Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Doaa. M. Salah"'
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-17 (2023)
Abstract In the present paper, the effects of magnetic field and heat transfer on the peristaltic flow of a Jeffery fluid through a porous medium in an asymmetric channel have been studied. The governing non-linear partial differential equations repr
Externí odkaz:
https://doaj.org/article/dea5133a06184e9cb944a940095d7f09
Autor:
Fatina I. Fadel, Samar Sabry, Mohamed A. Abdel Mawla, Rasha Essam Eldin Galal, Doaa M. Salah, Rasha Helmy, Yasmen Ramadan, Wessam Elzayat, May Abdelfattah, Eman Abobakr Abd Alazem
Publikováno v:
Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-9 (2022)
Abstract Background Chronic kidney disease stage 5 (CKD 5) populations have peculiar risk for severe Covid-19 infection. Moreover; pediatric data are sparse and lacking. The aim of this study is to report our experience in CKD 5 children treated by h
Externí odkaz:
https://doaj.org/article/ff5e2dcd35cf4313a4223bd6273a2e4b
Pediatric focal segmental glomerulosclerosis: favorable transplantation outcome with plasma exchange
Publikováno v:
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-8 (2021)
Abstract Background Although kidney transplantation (KTX) is the treatment of choice for pediatric end stage kidney disease (ESKD); concerns for recurrence in cases of focal segmental glomerulosclerosis (FSGS) are still present. This study aimed to i
Externí odkaz:
https://doaj.org/article/d78e113ce6b44e52a16d90808cf96dec
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
Autor:
Mervat Ismail, Fatina I. Fadel, Alaa Rashad, Doaa M. Salah, Maha Rasheed, Nagwa Kantoush, Mona H. Ibrahim, Mona R. Kafoury, Manal F. Elshamaa
Publikováno v:
Pediatria Polska. 98:1-7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8141c7ba6019bcf9d7b30b9c3bc2bfa7
https://doi.org/10.5114/polp.2023.125388
https://doi.org/10.5114/polp.2023.125388
Publikováno v:
The Medical Journal of Cairo University. 90:1833-1843
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3910c6a89aaa23110026373867a7e6e
https://doi.org/10.21608/mjcu.2022.272752
https://doi.org/10.21608/mjcu.2022.272752
Publikováno v:
Pediatric Nephrology. 38:847-858
Background Glucose metabolism after kidney transplantation (KT) is highly dynamic with the first post-transplantation year being the most critical period for new-onset diabetes after transplantation (NODAT) occurrence. The present study aimed to anal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70b0ce3813e84d4d79784381038729bf
https://doi.org/10.1007/s00467-022-05669-0
https://doi.org/10.1007/s00467-022-05669-0
Publikováno v:
Italian Journal of Pediatrics. 49
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 rejection. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a74018bdb5797cfebd066ab6514ee28
https://doi.org/10.1186/s13052-023-01469-w
https://doi.org/10.1186/s13052-023-01469-w
Publikováno v:
International journal of health sciences. :5483-5508
Background: Cardiovascular disease (CVD) is the most common cause of mortality and morbidity in children with end stage kidney disease (ESKD) which arises from the interaction of several risk factors. The aim of the study is to assess CV risk of ESKD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e30581e931aeab9a888a02c712472330
https://doi.org/10.53730/ijhs.v6ns4.6105
https://doi.org/10.53730/ijhs.v6ns4.6105
Autor:
Doaa M Salah, Ahmed H Aoun, Balsam Sherif Fahmy, Asmaa Hasan Mahaseb Abu Zeid, Yosra Aboelnaga Fahmy
Publikováno v:
Journal of Comprehensive Pediatrics. 14
Background: Nephrotic syndrome (NS) is a common glomerular disease in children, for which there are currently no noninvasive markers for predicting responsiveness to steroid treatment. Objectives: This study aimed to analyze the relationship between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::005e18d181aa748cb74ad2e4a152d7e2
https://doi.org/10.5812/compreped-130133
https://doi.org/10.5812/compreped-130133