Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Khawla A Rahim"'
Autor:
Ebtisam Ibraheem Al-Sadoon, Khawla A Rahim, Abdulkarim AlAnazi, Hassan Faqeehi, Sawsan AlBatati
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 31, Iss 1, Pp 176-181 (2020)
Glomerular diseases are considered to be a significant cause of chronic kidney disease. Kidney biopsy continues to be an essential diagnostic tool. We review the renal biopsies which were done on children below the age of 14 years in the past 10 year
Externí odkaz:
https://doaj.org/article/b700b01fcb4c48e9aed1bf1ddd7b13c1
Autor:
Khaled O Alsaad, Burhan Edrees, Khawla A Rahim, Abdulkareem Alanazi, Muawia Ahmad, Noura Aloudah
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 28, Iss 4, Pp 898-905 (2017)
Collagenofìbrotic (collagen type III) glomerulopathy (CG) is a rare nonimmune-mediated glomerular disease. It is characterized by massive deposition of organized collagen type III fibers, which is localized in the mesangial and subendothelial glomer
Externí odkaz:
https://doaj.org/article/d03e41181234455eb59dae280ea20b7f
Autor:
Sibi Varghese, Vernice Rose, Khawla A. Rahim, Meshail A. BinThunian, Dayel Alshahrani, Mohammed Alsuhaibani, Abdulkarim Al Anazi, Saeed M Alzabli
Publikováno v:
International Journal of Pediatrics and Adolescent Medicine, Vol 8, Iss 4, Pp 229-235 (2021)
International Journal of Pediatrics & Adolescent Medicine
International Journal of Pediatrics & Adolescent Medicine
Background and Objective: Peritoneal dialysis (PD) associated peritonitis is the most common cause of morbidity, mortality, and treatment failure in patients undergoing PD. We aimed to identify the incidence, pathogens, antibiotic susceptibility, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d987a2b371e3dd0f4a212a33c9ec320e
https://doi.org/10.1016/j.ijpam.2020.09.001
https://doi.org/10.1016/j.ijpam.2020.09.001
Autor:
Ian J. Wilson, Mohammed S. Al Riyami, Khawla A Rahim, Eric Olinger, Elisa Molinari, Laura Powell, Miguel Barroso-Gil, Abdulrahman Al-Hussaini, Naif A.M. Almontashiri, Shirlee Shril, John A. Sayer, Mohamed H Al-Hamed, Friedhelm Hildebrandt, Intisar Al Alawi, Colin G. Miles, Isa Al Salmi, Eissa Ali Faqeih
Publikováno v:
Hum Mutat
Half of patients with a ciliopathy syndrome remain unsolved after initial analysis of whole exome sequencing (WES) data, highlighting the need for improved variant filtering and annotation. By candidate gene curation of WES data, combined with homozy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acafb70264bfe00a165f44e4cacb7593
https://doi.org/10.1002/humu.24251
https://doi.org/10.1002/humu.24251
Publikováno v:
Journal of Medical Case Reports, Vol 15, Iss 1, Pp 1-6 (2021)
Journal of Medical Case Reports
Journal of Medical Case Reports
Background Encapsulating peritoneal sclerosis is a rare but potentially lethal complication of long-term peritoneal dialysis that is associated with significant morbidity and mortality. The occurrence of encapsulating peritoneal sclerosis varies worl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d02a67e91759294fa84ef9b8dfaa81f9
https://doaj.org/article/504a05b2cf6a4cec8f98bdb5170c7718
https://doaj.org/article/504a05b2cf6a4cec8f98bdb5170c7718
Publikováno v:
Kidney & Blood Pressure Research, Vol 45, Iss 6, Pp 939-954 (2020)
Introduction: Genetic defects that determine uncontrolled activation of the alternative complement pathway have been well documented, which account for approximately 40–60% of atypical hemolytic uremic syndrome (aHUS) cases worldwide. In Saudi Arab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69c15a4371384fa2bcbe3695a3c2eda9
https://www.karger.com/Article/FullText/510612
https://www.karger.com/Article/FullText/510612
Publikováno v:
BMC Nephrology, Vol 21, Iss 1, Pp 1-6 (2020)
BMC Nephrology
BMC Nephrology
Background Fungal peritonitis (FP) is an infrequent but serious complication in children undergoing peritoneal dialysis (PD). This study aimed to explore the risk factors, clinical manifestations, causative organisms, fungal susceptibility findings,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32c31af9c7afce5924308e6ef0ab6c93
http://link.springer.com/article/10.1186/s12882-020-02014-1
http://link.springer.com/article/10.1186/s12882-020-02014-1
Autor:
Sawsan AlBatati, Khawla A Rahim, Abdulkarim AlAnazi, Ebtisam Ibraheem Al-Sadoon, Hassan Y Faqeehi
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 31, Iss 1, Pp 176-181 (2020)
Glomerular diseases are considered to be a significant cause of chronic kidney disease. Kidney biopsy continues to be an essential diagnostic tool. We review the renal biopsies which were done on children below the age of 14 years in the past 10 year
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51691da5840f96cb53e13f300a21437c
https://doi.org/10.4103/1319-2442.279938
https://doi.org/10.4103/1319-2442.279938
Autor:
Khawla A. Rahim, Saeed M Alzabli
Publikováno v:
Journal of Nephrology & Therapeutics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96179d652c9db6564d4292e04d209771
https://doi.org/10.4172/2161-0959-c1-045
https://doi.org/10.4172/2161-0959-c1-045
Autor:
Abdulkarim Al Anazi, Saeed M Alzabli, Hassan Y Faqeehi, Khawla A Rahim, Mohamed E Suliman, Muhammad Amin Ur Rahman
Publikováno v:
Asian Journal of Pediatric Nephrology. 1:78
Background: Dense deposit disease (DDD), a subtype of C3 glomerulopathy, is a rare disease that occurs secondary to hyperactivity of the alternative complement pathway. Renal biopsy typically reveals electron-dense deposits in the glomerular basement
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfbac2f67c8d0f51da8d7eaf65fb1b06
https://doi.org/10.4103/ajpn.ajpn_30_18
https://doi.org/10.4103/ajpn.ajpn_30_18