Søvik O - Search Results

1

[Molecular genetic diagnostics in syndromes associated with the RAS/MAPK signalling pathway].

Molven A, Søvik O, von der Lippe C, Steine SJ, Njølstad PR, Houge G, Prescott TE. Molven A, et al. Among authors: sovik o. Tidsskr Nor Laegeforen. 2009 Nov 19;129(22):2358-61. doi: 10.4045/tidsskr.09.0267. Tidsskr Nor Laegeforen. 2009. PMID: 19935936 Free article. Norwegian.

2

[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: sovik o. Tidsskr Nor Laegeforen. 2005 Nov 3;125(21):2968-72. Tidsskr Nor Laegeforen. 2005. PMID: 16276383 Free article. Review. Norwegian.

3

[Progress in diabetes genetics].

Njølstad PR, Hertel JK, Søvik O, Raeder H, Johansson S, Molven A. Njølstad PR, et al. Among authors: sovik o. 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.

4

De novo HRAS and KRAS mutations in two siblings with short stature and neuro-cardio-facio-cutaneous features.

Søvik O, Schubbert S, Houge G, Steine SJ, Norgård G, Engelsen B, Njølstad PR, Shannon K, Molven A. Søvik O, et al. J Med Genet. 2007 Jul;44(7):e84. doi: 10.1136/jmg.2007.049361. J Med Genet. 2007. PMID: 17601930 Free PMC article.

5

De novo HRAS and KRAS mutations in two siblings with short stature and neuro-cardio-facio-cutaneous features.

Søvik O, Schubbert S, Houge G, Steine SJ, Norgård G, Engelsen B, Njølstad PR, Shannon K, Molven A. Søvik O, et al. BMJ Case Rep. 2009;2009:bcr07.2008.0550. doi: 10.1136/bcr.07.2008.0550. Epub 2009 Jan 23. BMJ Case Rep. 2009. PMID: 21686750 Free PMC article.

6

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

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

7

[Diagnosis and treatment of congenital hyperinsulinism--to Paris at any price?].

Søvik O, Njølstad PR, Reigstad H, Brackman D, Teslo I, Brunvand L. Søvik O, et al. Tidsskr Nor Laegeforen. 2001 Feb 20;121(5):612-4. Tidsskr Nor Laegeforen. 2001. PMID: 11301621 Free article. Norwegian.

8

Hunting for a hypoglycemia gene: severe neonatal hypoglycemia in a consanguineous family.

Molven A, Rishaug U, Matre GE, Njølstad PR, Søvik O. Molven A, et al. Among authors: sovik o. Am J Med Genet. 2002 Nov 15;113(1):40-6. doi: 10.1002/ajmg.10575. Am J Med Genet. 2002. PMID: 12400064

9

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: sovik o. J Clin Endocrinol Metab. 2003 Feb;88(2):920-31. doi: 10.1210/jc.2002-020945. J Clin Endocrinol Metab. 2003. PMID: 12574234

10

Permanent neonatal diabetes caused by glucokinase deficiency: inborn error of the glucose-insulin signaling pathway.

Njølstad PR, Sagen JV, Bjørkhaug L, Odili S, Shehadeh N, Bakry D, Sarici SU, Alpay F, Molnes J, Molven A, Søvik O, Matschinsky FM. Njølstad PR, et al. Among authors: sovik o. Diabetes. 2003 Nov;52(11):2854-60. doi: 10.2337/diabetes.52.11.2854. Diabetes. 2003. PMID: 14578306

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