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158 results
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Page 1
[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.
[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.
[Sense of coherence for parents of disabled children].
Grøholt EK, Nordhagen R, Heiberg A. Grøholt EK, et al. Among authors: heiberg a. Tidsskr Nor Laegeforen. 2007 Feb 15;127(4):422-6. Tidsskr Nor Laegeforen. 2007. PMID: 17304268 Free article. Norwegian.
[Dementia among younger persons and Huntington disease].
Frich JC, Heiberg A. Frich JC, et al. Among authors: heiberg a. Tidsskr Nor Laegeforen. 2011 Sep 6;131(17):1639; author reply 1639. doi: 10.4045/tidsskr.11.0791. Tidsskr Nor Laegeforen. 2011. PMID: 21901032 Free article. Norwegian. No abstract available.
[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.
[Charcot-Marie-Tooth disease. Peroneal muscular atrophy].
Hagen T, Jensen D Jr, Dietrichson P, Heiberg A. Hagen T, et al. Among authors: heiberg a. Tidsskr Nor Laegeforen. 1990 Oct 10;110(24):3110-5. Tidsskr Nor Laegeforen. 1990. PMID: 2237866 Norwegian.
[Genetic analysis in familial adenomatous polyposis].
Andresen PA, Gedde-Dahl T Jr, Fausa O, Eide TJ, Heiberg A. Andresen PA, et al. Among authors: heiberg a. Tidsskr Nor Laegeforen. 2001 Jan 10;121(1):64-8. Tidsskr Nor Laegeforen. 2001. PMID: 12013617 Free article. Norwegian.
[With the Red Cross against AIDS].
Heiberg A. Heiberg A. Tidsskr Nor Laegeforen. 2000 Nov 30;120(29):3597-8. Tidsskr Nor Laegeforen. 2000. PMID: 11188393 Free article. Norwegian. No abstract available.
[Genetic tests].
Heiberg A. Heiberg A. Tidsskr Nor Laegeforen. 2000 Aug 30;120(20):2378. Tidsskr Nor Laegeforen. 2000. PMID: 11475218 Free article. Norwegian. No abstract available.
[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.
[New knowledge does not always make it simpler].
Ruud E, Heiberg A. Ruud E, et al. Among authors: heiberg a. Tidsskr Nor Laegeforen. 2004 Dec 16;124(24):3256-7. Tidsskr Nor Laegeforen. 2004. PMID: 15608782 Free article. Norwegian. No abstract available.
The impact of an early truncating founder ATM mutation on immunoglobulins, specific antibodies and lymphocyte populations in ataxia-telangiectasia patients and their parents.
Stray-Pedersen A, Jónsson T, Heiberg A, Lindman CR, Widing E, Aaberge IS, Borresen-Dale AL, Abrahamsen TG. Stray-Pedersen A, et al. Among authors: heiberg a. Clin Exp Immunol. 2004 Jul;137(1):179-86. doi: 10.1111/j.1365-2249.2004.02492.x. Clin Exp Immunol. 2004. PMID: 15196260 Free PMC article.
Characterization of ATM mutations in 41 Nordic families with ataxia telangiectasia.
Laake K, Jansen L, Hahnemann JM, Brondum-Nielsen K, Lönnqvist T, Kääriäinen H, Sankila R, Lähdesmäki A, Hammarström L, Yuen J, Tretli S, Heiberg A, Olsen JH, Tucker M, Kleinerman R, Børresen-Dale AL. Laake K, et al. Among authors: heiberg a. Hum Mutat. 2000 Sep;16(3):232-46. doi: 10.1002/1098-1004(200009)16:3<232::AID-HUMU6>3.0.CO;2-L. Hum Mutat. 2000. PMID: 10980530
Neurofibromatosis type 2: Multiple intra-dermal tumors in a toddler.
Rustad CF, Dahl HM, Bowers NL, Sitek JC, Heiberg A, Huson S, Prescott T, Evans DGR. Rustad CF, et al. Among authors: heiberg a. Am J Med Genet A. 2017 May;173(5):1447-1449. doi: 10.1002/ajmg.a.38177. Epub 2017 Apr 3. Am J Med Genet A. 2017. PMID: 28371307 No abstract available.
[Rarity--a separate criterion used in prioritization?].
Heiberg A, Frich J, Røttingen JA. Heiberg A, et al. Tidsskr Nor Laegeforen. 2014 Mar 11;134(5):534-6. doi: 10.4045/tidsskr.14.0120. eCollection 2014 Mar 11. Tidsskr Nor Laegeforen. 2014. PMID: 24621914 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.
Parents' attitudes toward genetic research in autism spectrum disorder.
Johannessen J, Nærland T, Bloss C, Rietschel M, Strohmaier J, Gjevik E, Heiberg A, Djurovic S, Andreassen OA. Johannessen J, et al. Among authors: heiberg a. Psychiatr Genet. 2016 Apr;26(2):74-80. doi: 10.1097/YPG.0000000000000121. Psychiatr Genet. 2016. PMID: 26867185
Neurocranial morphology and growth in Williams syndrome.
