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Group by: Author | Type
Jump to: A | B | C | D | L | M | Q | R | S | V | W | Y
Number of items: 30.

A

Adalat, S; Bockenhauer, D; Ledermann, SE; Hennekam, RC; Woolf, AS; (2010) Renal malformations associated with mutations of developmental genes: messages from the clinic. PEDIATR NEPHROL , 25 (11) 2247 - 2255. 10.1007/s00467-010-1578-y.

Adalat, S; Papakrivopoulou, J; Woolf, AS; Bockenhauer, D; (2010) HNF1B and FXYD2 Co-Expression Helps Explain Renal Magnesium Wasting in the Renal Cysts and Diabetes Syndrome. PEDIATR NEPHROL , 25 (9) 1977 - 1977.

B

Bockenhauer, D; Carpentier, E; Rochdi, D; van't Hoff, W; Breton, B; Bernier, V; ... Bichet, DG; + view all (2010) Vasopressin type 2 receptor V88M mutation: molecular basis of partial and complete nephrogenic diabetes insipidus. Nephron Physiol , 114 (1) p1 - 10. 10.1159/000245059.

Bockenhauer, D; Reichold, M; Zdebik, A; Lieberer, E; Schmidt, K; Rapedius, M; ... Kleta, R; + view all (2010) Altered Renal Tubular Ultrastructure and Electrophysiology Caused by KCNJ10 Mutations in EAST Syndrome. PEDIATR NEPHROL , 25 (9) 1980 - 1980.

Bockenhauer, D; van't Hoff, W; Dattani, M; Lehnhardt, A; Subtirelu, M; Hildebrandt, F; Bichet, DG; (2010) Secondary Nephrogenic Diabetes Insipidus as a Complication of Inherited Renal Diseases. NEPHRON PHYSIOL , 116 (4) P23 - P29. 10.1159/000320117.

Bockenhauer, D; van't Hoff, W; Lehnhardt, A; Subtirelu, M; Hildebrandt, F; Bichet, DG; (2010) Secondary Inherited NDI: A Diagnostic Pitfall. PEDIATR NEPHROL , 25 (9) 1913 - 1914.

Borzych, D; Rees, L; Ha, IS; Chua, A; Valles, PG; Lipka, M; ... IPPN,; + view all (2010) The bone and mineral disorder of children undergoing chronic peritoneal dialysis. KIDNEY INTERNATIONAL , 78 (12) 1295 - 1304. 10.1038/ki.2010.316.

C

Chan, SK; Riley, PR; Price, KL; McElduff, F; Winyard, PJ; Welham, SJM; ... Long, DA; + view all (2010) Corticosteroid-induced kidney dysmorphogenesis is associated with deregulated expression of known cystogenic molecules, as well as indian hedgehog. AM J PHYSIOL-RENAL , 298 (2) F346 - F356. 10.1152/ajprenal.00574.2009.

Cordell, HJ; Darlay, R; Charoen, P; Stewart, A; Gullett, AM; Lambert, HJ; ... UK VUR Study Grp,; + view all (2010) Whole-Genome Linkage and Association Scan in Primary, Nonsyndromic Vesicoureteric Reflux. J AM SOC NEPHROL , 21 (1) 113 - 123. 10.1681/ASN.2009060624.

D

Daly, SB; Urquhart, JE; Hilton, E; McKenzie, EA; Kammerer, RA; Lewis, M; ... Newman, WG; + view all (2010) Mutations in HPSE2 Cause Urofacial Syndrome. AM J HUM GENET , 86 (6) 963 - 969. 10.1016/j.ajhg.2010.05.006.

L

Loubière, LS; Vasilopoulou, E; Bulmer, JN; Taylor, PM; Stieger, B; Verrey, F; ... Chan, SY; + view all (2010) Expression of thyroid hormone transporters in the human placenta and changes associated with intrauterine growth restriction. Placenta , 31 (4) 295 - 304. 10.1016/j.placenta.2010.01.013.

M

Matejas, V; Hinkes, B; Alkandari, F; Al-Gazali, L; Annexstad, E; Aytac, MB; ... Zenker, M; + view all (2010) Mutations in the Human Laminin beta 2 (LAMB2) Gene and the Associated Phenotypic Spectrum. HUM MUTAT , 31 (9) 992 - 1002. 10.1002/humu.21304.

Mekahli, D; Shaw, V; Ledermann, SE; Rees, L; (2010) Long-Term Outcome of Infants with Severe Chronic Kidney Disease. CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY , 5 (1) 10 - 17. 10.2215/CJN.05600809.

Mekahli, D; Woolf, AS; Bockenhauer, D; (2010) Similar renal outcomes in children with ADPKD diagnosed by screening or presenting with symptoms. PEDIATR NEPHROL , 25 (11) 2275 - 2282. 10.1007/s00467-010-1617-8.

Montini, G; Bockenhauer, D; Rees, L; Sebire, N; Tullus, K; van't Hoff, W; ... Marks, S; + view all (2010) A 20-Year Single Centre Experience of Congential and Infantile Nephrotic Syndrome. PEDIATR NEPHROL , 25 (9) 1878 - 1878.

