Zobrazeno 1 - 10
of 204
pro vyhledávání: '"PW Mathieson"'
Publikováno v:
QJM. 96:382-384
Sir, Proteinuric renal disease is common in Africa in both children and adults: in the 1960s it accounted for 2–3% of medical admissions.1 The condition is more severe than nephrotic syndrome in developed countries, incurring high mortality and typ
Autor:
CM Stirling, PW Mathieson, John Feehally, D Jayne, Dwomoa Adu, JM Boulton-Jones, Heather Murray
Publikováno v:
QJM : monthly journal of the Association of Physicians. 98(6)
Background: Focal segmental glomerulosclerosis (FSGS) is the least studied of the causes of idiopathic nephrotic syndrome, and there are few specific guidelines for treatment. Aim: To review data from five UK renal units to investigate whether adult
Publikováno v:
Cellular and molecular life sciences : CMLS. 59(3)
Genotypic variation in the human interleukin-10 (IL-10) promoter may account for marked inter-individual variation in IL-10 production and may influence susceptibility to autoimmune diseases. The G/A polymorphism at position -1082 has been linked to
Autor:
JH Miner, PW Mathieson
Publikováno v:
Nephron Experimental Nephrology. 106:e25-e26
Autor:
François Hirsch, C Dubay, Catherine Blanpied, Philippe Druet, K Gillespie, N Kermarrec, Dominique Gauguier, PW Mathieson, Mark Lathrop, B de Gouyon
Publikováno v:
Genomics. 31(1)
A subset of patients with rheumatoid arthritis occasionally develops skin reactions and glomerulonephritis and exhibits an increase in serum IgE concentration when treated with gold salts. Brown-Norway (BN) rats injected with aurothiopropanolsulfonat
Autor:
DK Peters, PW Mathieson
Publikováno v:
Nephron Clinical Practice. 96:c33-c34
Publikováno v:
Europe PubMed Central
The third component of complement (C3) exists in two main allotypic forms, C3S and C3F, distinguished at the DNA level by a single base change. An increased frequency of the rarer C3F allele has been reported in patients with the autoantibody nephrit
Publikováno v:
University of Bristol-PURE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::5e49cfd157e4021a2c7051c814541565
https://research-information.bris.ac.uk/en/publications/631b0114-4d27-4977-b5d7-c65e93aea8ff
https://research-information.bris.ac.uk/en/publications/631b0114-4d27-4977-b5d7-c65e93aea8ff
Publikováno v:
Europe PubMed Central
The third component of complement (C3) exists in two main allotypic forms, C3S and C3F, which can be distinguished at the molecular level using a variation of the polymerase chain reaction. An increased frequency of the C3F allele has been noted in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::552e237566138a3345533519f69c7287
http://europepmc.org/abstract/med/8525532
http://europepmc.org/abstract/med/8525532
Autor:
Patry C; Department of Pediatrics I, University Children's Hospital Heidelberg, 69120, Heidelberg, Germany.; Division of Cardiovascular Physiology, Institute of Physiology and Pathophysiology, University of Heidelberg, 69120, Heidelberg, Germany., Plotnicki K; Department of Pediatrics I, University Children's Hospital Heidelberg, 69120, Heidelberg, Germany., Betzen C; Department of Pediatrics I, University Children's Hospital Heidelberg, 69120, Heidelberg, Germany.; Division of Functional Genome Analysis, German Cancer Research Center (DKFZ), 69120, Heidelberg, Germany., Ortiz AP; Department of Neonatology, University Children's Hospital Mannheim, University of Heidelberg, 68167, Mannheim, Germany., Pappan KL; Metabolon, Inc., 617 Davis Drive, Suite 400, Durham, NC, 27713, USA., Satchell SC; Learning and Research Southmead Hospital Bristol, University of Bristol, Bristol, BS8 1TH, UK., Mathieson PW; The Principal's Office, University of Edinburgh, Edinburgh, EH8 9YL, UK., Bielaszewska M; Institute for Hygiene, University of Münster, 48149, Münster, Germany.; Reference Laboratory for E. coli and Shigella, National Public Health Institute, Srobarova 48, 10042, Prague, Czech Republic., Karch H; Institute for Hygiene, University of Münster, 48149, Münster, Germany., Tönshoff B; Department of Pediatrics I, University Children's Hospital Heidelberg, 69120, Heidelberg, Germany., Rafat N; Department of Pediatrics I, University Children's Hospital Heidelberg, 69120, Heidelberg, Germany. Neysan.Rafat@umm.de.; Department of Neonatology, University Children's Hospital Mannheim, University of Heidelberg, 68167, Mannheim, Germany. Neysan.Rafat@umm.de.; Department of Pharmaceutical Sciences, Bahá'í Institute of Higher Education (BIHE), Teheran, Iran. Neysan.Rafat@umm.de.
Publikováno v:
Metabolomics : Official journal of the Metabolomic Society [Metabolomics] 2019 Oct 01; Vol. 15 (10), pp. 131. Date of Electronic Publication: 2019 Oct 01.