Axelsson S, Kjaer I, Heiberg A, Bjørnland T, Storhaug K. Axelsson S, et al. Among authors: heiberg a. Eur J Orthod. 2005 Feb;27(1):32-47. doi: 10.1093/ejo/cjh065. Eur J Orthod. 2005. PMID: 15743861
[Reflex time and thyroid function].
Heiberg A. Heiberg A. Tidsskr Nor Laegeforen. 1969 Aug 15;89(16):1246-7. Tidsskr Nor Laegeforen. 1969. PMID: 5375346 Norwegian. No abstract available.
[Spray treatment for bronchial asthma].
Heiberg A. Heiberg A. Tidsskr Nor Laegeforen. 1967 Dec 15;87(24):2053-4. Tidsskr Nor Laegeforen. 1967. PMID: 5590476 Norwegian. No abstract available.
Biallelic variants in KIF14 cause intellectual disability with microcephaly.
Makrythanasis P, Maroofian R, Stray-Pedersen A, Musaev D, Zaki MS, Mahmoud IG, Selim L, Elbadawy A, Jhangiani SN, Coban Akdemir ZH, Gambin T, Sorte HS, Heiberg A, McEvoy-Venneri J, James KN, Stanley V, Belandres D, Guipponi M, Santoni FA, Ahangari N, Tara F, Doosti M, Iwaszkiewicz J, Zoete V, Backe PH, Hamamy H, Gleeson JG, Lupski JR, Karimiani EG, Antonarakis SE. Makrythanasis P, et al. Among authors: heiberg a. Eur J Hum Genet. 2018 Mar;26(3):330-339. doi: 10.1038/s41431-017-0088-9. Epub 2018 Jan 17. Eur J Hum Genet. 2018. PMID: 29343805 Free PMC article.
Growth and nutrition in 10 girls with Rett syndrome.
Thommessen M, Kase BF, Heiberg A. Thommessen M, et al. Among authors: heiberg a. Acta Paediatr. 1992 Sep;81(9):686-90. doi: 10.1111/j.1651-2227.1992.tb12334.x. Acta Paediatr. 1992. PMID: 1421909
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.
The doctor in the twenty first century.
Heiberg AN. Heiberg AN. Br Med J (Clin Res Ed). 1987 Dec 19-26;295(6613):1602-3. doi: 10.1136/bmj.295.6613.1602. Br Med J (Clin Res Ed). 1987. PMID: 3121090 Free PMC article. No abstract available.
Expanding the genotypic spectrum of Perrault syndrome.
Demain LA, Urquhart JE, O'Sullivan J, Williams SG, Bhaskar SS, Jenkinson EM, Lourenco CM, Heiberg A, Pearce SH, Shalev SA, Yue WW, Mackinnon S, Munro KJ, Newbury-Ecob R, Becker K, Kim MJ, O' Keefe RT, Newman WG. Demain LA, et al. Among authors: heiberg a. Clin Genet. 2017 Feb;91(2):302-312. doi: 10.1111/cge.12776. Epub 2016 Apr 1. Clin Genet. 2017. PMID: 26970254
Myofascial pain dysfunction (MPD) syndrome in twins.
Heiberg A, Helöe B, Heiberg AN, Helöe LA, Magnus P, Berg K, Nance WE. Heiberg A, et al. Among authors: heiberg an. Community Dent Oral Epidemiol. 1980 Dec;8(8):434-6. doi: 10.1111/j.1600-0528.1980.tb01323.x. Community Dent Oral Epidemiol. 1980. PMID: 6942960
Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response.
Rice GI, Bond J, Asipu A, Brunette RL, Manfield IW, Carr IM, Fuller JC, Jackson RM, Lamb T, Briggs TA, Ali M, Gornall H, Couthard LR, Aeby A, Attard-Montalto SP, Bertini E, Bodemer C, Brockmann K, Brueton LA, Corry PC, Desguerre I, Fazzi E, Cazorla AG, Gener B, Hamel BC, Heiberg A, Hunter M, van der Knaap MS, Kumar R, Lagae L, Landrieu PG, Lourenco CM, Marom D, McDermott MF, van der Merwe W, Orcesi S, Prendiville JS, Rasmussen M, Shalev SA, Soler DM, Shinawi M, Spiegel R, Tan TY, Vanderver A, Wakeling EL, Wassmer E, Whittaker E, Lebon P, Stetson DB, Bonthron DT, Crow YJ. Rice GI, et al. Among authors: heiberg a. Nat Genet. 2009 Jul;41(7):829-32. doi: 10.1038/ng.373. Epub 2009 Jun 14. Nat Genet. 2009. PMID: 19525956 Free PMC article.
Clinical and molecular phenotype of Aicardi-Goutieres syndrome.
