Katarina Lindahl
Uppsala, C, Sweden
Last Updated: 09/26/2026
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Found 9 publications
Homozygosity for CREB3L1 premature stop codon in first case of recessive osteogenesis imperfecta associated with OASIS-deficiency to survive infancy.
Journal: Bone
Published: April 10, 2018
Mutations in COL1A1 and COL1A2 and dental aberrations in children and adolescents with osteogenesis imperfecta - A retrospective cohort study.
Journal: PloS one
Published: December 19, 2016
Tooth agenesis in osteogenesis imperfecta related to mutations in the collagen type I genes.
Journal: Oral diseases
Published: June 08, 2016
Decreased fracture rate, pharmacogenetics and BMD response in 79 Swedish children with osteogenesis imperfecta types I, III and IV treated with Pamidronate.
Journal: Bone
Published: September 14, 2015
Genetic epidemiology, prevalence, and genotype-phenotype correlations in the Swedish population with osteogenesis imperfecta.
Journal: European journal of human genetics : EJHG
Published: July 17, 2015
Genetic epidemiology, prevalence, and genotype-phenotype correlations in the Swedish population with osteogenesis imperfecta.
Journal: European journal of human genetics : EJHG
Published: December 10, 2014
Treatment of osteogenesis imperfecta in adults.
Journal: European journal of endocrinology
Published: April 25, 2014
Allele dependent silencing of collagen type I using small interfering RNAs targeting 3'UTR Indels - a novel therapeutic approach in osteogenesis imperfecta.
Journal: International journal of medical sciences
Published: December 28, 2012
Heterozygosity for a coding SNP in COL1A2 confers a lower BMD and an increased stroke risk.
Journal: Biochemical and biophysical research communications
Published: April 29, 2009
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Last Updated: 09/26/2026