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Polymorphism of the solute carrier family 12 (sodium/chloride transporters) member 3, SLC12A3, gene at exon 23 (+78G/A: Arg913Gln) is associated with elevation of urinary albumin excretion in Japanese patients with type 2 diabetes: a 10-year longitudinal study

Keisuke Nishiyama, Yasushi Tanaka, Katsuyuki Nakajima, Atsuko Mokubo, Yosuke Atsumi, Katsuyoshi Matsuoka, Hirotaka Watada, T. Hirose, Takashi Nomiyama, Shiro Maeda,

Diabetologia · 2005 · 33 citations · 12 references

Open access

References

12

Multifactorial Intervention and Cardiovascular Disease in Patients with Type 2 Diabetes

Peter Gæde, Pernille Vedel, Nicolai Balle Larsen et al. · New England Journal of Medicine · 2003 · 4.4K citations · Full text

Medicine, Cardiology, Rehabilitation Medicine +17

Diagnosis and Classification of Diabetes Mellitus

Diabetes Care · 2004 · 1.7K citations · Full text

Medicine, Endocrinology, Internal Medicine +11

Gitelman's variant of Barter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na–Cl cotransporter

David B. Simon, Carol Nelson‐Williams, Margaret J. Bia et al. · Nature Genetics · 1996 · 1.2K citations

Life Sciences, Genetics, Human Genetics +2

Nephropathy in Diabetes

Diabetes Care · 2004 · 1K citations

Long-term results of the Kumamoto Study on optimal diabetes control in type 2 diabetic patients.

Masayoshi Shichiri, Hiroki Kishikawa, Y Ohkubo et al. · PubMed · 2000 · 739 citations

Medicine, Internal Medicine, Clinical Optometry +16