Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ambrose Gullett"'
Autor:
Mandy Wan, Craig Knott, Rachel Shute, William van’t Hoff, Lesley Rees, Sarah Ledermann, Bahee Manickavasagar, David Wells, Rukshana Shroff, Ambrose Gullett, Helen Aitkenhead
Publikováno v:
Clinical Journal of the American Society of Nephrology. 7:216-223
Summary Background and objectives Vitamin D deficiency is an important contributor to the development of hyperparathyroidism and is independently associated with cardiovascular and bone disease. The hypothesis was that nutritional vitamin D (ergocalc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edfa3f74d9e467e92247c0d1e1dc86a9
https://doi.org/10.2215/cjn.04760511
https://doi.org/10.2215/cjn.04760511
Publikováno v:
Pediatric Nephrology. 26:2227-2233
Vitamin D deficiency is common in adult renal transplant recipients, but data in children are scarce. Vitamin D is shown to have multiple effects on the cardiovascular system, renal function, and maintenance of bone health. We hypothesized that 25(OH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7cbade2ca9ba6b80464b8432182f226
https://doi.org/10.1007/s00467-011-1920-z
https://doi.org/10.1007/s00467-011-1920-z
Autor:
Eileen Brennan, Robert Kleta, Adrian S. Woolf, Kjell Tullus, Enriko Klootwijk, Stephen D. Marks, Ambrose Gullett, Graciana Jaureguiberry, Horia Stanescu
Publikováno v:
Pediatric Nephrology. 26:1857-1861
Renal fibromuscular dysplasia (FMD) can cause hypertension, and previous reports suggest that FMD is familial. We hypothesized that, in families containing an individual with proven FMD, relatives of index cases would have an increased risk of hypert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7afc8806ae1b771e7ffd2b20b013f982
https://doi.org/10.1007/s00467-011-1891-0
https://doi.org/10.1007/s00467-011-1891-0
Autor:
Heather J. Cordell, Judith A. Goodship, Aisling Stewart, Adrian S. Woolf, Timothy H.J. Goodship, Sue Malcolm, Heather J Lambert, Ambrose Gullett, Sally Feather
Publikováno v:
Clinical Journal of the American Society of Nephrology. 6:760-766
Primary vesicoureteric reflux (VUR) can coexist with reflux nephropathy (RN) and impaired renal function. VUR appears to be an inherited condition and is reported in approximately one third of siblings of index cases. The objective was to establish a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e13f36e80143dfe04fde2c629864961
https://doi.org/10.2215/cjn.04580510
https://doi.org/10.2215/cjn.04580510
Autor:
Sankar Sailesh, Detlef Bockenhauer, William van’t Hoff, Daniel G. Bichet, David Hampton, Ambrose Gullett, M D Penney
Publikováno v:
American Journal of Kidney Diseases. 59:566-568
Nephrogenic syndrome of inappropriate antidiuresis (NSIAD) is an X-linked disorder caused by activating mutations in arginine vasopressin receptor 2 (AVPR2), resulting in persistently concentrated urine. We report on a family affected by NSIAD with t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d00deac100e614f066a0ea79e8833ed
https://doi.org/10.1053/j.ajkd.2011.09.026
https://doi.org/10.1053/j.ajkd.2011.09.026
Urinary and dialysate losses of vitamin D-binding protein in children on chronic peritoneal dialysis
Autor:
Timothy McLean, Sarah Ledermann, Craig Knott, Rukshana Shroff, Michelle Cantwell, David Wells, Ambrose Gullett, Lesley Rees, Agnieszka Prytuła, Kimberly Hassen, Filipa Balona
Publikováno v:
Pediatric nephrology (Berlin, Germany). 27(4)
Vitamin D deficiency is widely prevalent in chronic kidney disease [CKD] patients. The aim of our study was to determine whether losses of vitamin D binding protein [VDBP] in urine and dialysate contribute to circulating 25-hydroxyvitamin D [25OHD] l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f01817a64ef397f4283ca717574a5bd
https://pubmed.ncbi.nlm.nih.gov/22081234
https://pubmed.ncbi.nlm.nih.gov/22081234
Autor:
Judith A. Goodship, Sue Malcolm, Heather J. Cordell, Timothy H.J. Goodship, Rebecca Darlay, Heather J Lambert, Sally Feather, Aisling Stewart, Ambrose Gullett, Pimphen Charoen, Rajko B. Kenda, Adrian S. Woolf
Primary vesicoureteric reflux accounts for approximately 10% of kidney failure requiring dialysis or transplantation, and sibling studies suggest a large genetic component. Here, we report a whole-genome linkage and association scan in primary, nonsy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef899b89ab0ca84fe1f4ba602f6d4364
https://europepmc.org/articles/PMC2799286/
https://europepmc.org/articles/PMC2799286/
Autor:
Lesley Rees, Ambrose Gullett, L. Krischock, Detlef Bockenhauer, Stephen D. Marks, Richard S. Trompeter
Publikováno v:
Pediatric transplantation. 13(4)
The aim of this study was to determine whether CNIs can be safely withdrawn in paediatric patients with declining renal allograft function receiving MMF and corticosteroids for long-term immunosuppression following renal transplantation. We performed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49cd1d77c6fdcb29c86fbb4402c9c15b
https://pubmed.ncbi.nlm.nih.gov/18992054
https://pubmed.ncbi.nlm.nih.gov/18992054
Autor:
David F.M. Thomas, Maria Bitner-Glindzicz, Adrian S. Woolf, Sue Malcolm, Chih-Chi Andrew Hu, Rachel Belk, Tung-Tien Sun, Jennifer Allison, Paul J.D. Winyard, Dagan Jenkins, Ambrose Gullett, Sally Feather
Publikováno v:
Journal of the American Society of Nephrology : JASN. 16(7)
Human renal adysplasia usually occurs sporadically, and bilateral disease is the most common cause of childhood end-stage renal failure, a condition that is lethal without intervention using dialysis or transplantation. De novo heterozygous mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52438c226f93b263c82c249b7514b9de
https://pubmed.ncbi.nlm.nih.gov/15888565
https://pubmed.ncbi.nlm.nih.gov/15888565