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Number of items: 108.
A
Abeyagunawardena, AS;
Thalgahagoda, RS;
Dissanayake, PV;
Abeyagunawardena, S;
Illangasekera, YA;
Karunadasa, UI;
Trompeter, RS;
(2017)
Short courses of daily prednisolone during upper respiratory tract infections reduce relapse frequency in childhood nephrotic syndrome.
Pediatric Nephrology
, 32
(8)
pp. 1377-1382.
10.1007/s00467-017-3640-5.
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Antonelou, M;
El-Kateb, S;
Davies, N;
Davenport, A;
(2017)
Changes in serum osmotic pressure following haemodialysis treatments lead to changes in bioimpedance spectroscopy estimates of lean and adipose tissue.
European Journal of Clinical Nutrition
, 71
(4)
pp. 564-565.
10.1038/ejcn.2016.270.
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Arno, G;
Carss, KJ;
Hull, S;
Zihni, C;
Robson, AG;
Fiorentino, A;
Hardcastle, AJ;
... Yu, P; + view all
(2017)
Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration.
The American Journal of Human Genetics
, 100
(2)
pp. 334-342.
10.1016/j.ajhg.2016.12.014.
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Aymé, S;
Bockenhauer, D;
Day, S;
(2017)
Aymé S, Bockenhauer D, Day S, et al. Common Elements in Rare Kidney Diseases: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. Kidney Int. 2017;92:796–808.
[Corrigendum].
Kidney International
, 92
(6)
p. 1558.
10.1016/j.kint.2017.10.004.
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 |
B
|
Bacchelli, C;
Moretti, FA;
Carmo, M;
Adams, S;
Stanescu, HC;
Pearce, K;
Madkaikar, M;
... Gaspar, HB; + view all
(2017)
Mutations in linker for activation of T cells (LAT) lead to a novel form of severe combined immunodeficiency.
Journal of Allergy and Clinical Immunology
, 139
(2)
pp. 634-642.
10.1016/j.jaci.2016.05.036.
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Baigent, C;
Herrington, WG;
Coresh, J;
Landray, MJ;
Levin, A;
Perkovic, V;
Pfeffer, MA;
... McMurray, JJV; + view all
(2017)
Challenges in conducting clinical trials in nephrology: conclusions from a Kidney Disease-Improving Global Outcomes (KDIGO) Controversies Conference.
Kidney International
, 92
(2)
pp. 297-305.
10.1016/j.kint.2017.04.019.
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Bajema, IM;
Bruijn, JA;
Casian, A;
Cid, MC;
Csernok, E;
van Daalen, E;
Harper, L;
... Jayne, D; + view all
(2017)
The European Vasculitis Society 2016 Meeting Report.
Kidney International Reports
, 2
(6)
pp. 1018-1031.
10.1016/j.ekir.2017.09.008.
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Bello, AK;
Alrukhaimi, M;
Ashuntantang, GE;
Basnet, S;
Rotter, RC;
Douthat, WG;
Kazancioglu, R;
... Moe, O; + view all
(2017)
Complications of chronic kidney disease: current state, knowledge gaps, and strategy for action.
[Review].
Kidney International Supplements
, 7
(2)
pp. 122-129.
10.1016/j.kisu.2017.07.007.
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Besouw, MTP;
Bienias, M;
Walsh, P;
Kleta, R;
van't Hoff, WG;
Ashton, E;
Jenkins, L;
(2017)
Erratum to: Clinical and molecular aspects of distal renal tubular acidosis in children.
[Corrigendum].
Pediatric Nephrology
, 32
(6)
p. 1095.
10.1007/s00467-017-3631-6.
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Blanchard, A;
Bockenhauer, D;
Bolignano, D;
Calò, LA;
Cosyns, E;
Devuyst, O;
Ellison, DH;
... Vargas-Poussou, R; + view all
(2017)
Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference.
Kidney International
, 91
(1)
pp. 24-33.
