Zobrazeno 1 - 10
of 125
pro vyhledávání: '"Nicholas J A, Webb"'
Autor:
Juliane Münch, Isabelle Sessler, Hans Martin Bosse, Manfred Wargenau, Janine D. Dreesen, Giulio Loforese, Nicholas J. A. Webb, Rama Sivasubramanian, Sibylle Reidemeister, Philipp Lustenberger, Viviane Klingmann
Publikováno v:
Pharmaceutics, Vol 15, Iss 6, p 1729 (2023)
Mini-tablets are advantageous over liquid formulations in overcoming challenges related to stability, taste, and dosage. This open-label, single-dose, cross-over study investigated the acceptability and safety of drug-free, film-coated mini-tablets i
Externí odkaz:
https://doaj.org/article/55e642951f544c44acb8c0aee35b83a4
Autor:
Andrew S, Bomback, David, Kavanagh, Marina, Vivarelli, Matthias, Meier, Yaqin, Wang, Nicholas J A, Webb, Angelo J, Trapani, Richard J H, Smith
Publikováno v:
Kidney International Reports. 7:2150-2159
Complement 3 glomerulopathy (C3G) is a rare kidney disease characterized by dysregulation of the alternative pathway (AP) of the complement system. About 50% of patients with C3G progress to kidney failure within 10 years of diagnosis. Currently, the
Autor:
Klingmann, Juliane Münch, Isabelle Sessler, Hans Martin Bosse, Manfred Wargenau, Janine D. Dreesen, Giulio Loforese, Nicholas J. A. Webb, Rama Sivasubramanian, Sibylle Reidemeister, Philipp Lustenberger, Viviane
Publikováno v:
Pharmaceutics; Volume 15; Issue 6; Pages: 1729
Mini-tablets are advantageous over liquid formulations in overcoming challenges related to stability, taste, and dosage. This open-label, single-dose, cross-over study investigated the acceptability and safety of drug-free, film-coated mini-tablets i
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
Autor:
Elena Levtchenko, Aude Servais, Sally A Hulton, Gema Ariceta, Francesco Emma, David S Game, Karin Lange, Risto Lapatto, Hong Liang, Rebecca Sberro-Soussan, Rezan Topaloglu, Anibh M Das, Nicholas J A Webb, Christoph Wanner
Publikováno v:
Scientia
Clinical recommendations; Cystinosis; Multidisciplinary care Recomendaciones clínicas; Cistinosis; Atención multidisciplinaria Recomanacions clíniques; Cistinosi; Atenció multidisciplinària Cystinosis, a rare autosomal recessive lysosomal storag
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
Autor:
Wendy Cook, Moin A. Saleem, Caroline Jones, Samir Mehta, Detlef Bockenhauer, Karl McKeever, Angela S Hall, Elizabeth Brettell, Martin Christian, Afentou Nafsika, Emma Frew, Shivaram Hegde, Nicholas J. A. Webb, Ania Koziell, Adam Khan, Natalie Ives, Hitesh Prajapati, Heather Maxwell, Rodney D. Gilbert, Rebecca Woolley, David V. Milford
Publikováno v:
Nephrology Dialysis Transplantation. 36
Background and Aims At least 80% of children with steroid sensitive nephrotic syndrome (SSNS) have relapses and many are triggered by upper respiratory tract infections (URTIs). Previous small studies (4 studies, 232 patients in total), mostly in chi
Autor:
Eiske M. Dorresteijn, Michiel F. Schreuder, Nicholas J. A. Webb, Anne M Schijvens, Steven Teerenstra, Nynke Teeninga
Publikováno v:
European Journal of Pediatrics, 180, 2849-2859
European Journal of Pediatrics
European Journal of Pediatrics, 180, 9, pp. 2849-2859
European Journal of Pediatrics, 180(9), 2849-2859. Springer-Verlag
European Journal of Pediatrics
European Journal of Pediatrics, 180, 9, pp. 2849-2859
European Journal of Pediatrics, 180(9), 2849-2859. Springer-Verlag
Steroids are the cornerstone of the treatment of childhood nephrotic syndrome. The optimal duration for the first episode remains a matter of debate. The aim of this study is to determine whether the 8 weeks International Study of Kidney Disease in C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51d1faa54469584e0f376d8c58850cb9
http://hdl.handle.net/2066/237507
http://hdl.handle.net/2066/237507
Publikováno v:
Pediatric Nephrology (Berlin, Germany)
Background Studies have shown that losartan reduces serum uric acid in adults, unlike angiotensin-converting enzyme inhibitors. A previous study demonstrated that losartan and enalapril had comparable effects on proteinuria in children. Methods We co
Autor:
Christoph Wanner, Elena Levtchenko, Aude Servais, Nicholas J. A. Webb, Sally A. Hulton, Anibh M. Das
Publikováno v:
Nephrology Dialysis Transplantation. 35
Background and Aims Cystinosis is a rare autosomal recessive lysosomal storage disorder caused by mutations in the CTNS gene on chromosome 17p13. It affects between 1:150,000–1:200,000 live births, with a prevalence of approximately 1.6 per million