4 results for author:"Soevik O." in Literature citations
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| Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction. Raeder H., Johansson S., Holm P.I., Haldorsen I.S., Mas E., Sbarra V., Nermoen I., Eide S.A., Grevle L., Bjoerkhaug L. et al. |
| Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy. Sagen J.V., Raeder H., Hathout E., Shehadeh N., Gudmundsson K., Baevre H., Abuelo D., Phornphutkul C., Molnes J., Bell G.I. et al. |
| Neonatal diabetes mellitus due to complete glucokinase deficiency. Njoelstad P.R., Soevik O., Cuesta-Munoz A., Bjoerkhaug L., Massa O., Barbetti F., Undlien D.E., Shiota C., Magnuson M.A., Molven A. et al. N. Engl. J. Med. 344:1588-1592(2001) · UniProtKB (1) · Mapped (3) |
| A novel syndrome of diabetes mellitus, renal dysfunction and genital malformation associated with a partial deletion of the pseudo-POU domain of hepatocyte nuclear factor-1beta. Lindner T.H., Njoelstad P.R., Horikawa Y., Bostad L., Bell G.I., Soevik O. Hum. Mol. Genet. 8:2001-2008(1999) · UniProtKB (1) |