Zobrazeno 1 - 10
of 188
pro vyhledávání: '"O Wrong"'
Autor:
O Wrong, Sian E. Piret, Jonathan D. Lippiat, L.P.W.J. van den Heuvel, Caroline M Gorvin, Elena Levtchenko, Rajesh V. Thakker, Parmjit S. Jat, Brian Harding, Martijn J. Wilmer
Publikováno v:
Proceedings of the National Academy of Sciences USA, 110, 17, pp. 7014-9
Proceedings of the National Academy of Sciences USA, 110, 7014-9
Proceedings of the National Academy of Sciences USA, 110, 7014-9
Contains fulltext : 117540.pdf (Publisher’s version ) (Closed access) Receptor-mediated endocytosis, involving megalin and cubilin, mediates renal proximal-tubular reabsorption and is decreased in Dent disease because of mutations of the chloride/p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7e3abb25f752293770cd87189079e1d
https://doi.org/10.1073/pnas.1302063110
https://doi.org/10.1073/pnas.1302063110
Autor:
O Wrong, Robert J. Unwin
Publikováno v:
Clinical Medicine. 12:s22-s25
The term ‘renal tubular acidosis’ (RTA) might logically be applied to any form of renal disease causing systemic acidosis, since the renal tubule is the only part of the kidney involved in acid excretion. By convention, however, the term is not u
Autor:
Andres Ruiz-Linares, Kaisu Nikali, Juliana Martinez, Robert J. Unwin, M. W. Burley, Juan José Vanegas, O Wrong, Sue Povey, Lina M. Lopez, Gabriel Bedoya
Publikováno v:
American Journal of Medical Genetics Part A. :2709-2712
Publikováno v:
Kidney International. 71(12):1310-1316
Distal renal tubular acidosis (RTA) can lead to rickets in children or osteomalacia in adults if undetected. This disorder is normally diagnosed by means of an oral ammonium chloride-loading test; however, the procedure often leads to vomiting and ab
Autor:
Taija K. Nicoli, Michael J. A. Tanner, Keng E. Choo, Lesley J. Bruce, O Wrong, Andres Ruiz-Linares
Publikováno v:
Pediatric Nephrology. 21:212-217
Mutations of the AE1 (SLC4A1, Anion-Exchanger 1) gene that codes for band 3, the renal and red cell anion exchanger, are responsible for many cases of familial distal renal tubular acidosis (dRTA). In Southeast Asia this disease is usually recessive,
Publikováno v:
Kidney International. 62(1):10-19
Band 3 mutations, distal renal tubular acidosis, and Southeast Asian ovalocytosis. Familial distal renal tubular acidosis (dRTA) and Southeast Asian ovalocytosis (SAO) may coexist in the same patient. Both can originate in mutations of the anion-exch
Publikováno v:
Urinary Stones: Medical and Surgical Management
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::050020e798a34fc15bc0eda4915c5e98
https://doi.org/10.1002/9781118405390.ch9
https://doi.org/10.1002/9781118405390.ch9
Publikováno v:
QJM : monthly journal of the Association of Physicians. 107(2)
A 78-year-old female presented in 1996 with bone pain, generalized muscular weakness and immobility. She had marked hypophosphataemia and osteomalacic fractures and a clinical diagnosis of oncogernic osteomalacia was made.1 No tumour could be identif
Publikováno v:
British Journal of Nutrition. 63:17-26
An in vitro faecal incubation system was used to study the metabolism of complex carbohydrates by intestinal bacteria. Homogenates of human faeces were incubated anaerobically with added lactulose, pectin, the hemicellulose arabinogalactan, and cellu
Publikováno v:
Biochemistry and cell biology = Biochimie et biologie cellulaire. 76(5)
In distal renal tubular acidosis (dRTA) the tubular secretion of hydrogen ion in the distal nephron is impaired, leading to the development of metabolic acidosis, frequently accompanied by hypokalemia, nephrocalcinosis, and metabolic bone disease. Th