10.1016/j.kint.2016.09.046.
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Bockenhauer, D;
(2017)
Hyponatremia and cyst growth in neonatal polycystic kidney disease: a case for aquaretics?
Pediatric Nephrology
, 32
(5)
pp. 721-723.
10.1007/s00467-017-3578-7.
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Bockenhauer, D;
Besouw, M;
Bienias, M;
Walsh, P;
Kleta, R;
Van't Hoff, WG;
Jenkins, L;
(2017)
Clinical and molecular aspects of distal renal tubular acidosis in children.
Pediatric Nephrology
, 32
(6)
pp. 987-996.
10.1007/s00467-016-3573-4.
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Bockenhauer, D;
Bichet, DG;
(2017)
Nephrogenic diabetes insipidus.
Current Opinion in Pediatrics
, 29
(2)
pp. 199-205.
10.1097/MOP.0000000000000473.
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Bockenhauer, D;
Hayes, W;
Boyle, S;
Carroll, A;
Marks, S;
(2017)
Hypomagnesemia and increased risk of new-onset diabetes mellitus after transplantation in pediatric renal transplant recipients.
Paediatric Nephrology
, 32
(5)
pp. 879-884.
10.1007/s00467-016-3571-6.
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Bockenhauer, D;
Kleta, R;
(2017)
Of dogs and men.
European Journal of Human Genetics
, 25
(2)
p. 161.
10.1038/ejhg.2016.161.
|
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Brocklebank, V;
Johnson, S;
Sheerin, TP;
Marks, SD;
Gilbert, RD;
Tyerman, K;
Kinoshita, M;
... Kavanagh, D; + view all
(2017)
Factor H autoantibody is associated with atypical hemolytic uremic syndrome in children in the United Kingdom and Ireland.
Kidney International
, 92
(5)
pp. 1261-1271.
10.1016/j.kint.2017.04.028.
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C
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Cabezas, OR;
Flanagan, S;
Stanescu, H;
Garcia-Martinez, E;
Caswell, R;
Lango-Allen, H;
Anton-Gamero, M;
... Bockenhauer, D; + view all
(2017)
Polycystic kidney disease with hyperinsulinemic hypoglycemia caused by a promoter mutation in PMM2.
Journal of the American Society of Nephrology
, 28
(8)
pp. 2529-2539.
10.1681/ASN.2016121312.
|
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Canetti, D;
Rendell, NB;
Di Vagno, L;
Gilbertson, JA;
Rowczenio, D;
Rezk, T;
Gillmore, JD;
... Taylor, GW; + view all
(2017)
Misidentification of transthyretin and immunoglobulin variants by proteomics due to methyl lysine formation in formalin-fixed paraffin-embedded amyloid tissue.
Amyloid
, 27
(4)
pp. 229-237.
10.1080/13506129.2017.1385452.
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Caplin, B;
Jakobsson, K;
Glaser, J;
Nitsch, D;
Jha, V;
Singh, A;
Correa-Rotter, R;
(2017)
International Collaboration for the Epidemiology of eGFR in Low and Middle Income Populations - Rationale and core protocol for the Disadvantaged Populations eGFR Epidemiology Study (DEGREE).
BMC Nephrology
, 18
, Article 1. 10.1186/s12882-016-0417-1.
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Caplin, B;
Nitsch, D;
(2017)
Urinary biomarkers of tubular injury in chronic kidney disease.
Kidney International
, 91
(1)
pp. 21-23.
10.1016/j.kint.2016.10.003.
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Caplin, BD;
Kim, L;
Cleary, F;
Hull, S;
Griffin, K;
Wheeler, D;
Nitsch, D;
(2017)
Accounting for overdispersion when determining primary care outliers for the identification of chronic kidney disease: learning from the National Chronic Kidney Disease Audit.
Nephrology, Dialysis and Transplantation
, 32
(Supp 2)
ii151-ii158.
10.1093/ndt/gfw398.
