Year |
Citation |
Score |
2023 |
Manzano A, Weging S, Bezdan D, Borg J, Cahill T, Carnero-Diaz E, Cope H, Deane CS, Etheridge T, Giacomello S, Hardiman G, Leys N, Madrigal P, Mastroleo F, Medina FJ, ... ... Walsh SB, et al. Enhancing European capabilities for application of multi-omics studies in biology and biomedicine space research. Iscience. 26: 107289. PMID 37636054 DOI: 10.1016/j.isci.2023.107289 |
0.707 |
|
2023 |
Olde Engberink RHG, van Oosten PJ, Weber T, Tabury K, Baatout S, Siew K, Walsh SB, Valenti G, Chouker A, Boutouyrie P, Heer M, Jordan J, Goswami N. Author Correction: The kidney, volume homeostasis and osmoregulation in space: current perspective and knowledge gaps. Npj Microgravity. 9: 60. PMID 37528092 DOI: 10.1038/s41526-023-00307-x |
0.731 |
|
2023 |
D'Ambrosio V, Wan ER, Hawkins-van der Cingel G, Siew K, Hawthorne M, Crawford C, Walsh SB. Hyperoxaluric acute kidney injury and frontotemporal dementia. Lancet (London, England). 401: 1530. PMID 37149308 DOI: 10.1016/S0140-6736(22)02601-0 |
0.725 |
|
2023 |
Wagner CA, Unwin R, Lopez-Garcia SC, Kleta R, Bockenhauer D, Walsh S. The pathophysiology of distal renal tubular acidosis. Nature Reviews. Nephrology. PMID 37016093 DOI: 10.1038/s41581-023-00699-9 |
0.547 |
|
2022 |
Wan ER, Iancu D, Ashton E, Siew K, Mohidin B, Sung CC, Nagano C, Bockenhauer D, Lin SH, Nozu K, Walsh SB. Machine Learning to Identify Genetic Salt-Losing Tubulopathies in Hypokalemic Patients. Kidney International Reports. 8: 556-565. PMID 36938092 DOI: 10.1016/j.ekir.2022.12.008 |
0.721 |
|
2021 |
Wan ER, Siew K, Heptinstall L, Walsh SB. Fumaric acid ester-induced renal Fanconi syndrome: evidence of mitochondrial toxicity. Clinical Kidney Journal. 14: 2085-2089. PMID 35261762 DOI: 10.1093/ckj/sfaa270 |
0.758 |
|
2021 |
Patel V, Klootwijk E, Whiting G, Bockenhauer D, Siew K, Walsh S, Bleich M, Himmerkus N, Jaureguiberry G, Issler N, Godovac-Zimmermann J, Kleta R, Wheeler J. Quantification of FAM20A in human milk and identification of calcium metabolism proteins. Physiological Reports. 9: e15150. PMID 34957696 DOI: 10.14814/phy2.15150 |
0.731 |
|
2021 |
Rezk T, Salota R, Gan JJ, Lachmann HJ, Fontana M, Siew K, Martinez-Naharro A, Guillotte C, Bass P, Sachchithanantham S, Mahmood S, Petrie A, Whelan CJ, Pinney JH, Dockrell M, ... ... Walsh SB, et al. Urinary retinol binding protein predicts renal outcome in systemic immunoglobulin light-chain (AL) amyloidosis. British Journal of Haematology. PMID 34374069 DOI: 10.1111/bjh.17706 |
0.743 |
|
2021 |
Wan ER, Unwin R, Walsh SB. COVID-19 2020: The Experience of a London Teaching Hospital's Nephrology Service. Kidney & Blood Pressure Research. 1-5. PMID 33823516 DOI: 10.1159/000515194 |
0.354 |
|
2020 |
Wan ER, Woolfson RG, Greenwood R, Walsh SB. Transient Renal Tubular Syndromes Associated With Acute COVID-19 Disease. Kidney International Reports. PMID 32838078 DOI: 10.1016/J.Ekir.2020.06.037 |
