Arvid Heiberg
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Author network for Arvid Heiberg by COREMINE medical


Publications 2016

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 (2016)
Expanding the genotypic spectrum of Perrault syndrome
Clin Genet, 91 (2), 302-312
PubMed 26970254

Johannessen J, Nærland T, Bloss C, Rietschel M, Strohmaier J, Gjevik E, Heiberg A, Djurovic S, Andreassen OA (2016)
Parents' attitudes toward genetic research in autism spectrum disorder
Psychiatr Genet, 26 (2), 74-80
PubMed 26867185

Nylenna M, Breivik N, Heiberg A, Larsen Ø (2016)
[«A most strange instance of illness in several siblings»--first description of a rare neurological disease in 1830?]
Tidsskr Nor Laegeforen, 136 (5), 437-40
PubMed 26983149

Publications 2014

Apelland T, Gude E, Strøm EH, Gullestad L, Eiklid KL, Månsson JE, Reinholt FP, Houge G, Dahl CP, Almaas VM, Heiberg A (2014)
Familial globotriaosylceramide-associated cardiomyopathy mimicking Fabry disease
Heart, 100 (22), 1793-8
PubMed 25031264

Geirdal AØ, Lund-Petersen I, Heiberg A (2014)
Understanding the experience of myotonic dystrophy. Mixed method study
J Genet Couns, 24 (1), 169-78
PubMed 25123360

Heiberg A, Frich J, Røttingen JA (2014)
[A. Heiberg and colleagues reply]
Tidsskr Nor Laegeforen, 134 (8), 809-10
PubMed 24780961

Heiberg A, Frich J, Røttingen JA (2014)
[Rarity--a separate criterion used in prioritization?]
Tidsskr Nor Laegeforen, 134 (5), 534-6
PubMed 24621914

Publications 2013

Yasmeen S, Lund K, De Paepe A, De Bie S, Heiberg A, Silva J, Martins M, Skjørringe T, Møller LB (2013)
Occipital horn syndrome and classical Menkes Syndrome caused by deep intronic mutations, leading to the activation of ATP7A pseudo-exon
Eur J Hum Genet, 22 (4), 517-21
PubMed 24002164

Publications 2012

Isaksen J, Bryn V, Diseth TH, Heiberg A, Schjølberg S, Skjeldal OH (2012)
Children with autism spectrum disorders - the importance of medical investigations
Eur J Paediatr Neurol, 17 (1), 68-76
PubMed 22954514

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 et al. (2012)
Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature
Nat Genet, 44 (11), 1243-8
PubMed 23001123

Østern R, Fagerheim T, Ørstavik K, Holmøy T, Heiberg A, Lund-Petersen I, Strom TM, Nilssen Ø, Dahl A (2012)
Hereditary motor neuron disease in a large Norwegian family with a "H46R" substitution in the superoxide dismutase 1 gene
Neuromuscul Disord, 22 (6), 511-21
PubMed 22475618

Publications 2011

Frich JC, Heiberg A (2011)
[Dementia among younger persons and Huntington disease]
Tidsskr Nor Laegeforen, 131 (17), 1639; author reply 1639
PubMed 21901032

Smith MJ, Kulkarni A, Rustad C, Bowers NL, Wallace AJ, Holder SE, Heiberg A, Ramsden RT, Evans DG (2011)
Vestibular schwannomas occur in schwannomatosis and should not be considered an exclusion criterion for clinical diagnosis
Am J Med Genet A, 158A (1), 215-9
PubMed 22105938

Publications 2010

Gjone H, Diseth TH, Fausa O, Nøvik TS, Heiberg A (2010)
Familial adenomatous polyposis: mental health, psychosocial functioning and reactions to genetic risk in adolescents
Clin Genet, 79 (1), 35-43
PubMed 21143468

Lundin A, Dietrichs E, Haghighi S, Göller ML, Heiberg A, Loutfi G, Widner H, Wiktorin K, Wiklund L, Svenningsson A, Sonesson C, Waters N, Waters S, Tedroff J (2010)
Efficacy and safety of the dopaminergic stabilizer Pridopidine (ACR16) in patients with Huntington's disease
Clin Neuropharmacol, 33 (5), 260-4
PubMed 20616707

Publications 2009

Elvsåshagen T, Solyga V, Bakke SJ, Heiberg A, Kerty E (2009)
[Neurofibromatosis type 2 and auditory brainstem implantation]
Tidsskr Nor Laegeforen, 129 (15), 1469-73
PubMed 19690597