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Carss, KJ;
Arno, G;
Erwood, M;
Stephens, J;
Sanchis-Juan, A;
Hull, S;
Megy, K;
... Raymond, FL; + view all
(2017)
Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease.
American Journal of Human Genetics
, 100
(1)
pp. 75-90.
10.1016/j.ajhg.2016.12.003.
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Chan, MMY;
Barnicoat, A;
Mumtaz, F;
Aitchison, M;
Side, L;
Brittain, H;
Bates, AWH;
(2017)
Cascade Fumarate Hydratase mutation screening allows early detection of kidney tumour: a case report.
BMC Medical Genetics
, 18
, Article 79. 10.1186/s12881-017-0436-1.
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Cherukuri, A;
Salama, AD;
Carter, CR;
Landsittel, D;
Arumugakani, G;
Clark, B;
Rothstein, DM;
(2017)
Reduced human transitional B cell T1/T2 ratio is associated with subsequent deterioration in renal allograft function.
Kidney International
, 91
(1)
pp. 183-195.
10.1016/j.kint.2016.08.028.
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Chong, LSH;
Sautenet, B;
Tong, A;
Hanson, CS;
Samuel, S;
Zappitelli, M;
Dart, A;
... Craig, JC; + view all
(2017)
Range and Heterogeneity of Outcomes in Randomized Trials of Pediatric Chronic Kidney Disease.
The Journal of Pediatrics
, 186
110-117.e11.
10.1016/j.jpeds.2017.03.034.
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Collins, L;
Sathiananthamoorthy, S;
Fader, M;
Malone-Lee, J;
(2017)
Intermittent catheterisation after botulinum toxin injections: the time to reassess our practice.
International Urogynecology Journal
, 28
(9)
pp. 1351-1356.
10.1007/s00192-017-3271-1.
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Connell, A;
Montgomery, H;
Morris, S;
Nightingale, C;
Stanley, S;
Emerson, M;
Jones, G;
... Laing, C; + view all
(2017)
Service evaluation of the implementation of a digitally-enabled care pathway for the recognition and management of acute kidney injury (version 1).
F1000Research
, 6
, Article 1033. 10.12688/f1000research.11637.1.
|
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Connell, A;
Montgomery, H;
Morris, S;
Nightingale, C;
Stanley, S;
Emerson, M;
Jones, G;
... Laing, C; + view all
(2017)
Service evaluation of the implementation of a digitally-enabled care pathway for the recognition and management of acute kidney injury (version 2).
F1000Res
, 6
, Article 1033. 10.12688/f1000research.11637.2.
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Connor, TM;
Hoer, S;
Mallett, A;
Gale, DP;
Gomez-Duran, A;
Posse, V;
Antrobus, R;
... Maxwell, PH; + view all
(2017)
Mutations in mitochondrial DNA causing tubulointerstitial kidney disease.
PLOS Genetics
, 13
(3)
, Article e1006620. 10.1371/journal.pgen.1006620.
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D
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Deschênes, G;
Vivarelli, M;
Peruzzi, L;
Alpay, H;
Alvaro Madrid, A;
Andersen, R;
Bald, M;
... Zurowska, A; + view all
(2017)
Variability of diagnostic criteria and treatment of idiopathic nephrotic syndrome across European countries.
European Journal of Pediatrics
, 176
(5)
pp. 647-654.
10.1007/s00431-017-2891-2.
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Dufek, S;
Booth, C;
Carroll, A;
van’t Hoff, W;
Kleta, R;
Bockenhauer, D;
(2017)
Urea is successful in treating inappropriate antidiuretic hormone secretion in an infant.
Acta Paediatrica
, 106
(3)
pp. 513-515.
10.1111/apa.13697.
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E
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Evangelidis, N;
Tong, A;
Manns, B;
Hemmelgarn, B;
Wheeler, DC;
Tugwell, P;
Crowe, S;
... Craig, JC; + view all
(2017)
Developing a Set of Core Outcomes for Trials in Hemodialysis: An International Delphi Survey.
