Early proximal tubular dysfunction in Lowe’s syndrome von Laube, G F, Russell-Eggitt, I M, van’t Hoff, W G

Volltext

Molecular developments in renal tubulopathies von VAN'T HOFF, WILLIAM G

Volltext

Combined liver-kidney transplantation in methylmalonic acidemia von van't Hoff, W.G., Dixon, M., Taylor, J., Mistry, P., Rolles, K., Rees, L., Leonard, J.V.

Volltext

The enzyme 4-hydroxy-2-oxoglutarate aldolase is deficient in primary hyperoxaluria type 3 von WILLIAM, Emma L, BOCKENHAUER, Detlef, VAN'T HOFF, William G, JOHRI, Nikhil, LAING, Chris, SINHA, Manish D, UNWIN, Robert, VILJOEN, Adie, RUMSBY, Gill

Volltext

Characterization of renal chloride channel (CLCN5) mutations in Dent's disease von YAMAMOTO, K, COX, J. P. D. T, YAMAOKA, K, JENTSCH, T. J, THAKKER, R. V, FRIEDRICH, T, CHRISTIE, P. T, BALD, M, HOUTMAN, P. N, LAPSLEY, M. J, PATZER, L, TSIMARATOS, M, VAN'T HOFF, W. G

Volltext

Catch‐up growth in Fanconi‐Bickel syndrome with uncooked cornstarch von Lee, P. J., Van't Hoff, W. G., Leonard, J. V.

Volltext

Renal tubular dysfunction in multiple acyl‐CoA dehydrogenase deficiency von Morris, A. A. M., Olpin, S. E., Van't Hoff, W. G., Johnson, A. W., Leonard, J. V.

Volltext

Treatment with recombinant human growth hormone in short children with nephropathic cystinosis : No evidence for increased deterioration rate of renal function von WÜHL, E, HAFFNER, D, GRETZ, N, OFFNER, G, VAN'T HOFF, W. G, BROYER, M, MEHLS, O

Volltext

The treatment of cystinosis with cysteamine and phosphocysteamine in the United Kingdom and Eire von VAN'T HOFF, W. G, GRETZ, N

Volltext

Atypical familial juvenile hyperuricemic nephropathy associated with a hepatocyte nuclear factor-1β gene mutation von Bingham, Coralie, Ellard, Sian, van't Hoff, William G., Simmonds, H. Anne, Marinaki, Anthony M., Badman, Michael K., Winocour, Peter H., Stride, Amanda, Lockwood, Christopher R., Nicholls, Anthony J., Owen, Katharine R., Spyer, Ghislaine, Pearson, Ewan R., Hattersley, Andrew T.

Volltext

Neonatal severe hyperparathyroidism: genotype/phenotype correlation and the use of pamidronate as rescue therapy von WALLER, Simon, KURZAWINSKI, Tom, SPITZ, Lewis, THAKKER, Rajesh, CRANSTON, Treena, PEARCE, Simon, CHEETHAM, Tim, VAN'T HOFF, William G

Volltext

Incompletely penetrant PKD1 alleles suggest a role for gene dosage in cyst initiation in polycystic kidney disease

Volltext

Glutathione depletion and increased apoptosis rate in human cystinotic proximal tubular cells von Laube, Guido F, Shah, Vanita, Stewart, Victoria C, Hargreaves, Iain P, Haq, Mushfequr R, Heales, Simon J R, van't Hoff, William G

Volltext

Incompletely penetrant PKD1 alleles suggest a role for gene dosage in cyst initiation in polycystic kidney disease

Volltext

Aetiological Factors in Paediatric Urolithiasis von van’t Hoff, William G.

Volltext

Early-onset chronic renal failure as a presentation of infantile nephropathic cystinosis von VAN'T HOFF, W. G, LEDERMANN, S. E, WALDRON, M, TROMPETER, R. S

Volltext

Immunolocalization of cystinosin, the protein defective in cystinosis von HAQ, Mushfequr R, KALATZIS, Vasiliki, GUBLER, Marie-Claire, TOWN, Margaret M, ANTIGNAC, Corinne, VAN'T HOFF, William G, WOOLF, Adrian S

Volltext

Neonatal nephrocalcinosis in association with glucose-galactose malabsorption von PAHARI, Amitava, MILLA, Peter J, VAN'T HOFF, William G

Volltext

Reproducibility of cerebral artery Doppler measurements von Moorthy, B, Colditz, P R, Ives, K N, Rees, D G, van't Hoff, W G, Hope, P L

Volltext

COMBINED LIVER AND KIDNEY TRANSPLANTATION IN THE TREATMENT OF VITAMIN B12 RESISTANT METHYLMALONIC ACIDAEMIA von Shah, S R, Barnes, E, Burroughs, A K, Leonard, J V, van't Hoff, W G, Rolles, K

Volltext