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Congenital hyperinsulinism.
Velde CD, Reigstad H, Tjora E, Guthe HJT, Hansen EV, Molven A, Njølstad PR. Velde CD, et al. Among authors: njolstad pr. Tidsskr Nor Laegeforen. 2023 Dec 11;143(18). doi: 10.4045/tidsskr.23.0425. Print 2023 Dec 12. Tidsskr Nor Laegeforen. 2023. PMID: 38088279 Free article. English, Norwegian.
[Molecular diagnostics in diabetes mellitus].
Bjørkhaug L, Johansson S, Raeder H, Thorsby PM, Undlien DE, Søvik O, Molven A, Sagen JV, Njølstad PR. Bjørkhaug L, et al. Among authors: njolstad pr. Tidsskr Nor Laegeforen. 2005 Nov 3;125(21):2968-72. Tidsskr Nor Laegeforen. 2005. PMID: 16276383 Free article. Review. Norwegian.
[Progress in diabetes genetics].
Njølstad PR, Hertel JK, Søvik O, Raeder H, Johansson S, Molven A. Njølstad PR, et al. Tidsskr Nor Laegeforen. 2010 Jun 3;130(11):1145-9. doi: 10.4045/tidsskr.09.1035. Tidsskr Nor Laegeforen. 2010. PMID: 20531501 Free article. Review. Norwegian.
[Tailored medicine or narcissomics?].
Ræder H, Molven A, Njølstad PR. Ræder H, et al. Among authors: njolstad pr. Tidsskr Nor Laegeforen. 2012 Sep 4;132(16):1844-5. doi: 10.4045/tidsskr.12.0582. Tidsskr Nor Laegeforen. 2012. PMID: 22986961 Free article. Norwegian. No abstract available.
Functional evaluation of 16 SCHAD missense variants: Only amino acid substitutions causing congenital hyperinsulinism of infancy lead to loss-of-function phenotypes in vitro.
Velasco K, St-Louis JL, Hovland HN, Thompson N, Ottesen Å, Choi MH, Pedersen L, Njølstad PR, Arnesen T, Fjeld K, Aukrust I, Myklebust LM, Molven A. Velasco K, et al. Among authors: njolstad pr. J Inherit Metab Dis. 2021 Jan;44(1):240-252. doi: 10.1002/jimd.12309. Epub 2020 Sep 28. J Inherit Metab Dis. 2021. PMID: 32876354
284 results