Browse by UCL people
Group by: Type | Date
Number of items: 10.
Article
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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Dufek, S;
Cheshire, C;
Levine, AP;
Trompeter, RS;
Issler, N;
Stubbs, M;
Mozere, M;
... Bockenhauer, D; + view all
(2019)
Genetic identification of two novel loci associated with steroid-sensitive nephrotic syndrome.
Journal of the American Society of Nephrology
, 30
(8)
pp. 1375-1384.
10.1681/ASN.2018101054.
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Dufek, S;
Holtta, T;
Trautmann, A;
Ylinen, E;
Alpay, H;
Ariceta, G;
Aufricht, C;
... Shroff, R; + view all
(2019)
Management of children with congenital nephrotic syndrome: challenging treatment paradigms.
Nephrology Dialysis Transplantation
, 34
(8)
pp. 1369-1377.
10.1093/ndt/gfy165.
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Dufek, S;
Khalil, A;
Mamode, N;
Sebire, NJ;
Marks, SD;
(2017)
Plasma-cell-rich infiltrates in paediatric renal transplant biopsies are associated with increased risk of renal allograft failure.
Pediatric Nephrology
, 32
(4)
pp. 679-684.
10.1007/s00467-016-3524-0.
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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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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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Lopez-Garcia, SC;
Emma, F;
Walsh, SB;
Fila, M;
Hooman, N;
Zaniew, M;
Bertholet-Thomas, A;
... Bockenhauer, D; + view all
(2019)
Treatment and long-term outcome in primary distal renal tubular acidosis.
Nephrology Dialysis Transplantation
, 34
(6)
pp. 981-991.
10.1093/ndt/gfy409.
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Webb, H;
Jaureguiberry, G;
Dufek, S;
Tullus, K;
Bockenhauer, D;
(2016)
Cyclophosphamide and rituximab in frequently relapsing/steroid-dependent nephrotic syndrome.
Pediatric Nephrology
, 31
(4)
pp. 589-594.
10.1007/s00467-015-3245-9.
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Xie, J;
Liu, L;
Mladkova, N;
Li, Y;
Ren, H;
Wang, W;
Cui, Z;
... Kiryluk, K; + view all
(2020)
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis.
Nature Communications
, 11
(1)
, Article 1600. 10.1038/s41467-020-15383-w.
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Thesis
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Dufek-Kamperis, Stephanie;
(2020)
Genome wide association study in steroid sensitive nephrotic syndrome.
Doctoral thesis (Ph.D), UCL (University College London).
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