0.424 |
|
2020 |
Levey AS, Eckardt KU, Dorman NM, Christiansen SL, Hoorn EJ, Ingelfinger JR, Inker LA, Levin A, Mehrotra R, Palevsky PM, Perazella MA, Tong A, Allison SJ, Bockenhauer D, Briggs JP, ... ... Walsh SB, et al. Nomenclature for kidney function and disease: report of a Kidney Disease: Improving Global Outcomes (KDIGO) Consensus Conference. Kidney International. PMID 32409237 DOI: 10.1016/J.Kint.2020.02.010 |
0.406 |
|
2020 |
Bertocchio JP, Genetet S, Da Costa L, Walsh SB, Knebelmann B, Galimand J, Bessenay L, Guitton C, De Lafaille R, Vargas-Poussou R, Eladari D, Mouro-Chanteloup I. Red Blood Cell AE1/Band 3 Transports in Dominant Distal Renal Tubular Acidosis Patients. Kidney International Reports. 5: 348-357. PMID 32154456 DOI: 10.1016/J.Ekir.2019.12.020 |
0.382 |
|
2020 |
Martin JL, Davis-Cochrane AGJ, Temelcos C, Unwin RJ, Walsh SB, Tam C, Goodman D. A rare case of genetically linked primary distal renal tubular acidosis and Southeast Asian ovalocytosis. Internal Medicine Journal. 50: 383-385. PMID 32141208 DOI: 10.1111/Imj.14752 |
0.575 |
|
2020 |
Govers LP, Toka HR, Hariri A, Walsh SB, Bockenhauer D. Mitochondrial DNA mutations in renal disease: an overview. Pediatric Nephrology (Berlin, Germany). PMID 31925537 DOI: 10.1007/S00467-019-04404-6 |
0.416 |
|
2019 |
Hureaux M, Ashton E, Dahan K, Houillier P, Blanchard A, Cormier C, Koumakis E, Iancu D, Belge H, Hilbert P, Rotthier A, Del Favero J, Schaefer F, Kleta R, Bockenhauer D, ... ... Walsh SB, et al. High-throughput sequencing contributes to the diagnosis of tubulopathies and familial hypercalcemia hypocalciuria in adults. Kidney International. PMID 31672324 DOI: 10.1016/J.Kint.2019.08.027 |
0.317 |
|
2019 |
Wan ER, Cross J, Sofat R, Walsh SB. 24-hour vs Spot Urinary Sodium and Potassium Measurements in Adult Hypertensive patients; A Cohort Validation Study. American Journal of Hypertension. PMID 31247068 DOI: 10.1093/Ajh/Hpz104 |
0.332 |
|
2019 |
Lopez-Garcia SC, Emma F, Walsh SB, Fila M, Hooman N, Zaniew M, Bertholet-Thomas A, Colussi G, Burgmaier K, Levtchenko E, Sharma J, Singhal J, Soliman NA, Ariceta G, Basu B, et al. Treatment and long-term outcome in primary distal renal tubular acidosis. Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. PMID 30773598 DOI: 10.1093/Ndt/Gfy409 |
0.352 |
|
2019 |
Oliveira B, Unwin R, Walsh SB. Inherited proximal tubular disorders and nephrolithiasis. Urolithiasis. 47: 35-42. PMID 30673801 DOI: 10.1007/S00240-018-01103-Z |
0.508 |
|
2019 |
Mumford E, Unwin RJ, Walsh SB. Liquorice, Liddle, Bartter or Gitelman-how to differentiate? Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. 34: 38-39. PMID 29982819 DOI: 10.1093/Ndt/Gfy199 |
0.507 |
|
2019 |
Wan ER, Walsh SB. Sp002Clinical And Biochemical Characteristics Of Hypokalaemic Patients: Predictors Of A Genetic Diagnosis Of Gitelman Or Bartter Syndrome Nephrology Dialysis Transplantation. 34. DOI: 10.1093/Ndt/Gfz103.Sp002 |
