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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2003 1
2004 2
2005 1
2007 4
2008 3
2009 3
2010 4
2011 5
2012 7
2013 6
2014 5
2015 1
2016 3
2017 3
2018 4
2021 1
2023 1
2024 1

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48 results

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Page 1
Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation.
Legius E, Messiaen L, Wolkenstein P, Pancza P, Avery RA, Berman Y, Blakeley J, Babovic-Vuksanovic D, Cunha KS, Ferner R, Fisher MJ, Friedman JM, Gutmann DH, Kehrer-Sawatzki H, Korf BR, Mautner VF, Peltonen S, Rauen KA, Riccardi V, Schorry E, Stemmer-Rachamimov A, Stevenson DA, Tadini G, Ullrich NJ, Viskochil D, Wimmer K, Yohay K; International Consensus Group on Neurofibromatosis Diagnostic Criteria (I-NF-DC); Huson SM, Evans DG, Plotkin SR. Legius E, et al. Genet Med. 2021 Aug;23(8):1506-1513. doi: 10.1038/s41436-021-01170-5. Epub 2021 May 19. Genet Med. 2021. PMID: 34012067 Free PMC article.
Søskenbarn bør kunne gifte seg.
Chaudhry FA, Sajjad TA, Heiberg A. Chaudhry FA, et al. Among authors: heiberg a. Tidsskr Nor Laegeforen. 2023 Nov 16;143(18). doi: 10.4045/tidsskr.23.0733. Print 2023 Dec 12. Tidsskr Nor Laegeforen. 2023. PMID: 38088291 Free article. Norwegian. No abstract available.
Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature.
Rice GI, Kasher PR, Forte GM, Mannion NM, Greenwood SM, Szynkiewicz M, Dickerson JE, Bhaskar SS, Zampini M, Briggs TA, Jenkinson EM, Bacino CA, Battini R, Bertini E, Brogan PA, Brueton LA, Carpanelli M, De Laet C, de Lonlay P, del Toro M, Desguerre I, Fazzi E, Garcia-Cazorla A, Heiberg A, Kawaguchi M, Kumar R, Lin JP, Lourenco CM, Male AM, Marques W Jr, Mignot C, Olivieri I, Orcesi S, Prabhakar P, Rasmussen M, Robinson RA, Rozenberg F, Schmidt JL, Steindl K, Tan TY, van der Merwe WG, Vanderver A, Vassallo G, Wakeling EL, Wassmer E, Whittaker E, Livingston JH, Lebon P, Suzuki T, McLaughlin PJ, Keegan LP, O'Connell MA, Lovell SC, Crow YJ. Rice GI, et al. Among authors: heiberg a. Nat Genet. 2012 Nov;44(11):1243-8. doi: 10.1038/ng.2414. Epub 2012 Sep 23. Nat Genet. 2012. PMID: 23001123 Free PMC article.
[Huntington's disease].
Heiberg A. Heiberg A. Tidsskr Nor Laegeforen. 2008 Oct 9;128(19):2214-7. Tidsskr Nor Laegeforen. 2008. PMID: 18846148 Free article. Review. Norwegian.
[A. Heiberg and colleagues reply].
Heiberg A, Frich J, Røttingen JA. Heiberg A, et al. Tidsskr Nor Laegeforen. 2014 Apr 29;134(8):809-10. doi: 10.4045/tidsskr.14.0451. eCollection 2014 Apr 29. Tidsskr Nor Laegeforen. 2014. PMID: 24780961 Free article. Norwegian. No abstract available.
[Complex craniofacial synostoses].
Meling TR, Ørstavik KH, Heiberg A. Meling TR, et al. Among authors: heiberg a. Tidsskr Nor Laegeforen. 2004 May 6;124(9):1230-4. Tidsskr Nor Laegeforen. 2004. PMID: 15131704 Free article. Review. Norwegian.
Myotonic dystrophy type 1 - a multiorgan disorder.
Ørstavik K, Solbakken G, Rasmussen M, Sanaker PS, Fossmo HL, Bryne E, Knutsen-Øy T, Elgsås T, Heiberg A. Ørstavik K, et al. Among authors: heiberg a. Tidsskr Nor Laegeforen. 2024 Apr 16;144(5). doi: 10.4045/tidsskr.23.0687. Print 2024 Apr 23. Tidsskr Nor Laegeforen. 2024. PMID: 38651711 English, Norwegian.
[Neurofibromatosis type 2 and auditory brainstem implantation].
Elvsåshagen T, Solyga V, Bakke SJ, Heiberg A, Kerty E. Elvsåshagen T, et al. Among authors: heiberg a. Tidsskr Nor Laegeforen. 2009 Aug 13;129(15):1469-73. doi: 10.4045/tidsskr.08.0151. Tidsskr Nor Laegeforen. 2009. PMID: 19690597 Free article. Review. Norwegian.
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: heiberg a. Mol Autism. 2018 Jan 8;9:2. doi: 10.1186/s13229-017-0185-1. eCollection 2018. Mol Autism. 2018. PMID: 29340132 Free PMC article.
48 results