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 et al. (2009)
Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response
Nat Genet, 41 (7), 829-32
PubMed 19525956

Publications 2008

Heiberg A (2008)
[Huntington's disease]
Tidsskr Nor Laegeforen, 128 (19), 2214-7
PubMed 18846148

Kaasen A, Prescott TE, Heiberg A, Scott H, Haugen G (2008)
Investigations as a prerequisite for genetic counseling after termination of pregnancy based on sonographic detection of serious central nervous system--or skeletal anomalies
Acta Obstet Gynecol Scand, 87 (10), 998-1005
PubMed 18798055

Malm G, Lund AM, Månsson JE, Heiberg A (2008)
Mucopolysaccharidoses in the Scandinavian countries: incidence and prevalence
Acta Paediatr, 97 (11), 1577-81
PubMed 18681890

Publications 2007

Grøholt EK, Nordhagen R, Heiberg A (2007)
[Sense of coherence for parents of disabled children]
Tidsskr Nor Laegeforen, 127 (4), 422-6
PubMed 17304268

Grøndahl J, Riise R, Heiberg A, Leren T, Christoffersen T, Bragadottir R (2007)
Autosomal dominant retinitis pigmentosa in Norway: a 20-year clinical follow-up study with molecular genetic analysis. Two novel rhodopsin mutations: 1003delG and I179F
Acta Ophthalmol Scand, 85 (3), 287-97
PubMed 17488458

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 et al. (2007)
Clinical and molecular phenotype of Aicardi-Goutieres syndrome
Am J Hum Genet, 81 (4), 713-25
PubMed 17846997

Riise R, Ygge J, Lindman C, Stray-Pedersen A, Bek T, Rødningen OK, Heiberg A (2007)
Ocular findings in Norwegian patients with ataxia-telangiectasia: a 5 year prospective cohort study
Acta Ophthalmol Scand, 85 (5), 557-62
PubMed 17376192

Publications 2006

Kaasen A, Tuveng J, Heiberg A, Scott H, Haugen G (2006)
Correlation between prenatal ultrasound and autopsy findings: A study of second-trimester abortions
Ultrasound Obstet Gynecol, 28 (7), 925-33
PubMed 17121414

Publications 2005

Axelsson S, Kjaer I, Heiberg A, Bjørnland T, Storhaug K (2005)
Neurocranial morphology and growth in Williams syndrome
Eur J Orthod, 27 (1), 32-47
PubMed 15743861

Publications 2004

Meling TR, Ørstavik KH, Heiberg A (2004)
[Complex craniofacial synostoses]
Tidsskr Nor Laegeforen, 124 (9), 1230-4
PubMed 15131704

Ruud E, Heiberg A (2004)
[New knowledge does not always make it simpler]
Tidsskr Nor Laegeforen, 124 (24), 3256-7
PubMed 15608782

Stray-Pedersen A, Jónsson T, Heiberg A, Lindman CR, Widing E, Aaberge IS, Borresen-Dale AL, Abrahamsen TG (2004)
The impact of an early truncating founder ATM mutation on immunoglobulins, specific antibodies and lymphocyte populations in ataxia-telangiectasia patients and their parents
Clin Exp Immunol, 137 (1), 179-86
PubMed 15196260

Publications 2003

Axelson S, Bjornland T, Kjaer I, Heiberg A, Storhaug K (2003)
Dental characteristics in Williams syndrome: a clinical and radiographic evaluation
Acta Odontol. Scand., 61 (3), 129-136

Axelsson S, Bjørnland T, Kjaer I, Heiberg A, Storhaug K (2003)
Dental characteristics in Williams syndrome: a clinical and radiographic evaluation
Acta Odontol Scand, 61 (3), 129-36
PubMed 12868685

Moyhuddin A, Baser ME, Watson C, Purcell S, Ramsden RT, Heiberg A, Wallace AJ, Evans DG (2003)
Somatic mosaicism in neurofibromatosis 2: prevalence and risk of disease transmission to offspring
J Med Genet, 40 (6), 459-63
PubMed 12807969

Publications 2001

Andresen PA, Gedde-Dahl T, Fausa O, Eide TJ, Heiberg A (2001)
[Genetic analysis in familial adenomatous polyposis]
Tidsskr Nor Laegeforen, 121 (1), 64-8
PubMed 12013617

