Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Rodney D Gilbert"'
Autor:
Natalie Ives, Rebecca Woolley, Moin A Saleem, Catherine A Moakes, Aoife Waters, Rodney D Gilbert, Hugh Jarrett, Elizabeth Brettell, Steve Nash, Louise K Farmer, Khadija Ourradi, Sally A Johnson
Publikováno v:
Efficacy and Mechanism Evaluation, Vol 11, Iss 11 (2024)
Background Shiga-toxin-producing Escherichia coli haemolytic uraemic syndrome affects ~100 United Kingdom children each year. Around half need dialysis, a quarter develop serious complications with long-term consequences and ~3% die. No effective int
Externí odkaz:
https://doaj.org/article/d211a98eb57e4132bc1c294a564bffab
Autor:
Martin T Christian, Nicholas JA Webb, Rebecca L Woolley, Nafsika Afentou, Samir Mehta, Emma Frew, Elizabeth A Brettell, Adam R Khan, David V Milford, Detlef Bockenhauer, Moin A Saleem, Angela S Hall, Ania Koziell, Heather Maxwell, Shivaram Hegde, Eric R Finlay, Rodney D Gilbert, Caroline Jones, Karl McKeever, Wendy Cook, Natalie Ives
Publikováno v:
Health Technology Assessment, Vol 26, Iss 3 (2022)
Background: Most children with steroid-sensitive nephrotic syndrome have relapses that are triggered by upper respiratory tract infections. Four small trials, mostly in children already taking maintenance corticosteroid in countries of different uppe
Externí odkaz:
https://doaj.org/article/7bfec51e091e4c2a9b8d1ac71146dfcf
Autor:
Gary Leggatt, Guo Cheng, Sumit Narain, Luis Briseño-Roa, Jean-Philippe Annereau, The Genomics England Research Consortium, Christine Gast, Rodney D. Gilbert, Sarah Ennis
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-12 (2023)
Abstract Autosomal recessive whole gene deletions of nephrocystin-1 (NPHP1) result in abnormal structure and function of the primary cilia. These deletions can result in a tubulointerstitial kidney disease known as nephronophthisis and retinal (Senio
Externí odkaz:
https://doaj.org/article/e0618627729740fcb92ea2c5b536e427
Autor:
Eleanor G. Seaby, Steven Turner, David J. Bunyan, Fariba Seyed‐Rezai, Jonathan Essex, Rodney D. Gilbert, Sarah Ennis
Publikováno v:
Clinical Genetics. 103:214-218
Renal Fanconi syndrome (RFS) is a generalised disorder of the proximal convoluted tubule. Many genes have been associated with RFS including those that cause systemic disorders such as cystinosis, as well as isolated RFS. We discuss the case of a 10-
Autor:
Nafsika, Afentou, Emma, Frew, Samir, Mehta, Natalie J, Ives, Rebecca L, Woolley, Elizabeth A, Brettell, Adam R, Khan, David V, Milford, Detlef, Bockenhauer, Moin A, Saleem, Angela S, Hall, Ania, Koziell, Heather, Maxwell, Shivaram, Hegde, Eric, Finlay, Rodney D, Gilbert, Caroline, Jones, Karl, McKeever, Wendy, Cook, Nicholas J A, Webb, Martin T, Christian, Annette, Bolger Team
Publikováno v:
PharmacoEconomics - Open. 6:605-617
Childhood steroid-sensitive nephrotic syndrome is a frequently relapsing disease with significant short- and long-term complications, leading to high healthcare costs and reduced quality of life for patients. The majority of relapses are triggered by
Publikováno v:
Clinical Kidney Journal. 16:192-194
Dent disease type 1 is suspected in the presence of a complete phenotype of low molecular weight (LMW) proteinuria, hypercalciuria and at least one of the following: nephrocalcinosis, nephrolithiasis, haematuria, hypophosphatemia or chronic kidney di
Autor:
Martin T. Christian, Nicholas J. A. Webb, Samir Mehta, Rebecca L. Woolley, Nafsika Afentou, Emma Frew, Elizabeth A. Brettell, Adam R. Khan, David V. Milford, Detlef Bockenhauer, Moin A. Saleem, Angela S. Hall, Ania Koziell, Heather Maxwell, Shivaram Hegde, Hitesh Prajapati, Rodney D. Gilbert, Caroline Jones, Karl McKeever, Wendy Cook, Natalie Ives
Publikováno v:
Christian, M T, Webb, N J A, Mehta, S, Woolley, R L, Afentou, N, Frew, E, Brettell, E A, Khan, A R, Milford, D V, Bockenhauer, D, Saleem, M A, Hall, A S, Koziell, A, Maxwell, H, Hegde, S, Prajapati, H, Gilbert, R D, Jones, C, McKeever, K, Cook, W & Ives, N 2021, ' Evaluation of Daily Low-Dose Prednisolone During Upper Respiratory Tract Infection to Prevent Relapse in Children With Relapsing Steroid-Sensitive Nephrotic Syndrome : The PREDNOS 2 Randomized Clinical Trial ', JAMA Pediatrics . https://doi.org/10.1001/jamapediatrics.2021.5189
JAMA Pediatrics
JAMA Pediatrics
Key Points Question In children with relapsing corticosteroid-sensitive nephrotic syndrome, does daily low-dose corticosteroid given at the time of upper respiratory tract infection prevent upper respiratory tract infection–related relapse? Finding
Publikováno v:
Abstracts.
BackgroundChildren and young people (CYP) with a long term condition (LTC) are known to have increased psychosocial needs. This is also true for siblings of CYP with a LTC.The current COVID-19 pandemic has had an adverse impact on the psycho-social w
Autor:
Nagra Arvind, Rodney D. Gilbert, Eleanor Stubbs, Sarah Shameti, Shuman Haq, Caroline Anderson
Publikováno v:
Abstracts.
Background Studies show that young people (YP) aged 16-30 years with a long-term condition (LTC) do less well than their healthy peers in terms of their mental health and employability. 30% of YP with a LTC have mental health issues compared to 15% o
Autor:
Gary Leggatt, Rodney D. Gilbert, Kristin Veighey, Christine Gast, Sarah Ennis, Tahmina Rahman
Publikováno v:
Nephrology Dialysis Transplantation. 36
Background and Aims Hemizygous variants in chloride voltage-gated channel 5 (CLCN5) on chromosome Xp11.22 cause Dent disease type 1, characterised by low-molecular-weight proteinuria, hypercalciuria, nephrocalcinosis, nephrolithiasis, and progressive