American Journal of Kidney Diseases
, 70
(4)
pp. 464-475.
10.1053/j.ajkd.2016.11.029.
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F
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Forsythe, E;
Sparks, K;
Best, S;
Borrows, S;
Hoskins, B;
Sabir, A;
Barrett, T;
... Beales, PL; + view all
(2017)
Risk Factors for Severe Renal Disease in Bardet-Biedl Syndrome.
Journal of the American Society of Nephrology
, 28
(3)
pp. 963-970.
10.1681/ASN.2015091029.
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G
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Gale, DP;
Molyneux, K;
Wimbury, D;
Higgins, P;
Levine, AP;
Caplin, B;
Ferlin, A;
... Barratt, J; + view all
(2017)
Galactosylation of IgA1 Is Associated with Common Variation in C1GALT1.
J Am Soc Nephrol
, 28
(7)
pp. 2158-2166.
10.1681/ASN.2016091043.
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Gao, H;
Li, D;
Yang, P;
Zhao, L;
Wei, L;
Chen, Y;
Ruan, XZ;
(2017)
Suppression of CD36 attenuates adipogenesis with a reduction of P2X7 expression in 3T3-L1 cells.
Biochemical and Biophysical Research Communications
10.1016/j.bbrc.2017.07.077.
|
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Godfrey, C;
Desviat, LR;
Smedsrød, B;
Piétri-Rouxel, F;
Denti, MA;
Disterer, P;
Lorain, S;
... Arechavala-Gomeza, V; + view all
(2017)
Delivery is key: lessons learnt from developing splice-switching antisense therapies.
EMBO Molecular Medicine
, 9
(3)
pp. 281-394.
10.15252/emmm.201607199.
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González-Quiroz, M;
Camacho, A;
Faber, D;
Aragón, A;
Wesseling, C;
Glaser, J;
Le Blond, J;
... Caplin, B; + view all
(2017)
Rationale, description and baseline findings of a community-based prospective cohort study of kidney function amongst the young rural population of Northwest Nicaragua.
BMC Nephrol
, 18
, Article 16. 10.1186/s12882-016-0422-4.
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Gupta, S;
Connolly, J;
Pepper, RJ;
Walsh, SB;
Yaqoob, MM;
Kleta, R;
Ashman, N;
(2017)
Membranous nephropathy: a retrospective observational study of membranous nephropathy in north east and central London.
BMC Nephrology
, 18
, Article 201. 10.1186/s12882-017-0615-5.
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Gupta, S;
Köttgen, A;
Hoxha, E;
Brenchley, P;
Bockenhauer, D;
Stanescu, HC;
Kleta, R;
(2017)
Genetics of membranous nephropathy.
Nephrol Dial Transplant
10.1093/ndt/gfx296.
(In press).
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H
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Hadinnapola, C;
Bleda, M;
Haimel, M;
Screaton, N;
Swift, A;
Dorfmuller, P;
Preston, SD;
... Morrell, NW; + view all
(2017)
Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension.
Circulation
, 136
(21)
pp. 2022-2033.
10.1161/CIRCULATIONAHA.117.028351.
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Hayer, MK;
Edwards, NC;
Slinn, G;
Moody, WE;
Steeds, RP;
Ferro, CJ;
Price, AM;
... Townend, JN; + view all
(2017)
A randomized, multicenter, open-label, blinded end point trial comparing the effects of spironolactone to chlorthalidone on left ventricular mass in patients with early-stage chronic kidney disease: Rationale and design of the SPIRO-CKD trial.
American Heart Journal
, 191
(C)
pp. 37-46.
10.1016/j.ahj.2017.05.008.
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Hayes, W;
Boyle, S;
Carroll, A;
Bockenhauer, D;
Marks, SD;
(2017)
Erratum to: Hypomagnesemia and increased risk of new-onset diabetes mellitus after transplantation in pediatric renal transplant recipients.
