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Health and Quality of Life Outcomes|May 6, 2005
Coping, quality of life, and hope in adults with primary antibody deficienciesHanne Marie Høybråten Sigstad, Asbjørg Stray-Pedersen, Stig S Frøland
Clinical Dysmorphology|December 6, 2008
Two brothers with a microduplication including the MECP2 gene: rapid head growth in infancy and resolution of susceptibility to infectionTrine E Prescott, Olaug K Rødningen, Alf Bjørnstad, et al.
Brain : a Journal of Neurology|April 3, 2009
Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based studyAnne Kjersti Erichsen, Jeanette Koht, Asbjørg Stray-Pedersen, et al.
International Journal of Neonatal Screening|December 22, 2023
Newborn Genetic Screening-Still a Role for Sanger Sequencing in the Era of NGSSilje Hogner, Emma Lundman, Janne Strand, et al.
Acta Ophthalmologica Scandinavica|March 23, 2007
Ocular findings in Norwegian patients with ataxia-telangiectasia: a 5 year prospective cohort studyRuth Riise, Jan Ygge, Carl Lindman, et al.
BMC Genomics|January 15, 2016
cnvScan: a CNV screening and annotation tool to improve the clinical utility of computational CNV prediction from exome sequencing dataPubudu Saneth Samarakoon, Hanne Sørmo Sorte, Asbjørg Stray-Pedersen, et al.
Journal of Pediatric Hematology/Oncology|April 29, 2020
Delayed Radiation Myelopathy in a Child With Hodgkin Lymphoma and ARTEMIS MutationBuket Kara, Nusret Seher, Hulya Ucaryilmaz, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|March 3, 2022
A man in his sixties with chondritis and bone marrow failureØyvind Midtvedt, Asbjørg Stray-Pedersen, Helena Andersson, et al.
Hematology (Amsterdam, Netherlands)|December 11, 2023
Adult presentation of ornithine transcarbamylase deficiency: a possible cause of hyperammonemia after high-dose chemotherapy and stem cell transplantationGalina Tsykunova, Erle Kristensen, Asbjørg Stray-Pedersen, et al.
Frontiers in Immunology|August 29, 2025
A Norwegian cohort with STAT1-related disease - further expanding the clinical phenotypeKaren Helene Bronken Martinsen, Torstein Øverland, Asbjørg Stray-Pedersen, et al.
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