0.308 |
|
2018 |
Stewart D, Iancu D, Ashton E, Courtney AE, Connor A, Walsh SB. Transplantation of a Gitelman Syndrome Kidney Ameliorates Hypertension: A Case Report. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. PMID 30201548 DOI: 10.1053/J.Ajkd.2018.06.030 |
0.389 |
|
2018 |
Garcia SCL, Emma F, Walsh S, Fila M, Hooman N, Marcin Z, Bertholet-thomas A, Colussi G, Ebner K, Levtchenko E, Sharma J, Singhal J, Soliman NA, Ariceta C, Basu B, et al. Long-Term Outcome and Treatment Practices in Distal Renal Tubular Acidosis Pediatric Nephrology. 33: 1817-1817. PMID 30194615 DOI: 10.1007/S00467-018-4028-X |
0.34 |
|
2018 |
Oliveira B, Cunningham J, Walsh SB. Magnesium Balance in Chronic and End-Stage Kidney Disease. Advances in Chronic Kidney Disease. 25: 291-295. PMID 29793669 DOI: 10.1053/J.Ackd.2018.01.004 |
0.342 |
|
2018 |
Reichold M, Klootwijk ED, Reinders J, Otto EA, Milani M, Broeker C, Laing C, Wiesner J, Devi S, Zhou W, Schmitt R, Tegtmeier I, Sterner C, Doellerer H, Renner K, ... ... Walsh SB, et al. Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure. Journal of the American Society of Nephrology : Jasn. PMID 29654216 DOI: 10.1681/Asn.2017111179 |
0.62 |
|
2018 |
Ashton EJ, Legrand A, Benoit V, Roncelin I, Venisse A, Zennaro MC, Jeunemaitre X, Iancu D, Van't Hoff WG, Walsh SB, Godefroid N, Rotthier A, Del Favero J, Devuyst O, Schaefer F, et al. Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies. Kidney International. PMID 29398133 DOI: 10.1016/J.Kint.2017.10.016 |
0.393 |
|
2017 |
Enerbäck S, Nilsson D, Edwards N, Heglind M, Alkanderi S, Ashton E, Deeb A, Kokash FEB, Bakhsh ARA, Van't Hoff W, Walsh SB, D'Arco F, Daryadel A, Bourgeois S, Wagner CA, et al. Acidosis and Deafness in Patients with Recessive Mutations in FOXI1. Journal of the American Society of Nephrology : Jasn. PMID 29242249 DOI: 10.1681/Asn.2017080840 |
0.384 |
|
2017 |
Walsh SB, Unwin R, Kleta R, Van't Hoff W, Bass P, Hussain K, Ellard S, Bockenhauer D. Fainting Fanconi syndrome clarified by proxy: a case report. Bmc Nephrology. 18: 230. PMID 28693455 DOI: 10.1186/S12882-017-0649-8 |
0.514 |
|
2017 |
Gupta S, Connolly J, Pepper RJ, Walsh SB, Yaqoob MM, Kleta R, Ashman N. Membranous nephropathy: a retrospective observational study of membranous nephropathy in north east and central London. Bmc Nephrology. 18: 201. PMID 28637442 DOI: 10.1186/S12882-017-0615-5 |
0.333 |
|
2017 |
Seys E, Andrini O, Keck M, Mansour-Hendili L, Courand PY, Simian C, Deschenes G, Kwon T, Bertholet-Thomas A, Bobrie G, Borde JS, Bourdat-Michel G, Decramer S, Cailliez M, Krug P, ... ... Walsh SB, et al. Clinical and Genetic Spectrum of Bartter Syndrome Type 3. Journal of the American Society of Nephrology : Jasn. PMID 28381550 DOI: 10.1681/Asn.2016101057 |
0.382 |
|
2017 |
