Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Tekman MC"'
Autor:
Downie ML, Gupta S, Tekman MC, Cheshire C, Arora S, Licht C, Robinson LA, Munoz M, Alvaro Madrid Aris, Al Attrach I, Brenchley PE, Gale DP, Stanescu H, Bockenhauer D, Kleta R
Publikováno v:
Kidney International Reports
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
INTRODUCTION: Membranous nephropathy (MN) is the most common cause of nephrotic syndrome (NS) in adults and is a leading cause of end-stage renal disease due to glomerulonephritis. Primary MN has a strong male predominance, accounting for approximate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2c8d9bbf4c30dd1a093e9b66216f4d5c
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=19806
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=19806
Autor:
Chris Cheshire, Mallory L. Downie, Alvaro Madrid Aris, Steven Arora, Horia Stanescu, Christoph Licht, Lisa A. Robinson, Robert Kleta, Mehmet Tekman, Paul Brenchley, Sanjana Gupta, Detlef Bockenhauer, Ibrahim Al Attrach, Marina Munoz, Daniel P. Gale
Publikováno v:
Scientia
Downie, M L, Gupta, S, Tekman, M C, Cheshire, C, Arora, S, Licht, C, Robinson, L A, Munoz, M, Aris, A M, Al Attrach, I, Brenchley, P E, Gale, D P, Stanescu, H, Bockenhauer, D & Kleta, R 2021, ' Identification of a Locus on the X Chromosome Linked to Familial Membranous Nephropathy ', Kidney International Reports, vol. 6, no. 6, pp. 1669-1676 . https://doi.org/10.1016/j.ekir.2021.02.025, https://doi.org/10.1016/j.ekir.2021.02.025
Kidney International Reports, Vol 6, Iss 6, Pp 1669-1676 (2021)
Kidney International Reports
Downie, M L, Gupta, S, Tekman, M C, Cheshire, C, Arora, S, Licht, C, Robinson, L A, Munoz, M, Aris, A M, Al Attrach, I, Brenchley, P E, Gale, D P, Stanescu, H, Bockenhauer, D & Kleta, R 2021, ' Identification of a Locus on the X Chromosome Linked to Familial Membranous Nephropathy ', Kidney International Reports, vol. 6, no. 6, pp. 1669-1676 . https://doi.org/10.1016/j.ekir.2021.02.025, https://doi.org/10.1016/j.ekir.2021.02.025
Kidney International Reports, Vol 6, Iss 6, Pp 1669-1676 (2021)
Kidney International Reports
Introduction Membranous nephropathy (MN) is the most common cause of nephrotic syndrome (NS) in adults and is a leading cause of end-stage renal disease due to glomerulonephritis. Primary MN has a strong male predominance, accounting for approximatel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a9b671ce8f79a81158554da990de90d
https://doi.org/10.1016/j.ekir.2021.02.025
https://doi.org/10.1016/j.ekir.2021.02.025