Pediatric Nephrology
, 32
(5)
p. 903.
10.1007/s00467-017-3609-4.
|
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He, K;
Zhu, X;
Liu, Y;
Miao, C;
Wang, T;
Li, P;
Zhao, L;
... Gong, J; + view all
(2017)
Inhibition of NLRP3 inflammasome by thioredoxin-interacting protein in mouse Kupffer cells as a regulatory mechanism for non-alcoholic fatty liver disease development.
Oncotarget
, 8
(23)
pp. 37657-37672.
10.18632/oncotarget.17489.
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Horn, A;
Wright, J;
Bockenhauer, D;
Van't Hoff, W;
Eastwood, DM;
(2017)
The orthopaedic management of lower limb deformity in hypophosphataemic rickets.
Journal of Children's Orthopaedics
, 11
(4)
pp. 298-305.
10.1302/1863-2548.11.170003.
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Huang, J;
Zhao, L;
Yang, P;
Chen, Z;
Ruan, XZ;
Huang, A;
Tang, N;
(2017)
Fatty acid translocase promoted hepatitis B virus replication by upregulating the levels of hepatic cytosolic calcium.
Experimental Cell Research
, 358
(2)
pp. 360-368.
10.1016/j.yexcr.2017.07.012.
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Hutt, DF;
Fontana, M;
Burniston, M;
Quigley, AM;
Petrie, A;
Ross, JC;
Page, J;
... Gillmore, JD; + view all
(2017)
Prognostic utility of the Perugini grading of 99mTc-DPD scintigraphy in transthyretin (ATTR) amyloidosis and its relationship with skeletal muscle and soft tissue amyloid.
European Heart Journal - Cardiovascular Imaging
, 18
(12)
pp. 1344-1350.
10.1093/ehjci/jew325.
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I
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Issler, N;
Dufek, S;
Kleta, R;
Bockenhauer, D;
Smeulders, N;
Van't Hoff, W;
(2017)
Epidemiology of paediatric renal stone disease: a 22-year single centre experience in the UK.
BMC Nephrology
, 18
(1)
, Article 136. 10.1186/s12882-017-0505-x.
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J
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Jiang, X-S;
Chen, X-M;
Wan, J-M;
Gui, H-B;
Ruan, X-Z;
Du, X-G;
(2017)
Autophagy Protects against Palmitic Acid-Induced Apoptosis in Podocytes in vitro.
Scientific Reports
, 7
, Article 42764. 10.1038/srep42764.
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K
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Kesselheim, A;
Ashton, E;
Bockenhauer, D;
(2017)
Potential and pitfalls in the genetic diagnosis of kidney diseases.
Clinical Kidney Journal
, 10
(5)
pp. 581-585.
10.1093/ckj/sfx075.
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Khan, KN;
El-Asrag, ME;
Ku, CA;
Holder, GE;
McKibbin, M;
Arno, G;
Poulter, JA;
... for NIHR BioResource-Rare Diseases and UK Inherited Retinal Dise, .; + view all
(2017)
Specific Alleles of CLN7/MFSD8, a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy.
Investigative Ophthalmology & Visual Science
, 58
(7)
pp. 2906-2914.
10.1167/iovs.16-20608.
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Khasriya, R;
Barcella, W;
De Iorio, M;
Swamy, S;
Gill, K;
Kupelian, A;
Malone-Lee, J;
(2017)
Lower urinary tract symptoms that predict microscopic pyuria.
International Urogynecology Journal
10.1007/s00192-017-3472-7.
(In press).
|
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Khoo, B;
Boshier, PR;
Freethy, A;
Tharakan, G;
Saeed, S;
Hill, N;
Williams, EL;
... Tan, T; + view all
(2017)
Re-defining the stress cortisol response to surgery.
Clinical Endocrinology
, 87
(5)
pp. 451-458.
