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Items: 4

1.

The Molecular Genetics of Gordon Syndrome.

Mabillard H, Sayer JA.

Genes (Basel). 2019 Nov 29;10(12). pii: E986. doi: 10.3390/genes10120986. Review.

2.

Human urine-derived renal epithelial cells provide insights into kidney-specific alternate splicing variants.

Molinari E, Decker E, Mabillard H, Tellez J, Srivastava S, Raman S, Wood K, Kempf C, Alkanderi S, Ramsbottom SA, Miles CG, Johnson CA, Hildebrandt F, Bergmann C, Sayer JA.

Eur J Hum Genet. 2018 Dec;26(12):1791-1796. doi: 10.1038/s41431-018-0212-5. Epub 2018 Jul 12.

3.

Large Retroperitoneal Haemorrhage Following Cyst Rupture in a Patient with Autosomal Dominant Polycystic Kidney Disease.

Mabillard H, Srivastava S, Haslam P, Karasek M, Sayer JA.

Case Rep Nephrol. 2017;2017:4653267. doi: 10.1155/2017/4653267. Epub 2017 Oct 18.

4.

Investigation and management of renal stone disease.

Mabillard HR, Tomson CRV.

Nephrol Dial Transplant. 2017 Dec 1;32(12):1984-1986. doi: 10.1093/ndt/gfx306. No abstract available.

PMID:
29145637

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