Morgenstern, DA; Hasan, F; Gibson, S; Winyard, P; Sebire, NJ; Anderson, J; (2010) PAX5 Expression in Nonhematopoietic Tissues. AM J CLIN PATHOL , 133 (3) 407 - 415. 10.1309/AJCPZPQNOLUGKMME.

Morgenstern, DA; Hasan, F; Gibson, S; Winyard, P; Sebire, NJ; Anderson, J; (2010) PAX5 expression in nonhematopoietic tissues. Reappraisal of previous studies. Am J Clin Pathol , 133 (3) 407 - 415. 10.1309/AJCPZPQN0LUGKMME.

Q

Quinlan, C; Cantwell, M; Rees, L; (2010) Eosinophilic peritonitis in children on chronic peritoneal dialysis. PEDIATRIC NEPHROLOGY , 25 (3) 517 - 522. 10.1007/s00467-009-1366-8.

R

Rees, L; Brandt, ML; (2010) Tube feeding in children with chronic kidney disease: technical and practical issues. In: PEDIATRIC NEPHROLOGY. (pp. 699 - 704).

Rees, L; Shroff, RC; (2010) Phosphate binders in CKD: chalking out the differences. PEDIATR NEPHROL , 25 (3) 385 - 394. 10.1007/s00467-009-1329-0.

Reichold, M; Zdebik, AA; Lieberer, E; Rapedius, M; Schmidt, K; Bandulik, S; ... Warth, R; + view all (2010) KCNJ10 gene mutations causing EAST syndrome (epilepsy, ataxia, sensorineural deafness, and tubulopathy) disrupt channel function. P NATL ACAD SCI USA , 107 (32) 14490 - 14495. 10.1073/pnas.1003072107.

S

Schoeb, DS; Chernin, G; Heeringa, SF; Matejas, V; Held, S; Vega-Warner, V; ... GPN Study Grp,; + view all (2010) Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS). NEPHROL DIAL TRANSPL , 25 (9) 2970 - 2976. 10.1093/ndt/gfq088.

Shroff, R; Knott, C; Rees, L; (2010) The virtues of vitamin D-but how much is too much? PEDIATRIC NEPHROLOGY , 25 (9) 1607 - 1620. 10.1007/s00467-010-1499-9.

Shroff, RC; Gullett, A; Hiorns, M; Shanahan, C; Rees, L; (2010) Accelerated Progression of Vascular Calcification in Paediatric CKD and Dialysis Patients Is Associated with Baseline Vessel Changes. PEDIATR NEPHROL , 25 (9) 1906 - 1906.

Shroff, RC; McNair, R; Skepper, JN; Figg, N; Schurgers, LJ; Deanfield, J; ... Shanahan, CM; + view all (2010) Chronic Mineral Dysregulation Promotes Vascular Smooth Muscle Cell Adaptation and Extracellular Matrix Calcification. J AM SOC NEPHROL , 21 (1) 103 - 112. 10.1681/ASN.2009060640.

V

Vasilopoulou, E; Loubière, LS; Martín-Santos, A; McCabe, CJ; Franklyn, JA; Kilby, MD; Chan, SY; (2010) Differential triiodothyronine responsiveness and transport by human cytotrophoblasts from normal and growth-restricted pregnancies. J Clin Endocrinol Metab , 95 (10) 4762 - 4770. 10.1210/jc.2010-0354.

W

Waters, AM; Bockenhauer, D; Tullus, K; Shroff, R; Marks, SD; Rees, L; ... Sebire, N; + view all (2010) Successful renal transplantation in factor H autoantibody associated HUS with CFHR1 and 3 deficiency and CFH variant G2850T: Case report. American Journal of Transplantation , 10 (1) 168 - 172. 10.1111/j.1600-6143.2009.02870.x.

Waters, AM; Pappworth, I; Marchbank, K; Bockenhauer, D; Tullus, K; Pickering, MC; ... Rees, L; + view all (2010) Successful Renal Transplantation in Factor H Autoantibody Associated HUS with CFHR1 and 3 Deficiency and CFH Variant G2850T. AM J TRANSPLANT , 10 (1) 168 - 172. 10.1111/j.1600-6143.2009.02870.x.

Winyard, P; (2010) FETAL HYDRONEPHROSIS - SHOULD WE DO A POST NATAL WORK UP OR NOT? CHILD CARE HEALTH AND DEVELOPMENT , 36 25 - 25.

Y

Yates, LL; Papakrivopoulou, J; Long, DA; Goggolidou, P; Connolly, JO; Woolf, AS; Dean, CH; (2010) The planar cell polarity gene Vangl2 is required for mammalian kidney-branching morphogenesis and glomerular maturation. HUM MOL GENET , 19 (23) 4663 - 4676. 10.1093/hmg/ddq397.

This list was generated on Sun Apr 20 11:35:11 2014 BST.