Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mohamed Gamal Fathallah"'
Autor:
Doaa M. Salah, Fatina I. Fadel, Mohamed A. Abdel Mawla, Hesham NAbdel Mooty, Mohamed El Ghobashy, Amr M. Salem, Mohamed Gamal Fathallah, Eman Abobakr Abd Alazem
Publikováno v:
Italian Journal of Pediatrics, Vol 50, Iss 1, Pp 1-9 (2024)
Abstract Background Hemodialysis (HD) success is dependent mainly on vascular access (VA). The aim of this study is to share the experience of Pediatric Nephrology Unit (PNU), Cairo University Children’s Hospital (CUCH), with VA-related obstacles i
Externí odkaz:
https://doaj.org/article/05ed50db7b454d3aad6057af4fcf0352
Autor:
Hoda A. Ahmed, Fatina I. Fadel, Mohamed A. Abdel Mawla, Doaa M. Salah, Mohamed Gamal Fathallah, Khalda Amr
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 8, Pp n/a-n/a (2022)
Abstract Background Primary hyperoxaluria (PH) is a rare heterogeneous, autosomal recessive disorder of glyoxylate metabolism. It is characterized by excessive hepatic production of oxalate resulting in a wide spectrum of clinical, imaging, and funct
Externí odkaz:
https://doaj.org/article/bfb62992f1d3463595a6e0b8e63fe037
Publikováno v:
Biomedical and Pharmacology Journal. 14:1397-1403
Objectives To assess the health related quality of life of living related donors after kidney transplantation and to evaluate clinical ,social and psychological condition post donation Study design This is an observational cross sectional study that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d4e6131c01ecf3a1ec3b9ee8cbc0a5a
https://doi.org/10.13005/bpj/2242
https://doi.org/10.13005/bpj/2242
Autor:
Amr Mohamed Salem, Mohamed A. Abdel Mawla, Doaa M. Salah, Fatina I. Fadel, Khalda Amr, Hoda Abdalla Ahmed, Mohamed Gamal Fathallah, Rasha M Hasanin, Magd A. Kotb
Publikováno v:
Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis TherapyREFERENCES. 26(1)
Introduction Primary hyperoxaluria type 1 (PH1) is a rare disease that is challenged by the overproduced oxalate and commonly presented with radiopaque renal stones or obstructive uropathy. This study aimed to report clinical presentations, renal rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8532451a05fed19e88f4df1dd13bbba2
https://pubmed.ncbi.nlm.nih.gov/33945205
https://pubmed.ncbi.nlm.nih.gov/33945205
Autor:
Shaimaa Sayed, Amr Mohamed Salem, Mohamed Gamal Fathallah, Mohamed ElGhonimy, Hafez M. Bazaraa, Fatma Mohammad Atia, Eman Fathy Eryan, Ahmed M. Shouman, Eman Abobakr Abd Alazem, Waleed Ghonima, Hesham Badawy, Sherif M Soaida, Yasmin Ramadan, Mohamed Salah Eldin, Rasha Helmy, Yosra Aboelnaga Fahmy, Mohamed A. Abdel Mawla, Hany A. Morsi, Fatina I. Fadel, Gamal Saadi, Ahmed I. Shoukry, Doaa M. Salah, Wesam Ismail
Publikováno v:
Pediatric transplantationREFERENCES. 24(6)
Pediatric kidney transplantation is a multidisciplinary therapy that needs special consideration and experience. In this study, we aimed to present CUCH experience; over a 10-year period, as a specialized center of kidney transplantation in children.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0adca51d6879a12c76ec6359cac2ef6
https://pubmed.ncbi.nlm.nih.gov/32388917
https://pubmed.ncbi.nlm.nih.gov/32388917