021.55630.1011
https://doi.org/10.21608/cupsj.2021.55630.1011
Autor:
Gamal H. El Tagy, Haytham Esmat, Alaa F. Hamza, Hesham Abd El Kader, Nahla Ibrahim Mohamed Fathy Sabry, Heba Amin Ragab, Ahmed El Hatw, Dalia S. Mosallam, Sherif M. Shehata, Hend Abd El Baky, Magd A. Kotb
Publikováno v:
Pediatric Sciences Journal. 1:34-40
Background: Chylous ascites (CA) is accumulation of lipid rich lymph in peritoneal cavity. CA is rare among children. In pediatric age, causes of CA varies according to the age group, leading primary causes include congenital malformation of lymphati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d829993a001de714ddc554e19a6b3940
https://doi.org/10.21608/cupsj.2020.31018.1001
https://doi.org/10.21608/cupsj.2020.31018.1001
Publikováno v:
Case Reports in Rheumatology
Case Reports in Rheumatology, Vol 2020 (2020)
Case Reports in Rheumatology, Vol 2020 (2020)
Osteoid osteoma (OO) is a benign bone tumor that usually presents between 10 and 35 years of age. The metaphysis and diaphysis of the femur and tibia are the typical locations. The diagnosis is usually straightforward when images reveal a radiolucent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::569dc20af4a908c9c22c583de2049c6e
https://doi.org/10.1155/2020/8810735
https://doi.org/10.1155/2020/8810735
Autor:
Magd A, Kotb, Lubna A, Fawaz, Rania A, Zeitoun, Yomna M, Shaalan, Nazira, Aly, Hesham, Abd El Kader, Gamal, El Tagy, Haytham, Esmat, Alaa F, Hamza, Hend, Abd El Baky
Publikováno v:
Medicine. 101:e31156
Liver transplantation (LT) is the definitive treatment of end-stage liver disease. The long-term survival following LT spurred more interest in improving the quality of life of patients. This was a cohort study that included 23 pediatric liver transp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::124099959a5c6d88339baa312e25fe74
https://doi.org/10.1097/md.0000000000031156
https://doi.org/10.1097/md.0000000000031156
Autor:
Haytham Esmat, Sally T. Mostafa El Sorogy, Hend Abd El Baky, Christine Ws Basanti, Iman H. Draz, Dalia S. Mosallam, Hesham M Abd Elkader, Magd A. Kotb
Publikováno v:
Clinical and Experimental Gastroenterology. 12:401-408
Purpose We aimed to define the clinical presentations, course and outcome of cholestasis in infants with Down syndrome (trisomy 21) who presented to the Pediatric Hepatology Clinic, New Children Hospital, Cairo University, Egypt. Methods Retrospectiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1841938741d3576f991c63c22ae26642
https://doi.org/10.2147/ceg.s216189
https://doi.org/10.2147/ceg.s216189