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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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A prospective cohort study investigating gross motor function, pain, and health‐related quality of life 17 years after selective dorsal rhizotomy in cerebral palsy

Developmental medicine and child neurology, 2015-05, Vol.57 (5), p.484-490

2015

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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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Does loss of spasticity matter? A 10‐year follow‐up after selective dorsal rhizotomy in cerebral palsy

Developmental medicine and child neurology, 2011-08, Vol.53 (8), p.724-729

2011

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Expanding the Clinical Spectrum of Phenotypes Caused by Pathogenic Variants in PLOD2

Journal of bone and mineral research, 2018-04, Vol.33 (4), p.753-760

2018

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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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No osteonecrosis in jaws of young patients with osteogenesis imperfecta treated with bisphosphonates

Journal of oral pathology & medicine, 2008-04, Vol.37 (4), p.196-200

2008

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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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Novel mutations in the LRP5 gene in patients with Osteoporosis‐pseudoglioma syndrome

American journal of medical genetics. Part A, 2017-12, Vol.173 (12), p.3132-3135

2017

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

A prospective cohort study investigating gross motor function, pain, and health‐related quality of life 17 years after selective dorsal rhizotomy in cerebral palsy

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

Does loss of spasticity matter? A 10‐year follow‐up after selective dorsal rhizotomy in cerebral palsy

Expanding the Clinical Spectrum of Phenotypes Caused by Pathogenic Variants in PLOD2

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

Clinical validation of a novel automated cell‐free DNA screening assay for trisomies 21, 13, and 18 in maternal plasma

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

No osteonecrosis in jaws of young patients with osteogenesis imperfecta treated with bisphosphonates

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

Novel mutations in the LRP5 gene in patients with Osteoporosis‐pseudoglioma syndrome

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

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