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 et al. (2001)
High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH
Hum Mol Genet, 10 (3), 271-82
PubMed 11159946

Heiberg A (2001)
[Aagenaes syndrome--lymphedema and intrahepatic cholestasis]
Tidsskr Nor Laegeforen, 121 (14), 1718-9
PubMed 11446017

Heiberg A (2001)
[Chronically ill and disabled children--a challenge for health services]
Tidsskr Nor Laegeforen, 121 (8), 898
PubMed 11332372

Heiberg A (2001)
Reflections on nursing in a new century
Int J Nurs Pract, 7 (1), 1
PubMed 11811341

Publications 2000

Heiberg A (2000)
[Genetic tests]
Tidsskr Nor Laegeforen, 120 (20), 2378
PubMed 11475218

Heiberg A (2000)
[With the Red Cross against AIDS]
Tidsskr Nor Laegeforen, 120 (29), 3597-8
PubMed 11188393

Jakobsen LB, Moum T, Heiberg A (2000)
[Need of better knowledge of genetic tests among Norwegian physicians]
Tidsskr Nor Laegeforen, 120 (20), 2419-22
PubMed 11475229

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 (2000)
Characterization of ATM mutations in 41 Nordic families with ataxia telangiectasia
Hum Mutat, 16 (3), 232-46
PubMed 10980530

Publications 1999

Jakobsen LB, Malt U, Nilsson B, Rosenlund S, Heiberg A (1999)
[Psychosocial consequences of presymptomatic genetic testing. A retrospective study of testing for Huntington disease]
Tidsskr Nor Laegeforen, 119 (13), 1913-6
PubMed 10382341

Publications 1998

Laake K, Telatar M, Geitvik GA, Hansen RO, Heiberg A, Andresen AM, Gatti R, Børresen-Dale AL (1998)
Identical mutation in 55% of the ATM alleles in 11 Norwegian AT families: evidence for a founder effect
Eur J Hum Genet, 6 (3), 235-44
PubMed 9781027

Publications 1997

Finne PH, Heiberg A, Holmström H (1997)
[Collagen analysis in fibroblasts in osteogenesis imperfecta. Clinical benefits]
Tidsskr Nor Laegeforen, 117 (10), 1469-73
PubMed 9178973

Heiberg A (1997)
[Dynamic mutations--new light on Huntington disease]
Tidsskr Nor Laegeforen, 117 (16), 2350-1
PubMed 9265284

Publications 1996

Bjłrnstad A, Heiberg A (1996)
[Neurofibromatosis type I in Norway. A clinical prevalence study based on a small project]
Tidsskr Nor Laegeforen, 116 (26), 3108-10
PubMed 8999570

von Tetzchner S, Jacobsen KH, Smith L, Skjeldal OH, Heiberg A, Fagan JF (1996)
Vision, cognition and developmental characteristics of girls and women with Rett syndrome
Dev Med Child Neurol, 38 (3), 212-25
PubMed 8631518

Publications 1995

Skjeldal OH, von Tetzchner S, Jacobsen K, Smith L, Heiberg A (1995)
Rett syndrome--distribution of phenotypes with special attention to the preserved speech variant
Neuropediatrics, 26 (2), 87
PubMed 7566462

Publications 1994

Heiberg A (1994)
[Problems of small patient groups, illustrated by Williams syndrome]
Tidsskr Nor Laegeforen, 114 (1), 14
PubMed 8296273

Publications 1992

Daniels RJ, Suthers GK, Morrison KE, Thomas NH, Francis MJ, Mathew CG, Loughlin S, Heiberg A, Wood D, Dubowitz V (1992)
Prenatal prediction of spinal muscular atrophy
J Med Genet, 29 (3), 165-70
PubMed 1348091

Heiberg A (1992)
[Frambu Health Center: information to families with functionally impaired members]
Nord Med, 107 (3), 88-90
PubMed 1532249

Heiberg A (1992)
[Expertise on examination and treatment of children with developmental and behavior disorders]
Tidsskr Nor Laegeforen, 112 (8), 1001-2
PubMed 1372769

Thommessen M, Heiberg A, Kase BF (1992)
Feeding problems in children with congenital heart disease: the impact on energy intake and growth outcome
Eur J Clin Nutr, 46 (7), 457-64
PubMed 1623850

Thommessen M, Kase BF, Heiberg A (1992)
Growth and nutrition in 10 girls with Rett syndrome
Acta Paediatr, 81 (9), 686-90
PubMed 1421909

