Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Mireille, El Ters"'
Autor:
Filippo Pinto e Vairo, Jennifer L. Kemppainen, Carolyn R. Rohrer Vitek, Denise A. Whalen, Kayla J. Kolbert, Kaitlin J. Sikkink, Sarah A. Kroc, Teresa Kruisselbrink, Gabrielle F. Shupe, Alyssa K. Knudson, Elizabeth M. Burke, Elle C. Loftus, Lorelei A. Bandel, Carri A. Prochnow, Lindsay A. Mulvihill, Brittany Thomas, Dale M. Gable, Courtney B. Graddy, Giovanna G. Moreno Garzon, Idara U. Ekpoh, Eva M. Carmona Porquera, Fernando C. Fervenza, Marie C. Hogan, Mireille El Ters, Kenneth J. Warrington, John M. Davis, Matthew J. Koster, Amir B. Orandi, Matthew L. Basiaga, Adrian Vella, Seema Kumar, Ana L. Creo, Aida N. Lteif, Siobhan T. Pittock, Peter J. Tebben, Ejigayehu G. Abate, Avni Y. Joshi, Elizabeth H. Ristagno, Mrinal S. Patnaik, Lisa A. Schimmenti, Radhika Dhamija, Sonia M. Sabrowsky, Klaas J. Wierenga, Mira T. Keddis, Niloy Jewel J. Samadder, Richard J. Presutti, Steven I. Robinson, Michael C. Stephens, Lewis R. Roberts, William A. Faubion, Sherilyn W. Driscoll, Lily C. Wong-Kisiel, Duygu Selcen, Eoin P. Flanagan, Vijay K. Ramanan, Lauren M. Jackson, Michelle L. Mauermann, Victor E. Ortega, Sarah A. Anderson, Stacy L. Aoudia, Eric W. Klee, Tammy M. McAllister, Konstantinos N. Lazaridis
Publikováno v:
Journal of Translational Medicine, Vol 21, Iss 1, Pp 1-10 (2023)
Abstract Background In the United States, rare disease (RD) is defined as a condition that affects fewer than 200,000 individuals. Collectively, RD affects an estimated 30 million Americans. A significant portion of RD has an underlying genetic cause
Externí odkaz:
https://doaj.org/article/379d322058a142068b8b67a35317dec9
Autor:
Filippo Pinto e Vairo, Jennifer L. Kemppainen, Carolyn R. Rohrer Vitek, Denise A. Whalen, Kayla J. Kolbert, Kaitlin J. Sikkink, Sarah A. Kroc, Teresa Kruisselbrink, Gabrielle F. Shupe, Alyssa K. Knudson, Elizabeth M. Burke, Elle C. Loftus, Lorelei A. Bandel, Carri A. Prochnow, Lindsay A. Mulvihill, Brittany Thomas, Dale M. Gable, Courtney B. Graddy, Giovanna G. Moreno Garzon, Idara U. Ekpoh, Eva M. Carmona Porquera, Fernando C. Fervenza, Marie C. Hogan, Mireille El Ters, Kenneth J. Warrington, John M. Davis, Matthew J. Koster, Amir B. Orandi, Matthew L. Basiaga, Adrian Vella, Seema Kumar, Ana L. Creo, Aida N. Lteif, Siobhan T. Pittock, Peter J. Tebben, Ejigayehu G. Abate, Avni Y. Joshi, Elizabeth H. Ristagno, Mrinal S. Patnaik, Lisa A. Schimmenti, Radhika Dhamija, Sonia M. Sabrowsky, Klaas J. Wierenga, Mira T. Keddis, Niloy Jewel J. Samadder, Richard J. Presutti, Steven I. Robinson, Michael C. Stephens, Lewis R. Roberts, William A. Faubion, Sherilyn W. Driscoll, Lily C. Wong-Kisiel, Duygu Selcen, Eoin P. Flanagan, Vijay K. Ramanan, Lauren M. Jackson, Michelle L. Mauermann, Victor E. Ortega, Sarah A. Anderson, Stacy L. Aoudia, Eric W. Klee, Tammy M. McAllister, Konstantinos N. Lazaridis
Publikováno v:
Journal of Translational Medicine, Vol 22, Iss 1, Pp 1-2 (2024)
Externí odkaz:
https://doaj.org/article/7330cbbda97649539c05138a79d450aa
Autor:
Filippo Pinto e Vairo, Carri Prochnow, Jennifer L. Kemppainen, Emily C. Lisi, Joan M. Steyermark, Teresa M. Kruisselbrink, Pavel N. Pichurin, Rhadika Dhamija, Megan M. Hager, Sam Albadri, Lynn D. Cornell, Konstantinos N. Lazaridis, Eric W. Klee, Sarah R. Senum, Mireille El Ters, Hatem Amer, Linnea M. Baudhuin, Ann M. Moyer, Mira T. Keddis, Ladan Zand, David J. Sas, Stephen B. Erickson, Fernando C. Fervenza, John C. Lieske, Peter C. Harris, Marie C. Hogan
Publikováno v:
Kidney Medicine, Vol 3, Iss 5, Pp 785-798 (2021)
Rationale & Objective: The etiology of kidney disease remains unknown in many individuals with chronic kidney disease (CKD). We created the Mayo Clinic Nephrology Genomics Clinic to improve our ability to integrate genomic and clinical data to identi
Externí odkaz:
https://doaj.org/article/04c369ed9d8440b18c17f55de117a3b3
Autor:
Mireille El Ters, Pengcheng Lu, Jonathan D. Mahnken, Jason R. Stubbs, Shiqin Zhang, Darren P. Wallace, Jared J. Grantham, Arlene B. Chapman, Vicente E. Torres, Peter C. Harris, Kyongtae Ty Bae, Douglas P. Landsittel, Frederic F. Rahbari-Oskoui, Michal Mrug, William M. Bennett, Alan S.L. Yu
Publikováno v:
Kidney International Reports, Vol 6, Iss 4, Pp 953-961 (2021)
