Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Shashi K. Nagaraj"'
Autor:
Holger Prokisch, Evan H. Baugh, Valentina Del Dotto, Michele Carbonelli, Rocco Liguori, Mirjana Gusic, Wolfgang Sperl, Tommaso Pippucci, Nicholas Stong, Pamela Magini, Enrico Bertini, William C. Copeland, Alessandra Maresca, Francesca Diomedi-Camassei, Shashi K. Nagaraj, Ioana Cutcutache, Bertil Macao, Alessandro Iannaccone, Francesco Emma, Piero Barboni, Marco Seri, Vandana Shashi, Zsolt Szilagyi, Farid Ullah, Camille Peron, Valerio Carelli, Chiara La Morgia, Ivano Di Meo, Martin Armstrong, Jennifer A. Sullivan, Saskia B. Wortmann, Nicholas Katsanis, Leonardo Caporali, Kamal Khan, Maria Falkenberg, Valeria Tiranti, Mays A. El-Dairi, Erica E. Davis, Maria Lucia Valentino, Margaret A. Gustafson, Claudia Zanna, Rosalba Carrozzo, Sylvia Boesch, Flavia Palombo, Francesca Tagliavini, Robert Kopajtich, Matthew Page
Publikováno v:
J. Clin. Invest. 130, 108-125 (2020)
Inherited optic neuropathies include complex phenotypes, mostly driven by mitochondrial dysfunction. We report an optic atrophy spectrum disorder, including retinal macular dystrophy and kidney insufficiency leading to transplantation, associated wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f59384a409cfa55c80cfd8e64162ba11
https://europepmc.org/articles/PMC6934201/
https://europepmc.org/articles/PMC6934201/
Autor:
Atif Awan, John W. Foreman, Shenal Thalgahagoda, Tracy E. Hunley, Deepa H. Chand, Arundhati S. Kale, Halima S. Janjua, Vladimir Belostotsky, Catherine O'Brien, Michelle P. Winn, Guanghong Wu, William E. Smoyer, Tarak Srivastava, Yi Cai, Adebowale Adeyemo, Joanna R. Ghali, Patrick D. Brophy, Alison Homstad, Nicholas J. A. Webb, Jen Jar Lin, Kathy Nicholls, Gina Marie Barletta, Gentzon Hall, Delbert R. Wigfall, Arvind Bagga, Rasheed Gbadegesin, Abiodun Aderogba Omoloja, Shashi K. Nagaraj, Elizabeth Abraham, Larry A. Greenbaum, A S Abeyagunawardena, Michelle N. Rheault, Aditi Sinha, David D. Milford, Debbie S. Gipson
Steroid-sensitive nephrotic syndrome (SSNS) accounts for >80% of cases of nephrotic syndrome in childhood. However, the etiology and pathogenesis of SSNS remain obscure. Hypothesizing that coding variation may underlie SSNS risk, we conducted an exom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0505b0a83a96425d66c53e6838a3ba95
https://europepmc.org/articles/PMC4483579/
https://europepmc.org/articles/PMC4483579/
Publikováno v:
Ambulatory Pediatrics. 5:249-252
Recurrent urinary tract infections are common in children, and the use of complementary therapies is common in other children with recurrent illnesses. However, little is known about the use of cranberry products by children with renal disease. We hy
Publikováno v:
Infection. 33(5-6)
Neisseria mucosa is part of the normal nasopharyngeal flora and rarely pathogenic in humans. Reports of serious infections associated with this pathogen are very unusual. A 17-year-old boy with end-stage renal disease due to IgA nephropathy presented
Autor:
Uptal D. Patel, Shashi K. Nagaraj, William A. Primack, Maria E. Ferris, Debbie S. Gipson, William Conley, James Bradley Layton, Susan F. Massengill
Publikováno v:
ResearcherID
Scopus-Elsevier
Europe PubMed Central
Scopus-Elsevier
Europe PubMed Central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92d65e51b3cdeb744a9244f3a502601a
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=MEDLINE&KeyUT=MEDLINE:18751354&KeyUID=MEDLINE:18751354
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=MEDLINE&KeyUT=MEDLINE:18751354&KeyUID=MEDLINE:18751354