Zobrazeno 1 - 10
of 85
pro vyhledávání: '"Samar A. Said"'
Publikováno v:
IEEE Access, Vol 10, Pp 97075-97088 (2022)
Nowadays, Big Data becomes a research focus in industrial, banking, social network, and other fields. In addition, the explosive increase of data and information require efficient processing solutions. Therefore, Spark is considered as a promising ca
Externí odkaz:
https://doaj.org/article/25df908e57ce448683fdbcff19826c06
Autor:
Samih H. Nasr, Julie A. Vrana, Surendra Dasari, Frank Bridoux, Mary E. Fidler, Sihem Kaaki, Nathalie Quellard, Alexia Rinsant, Jean Michel Goujon, Sanjeev Sethi, Fernando C. Fervenza, Lynn D. Cornell, Samar M. Said, Ellen D. McPhail, Loren P. Herrera Hernandez, Joseph P. Grande, Marie C. Hogan, John C. Lieske, Nelson Leung, Paul J. Kurtin, Mariam P. Alexander
Publikováno v:
Kidney International Reports, Vol 3, Iss 1, Pp 56-64 (2018)
Fibrillary glomerulonephritis (FGN) is a rare disease with unknown pathogenesis and a poor prognosis. Until now, the diagnosis of this disease has required demonstration of glomerular deposition of randomly oriented fibrils by electron microscopy tha
Externí odkaz:
https://doaj.org/article/5a6bfb80b6b44dfca60e41125f0467d5
Autor:
Vincent, Javaugue, Alejandro Best, Rocha, Samar M, Said, Dominick, Santoriello, Jean, Hou, Surendra, Dasari, Jason D, Theis, Julie A, Vrana, Ibrahim, Batal, Christopher, Larsen, Glen S, Markowitz, Vivette D, D'Agati, Ellen D, McPhail, Nelson, Leung, Samih H, Nasr
Publikováno v:
Kidney International. 102:926-929
Autor:
Samar M. Said, Mary E. Fidler, Anthony M. Valeri, Brooke McCann, Wade Fiedler, Lynn D. Cornell, Mariam Priya Alexander, Ahmed M. Alkhunaizi, Anne Sullivan, Carl H. Cramer, Marie C. Hogan, Samih H. Nasr
Publikováno v:
Kidney International Reports, Vol 2, Iss 1, Pp 44-52 (2017)
Alport syndrome (AS) is a genetic disorder characterized by progressive hematuric nephropathy with or without sensorineural hearing loss and ocular lesions. Previous studies on AS included mostly children. Methods: To determine the prognostic value o
Externí odkaz:
https://doaj.org/article/77bb12782c4b462ab2328ee13dd79917
Autor:
Nelson Leung, Samih H. Nasr, Christopher P. Larsen, Hassan B. Alkhateeb, Benjamin J. Madden, Sanjeev Sethi, Laurence H. Beck, M. Cristine Charlesworth, Samar M. Said
Publikováno v:
American Journal of Kidney Diseases. 79:904-908
Tubular basement membrane (TBM) deposits are very uncommon in non-lupus membranous nephropathy. We report 5 patients with membranous nephropathy and extensive TBM deposits following allogeneic hematopoietic cell transplant. Patients presented with ne
Publikováno v:
International Design Journal. 12:381-392
Publikováno v:
International Design Journal. 12:191-200
Publikováno v:
Proceedings of the 8th International Conference on Advanced Intelligent Systems and Informatics 2022 ISBN: 9783031206009
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd038d6b4212532eafdb749aefb92018
https://doi.org/10.1007/978-3-031-20601-6_10
https://doi.org/10.1007/978-3-031-20601-6_10
Autor:
Ellen D. McPhail, Samih H. Nasr, Paul J. Kurtin, Jason D. Theis, Benjamin J. Van Treeck, Surendra Dasari, Saba Yasir, Lizhi Zhang, Rondell P. Graham, Samar M. Said
Publikováno v:
Amyloid. 29:58-63
OBJECTIVE To report the clinicopathologic and proteomic characteristics of a novel form of amyloidosis derived from the precursor protein somatostatin. MATERIALS AND METHODS Cases were identified by searching the Mayo Clinic amyloid liquid chromatogr
Autor:
Samih H. Nasr, Satoru Kudose, Vincent Javaugue, Stéphanie Harel, Samar M. Said, Virginie Pascal, M. Barry Stokes, Julie A. Vrana, Surendra Dasari, Jason D. Theis, George A. Osuchukwu, Insara Jaffer Sathick, Arjun Das, Ali Kashkouli, Elliot J. Suchin, Yaakov Liss, Zalman Suldan, Jerome Verine, Bertrand Arnulf, Alexis Talbot, Sanjeev Sethi, Mohamad Zaidan, Jean-Michel Goujon, Anthony M. Valeri, Ellen D. Mcphail, Christophe Sirac, Nelson Leung, Frank Bridoux, Vivette D. D’Agati
Publikováno v:
Kidney international.
Monoclonal immunoglobulin light chain (LC) crystalline inclusions within podocytes is a rare, poorly characterized entity. To provide more insight, we now present the first clinicopathologic series of LC crystalline podocytopathy (LCCP) encompassing