Introduction: Autosomal dominant polycystic kidney disease (ADPKD) is characterized by progressive cyst growth and a loss of functioning renal mass, but a decline in glomerular filtration rate (GFR) and onset of end-stage renal disease (ESRD) occur l
Externí odkaz:
https://doaj.org/article/8beb5b69c3a14ce4bc60ffbad23c4ea5
Autor:
Massini A. Merzkani, MD, Andrew J. Bentall, MD, Byron H. Smith, PhD, Xiomara Benavides Lopez, MD, Matthew R. D’Costa, MD, Walter D. Park, BS, Walter K. Kremers, PhD, Naim Issa, MD, Andrew D. Rule, MD, Harini Chakkera, MD, Kunam Reddy, MD, Hasan Khamash, MD, Hani M. Wadei, MD, Martin Mai, MD, Mariam P. Alexander, MD, Hatem Amer, MD, Aleksandra Kukla, MD, Mireille El Ters, MD, Carrie A. Schinstock, MD, Manish J. Gandhi, MD, Raymond Heilman, MD, Mark D. Stegall, MD
Publikováno v:
Transplantation Direct, Vol 8, Iss 2, p e1273 (2022)
Background. Improving both patient and graft survival after kidney transplantation are major unmet needs. The goal of this study was to assess risk factors for specific causes of graft loss to determine to what extent patients who develop either deat
Externí odkaz:
https://doaj.org/article/1c76ac7fabe04f51b5f07c40fe28dcc2
Publikováno v:
Kidney International Reports, Vol 5, Iss 10, Pp 1840-1841 (2020)
Externí odkaz:
https://doaj.org/article/9f15d0c268c3446785d45c422684be30
Autor:
Martha Q. Lacy, Rahma Warsame, Mikel Prieto, Mireille El Ters, Angela Dispenzieri, Mark D. Stegall, Hatem Amer, Francis K. Buadi, David Dingli, Morie A. Gertz, Andrew Bentall, Cihan Heybeli, Carrie A. Schinstock, Shaji Kumar, S. Vincent Rajkumar, Naim Issa, Aleksandra Kukla, David L. Murray, Prashant Kapoor, Nelson Leung, Patrick G. Dean, Mariam P. Alexander, Samih H. Nasr, Eli Muchtar, Elizabeth C. Lorenz, Taxiarchis Kourelis
Publikováno v:
American Journal of Kidney Diseases. 79:202-216
Rationale & Objective Data on kidney transplantation outcomes among patients with monoclonal gammopathy of renal significance (MGRS) are lacking. Study Design Case series of patients with MGRS, some of whom received clone-directed therapies before ki
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a60d425176e84afdc5d1197c9e5098d1
https://doi.org/10.1053/j.ajkd.2021.04.015
https://doi.org/10.1053/j.ajkd.2021.04.015
Autor:
Stephen B. Erickson, Andrew Bentall, Mireille El Ters, Pavel N. Pichurin, Fernando C. Fervenza, Marie C. Hogan, Loren P. Herrera Hernandez, Ladan Zand, Jing Miao, Aleksandra Kukla, Eddie L. Greene, Konstantinos N. Lazaridis, Carri A. Prochnow, Sanjeev Sethi, Filippo Vairo, Emily C. Lisi
Publikováno v:
Mayo Clinic Proceedings. 96:2342-2353
Objective To increase the likelihood of finding a causative genetic variant in patients with a focal segmental glomerulosclerosis (FSGS) lesion, clinical and histologic characteristics were analyzed. Patients and Methods Individuals 18 years and olde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe57f7154815be2d3b4b098b8f3afbb4
https://doi.org/10.1016/j.mayocp.2021.01.037
https://doi.org/10.1016/j.mayocp.2021.01.037
Autor:
Mireille El Ters, Filippo Pinto e Vairo, Carri Prochnow, Carrie Schinstock, Patrick Dean, Jennifer Kemppainen, Konstantinos Lazaridis, Fernando Cosio, Fernando C. Fervenza, Lynn Cornell, Hatem Amer, Marie C. Hogan
Publikováno v:
Transplantation.
Recent studies identified underlying genetic causes in a proportion of patients with various forms of kidney disease. In particular, genetic testing reclassified some focal segmental glomerulosclerosis (FSGS) cases into collagen type 4 (COL4)-related
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbd611c93147e2c5c0607cff616707e6
https://pubmed.ncbi.nlm.nih.gov/36253919
https://pubmed.ncbi.nlm.nih.gov/36253919
Autor:
Mireille El Ters, Nelson Leung, S. Vincent Rajkumar, Ladan Zand, Sanjeev Sethi, Fernando C. Fervenza
Publikováno v:
Journal of the American Society of Nephrology. 32:1163-1173
Background Treatment of proliferative GN with monoclonal Ig deposits (PGNMID) is not established. A monoclonal anti-CD38 antibody (daratumumab) is effective in treating multiple myeloma. Abnormal plasma cell clones may play a role in the pathogenesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0fc984109784102504ff2443af39fd6
https://doi.org/10.1681/asn.2020101541
https://doi.org/10.1681/asn.2020101541