Viering DHHM, de Baaij JHF, Walsh SB, Kleta R, Bockenhauer D. Genetic causes of hypomagnesemia, a clinical overview. Pediatric Nephrology (Berlin, Germany). 32: 1123-1135. PMID 27234911 DOI: 10.1007/S00467-016-3416-3 |
0.365 |
|
2016 |
Oliveira B, Kleta R, Bockenhauer D, Walsh SB. Genetic, pathophysiological, and clinical aspects of nephrocalcinosis. American Journal of Physiology. Renal Physiology. 311: F1243-F1252. PMID 27605580 DOI: 10.1152/Ajprenal.00211.2016 |
0.384 |
|
2016 |
Shavit L, Chen L, Ahmed F, Ferraro PM, Moochhala S, Walsh SB, Unwin R. Selective screening for distal renal tubular acidosis in recurrent kidney stone formers: initial experience and comparison of the simultaneous furosemide and fludrocortisone test with the short ammonium chloride test. Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. PMID 26961999 DOI: 10.1093/Ndt/Gfv423 |
0.505 |
|
2016 |
Roksnoer LC, Heijnen BF, Nakano D, Peti-Peterdi J, Walsh SB, Garrelds IM, van Gool JM, Zietse R, Struijker-Boudier HA, Hoorn EJ, Danser AH. On the Origin of Urinary Renin: A Translational Approach. Hypertension. 67: 927-33. PMID 26928805 DOI: 10.1161/Hypertensionaha.115.07012 |
0.358 |
|
2016 |
Evans RD, Laing CM, Ciurtin C, Walsh SB. Tubulointerstitial nephritis in primary Sjögren syndrome: clinical manifestations and response to treatment. Bmc Musculoskeletal Disorders. 17: 2. PMID 26728714 DOI: 10.1186/S12891-015-0858-X |
0.356 |
|
2015 |
Walsh SB, Zdebik AA, Unwin RJ. Magnesium: The Disregarded Cation. Mayo Clinic Proceedings. 90: 993-5. PMID 26250724 DOI: 10.1016/j.mayocp.2015.06.011 |
0.387 |
|
2015 |
Evans R, Zdebik A, Ciurtin C, Walsh SB. Renal involvement in primary Sjögren's syndrome. Rheumatology (Oxford, England). PMID 26070939 DOI: 10.1093/Rheumatology/Kev223 |
0.416 |
|
2015 |
Shavit L, Ferraro PM, Johri N, Robertson W, Walsh SB, Moochhala S, Unwin R. Effect of being overweight on urinary metabolic risk factors for kidney stone formation. Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. 30: 607-13. PMID 25362001 DOI: 10.1093/Ndt/Gfu350 |
0.449 |
|
2014 |
Nadarajah L, Khosravi M, Dumitriu S, Klootwijk E, Kleta R, Yaqoob MM, Walsh SB. A novel claudin-16 mutation, severe bone disease, and nephrocalcinosis. Lancet (London, England). 383: 98. PMID 24388313 DOI: 10.1016/S0140-6736(13)62673-2 |
0.391 |
|
2012 |
Jaureguiberry G, De la Dure-Molla M, Parry D, Quentric M, Himmerkus N, Koike T, Poulter J, Klootwijk E, Robinette SL, Howie AJ, Patel V, Figueres ML, Stanescu HC, Issler N, Nicholson JK, ... ... Walsh SB, et al. Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations. Nephron. Physiology. 122: 1-6. PMID 23434854 DOI: 10.1159/000349989 |
0.564 |
|
2012 |
Walsh SB, Unwin RJ. Renal tubular disorders. Clinical Medicine (London, England). 12: 476-9. PMID 23101152 DOI: 10.7861/Clinmedicine.12-5-476 |
0.582 |
|
2012 |