Tommerup N, van der Hagen CB, Heiberg A (1992)
Tentative assignment of a locus for Rubinstein-Taybi syndrome to 16p13.3 by a de novo reciprocal translocation, t(7;16)(q34;p13.3)
Am J Med Genet, 44 (2), 237-41
PubMed 1456298

Publications 1991

Heiberg A, Lofterød B (1991)
[Prader-Willi syndrome]
Nord Med, 106 (6-7), 189-90
PubMed 1852594

Thommessen M, Heiberg A, Kase BF, Larsen S, Riis G (1991)
Feeding problems, height and weight in different groups of disabled children
Acta Paediatr Scand, 80 (5), 527-33
PubMed 1831317

Thommessen M, Kase BF, Riis G, Heiberg A (1991)
The impact of feeding problems on growth and energy intake in children with cerebral palsy
Eur J Clin Nutr, 45 (10), 479-87
PubMed 1782919

Thommessen M, Riis G, Kase BF, Larsen S, Heiberg A (1991)
Energy and nutrient intakes of disabled children: do feeding problems make a difference?
J Am Diet Assoc, 91 (12), 1522-5
PubMed 1960343

Publications 1990

Børresen AL, Andersen TI, Tretli S, Heiberg A, Møller P (1990)
Breast cancer and other cancers in Norwegian families with ataxia-telangiectasia
Genes Chromosomes Cancer, 2 (4), 339-40
PubMed 2268581

Hagen T, Jensen D, Dietrichson P, Heiberg A (1990)
[Charcot-Marie-Tooth disease. Peroneal muscular atrophy]
Tidsskr Nor Laegeforen, 110 (24), 3110-5
PubMed 2237866

Heutink P, van de Wetering BJ, Breedveld GJ, Weber J, Sandkuyl LA, Devor EJ, Heiberg A, Niermeijer MF, Oostra BA (1990)
No evidence for genetic linkage of Gilles de la Tourette syndrome on chromosomes 7 and 18
J Med Genet, 27 (7), 433-6
PubMed 2395161

Aakhus T, Brosstad F, Halse J, Ose L, Brodwall EK, Finne P, Natvig J, Stavem P, Heiberg A, Orstavik LA (1990)
[Are prosecuted parents allowed the benefit of the doubt in cases of child abuse?]
Tidsskr Nor Laegeforen, 110 (5), 627-8
PubMed 2309218

Publications 1988

MICHALSEN H, FOLLERAS S, BENTSEN BS, HEIBERG A (1988)
SOCIAL MEDICAL ASPECTS OF CYSTIC-FIBROSIS IN NORWAY .1. CHARACTERIZATION OF THE MATERIAL
Scand. J. Gastroenterol., 23 143, 52-55

Michalsen H, Follerås S, Bentsen BS, Heiberg A (1988)
Social-medical aspects of cystic fibrosis in Norway. I. Characterization of the material
Scand J Gastroenterol Suppl, 143, 52-5
PubMed 3164510

Publications 1987

Børresen AL, Heiberg A, Møller P, Berg K (1987)
Evidence for a sperm mutation resulting in Duchenne muscular dystrophy
Clin Genet, 32 (3), 187-91
PubMed 2887319

Publications 1986

Tommerup N, Aula P, Gustavii B, Heiberg A, Holmgren G, von Koskull H, Leisti J, Mikkelsen M, Mitelman F, Nielsen KB (1986)
Second trimester prenatal diagnosis of the fragile X
Am J Med Genet, 23 (1-2), 313-24
PubMed 2937296

Vilming ST, Dietrichson P, Isachsen MM, Løvvik L, Heiberg A (1986)
Late-onset hereditary myopathy with abnormal mitochondria and progressive dementia
Acta Neurol Scand, 73 (5), 502-6
PubMed 3727928

Publications 1985

Donald JA, Wallis SC, Kessling A, Tippett P, Robson EB, Ball S, Davies KE, Scambler P, Berg K, Heiberg A (1985)
Linkage relationships of the gene for apolipoprotein CII with loci on chromosome 19
Hum Genet, 69 (1), 39-43
PubMed 3855405

Publications 1984

Humphries SE, Donald JA, McFadden JJ, Shull S, Williamson R, Jowett NI, Galton DJ, Julsrud JO, Berg K, Heiberg A (1984)
The use of polymorphic DNA and protein markers for the third complement component for determining linkage of familial hypercholesterolaemia
Atherosclerosis, 52 (3), 267-78
PubMed 6497930

