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Number of items: 18.

B

Bockenhauer, D and Medlar, AJ and Ashton, E and Kleta, R and Lench, N (2012) Genetic testing in renal disease. Pediatr Nephrol , 27 (6) 873 - 883. 10.1007/s00467-011-1865-2.

Bockenhauer, D and Penney, MD and Hampton, D and van't Hoff, W and Gullett, A and Sailesh, S and Bichet, DG (2012) A family with hyponatremia and the nephrogenic syndrome of inappropriate antidiuresis. Am J Kidney Dis , 59 (4) 566 - 568. 10.1053/j.ajkd.2011.09.026.

Boyden, LM and Choi, M and Choate, KA and Nelson-Williams, CJ and Farhi, A and Toka, HR and Tikhonova, IR and Bjornson, R and Mane, SM and Colussi, G and Lebel, M and Gordon, RD and Semmekrot, BA and Poujol, A and Välimäki, MJ and De Ferrari, ME and Sanjad, SA and Gutkin, M and Karet, FE and Tucci, JR and Stockigt, JR and Keppler-Noreuil, KM and Porter, CC and Anand, SK and Whiteford, ML and Davis, ID and Dewar, SB and Bettinelli, A and Fadrowski, JJ and Belsha, CW and Hunley, TE and Nelson, RD and Trachtman, H and Cole, TR and Pinsk, M and Bockenhauer, D and Shenoy, M and Vaidyanathan, P and Foreman, JW and Rasoulpour, M and Thameem, F and Al-Shahrouri, HZ and Radhakrishnan, J and Gharavi, AG and Goilav, B and Lifton, RP (2012) Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities. Nature , 482 (7383) 98 - 102. 10.1038/nature10814.

Brockschmidt, A and Chung, B and Weber, S and Fischer, DC and Kolatsi-Joannou, M and Christ, L and Heimbach, A and Shtiza, D and Klaus, G and Simonetti, GD and Konrad, M and Winyard, P and Haffner, D and Schaefer, F and Weber, RG (2012) CHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT). Nephrol Dial Transplant , 27 (6) 2355 - 2364. 10.1093/ndt/gfr649.

H

Harteneck, C and Weber, S and Buescher, A and Riehle, M and Hoyer, P and Jeruschke, S and Kolatsie, M and Nagel, M and Winyard, P and Gollasch, M (2012) Mutations in TRPC6 ion channels in patients suffering from familial focal segmental glomerolusclerosis. In: NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY. (pp. 34 - 34).

Has, C and Spartà, G and Kiritsi, D and Weibel, L and Moeller, A and Vega-Warner, V and Waters, A and He, Y and Anikster, Y and Esser, P and Straub, BK and Hausser, I and Bockenhauer, D and Dekel, B and Hildebrandt, F and Bruckner-Tuderman, L and Laube, GF (2012) Integrin α3 mutations with kidney, lung, and skin disease. N Engl J Med , 366 (16) 1508 - 1514. 10.1056/NEJMoa1110813.

Huang, JL and Woolf, AS and Long, DA (2012) Angiogenesis and autosomal dominant polycystic kidney disease. Pediatr Nephrol 10.1007/s00467-012-2305-7.

J

Jaureguiberry, G and De la Dure-Molla, M and Parry, D and Quentric, M and Himmerkus, N and Koike, T and Poulter, J and Klootwijk, E and Robinette, SL and Howie, AJ and Patel, V and Figueres, ML and Stanescu, HC and Issler, N and Nicholson, JK and Bockenhauer, D and Laing, C and Walsh, SB and McCredie, DA and Povey, S and Asselin, A and Picard, A and Coulomb, A and Medlar, AJ and Bailleul-Forestier, I and Verloes, A and Le Caignec, C and Roussey, G and Guiol, J and Isidor, B and Logan, C and Shore, R and Johnson, C and Inglehearn, C and Al-Bahlani, S and Schmittbuhl, M and Clauss, F and Huckert, M and Laugel, V and Ginglinger, E and Pajarola, S and Spartà, G and Bartholdi, D and Rauch, A and Addor, MC and Yamaguti, PM and Safatle, HP and Acevedo, AC and Martelli-Júnior, H and Dos Santos Netos, PE and Coletta, RD and Gruessel, S and Sandmann, C and Ruehmann, D and Langman, CB and Scheinman, SJ and Ozdemir-Ozenen, D and Hart, TC and Hart, PS and Neugebauer, U and Schlatter, E and Houillier, P and Gahl, WA and Vikkula, M and Bloch-Zupan, A and Bleich, M and Kitagawa, H and Unwin, RJ and Mighell, A and Berdal, A and Kleta, R (2012) Nephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal Recessive FAM20A Mutations. Nephron Physiol , 122 (1-2) 1 - 6. 10.1159/000349989.

