Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Mojgan, Mazaheri"'
Publikováno v:
Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy. 42:690-696
The comparative safety and efficacy of maintenance mycophenolate mofetil (MMF) and cyclosporine (CYC) following rituximab (RTX) in children with steroid-resistance nephrotic syndrome are uncertain.Multicenter randomized controlled trial.Sixty-six chi
Autor:
Farahnak Assadi, Anoush Azarfar, Behnaz Bazargani, Ali Derakhshan, Arash Abassi, Mehryar Mehrkash, Mastaneh Moghtaderi, Mitra Basiratnia, Mojgan Mazaheri, Afshin Safaeiasl, Alireza Eskandarifar, Fatemeh Ghane Sharbaf, Hamidreza Badeli, Rama Naghshizadian
Publikováno v:
Pediatric Emergency Care.
Autor:
Mojgan Mazaheri
Publikováno v:
International Journal of Preventive Medicine, Vol 12, Iss 1, Pp 2-2 (2021)
Background: Pyelonephritis is the most common bacterial infection in children that can cause renal failure if not diagnosed or treated early. We used serum biomarker interleukins (IL-6 and IL-8) and then confirmed the results by the findings dimercap
Externí odkaz:
https://doaj.org/article/0f714b4a55be47e392ded24147877600
Autor:
Ambika P. Ashraf, Farahnak Assadi, Thomas M. Barber, Filippo Ceccato, Stuti Fernandes, Cornelius J. Fernandesz, Maria Fleseriu, Rousseau Gama, David S. Geller, Iuri Martin Goemann, Guido Grassi, Tulay Guran, Fahmy W.F. Hanna, Nakysa Hooman, Pieter Jansen, Felix Jebasingh, Márta Korbonits, Ana Luiza Maia, Franco Mantero, Mojgan Mazaheri, Gabriela Mihai, Matthew A. Nazari, Dominic Oduro-Donkor, Katherine Ordidge, Karel Pacak, Joseph M. Pappachan, Ondřej Petrák, Oskar Ragnarsson, Anju Sahdev, Anna Sanders, Ute I. Scholl, Gino Seravalle, Fatemeh Ghane Sharbaf, Michael Stowasser, Constantine A. Stratakis, Naomi Szwarcbard, Nihal Thomas, Irene Tizianel, Duncan J. Topliss, Busra Gurpinar Tosun, Badhma Valaiyapathi, Elena V. Varlamov, Giacomo Voltan, Martin Wolley, Tomáš Zelinka
Publikováno v:
Endocrine Hypertension ISBN: 9780323961202
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d95b4fa36590a54b213c914f605d1b4
https://doi.org/10.1016/b978-0-323-96120-2.01002-5
https://doi.org/10.1016/b978-0-323-96120-2.01002-5
Publikováno v:
Endocrine Hypertension ISBN: 9780323961202
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a7f6d016dafbe5ed2d2f3b829474ba0
https://doi.org/10.1016/b978-0-323-96120-2.00001-7
https://doi.org/10.1016/b978-0-323-96120-2.00001-7
Autor:
Mojgan Mazaheri, Farahnak Assadi
Publikováno v:
International Journal of Preventive Medicine, Vol 10, Iss 1, Pp 35-35 (2019)
Background: Proteinuria is a common laboratory finding among children and adolescents. It can be identified as either a transient or a persistent finding and can represent a benign condition or a serious disease. Methods: Pertinent medical literature
Externí odkaz:
https://doaj.org/article/7240634158db4f469dc8dc8391234cd0
Autor:
Farahnak, Assadi, Nakysa, Hooman, Abdolhassan, Seyedzadeh, Anoush, Azarfar, Elaheh, Malakan Rad, Behnaz, Bazargani, Arash, Abasi, Mastaneh, Moghtaderi, Afshin, Safaeiasl, Nasrin, Esfandiar, Ali, Derakhsan, Hamidreza, Badeli, Alireza, Eskandarifar, Mojgan, Mazaheri, Fatemeh, Ghane Sharbaf
Publikováno v:
Iranian journal of kidney diseases. 16(6)
The newest Kidney Disease Improving Global Outcomes (KDIGO) guideline recommendations were investigated mainly for the care of adult kidney transplant recipients, but no guideline exists for the management of pediatric transplant recipients. This rev
Autor:
Mojgan Mazaheri, Farahnak Assadi
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 34:137-140
Objectives Clinical and laboratory data of reset osmostat (RO) and cerebral/renal salt wasting (C/RSW) mimic syndrome of inappropriate antidiuretic hormone (SIADH) and can pose diagnostic challenges because of significant overlapping between clinical
Publikováno v:
Integrated Science ISBN: 9783030853563
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fdec3485a92dfd97a75ed361c67747a2
https://doi.org/10.1007/978-3-030-85357-0_2
https://doi.org/10.1007/978-3-030-85357-0_2
Publikováno v:
International Urology and Nephrology. 52:121-128
Bartter syndrome is a rare hereditary salt-losing tubulopathy caused by mutations of several genes in the thick ascending limb of Henle’s loop, characterized by polyuria, hypokalemic metabolic alkalosis, growth retardation and normal blood pressure