Showing results (1-10 of 46) with videos related to
Sort By:
Pageof 5
Case Reports in Endocrinology|September 15, 2015
Chylous Ascites: A Rare Adverse Effect of Methimazole Treatment for Grave's Disease-A Case Report and Review of the LiteratureTawfik Khoury, Ronen SchneiderJournal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|May 12, 2015
A heart breaking case of rapidly developing severe hemophagocytic syndrome secondary to chronic active EBV infection; a case report and review of the literatureKhoury Tawfik, Yosha Liron, Abu Rmieleh Ayman, et al.Annals of Translational Medicine|May 2, 2020
Donor-derived hypouricemia in irrelevant recipients caused by kidney transplantationLisha Teng, Yanling Zhang, Luxi Ye, et al.Research Square|April 25, 2024
Recessive variants in MYO1C as a potential novel cause of proteinuric kidney diseaseIzzeldin Elmubarak, Shirlee Shril, Bshara Mansour, et al.Kidney International|February 5, 2022
Inhibition of endoplasmic reticulum stress signaling rescues cytotoxicity of human apolipoprotein-L1 risk variants in DrosophilaLea Gerstner, Mengmeng Chen, Lina L Kampf, et al.BMC Medical Education|September 17, 2014
The effect of medical students' gender, ethnicity and attitude towards poetry-reading on the evaluation of a required, clinically-integrated poetry-based educational interventionMordechai Muszkat, Orly Barak, Gadi Lalazar, et al.Acta Paediatrica (Oslo, Norway : 1992)|February 27, 2023
Genetic stratification reveals COL4A variants and spontaneous remission in Egyptian children with proteinuria in the first 2 years of lifeSamar Atef Elshafey, Mohamed Alaa Eldin Hassan Thabet, Reham Abdel Haleem Abo Elwafa, et al.Pediatric Nephrology (Berlin, Germany)|June 21, 2024
Recessive variants in MYO1C as a potential novel cause of proteinuric kidney diseaseIzzeldin Elmubarak, Shirlee Shril, Bshara Mansour, et al.Kidney International|April 24, 2019
Corticosteroid treatment exacerbates nephrotic syndrome in a zebrafish model of magi2a knockoutTilman Jobst-Schwan, Charlotte A Hoogstraten, Caroline M Kolvenbach, et al.Pediatric Nephrology (Berlin, Germany)|September 5, 2023
Copy number variation analysis in 138 families with steroid-resistant nephrotic syndrome identifies causal homozygous deletions in PLCE1 and NPHS2 in two familiesDalia Pantel, Nils D Mertens, Ronen Schneider, et al.Pageof 5