[HTML][HTML] Bioinspired mineralized collagen scaffolds for bone tissue engineering

Z Li, T Du, C Ruan, X Niu - Bioactive materials, 2021 - Elsevier
Successful regeneration of large segmental bone defects remains a major challenge in
clinical orthopedics, thus it is of important significance to fabricate a suitable alternative …

Management of endocrine disease: Osteogenesis imperfecta: An update on clinical features and therapies

R Marom, BM Rabenhorst… - European journal of …, 2020 - academic.oup.com
Osteogenesis imperfecta (OI) is an inherited skeletal dysplasia characterized by bone
fragility and skeletal deformities. While the majority of cases are associated with pathogenic …

Osteogenesis imperfecta: mechanisms and signaling pathways connecting classical and rare OI types

M Jovanovic, G Guterman-Ram, JC Marini - Endocrine reviews, 2022 - academic.oup.com
Osteogenesis imperfecta (OI) is a phenotypically and genetically heterogeneous skeletal
dysplasia characterized by bone fragility, growth deficiency, and skeletal deformity …

Osteogenesis imperfecta

JC Marini, WA Cabral - Genetics of bone biology and skeletal disease, 2018 - Elsevier
Osteogenesis imperfecta is a genetic disorder characterized by low bone mass, decreased
bone strength, increased bone fragility, and shortened stature. Autosomal dominant …

Collagen transport and related pathways in Osteogenesis Imperfecta

L Claeys, S Storoni, M Eekhoff, M Elting, L Wisse… - Human genetics, 2021 - Springer
Osteogenesis Imperfecta (OI) comprises a heterogeneous group of patients who share bone
fragility and deformities as the main characteristics, albeit with different degrees of severity …

Mechanisms of bone fragility: from osteogenesis imperfecta to secondary osteoporosis

A El-Gazzar, W Högler - International Journal of Molecular Sciences, 2021 - mdpi.com
Bone material strength is determined by several factors, such as bone mass, matrix
composition, mineralization, architecture and shape. From a clinical perspective, bone …

Osteogenesis imperfecta—Pathophysiology and therapeutic options

J Etich, L Leßmeier, M Rehberg, H Sill… - Molecular and cellular …, 2020 - Springer
Osteogenesis imperfecta (OI) is a rare congenital disease with a wide spectrum of severity
characterized by skeletal deformity and increased bone fragility as well as additional …

Osteogenesis imperfecta and therapeutics

R Morello - Matrix Biology, 2018 - Elsevier
Osteogenesis imperfecta, or brittle bone disease, is a congenital disease that primarily
causes low bone mass and bone fractures but it can negatively affect other organs. It is …

Genetic causes and mechanisms of osteogenesis imperfecta

J Lim, I Grafe, S Alexander, B Lee - Bone, 2017 - Elsevier
Osteogenesis Imperfecta (OI) is a genetic disorder characterized by various clinical features
including bone deformities, low bone mass, brittle bones, and connective tissue …

Managing the patient with osteogenesis imperfecta: a multidisciplinary approach

C Marr, A Seasman, N Bishop - Journal of multidisciplinary …, 2017 - Taylor & Francis
Osteogenesis imperfecta (OI) is a heterogeneous heritable connective tissue disorder
characterized by low bone density. The type and severity of OI are variable. The primary …