Publications 1982

Møller P, Heiberg A, Berg K (1982)
The atrioventricular conduction time - a heritable trait? III. Twin studies
Clin Genet, 21 (3), 181-3
PubMed 7201363

Publications 1981

Heiberg A, Magnus P, Berg K, Nance WE (1981)
Blood pressure in Norwegian twins
Prog Clin Biol Res, 69 Pt C, 163-8
PubMed 7198238

Publications 1980

Heiberg A, Helöe B, Heiberg AN, Helöe LA, Magnus P, Berg K, Nance WE (1980)
Myofascial pain dysfunction (MPD) syndrome in twins
Community Dent Oral Epidemiol, 8 (8), 434-6
PubMed 6942960

Møller P, Heiberg A (1980)
Atrioventricular conduction time--a heritable trait?
Clin Genet, 18 (6), 450-3
PubMed 7449185

Møller P, Heiberg A (1980)
Atrioventricular conduction time--a heritable trait?
Clin Genet, 18 (6), 454-5
PubMed 7449186

Publications 1979

Askevold F, Heiberg A (1979)
Anorexia nervosa--two cases in discordant MZ twins
Psychother Psychosom, 32 (1-4), 223-8
PubMed 550176

Publications 1978

Berg K, Heiberg A (1978)
Linkage between familial hypercholesterolemia with xanthomatosis and the C3 polymorphism confirmed
Cytogenet Cell Genet, 22 (1-6), 621-3
PubMed 752554

Dahl AA, Dahl CI, Heiberg A, Husby R, Olafsen OM, Sørensen T, Weisaeth L (1978)
A presentation of short-term psychotherapy project at the Oslo University Psychiatric Clinic
Psychother Psychosom, 29 (1-4), 299-304
PubMed 724946

Heiberg A (1978)
The main lines of the short-term psychotherapy project in Oslo
Psychother Psychosom, 29 (1-4), 309-11
PubMed 724949

Heiberg AN, Heiberg A (1978)
A possible genetic contribution to the alexithymia trait
Psychother Psychosom, 30 (3-4), 205-10
PubMed 570290

Wille LE, Heiberg A, Gjone E (1978)
Studies on serum pre-alpha-lipoprotein. An albumin-ApoA-I-lysolecithin-containing lipoprotein family (AAL)
Scand J Clin Lab Invest Suppl, 150, 59-65
PubMed 85328

WILLE LE, HEIBERG A, GJONE E (1978)
STUDIES ON SERUM PRE-ALPHA-LIPOPROTEIN - ALBUMIN-APOA-I-LYSOLECITHIN-CONTAINING LIPOPROTEIN FAMILY (AAL)
Scand. J. Clin. Lab. Invest., 38 150, 59-65

Publications 1977

Heiberg A, Heiberg A (1977)
Alexithymia -- an inherited trait?
Psychother Psychosom, 28 (1-4), 221-5
PubMed 565064

Heiberg A, Slack J (1977)
Family similarities in the age at coronary death in familial hypercholesterolaemia
Br Med J, 2 (6085), 493-5
PubMed 890365

Helöe B, Helöe LA, Heiberg A (1977)
Relationship between sociomedical factors and TMJ-symptoms in Norwegians with myofascial pain-dysfunction syndrome
Community Dent Oral Epidemiol, 5 (5), 207-12
PubMed 269766

Publications 1976

Berg K, Heiberg A (1976)
Linkage studies on familial hyperlipoproteinemia with xanthomatosis: normal lipoprotein markers and the C3 polymorphism
Cytogenet Cell Genet, 16 (1-5), 266-70
PubMed 975887

Berg K, Heiberg A (1976)
Linkage studies on familial hyperlipoproteinemia with xanthomatosis: normal lipoprotein markers and the C3 polymorphism
Birth Defects Orig Artic Ser, 12 (7), 266-70
PubMed 1024622

Heiberg A (1976)
Inheritance of xanthomatosis and hyper-beta-lipoproteinaemia. A study of 7 large kindreds
Clin Genet, 9 (1), 92-111
PubMed 174850

Heiberg A (1976)
Indications for psychotherapy in a psychiatric clinic population. Reliability and validity of evaluations
Psychother Psychosom, 27 (1), 18-25
PubMed 1052185

Heiberg A, Berg K (1976)
The inheritance of hyperlipoproteinaemia with xanthomatosis. A study of 132 kindreds
Clin Genet, 9 (2), 203-33
PubMed 174852

