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Plos One|May 13, 2017
Mutations in COL1A1 and COL1A2 and dental aberrations in children and adolescents with osteogenesis imperfecta - A retrospective cohort studyKristofer Andersson, Göran Dahllöf, Katarina Lindahl, et al.Calcified Tissue International|May 27, 2020
Bisphosphonate Therapy and Tooth Development in Children and Adolescents with Osteogenesis ImperfectaBarbro Malmgren, Georgios Tsilingaridis, Nina Monsef-Johansson, et al.European Journal of Human Genetics : EJHG|May 7, 2015
Genetic epidemiology, prevalence, and genotype-phenotype correlations in the Swedish population with osteogenesis imperfectaKatarina Lindahl, Eva Åström, Carl-Johan Rubin, et al.Plos One|March 16, 2017
Reverse lectin ELISA for detecting fucosylated forms of α1-acid glycoprotein associated with hepatocellular carcinomaEva Åström, Per Stål, Robin Zenlander, et al.Neurology|January 2, 2024
Bisphosphonates in Glucocorticoid-Treated Patients With Duchenne Muscular Dystrophy: A Systematic Review and Grading of the EvidenceErik Landfeldt, Kim Phung, Farasat Zaman, et al.American Journal of Medical Genetics. Part A|March 29, 2014
Autosomal dominant brachyolmia in a large Swedish family: phenotypic spectrum and natural courseGiedre Grigelioniene, Stefan Geiberger, Eva Horemuzova, et al.American Journal of Medical Genetics. Part A|November 8, 2024
Structural Variants in COL1A1 and COL1A2 in Osteogenesis ImperfectaDominyka Batkovskyte, Diana Swolin-Eide, Anna Hammarsjö, et al.Bone|June 25, 2018
Homozygosity for CREB3L1 premature stop codon in first case of recessive osteogenesis imperfecta associated with OASIS-deficiency to survive infancyKatarina Lindahl, Eva Åström, Anca Dragomir, et al.European Journal of Human Genetics : EJHG|June 30, 2026
Parent and professional experiences of a clinical trial of prenatal and postnatal stem cell therapy for severe osteogenesis imperfectaBikiran Behera, Charlotta Ingvoldstad Malmgren, Eva Åström, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 28, 2017
Expanding the Clinical Spectrum of Phenotypes Caused by Pathogenic Variants in PLOD2Gabriela Ferraz Leal, Gen Nishimura, Ulrika Voss, et al.Pageof 3