The patient clinical journey and socioeconomic impact of osteogenesis imperfecta: a systematic scoping review
M Rapoport, MB Bober, C Raggio, LL Wekre… - Orphanet Journal of …, 2023 - Springer
Background Osteogenesis imperfecta (OI) is a rare heritable connective tissue disorder
primarily characterised by skeletal deformity and fragility, and an array of secondary …
primarily characterised by skeletal deformity and fragility, and an array of secondary …
The role of environment in the pathogenesis of keratoconus
O de Azevedo Magalhães, MC Gonçalves… - Current opinion in …, 2021 - journals.lww.com
The literature shows that mechanical manipulation may be the common underlying factor or
the indispensable act precipitating the cascade of events leading to permanent corneal …
the indispensable act precipitating the cascade of events leading to permanent corneal …
The stimulating effect of rosmarinic acid and extracts from rosemary and lemon balm on collagen type I biosynthesis in osteogenesis imperfecta type I skin fibroblasts
J Sutkowska, N Hupert, K Gawron, JW Strawa… - Pharmaceutics, 2021 - mdpi.com
Rosemary extract (RE) and lemon balm extract (LBE) attract particular attention of
pharmacists due to their high therapeutic potential. Osteogenesis imperfecta (OI) type I is a …
pharmacists due to their high therapeutic potential. Osteogenesis imperfecta (OI) type I is a …
Collagen I defect corneal profiles in osteogenesis imperfecta
OA Magalhaes, HC Rohenkohl, LT de Souza… - Cornea, 2018 - journals.lww.com
Purpose: The goal of this study was to evaluate corneal profiles of patients with
osteogenesis imperfecta (OI) due to a collagen I gene mutation. Methods: This was a cross …
osteogenesis imperfecta (OI) due to a collagen I gene mutation. Methods: This was a cross …
Cyclic pamidronate treatment for osteogenesis imperfecta: Report from a Brazilian reference center
B Pinheiro, MB Zambrano, AP Vanz… - … and Molecular Biology, 2019 - SciELO Brasil
Abstract Treatment of moderate and severe forms of osteogenesis imperfecta (OI) with cyclic
pamidronate at the Reference Center for OI Treatment in Southern Brazil was studied. A …
pamidronate at the Reference Center for OI Treatment in Southern Brazil was studied. A …
Determinant Factors of the Quality of Life in Children with Osteogenesis Imperfecta during the COVID-19 Pandemic
N Rochmah, RI Mustikasari… - … Macedonian Journal of …, 2022 - repository.unair.ac.id
BACKGROUND: Osteogenesis imperfecta (OI) is a common chronic illness with increasing
prevalence. Coronavirus disease 2019 (COVID-19) and large society restriction policies in …
prevalence. Coronavirus disease 2019 (COVID-19) and large society restriction policies in …
[HTML][HTML] Resveratrol Delivery via Gene Therapy: Entering the Modern Era
G Singh - Turkish Journal of Pharmaceutical Sciences, 2022 - ncbi.nlm.nih.gov
Resveratrol is a natural compound (an antioxidant) and exhibits numerous therapeutic
activities. From a pharmacokinetic perspective, it is unclear whether resveratrol targets the …
activities. From a pharmacokinetic perspective, it is unclear whether resveratrol targets the …
Quality of Life among Children with Osteogenesis Imperfecta Receiving Bisphosphonate Therapy Before and during the 1st Year of the COVID-19 Pandemic in Dr …
BACKGROUND: Osteogenesis imperfecta (OI) is a chronic illness caused by a connective
tissue disorder that may lead to frequent fractures. Therefore, it may influence the quality of …
tissue disorder that may lead to frequent fractures. Therefore, it may influence the quality of …
[PDF][PDF] Determinant Factors of the Quality of Life in Children with Osteogenesis Imperfecta during the COVID-19 Pandemic. Open Access Maced J Med Sci. 2022 Apr …
BACKGROUND: Osteogenesis imperfecta (OI) is a common chronic illness with increasing
prevalence. Coronavirus disease 2019 (COVID-19) and large society restriction policies in …
prevalence. Coronavirus disease 2019 (COVID-19) and large society restriction policies in …
Анализ спектра мутаций в генах COL1A1 и COL1A2 с использованием массового параллельного секвенирования у больных несовершенным остеогенезом в …
НА Скрябин, ОЮ Васильева, АА Сивцев… - Медицинская …, 2020 - medgen-journal.ru
Аннотация Проведен поиск мутаций в генах COL1A1 и COL1A2 с использованием
массового параллельного секвенирования у 16 больных из 10 семей с несовершенным …
массового параллельного секвенирования у 16 больных из 10 семей с несовершенным …