Khositseth S, Bruce LJ, Walsh SB, Bawazir WM, Ogle GD, Unwin RJ, Thong MK, Sinha R, Choo KE, Chartapisak W, Kingwatanakul P, Sumboonnanonda A, Vasuvattakul S, Yenchitsomanus P, wrong O. Tropical distal renal tubular acidosis: Clinical and epidemiological studies in 78 patients Qjm. 105: 861-877. PMID 22919024 DOI: 10.1093/Qjmed/Hcs139 |
0.343 |
|
2012 |
Hoorn EJ, Walsh SB, McCormick JA, Zietse R, Unwin RJ, Ellison DH. Pathogenesis of calcineurin inhibitor-induced hypertension. Journal of Nephrology. 25: 269-75. PMID 22573529 DOI: 10.5301/Jn.5000174 |
0.539 |
|
2012 |
Hoorn EJ, Walsh SB, Unwin RJ, Ellison DH. Hypertension after kidney transplantation: calcineurin inhibitors increase salt-sensitivity. Journal of Hypertension. 30: 832-3; author reply . PMID 22418915 DOI: 10.1097/Hjh.0B013E32835165E4 |
0.52 |
|
2011 |
Hoorn EJ, Walsh SB, McCormick JA, Fürstenberg A, Yang CL, Roeschel T, Paliege A, Howie AJ, Conley J, Bachmann S, Unwin RJ, Ellison DH. The calcineurin inhibitor tacrolimus activates the renal sodium chloride cotransporter to cause hypertension. Nature Medicine. 17: 1304-9. PMID 21963515 DOI: 10.1038/Nm.2497 |
0.569 |
|
2011 |
Walsh SB, Unwin E, Vargas-Poussou R, Houillier P, Unwin R. Does hypokalaemia cause nephropathy? An observational study of renal function in patients with Bartter or Gitelman syndrome. Qjm : Monthly Journal of the Association of Physicians. 104: 939-44. PMID 21705784 DOI: 10.1093/qjmed/hcr095 |
0.563 |
|
2010 |
Walsh SB, Unwin RJ. Clinical hypokalemia and hyperkalemia at the bedside. Journal of Nephrology. 23: S105-11. PMID 21170866 |
0.433 |
|
2009 |
Walsh S, Borgese F, Gabillat N, Guizouarn H. Southeast Asian AE1 associated renal tubular acidosis: cation leak is a class effect. Biochemical and Biophysical Research Communications. 382: 668-672. PMID 19289107 DOI: 10.1016/J.Bbrc.2009.03.062 |
0.332 |
|
2008 |
Walsh S, Borgese F, Gabillat N, Unwin R, Guizouarn H. Cation transport activity of anion exchanger 1 mutations found in inherited distal renal tubular acidosis. American Journal of Physiology. Renal Physiology. 295: F343-50. PMID 18524859 DOI: 10.1152/ajprenal.00587.2007 |
0.477 |
|
2007 |
Walsh SB, Shirley DG, Wrong OM, Unwin RJ. Urinary acidification assessed by simultaneous furosemide and fludrocortisone treatment: an alternative to ammonium chloride. Kidney International. 71: 1310-6. PMID 17410104 DOI: 10.1038/SJ.KI.5002220 |
0.472 |
|
2007 |
Walsh S, Turner CM, Toye A, Wagner C, Jaeger P, Laing C, Unwin R. Immunohistochemical comparison of a case of inherited distal renal tubular acidosis (with a unique AE1 mutation) with an acquired case secondary to autoimmune disease. Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. 22: 807-12. PMID 17205967 DOI: 10.1093/Ndt/Gfl662 |
0.564 |
|
2007 |
Shirley DG, Walsh SB, Wrong OM, Unwin RJ. Response to ‘Simultaneous fludrocortisone and furosemide for assessment of urinary acidification’ Kidney International. 72: 1164-1164. DOI: 10.1038/Sj.Ki.5002535 |
0.475 |
|
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