Cargando…

A rare case of osteogenesis imperfecta (OI): clinical image

Detalles Bibliográficos
Autores principales:	Dhage, Prasad Pramod, Kulkarni, Chaitanya Ajay
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The African Field Epidemiology Network 2022
Materias:	Images in Clinical Medicine
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8797033/ https://www.ncbi.nlm.nih.gov/pubmed/35145601 http://dx.doi.org/10.11604/pamj.2022.41.9.32859

Ejemplares similares

Brittle bone disease (osteogenesis imperfecta): a rare condition
por: Dhage, Prasad Pramod, et al.
Publicado: (2022)

Eradicated and bygone Hansen’s disease with unusual features (leprosy)
por: Kulkarni, Chaitanya Ajay, et al.
Publicado: (2022)

Genetic evaluation of suspected osteogenesis imperfecta (OI)
por: Byers, Peter H., et al.
Publicado: (2006)

Evaluation of Stomatognathic Problems in Children with Osteogenesis Imperfecta (Osteogenesis Imperfecta − OI) − Preliminary Study
por: Smoląg, Danuta, et al.
Publicado: (2017)

Osteogenesis imperfecta: an unusual presentation
por: Patel, Hardik, et al.
Publicado: (2023)

Living with OI = Osteogenesis imperfecta = brittle bone disease
por: Wallentin, Ute
Publicado: (2010)

Osteogenesis imperfecta
por: Vitturi, Bruno Kusznir, et al.
Publicado: (2018)

CBCT of Osteogenesis Imperfecta of the Inner Ear
por: Gillardin, Patrick, et al.
Publicado: (2015)

Patient-reported experience of clinical care of osteogenesis imperfecta (OI) during the COVID-19 pandemic
por: Smyth, Debra, et al.
Publicado: (2023)

Targeting TGF-β for treatment of osteogenesis imperfecta
por: Song, I-Wen, et al.
Publicado: (2022)

Involving Families with Osteogenesis Imperfecta in Health Service Research: Joint Development of the OI/ECE Questionnaire
por: Dogba, Maman Joyce, et al.
Publicado: (2016)

The prevalence of musculoskeletal pain and therapy needs in adults with Osteogenesis Imperfecta (OI) a cross-sectional analysis
por: Barlow, Sophie, et al.
Publicado: (2022)

Giving Children With Osteogenesis Imperfecta a Voice: Participatory Approach for the Development of the Interactive Assessment and Communication Tool Sisom OI
por: Siedlikowski, Maia, et al.
Publicado: (2020)

Monomelic amyotrophy: a rare disease with unusual features (Hirayama disease)
por: Kulkarni, Chaitanya, et al.
Publicado: (2022)

Dissecting the phenotypic variability of osteogenesis imperfecta
por: Garibaldi, Nadia, et al.
Publicado: (2022)

Osteogenesis Imperfecta Affecting Two Generations
por: Gibson, Henry J. C.
Publicado: (1923)

Osteogenesis Imperfecta
por: Sam, Justin Easow, et al.
Publicado: (2017)

Live large flatworm in intestine
por: Joshi, Medhavi Vivek, et al.
Publicado: (2021)

Experiences of Children With Osteogenesis Imperfecta in the Co-design of the Interactive Assessment and Communication Tool Sisom OI: Secondary Analysis of Qualitative Design Sessions
por: Siedlikowski, Maia, et al.
Publicado: (2021)

Dentinogenesis imperfecta associated with osteogenesis imperfecta
por: Biria, Mina, et al.
Publicado: (2012)

Educational Case: Osteogenesis imperfecta
por: Light, Jonathan, et al.
Publicado: (2022)

Osteogenesis imperfect
por: Natarajan, Surya Besant, et al.
Publicado: (2021)

Clinical Application of Antenatal Genetic Diagnosis of Osteogenesis Imperfecta Type IV
por: Yuan, Jing, et al.
Publicado: (2015)

A novel splicing pathogenic variant in COL1A1 causing osteogenesis imperfecta (OI) type I in a Chinese family
por: Han, Yaxin, et al.
Publicado: (2020)

Micro Ribonucleic Acid−29a (miR−29a) Antagonist Normalizes Bone Metabolism in Osteogenesis Imperfecta (OI) Mice Model
por: Ko, Jih-Yang, et al.
Publicado: (2023)

A case of “ainhum”: a rare clinical image
por: Vikas, Madasu Sai
Publicado: (2023)

Management of Osteogenesis Imperfecta
por: Ralston, Stuart H., et al.
Publicado: (2020)

A rare case of meconium peritonitis in a neonate: a rare clinical image
por: Kiran, Adithya, et al.
Publicado: (2023)

Temporal Bone Imaging Features in Osteogenesis Imperfecta
por: Hermie, Isabeau, et al.
Publicado: (2017)

Femoral neck fractures in osteogenesis imperfecta treated with bisphosphonates
por: Papanna, M. C., et al.
Publicado: (2017)

Pathophysiology of respiratory failure in patients with osteogenesis imperfecta: a systematic review
por: Storoni, S., et al.
Publicado: (2021)

Mutations in SERPINF1 Cause Osteogenesis Imperfecta Type VI
por: Homan, Erica P, et al.
Publicado: (2011)

Anencephaly: a rare clinical image
por: Wanjari, Mayur Bhaskar, et al.
Publicado: (2022)

A rare clinical image of anencephaly
por: Sulochana, Nycy Babu, et al.
Publicado: (2023)

Mastocytosis: a rare clinical image
por: Chitmulwar, Vaibhavi, et al.
Publicado: (2023)

Osteogenesis Imperfecta in a Family
por: Bose, K. S.
Publicado: (1953)

Amelogenesis imperfecta and nephrocalcinosis syndrome
por: Chaitanya, V., et al.
Publicado: (2014)

A rare case of subdural hygroma in an adult male: a clinical image
por: Sheikh, Taj Afreen, et al.
Publicado: (2023)

Metaphyseal bands in osteogenesis imperfecta
por: Suresh, SS, et al.
Publicado: (2010)

Radiographic features of osteogenesis imperfecta
por: Renaud, Armelle, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_9dmit46nm0lo3cofitd9sg3k2m