10.1111/cen.13439.
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Klootwijk, E;
Dufek, S;
Issler, N;
Bockenhauer, D;
Kleta, R;
(2017)
Pathophysiology, current treatments and future targets in hereditary forms of renal Fanconi syndrome.
Expert Opinion on Orphan Drugs
, 5
(1)
pp. 45-54.
10.1080/21678707.2017.1259560.
|
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Kokkinopoulos, I;
Wong, MM;
Potter, CMF;
Xie, Y;
Yu, B;
Warren, DT;
Nowak, WN;
... Xu, Q; + view all
(2017)
Adventitial SCA-1(+) Progenitor Cell Gene Sequencing Reveals the Mechanisms of Cell Migration in Response to Hyperlipidemia.
Stem Cell Reports
, 9
(2)
pp. 681-696.
10.1016/j.stemcr.2017.06.011.
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L
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Le Quesne Stabej, P;
James, C;
Ocaka, L;
Tekman, M;
Grunewald, S;
Clement, E;
Stanescu, HC;
... Bitner-Glindzicz, M; + view all
(2017)
An example of the utility of genomic analysis for fast and accurate clinical diagnosis of complex rare phenotypes.
Orphanet Journal of Rare Diseases
, 12
, Article 24. 10.1186/s13023-017-0582-8.
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Levin, A;
Tonelli, M;
Bonventre, J;
Coresh, J;
Donner, J-A;
Fogo, AB;
Fox, CS;
... ISN Global Kidney Health Summit participants; + view all
(2017)
Global kidney health 2017 and beyond: a roadmap for closing gaps in care, research, and policy.
The Lancet
, 390
(10105)
pp. 1888-1917.
10.1016/S0140-6736(17)30788-2.
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Li, F;
Ruan, X;
Min, L;
(2017)
Targeting both sides of the GDF15-GFRAL-RET receptor complex: A new approach to achieve body weight homeostasis.
Genes & Diseases
, 4
(4)
pp. 183-184.
10.1016/j.gendis.2017.11.004.
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Liou, N;
Currie, J;
James, C;
Malone-Lee, JG;
David, AL;
(2017)
Urothelial cells may indicate underlying bacteriuria in pregnancy at term: a comparative study.
BMC Pregnancy and Childbirth
, 17
, Article 414. 10.1186/s12884-017-1606-z.
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Luyckx, VA;
Tuttle, KR;
Garcia-Garcia, G;
Gharbi, MB;
Heerspink, HJL;
Johnson, DW;
Liu, Z-H;
... White, SL; + view all
(2017)
Reducing major risk factors for chronic kidney disease.
[Review].
Kidney International Supplements
, 7
(2)
pp. 71-87.
10.1016/j.kisu.2017.07.003.
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M
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Mafham, MM;
Staplin, N;
Emberson, J;
Haynes, R;
Herrington, W;
Reith, C;
Wanner, C;
... SHARP Collaborative Group, .; + view all
(2017)
Prognostic utility of estimated albumin excretion rate in chronic kidney disease: results from the Study of Heart and Renal Protection.
Nephrology Dialysis Transplantation
10.1093/ndt/gfw396.
(In press).
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Mangione, PP;
Mazza, G;
Gilbertson, JA;
Rendell, NB;
Canetti, D;
Giorgetti, S;
Frenguelli, L;
... Bellotti, V; + view all
(2017)
Increasing the accuracy of proteomic typing by decellularisation of amyloid tissue biopsies.
Journal of Proteomics
, 165
pp. 113-118.
10.1016/j.jprot.2017.06.016.
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Martinez-Naharro, A;
Treibel, TA;
Abdel-Gadir, A;
Bulluck, H;
Zumbo, G;
Knight, DS;
Kotecha, T;
... Fontana, M; + view all
(2017)
Magnetic Resonance in Transthyretin Cardiac Amyloidosis.
Journal of the American College of Cardiology
, 70
(4)
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