Rice G, Patrick T, Parmar R, Taylor CF, Aeby A, Aicardi J, Artuch R, Montalto SA, Bacino CA, Barroso B, Baxter P, Benko WS, Bergmann C, Bertini E, Biancheri R, Blair EM, Blau N, Bonthron DT, Briggs T, Brueton LA, Brunner HG, Burke CJ, Carr IM, Carvalho DR, Chandler KE, Christen HJ, Corry PC, Cowan FM, Cox H, D'Arrigo S, Dean J, De Laet C, De Praeter C, Dery C, Ferrie CD, Flintoff K, Frints SG, Garcia-Cazorla A, Gener B, Goizet C, Goutieres F, Green AJ, Guet A, Hamel BC, Hayward BE, Heiberg A, Hennekam RC, Husson M, Jackson AP, Jayatunga R, Jiang YH, Kant SG, Kao A, King MD, Kingston HM, Klepper J, van der Knaap MS, Kornberg AJ, Kotzot D, Kratzer W, Lacombe D, Lagae L, Landrieu PG, Lanzi G, Leitch A, Lim MJ, Livingston JH, Lourenco CM, Lyall EG, Lynch SA, Lyons MJ, Marom D, McClure JP, McWilliam R, Melancon SB, Mewasingh LD, Moutard ML, Nischal KK, Ostergaard JR, Prendiville J, Rasmussen M, Rogers RC, Roland D, Rosser EM, Rostasy K, Roubertie A, Sanchis A, Schiffmann R, Scholl-Burgi S, Seal S, Shalev SA, Corcoles CS, Sinha GP, Soler D, Spiegel R, Stephenson JB, Tacke U, Tan TY, Till M, Tolmie JL, Tomlin P, Vagnarelli F, Valente EM, Van Coster RN, Van der Aa N, Vanderver A, Vles JS, Voit T, Wassmer E, Weschke B, Whiteford ML, Willemsen MA, Zankl A, Zuberi SM, Orcesi S, Fazzi E, Lebon P, Crow YJ. Rice G, et al. Among authors: heiberg a. Am J Hum Genet. 2007 Oct;81(4):713-25. doi: 10.1086/521373. Epub 2007 Sep 4. Am J Hum Genet. 2007. PMID: 17846997 Free PMC article.
[Iron lung (siderosis)].
Heiberg A. Heiberg A. Tidsskr Nor Laegeforen. 1970 Mar 1;90(5):499-500. Tidsskr Nor Laegeforen. 1970. PMID: 5426199 Norwegian. No abstract available.
Prenatal prediction of spinal muscular atrophy.
Daniels RJ, Suthers GK, Morrison KE, Thomas NH, Francis MJ, Mathew CG, Loughlin S, Heiberg A, Wood D, Dubowitz V, et al. Daniels RJ, et al. Among authors: heiberg a. J Med Genet. 1992 Mar;29(3):165-70. doi: 10.1136/jmg.29.3.165. J Med Genet. 1992. PMID: 1348091 Free PMC article.
High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH.
Bruder CE, Hirvelä C, Tapia-Paez I, Fransson I, Segraves R, Hamilton G, Zhang XX, Evans DG, Wallace AJ, Baser ME, Zucman-Rossi J, Hergersberg M, Boltshauser E, Papi L, Rouleau GA, Poptodorov G, Jordanova A, Rask-Andersen H, Kluwe L, Mautner V, Sainio M, Hung G, Mathiesen T, Möller C, Pulst SM, Harder H, Heiberg A, Honda M, Niimura M, Sahlén S, Blennow E, Albertson DG, Pinkel D, Dumanski JP. Bruder CE, et al. Among authors: heiberg a. Hum Mol Genet. 2001 Feb 1;10(3):271-82. doi: 10.1093/hmg/10.3.271. Hum Mol Genet. 2001. PMID: 11159946 Free article.
Second trimester prenatal diagnosis of the fragile X.
Tommerup N, Aula P, Gustavii B, Heiberg A, Holmgren G, von Koskull H, Leisti J, Mikkelsen M, Mitelman F, Nielsen KB, et al. Tommerup N, et al. Among authors: heiberg a. Am J Med Genet. 1986 Jan-Feb;23(1-2):313-24. doi: 10.1002/ajmg.1320230124. Am J Med Genet. 1986. PMID: 2937296
Atrioventricular conduction time--a heritable trait?
Møller P, Heiberg A. Møller P, et al. Among authors: heiberg a. Clin Genet. 1980 Dec;18(6):450-3. doi: 10.1111/j.1399-0004.1980.tb01792.x. Clin Genet. 1980. PMID: 7449185
Atrioventricular conduction time--a heritable trait?
Møller P, Heiberg A. Møller P, et al. Among authors: heiberg a. Clin Genet. 1980 Dec;18(6):454-5. doi: 10.1111/j.1399-0004.1980.tb01793.x. Clin Genet. 1980. PMID: 7449186
158 results