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1

Effect of epilepsy on autism symptoms in Angelman syndrome

Bakke, Kristin A., Howlin, Patricia, Retterstøl, Lars, Kanavin, Øivind J., Heiberg, Arvid, Nærland, Terje

Journal:

Molecular Autism

Year:

2018

Language:

english

File:

PDF, 598 KB

english, 2018

2

THE UNIVERSITY BOAT RACE.

Eeg-Olofsson, Orvar, Heiberg, Arvid, Nesse, Trond, Skjeldal, Ola H.

Journal:

Year:

1914

Language:

english

File:

PDF, 178 KB

english, 1914

3

Do disabled adolescents view themselves differently from other young people?

Grue, Lars, Heiberg, Arvid

Journal:

Scandinavian Journal of Disability Research

Year:

2000

Language:

english

File:

PDF, 1.15 MB

english, 2000

4

Occipital horn syndrome and classical Menkes Syndrome caused by deep intronic mutations, leading to the activation of ATP7A pseudo-exon

Yasmeen, Saiqa, Lund, Katrine, De Paepe, Anne, De Bie, Sylvia, Heiberg, Arvid, Silva, João, Martins, Márcia, Skjørringe, Tina, Møller, Lisbeth B

Journal:

European Journal of Human Genetics

Year:

2014

Language:

english

File:

PDF, 327 KB

english, 2014

5

Notes on the History of Normality – Reflections on the Work of Quetelet and Galton

Grue, Lars, Heiberg, Arvid

Journal:

Scandinavian Journal of Disability Research

Year:

2006

Language:

english

File:

PDF, 188 KB

english, 2006

6

Identical mutation in 55% of the ATM alleles in 11 Norwegian AT families: evidence for a founder effect

Laake, Kirsten, Telatar, Milhan, Geitvik, Gry A, Hansen, Rita Øien, Heiberg, Arvid, Andresen, Anne Marie, Gatti, Richard, Børresen-Dale, Anne-Lise

Journal:

European Journal of Human Genetics

Year:

1998

Language:

english

File:

PDF, 484 KB

english, 1998

7

On the relationship between Lp(a) Iipoprotein, “sinking pre-β-lipoprotein” and inherited hyper-β-lipoproteinaemia

Arvid Heiberg, Kåre Berg

Journal:

Clinical Genetics

Year:

1974

Language:

english

File:

PDF, 700 KB

english, 1974

8

Children with autism spectrum disorders – The importance of medical investigations

Isaksen, Jørn, Bryn, Vesna, Diseth, Trond H., Heiberg, Arvid, Schjølberg, Synnve, Skjeldal, Ola H.

Journal:

European Journal of Paediatric Neurology

Year:

2013

Language:

english

File:

PDF, 871 KB

english, 2013

9

Second trimester prenatal diagnosis of the fragile X

Niels Tommerup, Pertti Aula, Björn Gustavii, Arvid Heiberg, Gösta Holmgren, Harriet von Koskull, Jaakko Leisti, Margareta Mikkelsen, Felix Mitelman, Karen B. Nielsen, Peter Steinbach, Sabine Stengel-R

Journal:

American Journal of Medical Genetics Part A

Year:

1986

Language:

english

File:

PDF, 603 KB

english, 1986

10

The heritability of serum lipoprotein and lipid concentrations. A twin study

Journal:

Clinical Genetics

Year:

1974

Language:

english

File:

PDF, 513 KB

english, 1974

11

Inheritance of xanthomatosis and hyper-β-lipoproteinaemia: A study of 7 large kind reds

Journal:

Clinical Genetics

Year:

1976

Language:

english

File:

PDF, 985 KB

english, 1976

12

Studies on Serum Pre-Alpha-Lipoprotein. An Albumin-ApoA-I-Lysolecithin-Containing Lipoprotein Family (AAL)

Wille, Leif E., Heiberg, Arvid, Gjone, Egil

Journal:

Scandinavian Journal of Clinical & Laboratory Investigation

Year:

1978

Language:

english

File:

PDF, 560 KB

english, 1978

13

Ocular findings in Norwegian patients with ataxia-telangiectasia: a 5 year prospective cohort study

Ruth Riise, Jan Ygge, Carl Lindman, Asbjørg Stray-Pedersen, Toke Bek, Olaug Kristin Rødningen, Arvid Heiberg

Journal:

Acta Ophthalmologica (Blackwell)

Year:

2007

Language:

english

File:

PDF, 849 KB

english, 2007

14

Alexithymia – an Inherited Trait?

Heiberg, Astrid, Heiberg, Arvid

Journal:

Psychotherapy and Psychosomatics

Year:

1977

File:

PDF, 2.29 MB

1977

15

Neurofibromatosis type 2: Multiple intra-dermal tumors in a toddler

Rustad, Cecilie F., Dahl, Hilde M., Bowers, Naomi L., Sitek, Jan C., Heiberg, Arvid, Huson, Susan, Prescott, Trine, Evans, D. Gareth R.

