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Whole-exome sequencing for diagnosis of hereditary ichthyosis.
Sitek JC, Kulseth MA, Rypdal KB, Skodje T, Sheng Y, Retterstøl L. Sitek JC, et al. Among authors: retterstol l. J Eur Acad Dermatol Venereol. 2018 Jun;32(6):1022-1027. doi: 10.1111/jdv.14870. Epub 2018 Mar 9. J Eur Acad Dermatol Venereol. 2018. PMID: 29444371
Effect of epilepsy on autism symptoms in Angelman syndrome.
Bakke KA, Howlin P, Retterstøl L, Kanavin ØJ, Heiberg A, Nærland T. Bakke KA, et al. Among authors: retterstol l. Mol Autism. 2018 Jan 8;9:2. doi: 10.1186/s13229-017-0185-1. eCollection 2018. Mol Autism. 2018. PMID: 29340132 Free PMC article.
[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.
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.
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.
41 results