Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Matthew Edey"'
Autor:
Peter F Zipfel, Matthew Edey, Stefan Heinen, Mihály Józsi, Heiko Richter, Joachim Misselwitz, Bernd Hoppe, Danny Routledge, Lisa Strain, Anne E Hughes, Judith A Goodship, Christoph Licht, Timothy H J Goodship, Christine Skerka
Publikováno v:
PLoS Genetics, Vol 3, Iss 3, p e41 (2007)
Atypical hemolytic uremic syndrome (aHUS) is associated with defective complement regulation. Disease-associated mutations have been described in the genes encoding the complement regulators complement factor H, membrane cofactor protein, factor B, a
Externí odkaz:
https://doaj.org/article/5dbab60a997e4d30ae0bf040891b6ada
Autor:
David Philip Lowe, Matthew Edey, Habib Kashi, Daniel Zehnder, Nithya Krishnan, Rizwan Hamer, Klaus Chen, M. Hathaway, Robert Higgins, C. Imray, Clare Williams, Sunil Daga, Simon Fletcher, David Briggs, Lam Chin Tan, For T. Lam
Publikováno v:
Transplantation. 92:900-906
Background. Human leukocyte antigen (HLA) antibody-incompatible renal transplantation has been increasingly performed since 2000 but with few data on the medium-term outcomes. Methods. Between 2003 and 2011, 84 patients received renal transplants wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::378d60b8f5423381fecdbb9781159766
https://doi.org/10.1097/tp.0b013e31822dc38d
https://doi.org/10.1097/tp.0b013e31822dc38d
Publikováno v:
Nephrology. 15:137-145
The incidence of hepatitis B virus (HBV) infection in dialysis populations has declined over recent decades, largely because of improvements in infection control and widespread implementation of HBV vaccination. Regardless, outbreaks of infection con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f07b4669cad9cff3738063b1587c8ef
https://doi.org/10.1111/j.1440-1797.2009.01268.x
https://doi.org/10.1111/j.1440-1797.2009.01268.x
Publikováno v:
Molecular Immunology. 46:1405-1408
There is substantial evidence to suggest that complement activation plays a pivotal role in the pathogenesis of IgA nephropathy. Mesangial C3 deposition is seen in approximately 90% of patients and polymeric IgA has been shown to activate the alterna
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4baead4c5cc937afbd116bad442e12a2
https://doi.org/10.1016/j.molimm.2008.12.002
https://doi.org/10.1016/j.molimm.2008.12.002
Autor:
David J. Kavanagh, Martha Diaz-Torres, Frida C Bergstrom, Carol Inward, Judith A. Goodship, Matthew Edey, Nadeem E. Moghal, Bruno O. Villoutreix, Véronique Frémeaux-Bacchi, Lisa Strain, Timothy H.J. Goodship, Charles R.V. Tomson, AK Lampe, Mary McHugh, Anna M. Blom
Publikováno v:
Scopus-Elsevier
ResearcherID
ResearcherID
Atypical hemolytic uremic syndrome (aHUS) is a disorder characterized by hemolytic anemia, thrombocytopenia, and acute renal failure. Mutations, polymorphisms, and copy number variation in complement factors and inhibitors are associated with aHUS. I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::436f769df4c517c45af6802d45aabce7
https://doi.org/10.4049/jimmunol.180.9.6385
https://doi.org/10.4049/jimmunol.180.9.6385
Autor:
Johan B. Rosman, David W. Johnson, Stephen P. McDonald, Kathryn J. Wiggins, Fiona G. Brown, Carmel M. Hawley, Matthew Edey, Kym M. Bannister
Publikováno v:
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. 25(4)
Background. Enterococcal peritonitis is a serious complication of peritoneal dialysis (PD), although reports of this condition in the literature are exceedingly limited.Methods. The frequency, predictors, treatment and clinical outcomes of enterococc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92f8a18265873f23cd04a5ccede27b95
https://pubmed.ncbi.nlm.nih.gov/19948875
https://pubmed.ncbi.nlm.nih.gov/19948875
Autor:
Paul A. Mead, Stephen J. Perkins, N. Suren Kanagasundaram, Lisa Strain, Timothy H.J. Goodship, Rebecca E. Saunders, Matthew Edey
Publikováno v:
American journal of kidney diseases : the official journal of the National Kidney Foundation. 51(3)
Hemolytic uremic syndrome (HUS) takes 2 forms: diarrheal HUS and nondiarrheal HUS. As its name suggests, diarrheal HUS classically follows an enteric infection. The classic infective organism is the Escherichia coli O157 serotype, although other bact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17f8343b9fc98bd27e82165dc4ac8e8c
https://pubmed.ncbi.nlm.nih.gov/18295065
https://pubmed.ncbi.nlm.nih.gov/18295065
Autor:
Judith A. Goodship, Matthew Edey, Stefan Heinen, Lisa Strain, Danny Routledge, Peter F. Zipfel, Mihály Józsi, Timothy H.J. Goodship, Anne E. Hughes, Heiko Richter, Christoph Licht, Bernd Hoppe, Christine Skerka, Joachim Misselwitz
Publikováno v:
PLoS Genetics
PLoS Genetics, Vol 3, Iss 3, p e41 (2007)
PLoS Genetics, Vol 3, Iss 3, p e41 (2007)
Atypical hemolytic uremic syndrome (aHUS) is associated with defective complement regulation. Disease-associated mutations have been described in the genes encoding the complement regulators complement factor H, membrane cofactor protein, factor B, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::354b4e04a757954abe6c689ecf4d5289
http://europepmc.org/articles/PMC1828695
http://europepmc.org/articles/PMC1828695
Publikováno v:
New England Journal of Medicine. 353:846-847
To the Editor: The regression of Kaposi's sarcoma in renal-graft recipients after switching from treatment with cyclosporine and mycophenolate mofetil to sirolimus, as reported by Stallone et al. (March 31 issue),1 is remarkable and confirms earlier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9970655186d826634680047a60226930
https://doi.org/10.1056/nejmc058158
https://doi.org/10.1056/nejmc058158
Autor:
Matthew Edey
Publikováno v:
New England Journal of Medicine. 361:1511-1511
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2cb7d842ce111a96af0b6e5bf4e56d30
https://doi.org/10.1056/nejmc091704
https://doi.org/10.1056/nejmc091704