Publications 1975

Eitinger L, Heiberg A, Sifneos P, Waldenstrom E (1975)
Psychotherapeutic problems, research and plans at the Psychiatric Department, University of Oslo
Psychother Psychosom, 25 (1-6), 221-4
PubMed 1129413

Heiberg A (1975)
The lipoprotein and lipid pattern in xanthomatosis
Acta Med Scand, 198 (3), 183-95
PubMed 1180126

Heiberg A (1975)
The risk of atherosclerotic vascular disease in subjects with xanthomatosis
Acta Med Scand, 198 (4), 249-61
PubMed 1189982

Heiberg A (1975)
Indications for psychotherapy in a psychiatric clinic population. A survey
Psychother Psychosom, 26 (3), 156-66
PubMed 1215453

Heiberg A, Berg K (1975)
Linkage data on the MNSs blood group-red cell acid phosphatase realationship
Hum Hered, 25 (2), 93-4
PubMed 1150305

Heiberg A, Sorensen T, Olafsen OM (1975)
Short-term dynamic psychotherapy; three models of treatment
Psychother Psychosom, 26 (4), 229-36
PubMed 1226419

Publications 1974

Heiberg A (1974)
The heritability of serum lipoprotein and lipid concentrations. A twin study
Clin Genet, 6 (4), 307-16
PubMed 4474930

Heiberg A, Berg K (1974)
On the relationship between Lp(a) lipoprotein, "sinking pre-beta-lipoprotein" and inherited hyper-beta-lipoproteinaemia
Clin Genet, 5 (2), 144-56
PubMed 4364245

Heiberg A, Grieg A (1974)
Serum lipid and lipoprotein concentrations in a Norwegian population sample
Acta Med Scand, 196 (3), 155-60
PubMed 4371219

Publications 1973

Heiberg A (1973)
A comparative study of different electrophoretic techniques for classification of hereditary hyperlipoproteinaemias
Clin Genet, 4 (5), 450-60
PubMed 4127396

Heiberg A, Amundsen S (1973)
Red cell acid phosphatase polymorphism in a Norwegian population sample
Hum Hered, 23 (4), 352-6
PubMed 4775459

Publications 1972

Heiberg A, Lingjaerde O (1972)
A controlled study on the possible effect of dihydroergotamine against dryness of the mouth in patients treated with tricyclic antidepressants
Acta Psychiatr Scand, 48 (4), 353-9
PubMed 4566565

Publications 1970

Heiberg A (1970)
[Iron lung (siderosis)]
Tidsskr Nor Laegeforen, 90 (5), 499-500
PubMed 5426199

Publications 1969

Heiberg A (1969)
[Delirious reactions in acute pancreatitis]
Nord Med, 82 (37), 1130-2
PubMed 5307785

Heiberg A (1969)
[Familial sarcoidosis]
Nord Med, 81 (18), 565-6
PubMed 5768310

Heiberg A (1969)
[Reflex time and thyroid function]
Tidsskr Nor Laegeforen, 89 (16), 1246-7
PubMed 5375346

Heiberg A (1969)
[Nicotinyl alcohol as a cholesterol-lowering agent]
Nord Med, 81 (22), 698-700
PubMed 5796529

Publications 1967

Heiberg A (1967)
[Spray treatment for bronchial asthma]
Tidsskr Nor Laegeforen, 87 (24), 2053-4
PubMed 5590476

Larsen O, Heiberg A (1967)
[Diagram of hemoglobin-hematocrit-MCHC correlations as a record form in anemia therapy]
Nord Med, 78 (37), 1190-2
PubMed 6054467

Publications 1966

Heiberg A (1966)
[Achilles tendon reflex time as a measure of thyroid function]
Tidsskr Nor Laegeforen, 86 (24), 1736-8 passim
PubMed 5980417

Publications 1964

HEIBERG A (1964)
[ACUTE TOLUENE POISONING. AN ACCIDENTAL CASE WHILE PAINTING IN A SILO]
Tidsskr Nor Laegeforen, 84, 623-4
PubMed 14144342

Publications 1963

HEIBERG A (1963)
[2 CASES OF THROMBOCYTOPENIC PURPURA AFTER ACUTE EXANTHEMATOUS CHILDHOOD DISEASES]
Tidsskr Nor Laegeforen, 83, 1465-6
PubMed 14055690