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

A

Adalat, S and Bockenhauer, D and Ledermann, SE and Hennekam, RC and 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 and Papakrivopoulou, J and Woolf, AS and 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.

Adalat, S and Sebire, NJ and Marks, SD (2010) The Integral Role of Renal Allograft Biopsies. PEDIATR NEPHROL , 25 (9) 1810 - 1810.

Adalat, S and Taylor, J and Booth, C and McCullough, M and Waller, S and Rigden, S and Sinha, M and Kozicll, A (2010) Efficacy of Rituximab in Childhood Nephrotic Syndrome. PEDIATR NEPHROL , 25 (9) 1795 - 1795.

B

Bockenhauer, D and Carpentier, E and Rochdi, D and van't Hoff, W and Breton, B and Bernier, V and Bouvier, M and Bichet, DG (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 and Reichold, M and Zdebik, A and Lieberer, E and Schmidt, K and Rapedius, M and Bandulik, S and Sterner, C and Tegtmeier, I and Baukrowitz, T and Hulton, SA and Ben-Zeev, B and Howie, AJ and Warth, R and Kleta, R (2010) Altered Renal Tubular Ultrastructure and Electrophysiology Caused by KCNJ10 Mutations in EAST Syndrome. PEDIATR NEPHROL , 25 (9) 1980 - 1980.

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

Borzych, D and Rees, L and Ha, IS and Chua, A and Valles, PG and Lipka, M and Zambrano, P and Ahlenstiel, T and Bakkaloglu, SA and Spizzirri, AP and Lopez, L and Ozaltin, F and Printza, N and Hari, P and Klaus, G and Bak, M and Vogel, A and Ariceta, G and Yap, HK and Warady, BA and Schaefer, F and IPPN, (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 and Riley, PR and Price, KL and McElduff, F and Winyard, PJ and Welham, SJM and Woolf, AS and Long, DA (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 and Darlay, R and Charoen, P and Stewart, A and Gullett, AM and Lambert, HJ and Malcolm, S and Feather, SA and Goodship, THJ and Woolf, AS and Kenda, RB and Goodship, JA and UK VUR Study Grp, (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 and Urquhart, JE and Hilton, E and McKenzie, EA and Kammerer, RA and Lewis, M and Kerr, B and Stuart, H and Donnai, D and Long, DA and Burgu, B and Aydogdu, O and Derbent, M and Garcia-Minaur, S and Reardon, W and Gener, B and Shalev, S and Smith, R and Woolf, AS and Black, GC and Newman, WG (2010) Mutations in HPSE2 Cause Urofacial Syndrome. AM J HUM GENET , 86 (6) 963 - 969. 10.1016/j.ajhg.2010.05.006.

L

Lewis, MA and Shaw, J and Sinha, MD and Adalat, S and Hussain, F and Castledine, C and van Schalkwyk, D and Inward, C (2010) UK Renal Registry 12th Annual Report (December 2009): Chapter 14 Demography of the UK Paediatric Renal Replacement Therapy population in 2008. NEPHRON CLIN PRACT , 115 C279 - C288. 10.1159/000301237.

M

Matejas, V and Hinkes, B and Alkandari, F and Al-Gazali, L and Annexstad, E and Aytac, MB and Barrow, M and Blahova, K and Bockenhauer, D and Cheong, HI and Maruniak-Chudek, I and Cochat, P and Dotsch, J and Gajjar, P and Hennekam, RC and Janssen, F and Kagan, M and Kariminejad, A and Kemper, MJ and Koenig, J and Kogan, J and Kroes, HY and Kuwertz-Broking, E and Lewanda, AF and Medeira, A and Muscheites, J and Niaudet, P and Pierson, M and Saggar, A and Seaver, L and Suri, M and Tsygin, A and Wuhl, E and Zurowska, A and Uebe, S and Hildebrandt, F and Antignac, C and Zenker, M (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 and Shaw, V and Ledermann, SE and 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 and Woolf, AS and 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 and Bockenhauer, D and Rees, L and Sebire, N and Tullus, K and van't Hoff, W and Waters, A and Marks, S (2010) A 20-Year Single Centre Experience of Congential and Infantile Nephrotic Syndrome. PEDIATR NEPHROL , 25 (9) 1878 - 1878.

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

Morgenstern, DA and Hasan, F and Gibson, S and Winyard, P and Sebire, NJ and 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 and Cantwell, M and 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 and Brandt, ML (2010) Tube feeding in children with chronic kidney disease: technical and practical issues. In: PEDIATRIC NEPHROLOGY. (pp. 699 - 704).

Rees, L and 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 and Zdebik, AA and Lieberer, E and Rapedius, M and Schmidt, K and Bandulik, S and Sterner, C and Tegtmeier, I and Penton, D and Baukrowitz, T and Hulton, SA and Witzgall, R and Ben-Zeev, B and Howie, AJ and Kleta, R and Bockenhauer, D and Warth, R (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 and Chernin, G and Heeringa, SF and Matejas, V and Held, S and Vega-Warner, V and Bockenhauer, D and Vlangos, CN and Moorani, KN and Neuhaus, TJ and Kari, JA and MacDonald, J and Saisawat, P and Ashraf, S and Ovunc, B and Zenker, M and Hildebrandt, F and GPN Study Grp, (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 and Knott, C and 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 and McNair, R and Skepper, JN and Figg, N and Schurgers, LJ and Deanfield, J and Rees, L and Shanahan, CM (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.

W

Waters, AM and Pappworth, I and Marchbank, K and Bockenhauer, D and Tullus, K and Pickering, MC and Strain, L and Sebire, N and Shroff, R and Marks, SD and Goodship, THJ and Rees, L (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.

Waters, AM and Pappworth, I and Marchbank, K and Bockenhauer, D and Tullus, K and Pickering, MC and Strain, L and Sebire, N and Shroff, R and Marks, SD and Goodship, THJ and Rees, L (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.

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 and Papakrivopoulou, J and Long, DA and Goggolidou, P and Connolly, JO and Woolf, AS and 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 Sat May 25 07:05:48 2013 BST.