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Mutations in COL1A1 and COL1A2 and dental aberrations in children and adolescents with osteogenesis imperfecta - A retrospective cohort study

PloS one, 2017-05, Vol.12 (5), p.e0176466-e0176466

2017

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Genetic epidemiology, prevalence, and genotype-phenotype correlations in the Swedish population with osteogenesis imperfecta

European journal of human genetics : EJHG, 2015-08, Vol.23 (8), p.1042-1050

2015

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Determination of Fucose Concentration in a Lectin-Based Displacement Microfluidic Assay

Applied biochemistry and biotechnology, 2019-07, Vol.188 (3), p.868-877

2019

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Abnormalities in Tooth Formation after Early Bisphosphonate Treatment in Children with Osteogenesis Imperfecta

Calcified tissue international, 2021-08, Vol.109 (2), p.121-131

2021

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Reverse lectin ELISA for detecting fucosylated forms of alpha 1-acid glycoprotein associated with hepatocellular carcinoma

PloS one, 2017-03, Vol.12 (3)

2017

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Mesenchymal Stem Cell Therapy for Osteogenesis Imperfecta

Clinical obstetrics and gynecology, 2021-12, Vol.64 (4), p.898

2021

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Bisphosphonate Therapy and Tooth Development in Children and Adolescents with Osteogenesis Imperfecta

Calcified tissue international, 2020-08, Vol.107 (2), p.143-150

2020

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Homozygosity for CREB3L1 premature stop codon in first case of recessive osteogenesis imperfecta associated with OASIS-deficiency to survive infancy

Bone (New York, N.Y.), 2018-09, Vol.114, p.268-277

2018

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Reverse lectin ELISA for detecting fucosylated forms of α1-acid glycoprotein associated with hepatocellular carcinoma

PloS one, 2017, Vol.12 (3), p.e0173897-e0173897

2017

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Disialo–trisialo bridging of transferrin is due to increased branching and fucosylation of the carbohydrate moiety

Clinica chimica acta, 2012-12, Vol.414, p.58-64

2012

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Exploring pain interference and self-perceived health status in children with osteogenesis imperfecta - a cross-sectional study

BMC musculoskeletal disorders, 2022-09, Vol.23 (1), p.1-876, Article 876

2022

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Imaging single DNA molecules for high precision NIPT

Scientific reports, 2018-03, Vol.8 (1), p.4549-8, Article 4549

2018

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Elucidating the selectivity of recombinant forms of Aleuria aurantia lectin using weak affinity chromatography

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2012-02, Vol.885-886, p.66-72

2012

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Intravenous pamidronate treatment of infants with severe osteogenesis imperfecta

Archives of disease in childhood, 2007-04, Vol.92 (4), p.332-338

2007

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The impact of foot orthoses on gait in children with Osteogenesis Imperfecta type I, III and IV – a cross-sectional study

BMC musculoskeletal disorders, 2024-07, Vol.25 (1), p.1-12, Article 560

2024

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Production and characterization of a monomeric form and a single-site form of Aleuria aurantia lectin

Glycobiology (Oxford), 2011-01, Vol.21 (1), p.34-44

2011

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Mutations in COL1A1/A2 and CREB3L1 are associated with oligodontia in osteogenesis imperfecta

Orphanet journal of rare diseases, 2020-03, Vol.15 (1), p.80-80, Article 80

2020

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Pre‐ and Postnatal Transplantation of Fetal Mesenchymal Stem Cells in Osteogenesis Imperfecta: A Two‐Center Experience

Stem cells translational medicine, 2014-02, Vol.3 (2), p.255-264

2014

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Changes in the Expression of Nephrin Gene and Protein in Experimental Diabetic Nephropathy

Laboratory investigation, 2001-09, Vol.81 (9), p.1185-1190

2001

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Intravenous Pamidronate Treatment Improves Growth in Prepubertal Osteogenesis Imperfecta Patients

Hormone research in paediatrics, 2011-01, Vol.75 (5), p.354-361

2011

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Bisphosphonates in Glucocorticoid-Treated Patients With Duchenne Muscular Dystrophy: A Systematic Review and Grading of the Evidence

Neurology, 2024-01, Vol.102 (2), p.e207948

2024

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Fetal mesenchymal stem-cell engraftment in bone after in utero transplantation in a patient with severe osteogenesis imperfecta

Transplantation, 2005-06, Vol.79 (11), p.1607

2005

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Governance through Institutionalized Evaluation: Recentralization and Influences at Local Levels in Higher Education in Sweden

Evaluation (London, England. 1995), 2007-01, Vol.13 (1), p.48-67

2007

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A novel protein, densin, expressed by glomerular podocytes

Journal of the American Society of Nephrology, 2003-07, Vol.14 (7), p.1731-1737

2003

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Mutations in COL1A1 and COL1A2 and dental aberrations in children and adolescents with osteogenesis imperfecta - A retrospective cohort study

Genetic epidemiology, prevalence, and genotype-phenotype correlations in the Swedish population with osteogenesis imperfecta

Determination of Fucose Concentration in a Lectin-Based Displacement Microfluidic Assay

Abnormalities in Tooth Formation after Early Bisphosphonate Treatment in Children with Osteogenesis Imperfecta

Reverse lectin ELISA for detecting fucosylated forms of alpha 1-acid glycoprotein associated with hepatocellular carcinoma

Mesenchymal Stem Cell Therapy for Osteogenesis Imperfecta

An exploratory open-label multicentre phase I/II trial evaluating the safety and efficacy of postnatal or prenatal and postnatal administration of allogeneic expanded fetal mesenchymal stem cells for the treatment of severe osteogenesis imperfecta in infants and fetuses: the BOOSTB4 trial protocol

Bisphosphonate Therapy and Tooth Development in Children and Adolescents with Osteogenesis Imperfecta

Homozygosity for CREB3L1 premature stop codon in first case of recessive osteogenesis imperfecta associated with OASIS-deficiency to survive infancy

Reverse lectin ELISA for detecting fucosylated forms of α1-acid glycoprotein associated with hepatocellular carcinoma

Disialo–trisialo bridging of transferrin is due to increased branching and fucosylation of the carbohydrate moiety

Exploring pain interference and self-perceived health status in children with osteogenesis imperfecta - a cross-sectional study

Imaging single DNA molecules for high precision NIPT

Elucidating the selectivity of recombinant forms of Aleuria aurantia lectin using weak affinity chromatography

Intravenous pamidronate treatment of infants with severe osteogenesis imperfecta

The impact of foot orthoses on gait in children with Osteogenesis Imperfecta type I, III and IV – a cross-sectional study

Production and characterization of a monomeric form and a single-site form of Aleuria aurantia lectin

Mutations in COL1A1/A2 and CREB3L1 are associated with oligodontia in osteogenesis imperfecta

Pre‐ and Postnatal Transplantation of Fetal Mesenchymal Stem Cells in Osteogenesis Imperfecta: A Two‐Center Experience

Changes in the Expression of Nephrin Gene and Protein in Experimental Diabetic Nephropathy

Intravenous Pamidronate Treatment Improves Growth in Prepubertal Osteogenesis Imperfecta Patients

Bisphosphonates in Glucocorticoid-Treated Patients With Duchenne Muscular Dystrophy: A Systematic Review and Grading of the Evidence

Fetal mesenchymal stem-cell engraftment in bone after in utero transplantation in a patient with severe osteogenesis imperfecta

Governance through Institutionalized Evaluation: Recentralization and Influences at Local Levels in Higher Education in Sweden

A novel protein, densin, expressed by glomerular podocytes

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