Njølstad PR - Search Results

1

The genetic abnormality in the beta cell determines the response to an oral glucose load.

Stride A, Vaxillaire M, Tuomi T, Barbetti F, Njølstad PR, Hansen T, Costa A, Conget I, Pedersen O, Søvik O, Lorini R, Groop L, Froguel P, Hattersley AT. Stride A, et al. Among authors: njolstad pr. Diabetologia. 2002 Mar;45(3):427-35. doi: 10.1007/s00125-001-0770-9. Diabetologia. 2002. PMID: 11914749

2

[Non-insulin dependent diabetes in children and adolescents].

Njølstad PR, Søvik O, Bell GI, Cockburn BN, Følling I, Sagen J. Njølstad PR, et al. Tidsskr Nor Laegeforen. 1998 Mar 10;118(7):1054-7. Tidsskr Nor Laegeforen. 1998. PMID: 9531829 Norwegian.

3

Hyperexcitability to sulphonylurea in MODY3.

Søvik O, Njølstad P, Følling I, Sagen J, Cockburn BN, Bell GI. Søvik O, et al. Diabetologia. 1998 May;41(5):607-8. doi: 10.1007/s001250050956. Diabetologia. 1998. PMID: 9628283 No abstract available.

4

A missense mutation, Val62Ala, in the glucokinase gene in a Norwegian family with maturity-onset diabetes of the young.

Njølstad PR, Cockburn BN, Bell GI, Søvik O. Njølstad PR, et al. Acta Paediatr. 1998 Aug;87(8):853-6. doi: 10.1080/080352598750013626. Acta Paediatr. 1998. PMID: 9736233

5

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 TH, Njolstad PR, Horikawa Y, Bostad L, Bell GI, Sovik O. Lindner TH, et al. Among authors: njolstad pr. Hum Mol Genet. 1999 Oct;8(11):2001-8. doi: 10.1093/hmg/8.11.2001. Hum Mol Genet. 1999. PMID: 10484768

6

A simple test for the high-frequency P291fsinsC mutation in the HNF1 alpha/MODY3 gene.

Bjørkhaug L, Søvik O, Bell GI, Njølstad PR, Molven A. Bjørkhaug L, et al. Among authors: njolstad pr. Diabetologia. 2000 Jun;43(6):818-9. doi: 10.1007/s001250051383. Diabetologia. 2000. PMID: 10907131 No abstract available.

7

MODY associated with two novel hepatocyte nuclear factor-1alpha loss-of-function mutations (P112L and Q466X).

Bjørkhaug L, Ye H, Horikawa Y, Søvik O, Molven A, Njølstad PR. Bjørkhaug L, et al. Among authors: njolstad pr. Biochem Biophys Res Commun. 2000 Dec 29;279(3):792-8. doi: 10.1006/bbrc.2000.4024. Biochem Biophys Res Commun. 2000. PMID: 11162430

8

Neonatal diabetes mellitus due to complete glucokinase deficiency.

Njølstad PR, Søvik O, Cuesta-Muñoz A, Bjørkhaug L, Massa O, Barbetti F, Undlien DE, Shiota C, Magnuson MA, Molven A, Matschinsky FM, Bell GI. Njølstad PR, et al. N Engl J Med. 2001 May 24;344(21):1588-92. doi: 10.1056/NEJM200105243442104. N Engl J Med. 2001. PMID: 11372010 Free article. No abstract available.

9

Reduced prevalence of late-diabetic complications in MODY3 with early diagnosis.

Sagen JV, Njølstad PR, Søvik O. Sagen JV, et al. Among authors: njolstad pr. Diabet Med. 2002 Aug;19(8):697-8. doi: 10.1046/j.1464-5491.2002.00688_1.x. Diabet Med. 2002. PMID: 12147154 No abstract available.

10

Hepatocyte nuclear factor-1 alpha gene mutations and diabetes in Norway.

Bjørkhaug L, Sagen JV, Thorsby P, Søvik O, Molven A, Njølstad PR. Bjørkhaug L, et al. Among authors: njolstad pr. J Clin Endocrinol Metab. 2003 Feb;88(2):920-31. doi: 10.1210/jc.2002-020945. J Clin Endocrinol Metab. 2003. PMID: 12574234

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

293 results

Search Page

Filters