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List of works by Arvid Heiberg

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

scientific article published in May 2007

Children with autism spectrum disorders – The importance of medical investigations ⬇️

scientific article published on September 3, 2012

Clinical and genetic characteristics of late-onset Huntington's disease

scientific article

Clinical and molecular phenotype of Aicardi-Goutieres syndrome

scientific article

Dental characteristics in Williams syndrome: a clinical and radiographic evaluation

scientific article published in June 2003

Effect of epilepsy on autism symptoms in Angelman syndrome

scientific article published on 8 January 2018

Efficacy and safety of the dopaminergic stabilizer Pridopidine (ACR16) in patients with Huntington's disease

scientific article published on September 2010

Fabry disease in donor kidneys with 3- and 12-year follow-up after transplantation

scientific article published on 8 April 2010

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

scientific article published on 10 February 2018

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

scientific article published on January 2008

Mucopolysaccharidoses in the Scandinavian countries: incidence and prevalence

scientific article published on 4 August 2008

Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature

scientific article

Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response

scientific article

Neurocranial morphology and growth in Williams syndrome

scientific article

Neurofibromatosis type 2 and auditory brainstem implantation

scientific article published in August 2009

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

scientific article published on 04 September 2013

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

scientific article published on 22 March 2007

Parents' Attitudes toward Clinical Genetic Testing for Autism Spectrum Disorder-Data from a Norwegian Sample

scientific article

Parents' attitudes toward genetic research in autism spectrum disorder

scientific article

Understanding the experience of myotonic dystrophy. Mixed method study

scientific article

[A. Heiberg and colleagues reply]

scientific article published on 29 April 2014

[Complex craniofacial synostoses]

scientific article published on 01 May 2004

«A most strange instance of illness in several siblings»--first description of a rare neurological disease in 1830?

scientific article

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