au.\*:("FARHI, Anita")
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Sequence variants in SLITRK1 are associated with Tourette's syndromeABELSON, Jesse F; KWAN, Kenneth Y; DAVIS, Nicole R et al.Science (Washington, D.C.). 2005, Vol 310, Num 5746, pp 317-320, issn 0036-8075, 4 p.Article
Mitotic Recombination in Patients with Ichthyosis Causes Reversion of Dominant Mutations in KRT10CHOATE, Keith A; YIN LU; BREE, Alanna et al.Science (Washington, D.C.). 2010, Vol 329, Num 6000, pp 94-97, issn 0036-8075, 4 p.Article
High bone density due to a mutation in LDL-receptor-related protein 5BOYDEN, Lynn M; JUNHAO MAO; BELSKY, Joseph et al.The New England journal of medicine. 2002, Vol 346, Num 20, pp 1513-1521, issn 0028-4793Article
A novel SGLT2 mutation in a patient with autosomal recessive renal glucosuriaFRANCIS, Jean; JUNHUI ZHANG; FARHI, Anita et al.Nephrology, dialysis, transplantation (Print). 2004, Vol 19, Num 11, pp 2893-2895, issn 0931-0509, 3 p.Article
Mutations in the Na-Cl cotransporter reduce blood pressure in humansCRUZ, Dinna N; SIMON, David B; NELSON-WILLIAMS, Carol et al.Hypertension (Dallas, Tex. 1979). 2001, Vol 37, Num 6, pp 1458-1464, issn 0194-911XArticle
IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22-23GHARAVI, Ali G; YAN YAN; CARIDI, Gianluca et al.Nature genetics. 2000, Vol 26, Num 3, pp 354-357, issn 1061-4036Article