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Authors whose works are in public domain in at least one jurisdiction

List of works by Arvid Heiberg

A. Heiberg and colleagues reply

scientific article published on 29 April 2014

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

Complex craniofacial synostoses

scientific article published on 01 May 2004

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

scientific article

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