Shahriar Moossavi, MD, PhD
- Clinical Professor, Nephrology
Shahriar Moossavi, MD, PhD
- Education
- MD, Bayerische Julius Maximilians Universitat Wurzburg, 1994
- Residency
- Internal Medicine, University Hospital State University of New York Health Science Center Stony Brook, 2000
- Fellowship
- Nephrology, University Hospital State University of New York Health Science Center Stony Brook, 2002
- Board Certifications
- American Board of Internal Medicine, Internal Medicine
- American Board of Internal Medicine, Nephrology
- Memberships
- American Society of Nephrology
- American Society of Diagnostic and Interventional Nephrology
- Positions
- Clinical Professor, Nephrology
- Departments and Affiliations
- Nephrology
Research
- Renal replacement treatment initiation with twice-weekly versus thrice-weekly haemodialysis in patients with incident dialysis-dependent kidney disease: rationale and design of the TWOPLUS pilot clinical trial. Murea M, Moossavi S, Fletcher AJ, Jones DN, Sheikh HI, Russell G, Kalantar-Zadeh K. BMJ Open. 2021 05; 11(5):e047596.
- Arteriovenous Fistula Versus Graft Access Strategy in Older Adults Receiving Hemodialysis: A Pilot Randomized Trial. Robinson T, Geary RL, Davis RP, Hurie JB, Williams TK, Velazquez-Ramirez G, Moossavi S, Chen H, Murea M. Kidney Med. ; 3(2):248-256.e1.
- A randomized pilot study to evaluate graft versus fistula vascular access strategy in older patients with advanced kidney disease: results of a feasibility study. Murea M, Geary RL, Houston DK, Edwards MS, Robinson TW, Davis RP, Hurie JB, Williams TK, Velazquez-Ramirez G, Bagwell B, Tuttle AB, Moossavi S, Rocco MV, Freedman BI, Williamson JD, Chen H, Divers J. . 2020; 6:86.
- Narrative Review of Incremental Hemodialysis. Murea M, Moossavi S, Garneata L, Kalantar-Zadeh K. . 2020 Feb; 5(2):135-148.
- Outcomes of patient self-referral for the diagnosis of several rare inherited kidney diseases. Bleyer AJ, Kidd K, Robins V, Martin L, Taylor A, Santi A, Tsoumas G, Hunt A, Swain E, Abbas M, Akinbola E, Vidya S, Moossavi S, Bleyer AJ, Živná M, Hartmannová H, Hodanová K, Vyletal P, Votruba M, Harden M, Blumenstiel B, Greka A, Kmoch S. Genet Med. 2020 01; 22(1):142-149.