Journal:

American Journal of Medical Genetics Part A

Year:

2017

Language:

english

File:

PDF, 315 KB

english, 2017

16

Vestibular schwannomas occur in schwannomatosis and should not be considered an exclusion criterion for clinical diagnosis

Miriam J. Smith, Anjana Kulkarni, Cecilie Rustad, Naomi L. Bowers, Andrew J. Wallace, Susan E. Holder, Arvid Heiberg, Richard T. Ramsden, D. Gareth Evans

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 108 KB

english, 2012

17

Anorexia Nervosa – Two Cases in Discordant MZ Twins

Askevold, Finn, Heiberg, Arvid

Journal:

Psychotherapy and Psychosomatics

Year:

1979

Language:

english

File:

PDF, 547 KB

english, 1979

18

Atrioventricular conduction time -a heritable trait? : I. Routine tracings in adult Norwegians

PÅL Møller, Arvid Heiberg

Journal:

Clinical Genetics

Year:

1980

Language:

english

File:

PDF, 215 KB

english, 1980

19

Parents’ Attitudes toward Clinical Genetic Testing for Autism Spectrum Disorder—Data from a Norwegian Sample

Johannessen, Jarle, Nærland, Terje, Hope, Sigrun, Torske, Tonje, Høyland, Anne, Strohmaier, Jana, Heiberg, Arvid, Rietschel, Marcella, Djurovic, Srdjan, Andreassen, Ole

Journal:

International Journal of Molecular Sciences

Year:

2017

Language:

english

File:

PDF, 246 KB

english, 2017

20

VISION, COGNITION AND DEVELOPMENTAL CHARACTERISTICS OF GIRLS AND WOMEN WITH RETT SYNDROME

Stephen von Tetzchner, Karl H Jacobsen, Lars Smith, Ola H Skjeldal, Arvid Heiberg, Joseph F Fagan

Journal:

Developmental Medicine & Child Neurology

Year:

1996

Language:

english

File:

PDF, 1.04 MB

english, 1996

21

Atrioventricular conduction time - a heritable trait? : II. Family studies

Pål Møller, Arvid Heiberg

Journal:

Clinical Genetics

Year:

1980

Language:

english

File:

PDF, 96 KB

english, 1980

22

Tentative assignment of a locus for Rubinstein-Taybi syndrome to 16p13.3 by a de novo reciprocal translocation, t(7;16)(q34;p13.3)

Niels Tommerup, Carl B. Van Der Hagen, Arvid Heiberg

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 425 KB

english, 1992

23

Autosomal dominant retinitis pigmentosa in Norway: a 20-year clinical follow-up study with molecular genetic analysis. Two novel rhodopsin mutations: 1003delG and I179F

Jan Grøndahl, Ruth Riise, Arvid Heiberg, Trond Leren, Terje Christoffersen, Ragnheidur Bragadottir

Journal:

Acta Ophthalmologica (Blackwell)

Year:

2007

Language:

english

File:

PDF, 1.11 MB

english, 2007

24

The Lipoprotein and Lipid Pattern in Xanthomatosis

Journal:

Journal of Internal Medicine

Year:

1975

Language:

english

File:

PDF, 834 KB

english, 1975

25

Investigations as a prerequisite for genetic counseling after termination of pregnancy based on sonographic detection of serious central nervous system – or skeletal anomalies

ANNE KAASEN, TRINE E. PRESCOTT, ARVID HEIBERG, HELGE SCOTT, GUTTORM HAUGEN

Journal:

Acta Obstetricia et Gynecologica Scandinavica

Year:

2008

Language:

english

File:

PDF, 74 KB

english, 2008

26

Mucopolysaccharidoses in the Scandinavian countries: incidence and prevalence

Gunilla Malm, Allan M. Lund, Jan-Eric Månsson, Arvid Heiberg

Journal:

Acta Paediatrica

Year:

2008

Language:

english

File:

PDF, 104 KB

english, 2008

27

Dental characteristics in Williams syndrome: a clinical and radiographic evaluation

Axelsson, Stefan, Bjørnland, Tore, Kjær, Inger, Heiberg, Arvid, Storhaug, Kari

Journal:

Acta Odontologica Scandinavica

Year:

2003

Language:

english

File:

PDF, 145 KB

english, 2003

28

Studies on the genetic polymorphism of the C'3 of human serum

Ure Berg, Grethe Noer, Arvid Heiberg

Journal:

Clinical Genetics

Year:

1970

Language:

english

File:

PDF, 222 KB

english, 1970

29

Rett syndrome: Familial or geographical clustering of 3 cases in a Norwegian kindred

Eeg-Olofsson, Orvar, Heiberg, Arvid, Nesse, Trond, Skjeldal, Ola H.

