Retterstøl L - Search Results

1

De novo 19p13.2 microdeletion encompassing the insulin receptor and resistin genes in a patient with obesity and learning disability.

Wangensteen T, Retterstøl L, Rødningen OK, Hjelmesaeth J, Aukrust P, Halvorsen B. Wangensteen T, et al. Among authors: retterstol l. Am J Med Genet A. 2013 Jun;161A(6):1480-6. doi: 10.1002/ajmg.a.35927. Epub 2013 May 1. Am J Med Genet A. 2013. PMID: 23637016

2

[Genetic causes of obesity].

Wangensteen T, Undlien D, Tonstad S, Retterstøl L. Wangensteen T, et al. Among authors: retterstol l. Tidsskr Nor Laegeforen. 2005 Nov 17;125(22):3090-3. Tidsskr Nor Laegeforen. 2005. PMID: 16299561 Free article. Review. Norwegian.

3

A common haplotype in NAPEPLD is associated with severe obesity in a Norwegian population-based cohort (the HUNT study).

Wangensteen T, Akselsen H, Holmen J, Undlien D, Retterstøl L. Wangensteen T, et al. Among authors: retterstol l. Obesity (Silver Spring). 2011 Mar;19(3):612-7. doi: 10.1038/oby.2010.219. Epub 2010 Sep 30. Obesity (Silver Spring). 2011. PMID: 20885390 Free article.

4

Mutations in the melanocortin 4 receptor (MC4R) gene in obese patients in Norway.

Wangensteen T, Kolsgaard ML, Mattingsdal M, Joner G, Tonstad S, Undlien D, Retterstol L. Wangensteen T, et al. Among authors: retterstol l. Exp Clin Endocrinol Diabetes. 2009 Jun;117(6):266-73. doi: 10.1055/s-0028-1102942. Epub 2009 Mar 19. Exp Clin Endocrinol Diabetes. 2009. PMID: 19301229 Clinical Trial.

5

FTO genotype and weight gain in obese and normal weight adults from a Norwegian population based cohort (the HUNT study).

Wangensteen T, Egeland T, Akselsen H, Holmen J, Undlien D, Retterstøl L. Wangensteen T, et al. Among authors: retterstol l. Exp Clin Endocrinol Diabetes. 2010 Oct;118(9):649-52. doi: 10.1055/s-0030-1249636. Epub 2010 Apr 6. Exp Clin Endocrinol Diabetes. 2010. PMID: 20373279

6

Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor.

Farooqi IS, Wangensteen T, Collins S, Kimber W, Matarese G, Keogh JM, Lank E, Bottomley B, Lopez-Fernandez J, Ferraz-Amaro I, Dattani MT, Ercan O, Myhre AG, Retterstol L, Stanhope R, Edge JA, McKenzie S, Lessan N, Ghodsi M, De Rosa V, Perna F, Fontana S, Barroso I, Undlien DE, O'Rahilly S. Farooqi IS, et al. Among authors: retterstol l. N Engl J Med. 2007 Jan 18;356(3):237-47. doi: 10.1056/NEJMoa063988. N Engl J Med. 2007. PMID: 17229951 Free PMC article.

7

Temple syndrome as a differential diagnosis to Prader-Willi syndrome: Identifying three new patients.

Lande A, Kroken M, Rabben K, Retterstøl L. Lande A, et al. Among authors: retterstol l. Am J Med Genet A. 2018 Jan;176(1):175-180. doi: 10.1002/ajmg.a.38533. Epub 2017 Nov 21. Am J Med Genet A. 2018. PMID: 29159982

8

Associations between persistent organic pollutants and metabolic syndrome in morbidly obese individuals.

Dusanov S, Ruzzin J, Kiviranta H, Klemsdal TO, Retterstøl L, Rantakokko P, Airaksinen R, Djurovic S, Tonstad S. Dusanov S, et al. Among authors: retterstol l. Nutr Metab Cardiovasc Dis. 2018 Jul;28(7):735-742. doi: 10.1016/j.numecd.2018.03.004. Epub 2018 Mar 13. Nutr Metab Cardiovasc Dis. 2018. PMID: 29699815

9

Adrenoleukodystrophy in Norway: high rate of de novo mutations and age-dependent penetrance.

Horn MA, Retterstøl L, Abdelnoor M, Skjeldal OH, Tallaksen CM. Horn MA, et al. Among authors: retterstol l. Pediatr Neurol. 2013 Mar;48(3):212-9. doi: 10.1016/j.pediatrneurol.2012.12.007. Pediatr Neurol. 2013. PMID: 23419472

10

[Acute psychosis--an unusual clinical manifestation of primary hyperparathyroidism].

Retterstøl L, Svane S. Retterstøl L, et al. Tidsskr Nor Laegeforen. 1995 Nov 30;115(29):3623-4. Tidsskr Nor Laegeforen. 1995. PMID: 8539717 Norwegian.

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