Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Ayman Hammad"'
Autor:
Manar Mansour, Ali H. Elmokadem, Ahmed A. Abd Elrazek, Ayman Hammad, Marwa R. Abd-Almoaty, Khadiga M. Ali, Dina Abdalla Ibrahim, Tarek Elsayed Barakat
Publikováno v:
The Egyptian Journal of Radiology and Nuclear Medicine, Vol 55, Iss 1, Pp 1-8 (2024)
Abstract Background Children with chronic kidney disease (CKD) usually present with disease impact on growth besides cardiovascular problems that not only impact the patient's health during childhood but also affect their adult life. We aimed to iden
Externí odkaz:
https://doaj.org/article/839ea774139a406cbd05bccdccbe3554
Autor:
Hanan El-Halaby, Riham Eid, Ahmed Elagamy, Ahmed El-Hussiny, Fatma Moustafa, Ayman Hammad, Mayada Zeid
Publikováno v:
Italian Journal of Pediatrics, Vol 50, Iss 1, Pp 1-11 (2024)
Abstract Background Acute kidney injury (AKI) in patients with multisystem inflammatory syndrome (MIS), COVID-19 related infection has been increasingly recognized with a paucity of data on AKI incidence, related mortality, and the requirement of ren
Externí odkaz:
https://doaj.org/article/a8cd43ca5c6d40a49c0fdbce5100dd8d
Publikováno v:
Italian Journal of Pediatrics, Vol 49, Iss 1, Pp 1-13 (2023)
Abstract Background Tacrolimus is the backbone drug in kidney transplantation. Single nucleotide polymorphism of Multidrug resistant 1 gene can affect tacrolimus metabolism consequently it can affect tacrolimus trough level and incidence of acute rej
Externí odkaz:
https://doaj.org/article/1fa7967ea6684fbd9badb8b59ee49ee2
Autor:
Bahia Moustafa, Sawsan Moselhy, Moftah Rabie, Ayman Hammad, Doaa Youssef, Mohamed Shouman, Samuel Makar, Ahmed Badr, Sameh Mansour, Dina Ebrahim, Marwa Nabhan, Fatma Ateia, Hend Abdel-Nabi, Ahmed Hussein, Manal Salman, Mai S. Korkor, Esraa A. Elbahkiry, Marwa Dagher, Abeer Selim, Yasser S. Amer, Tarek Omar, Ashraf Abdel Baky, on behalf of the Egyptian Pediatric Clinical Practice Guidelines (EPG) Committee (Chairman Ashraf Abdel Baky), SRNS Clinical & Methodology work group
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 71, Iss 1, Pp 1-18 (2023)
Abstract Background Nephrotic syndrome is one of the most common chronic kidney diseases in children. Steroid sensitive type (SSNS) constitutes about 85–90%, whereas steroid-resistant type (SRNS) only 15–20% (Mickinney et al. Pediatr Nephrol 16:1
Externí odkaz:
https://doaj.org/article/38f3d4a8309d483eb32f8c7082fe7217
Publikováno v:
Anales de Pediatría, Vol 95, Iss 6, Pp 406-412 (2021)
Resumen: Introducción: El síndrome nefrótico (SN) primario es una glomerulopatía común en la edad pediátrica. Se evaluaron los genotipos y frecuencias alélicas del polimorfismo rs5370 del gen EDN1 en niños con SN primario. Pacientes y método
Externí odkaz:
https://doaj.org/article/80b516dbc38941f48012dea1bff3caaa
Publikováno v:
Anales de Pediatría (English Edition), Vol 95, Iss 6, Pp 406-412 (2021)
Introduction: Primary nephrotic syndrome (NS) is a common glomerular disease in children. We assessed the genotypes and frequency of the rs5370 allelic variant of the EDN1 gene in children with primary NS. Patients and methods: We conducted a case-co
Externí odkaz:
https://doaj.org/article/bfc81de8e83f44989c303ab361861592
Autor:
Bahia Moustafa, Sawsan Moselhy, Moftah Rabie, Ayman Hammad, Doaa Youssef, Mohamed Shouman, Samuel Makar, Ahmed Badr, Sameh Mansour, Dina Ebrahim, Marwa Nabhan, Fatma Ateia, Hend Abdel-Nabi, Ahmed Hussein, Manal Salman, Mai S. Korkor, Esraa A. Elbahkiry, Marwa Dagher, Abeer Selim, Yasser S. Amer, Tarek Omar, Ashraf Abdel Baky, the Egyptian Pediatric Clinical Practice Guidelines (EPG) Committee (Chairman Ashraf Abdel Baky), SRNS Clinical, Methodology work group
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 71, Iss 1, Pp 1-2 (2023)
Externí odkaz:
https://doaj.org/article/7f352ddc4aa94c78ad44230bce462d61
Autor:
Riham Eid, Ashraf Bakr, Atef Elmougy, Mohamed M Zedan, Nahla A Allam, Amr Sarhan, Ayman Hammad, Ahmed M El-Refaey, Nashwa Hamdy
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 31, Iss 6, Pp 1376-1387 (2020)
Hemolytic-uremic syndrome (HUS) is a leading cause of childhood acute kidney injury (AKI) worldwide, with its postdiarrheal (D+HUS) form being the most common. Scarce data are available regarding D+HUS epidemiology from developing countries. This stu
Externí odkaz:
https://doaj.org/article/e36e690c02d5460dbf66accefdb7cca0
Autor:
Mohammad Al-Haggar, Ashraf Bakr, Yahya Wahba, Paul J Coucke, Fatma El-Hussini, Mona Hafez, Riham Eid, Abdel-Rahman Eid, Amr Sarhan, Ali Shaltout, Ayman Hammad, Sohier Yahia, Ahmad El-Rifaie, Dina Abdel-Hadi
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 28, Iss 1, Pp 141-148 (2017)
Marfan syndrome (MFS), the founding member of connective tissue disorder, is an autosomal dominant disease; it is caused by a deficiency of the microfibrillar protein fibrillin-1 (FBN1) and characterized by involvement of three main systems; skeletal
Externí odkaz:
https://doaj.org/article/1243858dedaa4cd682a50f0b8764c30f
Autor:
Ashraf Bakr, Riham Eid, Amr Sarhan, Ayman Hammad, Ahmed Mahmoud El-Refaey, Atef El-Mougy, Mohammed Magdy Zedan, Fatma ElHusseini
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 26, Iss 5, Pp 987-991 (2015)
Schimke immune-osseous dysplasia (SIOD) is a rare autosomal recessive disorder characterized by spondylo-epiphyseal dysplasia (SED), progressive renal insufficiency beginning as steroid-resistant nephrotic syndrome (SRNS) and defective cellular immun
Externí odkaz:
https://doaj.org/article/a1251d1df712477d86a623b546f49b4e