Journal:

Pediatric Neurology

Year:

1992

Language:

english

File:

PDF, 122 KB

english, 1992

30

The inheritance of hyperipoproteinaemia with xanthomatosis:A study of 132 kindreds

Arvid Heiberg, Kåre Berg

Journal:

Clinical Genetics

Year:

1976

Language:

english

File:

PDF, 1.62 MB

english, 1976

31

Breast cancer and other cancers in Norwegian families with ataxia-telangiectasia

Dr. Anne-Lise Børresen, Tone Ikdahl Andersen, Steinar Tretli, Arvid Heiberg, Pål Møller

Journal:

Genes, Chromosomes and Cancer

Year:

1990

Language:

english

File:

PDF, 178 KB

english, 1990

32

THE INDIAN MEDICAL SERVICE.

Eeg-Olofsson, Orvar, Heiberg, Arvid, Nesse, Trond, Skjeldal, Ola H.

Journal:

Year:

1890

Language:

english

File:

PDF, 407 KB

english, 1890

33

Expanding the Genotypic Spectrum of Perrault syndrome

Demain, Leigh A. M., Urquhart, Jill E., O'Sullivan, James, Williams, Simon G., Bhaskar, Sanjeev S., Jenkinson, Emma M., Lourenco, Charles M., Heiberg, Arvid, Pearce, Simon H., Shalev, Stavit A., Yue,

Journal:

Clinical Genetics

Year:

2016

Language:

english

File:

PDF, 911 KB

english, 2016

34

Parents’ attitudes toward genetic research in autism spectrum disorder

Johannessen, Jarle, Nærland, Terje, Bloss, Cinnamon, Rietschel, Marcella, Strohmaier, Jana, Gjevik, Elen, Heiberg, Arvid, Djurovic, Srdjan, Andreassen, Ole A.

Journal:

Psychiatric Genetics

Year:

2016

Language:

english

File:

PDF, 129 KB

english, 2016

35

A comparative study of different electrophoretic techniques for classification of hereditary hyperlipoproteinaemias

Journal:

Clinical Genetics

Year:

1973

Language:

english

File:

PDF, 801 KB

english, 1973

36

A Possible Genetic Contribution to the Alexithymia Trait

Heiberg, Astrid Nøklebye, Heiberg, Arvid

Journal:

Psychotherapy and Psychosomatics

Year:

1978

File:

PDF, 1.11 MB

1978

37

The Risk of Atherosclerotic Vascular Disease in Subjects with Xanthomatosis

Journal:

Journal of Internal Medicine

Year:

1975

Language:

english

File:

PDF, 780 KB

english, 1975

38

The atrioventricular conduction time - a heritable trait?: III Twin studies

Pål Møller, Arvid Heiberg, Kåre Berg

Journal:

Clinical Genetics

Year:

1982

Language:

english

File:

PDF, 189 KB

english, 1982

39

Enzyme replacement therapy in MPS II patients over 20years of age or older at treatment initiation: An international case series from the Hunter Outcome Survey (HOS)

Whiteman, David, Heiberg, Arvid, Lampe, Christina

Journal:

Molecular Genetics and Metabolism

Year:

2013

Language:

english

File:

PDF, 63 KB

english, 2013

40

SERUM LIPID AND LIPOPROTEIN CONCENTRATIONS IN A NORWEGIAN POPULATION SAMPLE

Arvid Heiberg, Arne Grieg

Journal:

Journal of Internal Medicine

Year:

1974

Language:

english

File:

PDF, 351 KB

english, 1974

41

Retour d’experience RIS/PACS

Whiteman, David, Heiberg, Arvid, Lampe, Christina

Journal:

Journal de Radiologie

Year:

2005

Language:

french

File:

PDF, 692 KB

french, 2005

42

Health Survey of Adults with Neurofibromatosis 1 Compared to Population Study Controls

Fjermestad, Krister W., Nyhus, Livø, Kanavin, Øivind J., Heiberg, Arvid, Hoxmark, Lise B.

Journal:

Journal of Genetic Counseling

Year:

2018

Language:

english

File:

PDF, 472 KB

english, 2018

43

Understanding the Experience of Myotonic Dystrophy. Mixed Method Study

Geirdal, Amy Østertun, Lund-Petersen, Inger, Heiberg, Arvid

Journal:

Journal of Genetic Counseling

Year:

2015

Language:

english

File:

PDF, 227 KB

english, 2015

44

Hereditary motor neuron disease in a large Norwegian family with a “H46R” substitution in the superoxide dismutase 1 gene

Rune Østern, Toril Fagerheim, Kristin Ørstavik, Trygve Holmøy, Arvid Heiberg, Inger Lund-Petersen, Tim M. Strom, Øivind Nilssen, Arve Dahl

Journal:

Neuromuscular Disorders

Year:

2012

Language:

english

File:

PDF, 360 KB

english, 2012

45

Efficacy and Safety of the Dopaminergic Stabilizer Pridopidine (ACR16) in Patients With Huntington's Disease

Lundin, Anders, Dietrichs, Espen, Haghighi, Sara, Göller, Marie-Louise, Heiberg, Arvid, Loutfi, Ghada, Widner, Håkan, Wiktorin, Klas, Wiklund, Leif, Svenningsson, Anders, Sonesson, Clas, Waters, Nicho

Journal:

Clinical Neuropharmacology

Year:

2010

Language:

english

File:

PDF, 157 KB

english, 2010

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