Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Barbro Malmgren"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Abstract Background Osteogenesis imperfecta (OI) is a heterogeneous connective tissue disorder characterized by an increased tendency for fractures throughout life. Autosomal dominant (AD) mutations in COL1A1 and COL1A2 are causative in approximately
Externí odkaz:
https://doaj.org/article/b3f74a87cb05479faea9c91fdaf690bc
Autor:
Kristofer Andersson, Göran Dahllöf, Katarina Lindahl, Andreas Kindmark, Giedre Grigelioniene, Eva Åström, Barbro Malmgren
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0176466 (2017)
Osteogenesis imperfecta (OI) is a heterogeneous group of disorders of connective tissue, caused mainly by mutations in the collagen I genes (COL1A1 and COL1A2). Dentinogenesis imperfecta (DGI) and other dental aberrations are common features of OI. W
Externí odkaz:
https://doaj.org/article/00a0e237b4d34705b538f4610e27dbf4
Publikováno v:
Calcified Tissue International
Treatment with intravenous bisphosphonate (BP) in children and adolescents with osteogenesis imperfecta (OI) started in Sweden in 1991. No human studies on the role of BP therapy in development of disturbances in tooth mineralization or tooth morphol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f75d0e7ab1107e6a1b3b38afe2f9fb8
https://doi.org/10.1007/s00223-021-00835-2
https://doi.org/10.1007/s00223-021-00835-2
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Osteogenesis imperfecta (OI) is a heterogeneous connective tissue disorder characterized by an increased tendency for fractures throughout life. Autosomal dominant (AD) mutations in COL1A1 and COL1A2 are causative in approximately 85% of c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::962019e77f5dd1734bf5daab40ad5298
http://link.springer.com/article/10.1186/s13023-020-01361-4
http://link.springer.com/article/10.1186/s13023-020-01361-4
Autor:
Barbro Malmgren, Zaina Haif Al Qahtani, Nina Monsef-Johansson, Göran Dahllöf, Georgios Tsilingaridis, Eva Åström
Publikováno v:
Calcified Tissue International
Osteogenesis imperfecta (OI) is a heterogeneous connective tissue disorder characterized by repeated fractures and skeletal disorders. At present, bisphosphonate (BP) therapy is the gold standard for OI treatment. The present retrospective study eval
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8a73d1353c5e4d99ae2edc2093350aa
https://pubmed.ncbi.nlm.nih.gov/32451573
https://pubmed.ncbi.nlm.nih.gov/32451573
Autor:
Göran Dahllöf, Andreas Kindmark, Giedre Grigelioniene, Kristofer Andersson, Barbro Malmgren, Vasilios Zachariadis, Eva Åström, Katarina Lindahl
Publikováno v:
Oral Diseases. 23:42-49
Background Osteogenesis imperfecta (OI) is a heterogeneous group of disorders of connective tissue, mainly caused by mutations in the collagen type I genes (COL1A1 and COL1A2). Tooth agenesis is a common feature of OI. We investigated the association
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03425cfcb5ceed7e0e4f0d25bd43e8cf
https://doi.org/10.1111/odi.12568
https://doi.org/10.1111/odi.12568
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-7 (2018)
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-7 (2018)
Background Dentinogenesis imperfecta (DGI) is a heritable disorder of dentin. Genetic analyses have found two subgroups in this disorder: DGI type I, a syndromic form associated with osteogenesis imperfecta (OI), and DGI type II, a non-syndromic form
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::371d099888e7af34e15b1bc6ef109091
http://europepmc.org/articles/PMC6106925
http://europepmc.org/articles/PMC6106925
Publikováno v:
Dental Traumatology. 31:171-176
Background/Aim Tooth avulsion in young growing individuals is an uncommon but very severe dental trauma. The aim of this retrospective case–control study was to evaluate the effect of topical treatment with doxycycline on avulsed permanent teeth co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e24e6ecdb164c06ffb5554fb1b11a1b
https://doi.org/10.1111/edt.12161
https://doi.org/10.1111/edt.12161
Autor:
Barbro, Malmgren, Jens O, Andreasen, Marie Therese, Flores, Agneta, Robertson, Anthony J, DiAngelis, Lars, Andersson, Giacomo, Cavalleri, Nestor, Cohenca, Peter, Day, Morris Lamar, Hicks, Olle, Malmgren, Alex J, Moule, Juan, Onetto, Mitsuhiro, Tsukiboshi
Publikováno v:
Pediatric dentistry. 39(6)
Traumatic injuries to the primary dentition present special problems and the management is often different as compared with the permanent dentition. The International Association of Dental Traumatology (IADT) has developed a consensus statement after
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::c261e798a70eb4b119fff1bbe1b011a1
https://pubmed.ncbi.nlm.nih.gov/29179384
https://pubmed.ncbi.nlm.nih.gov/29179384
Autor:
Katarina Lindahl, Kristofer Andersson, Eva Åström, Barbro Malmgren, Andreas Kindmark, Göran Dahllöf, Giedre Grigelioniene
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0176466 (2017)
PLoS ONE
PLoS ONE
Osteogenesis imperfecta (OI) is a heterogeneous group of disorders of connective tissue, caused mainly by mutations in the collagen I genes (COL1A1 and COL1A2). Dentinogenesis imperfecta (DGI) and other dental aberrations are common features of OI. W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfcc4a9e21579666fef336593fe04b7d
http://europepmc.org/articles/PMC5428910?pdf=render
http://europepmc.org/articles/PMC5428910?pdf=render