K

Kerecuk, L and Long, DA and Ali, Z and Anders, C and Kolatsi-Joannou, M and Scambler, PJ and Woolf, AS (2012) Expression of Fraser syndrome genes in normal and polycystic murine kidneys. Pediatr Nephrol 10.1007/s00467-012-2100-5.

L

Long, DA and Lennon, R (2012) The renal archaeologist: digging for clues in archived tissues to understand diabetic kidney disease. Nephrol Dial Transplant , 27 (5) 1693 - 1695. 10.1093/ndt/gfs025.

Long, DA and Norman, JT and Fine, LG (2012) Restoring the renal microvasculature to treat chronic kidney disease. Nat Rev Nephrol , 8 (4) 244 - 250. 10.1038/nrneph.2011.219.

O

Ovunc, B and Ashraf, S and Vega-Warner, V and Bockenhauer, D and Elshakhs, NA and Joseph, M and Hildebrandt, F and Gesellschaft für Pädiatrische Nephrologie (GPN) Study Group, (2012) Mutation analysis of NPHS1 in a worldwide cohort of congenital nephrotic syndrome patients. Nephron Clin Pract , 120 (3) c139 - c146. 10.1159/000337379.

P

Papakrivopoulou, E and Lillywhite, S and Davenport, A (2012) Is N-terminal probrain-type natriuretic peptide a clinically useful biomarker of volume overload in peritoneal dialysis patients? Nephrol Dial Transplant , 27 (1) 396 - 401. 10.1093/ndt/gfr338.

Prytua, A and Wells, D and McLean, T and Balona, F and Gullett, A and Knott, C and Cantwell, M and Hassen, K and Ledermann, S and Rees, L and Shroff, R (2012) Urinary and dialysate losses of vitamin D-binding protein in children on chronic peritoneal dialysis. PEDIATRIC NEPHROLOGY , 27 (4) 643 - 649. 10.1007/s00467-011-2045-0.

Q

Quinlan, C and Guegan, K and Offiah, A and Neill, RO and Hiorns, MP and Ellard, S and Bockenhauer, D and Hoff, WV and Waters, AM (2012) Growth in PHEX-associated X-linked hypophosphatemic rickets: the importance of early treatment. Pediatr Nephrol , 27 (4) 581 - 588. 10.1007/s00467-011-2046-z.

S

Shroff, R and Wan, M and Gullett, A and Ledermann, S and Shute, R and Knott, C and Wells, D and Aitkenhead, H and Manickavasagar, B and van't Hoff, W and Rees, L (2012) Ergocalciferol Supplementation in Children with CKD Delays the Onset of Secondary Hyperparathyroidism: A Randomized Trial. CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY , 7 (2) 216 - 223. 10.2215/CJN.04760511.

Sparta', G and Has, C and Kiritsi, D and Weibel, L and Moeller, A and Vega-Warner, V and Waters, A and He, Y and Anikster, Y and Esser, P and Straub, BK and Hausser, I and Bockenhauer, D and Dekel, B and Hildebrandt, F and Bruckner-Tuderman, L and Laube, GF (2012) NEP-SYNDROME: A NEW GENETIC CONDITION WITH NEPHROTIC SYNDROME, EPIDERMOLYSIS BULLOSA AND PULMONARY DISEASE BASED ON INTEGRIN alpha 3 MUTATION. PEDIATRIC NEPHROLOGY , 27 (9) 1611 - 1611.

W

Williams, EL and Bockenhauer, D and van't Hoff, WG and Johri, N and Laing, C and Sinha, MD and Unwin, R and Viljoen, A and Rumsby, G (2012) The enzyme 4-hydroxy-2-oxoglutarate aldolase is deficient in primary hyperoxaluria type 3. Nephrol Dial Transplant , 27 (8) 3191 - 3195. 10.1093/ndt/gfs039.

This list was generated on Thu May 23 09:20:45 2013 BST.