Zobrazeno 1 - 7
of 7
pro vyhledávání: '"aggrecanopathy"'
Autor:
Antoine Denis, Sami Chergui, Shuaa Basalom, Philippe M. Campeau, Chantal Janelle, Thierry Pauyo
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 1, Pp n/a-n/a (2022)
Abstract Background Osteochondritis dissecans is a condition wherein there is a subchondral bone lesion that causes pain, inflammation, and cartilage damage. Dominant Familial Osteochondritis Dissecans is a rare and severe form of osteochondritis dis
Externí odkaz:
https://doaj.org/article/643348b172e24b38a7ca0daf5462fbbb
Autor:
Angelo Florio, Riccardo Papa, Roberta Caorsi, Alessandro Consolaro, Roberto Gastaldi, Marco Gattorno, Paolo Picco
Publikováno v:
Italian Journal of Pediatrics, Vol 45, Iss 1, Pp 1-3 (2019)
Abstract Heterozygous mutations of the ACAN gene have been associated with a broad spectrum of non-lethal skeletal dysplasias, called Aggrecanopathies. We report a case of a child with severe inflammatory elbow involvement mimicking septic arthritis
Externí odkaz:
https://doaj.org/article/23d7151bef134996b5d8fa77ab79cdb0
Autor:
Antoine Denis, Sami Chergui, Shuaa Basalom, Philippe M. Campeau, Chantal Janelle, Thierry Pauyo
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 10, Iss 1, Pp n/a-n/a (2022)
Molecular Genetics & Genomic Medicine, Vol 10, Iss 1, Pp n/a-n/a (2022)
Background Osteochondritis dissecans is a condition wherein there is a subchondral bone lesion that causes pain, inflammation, and cartilage damage. Dominant Familial Osteochondritis Dissecans is a rare and severe form of osteochondritis dissecans (O
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e97c4e2422934896272922d820df3a2c
https://doi.org/10.1002/mgg3.1773
https://doi.org/10.1002/mgg3.1773
Autor:
Alessandro Consolaro, Roberto Gastaldi, Roberta Caorsi, Riccardo Papa, Paolo Picco, Angelo Florio, Marco Gattorno
Publikováno v:
Italian Journal of Pediatrics
Italian Journal of Pediatrics, Vol 45, Iss 1, Pp 1-3 (2019)
Italian Journal of Pediatrics, Vol 45, Iss 1, Pp 1-3 (2019)
Heterozygous mutations of the ACAN gene have been associated with a broad spectrum of non-lethal skeletal dysplasias, called Aggrecanopathies. We report a case of a child with severe inflammatory elbow involvement mimicking septic arthritis who carri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da5e0bf3913df05a1c4859c9ae6a5c41
http://europepmc.org/articles/PMC6868685
http://europepmc.org/articles/PMC6868685
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Autor:
Denis A; Shriners Hospitals for Children, Montreal, Quebec, Canada., Chergui S; Shriners Hospitals for Children, Montreal, Quebec, Canada., Basalom S; Shriners Hospitals for Children, Montreal, Quebec, Canada., Campeau PM; Shriners Hospitals for Children, Montreal, Quebec, Canada., Janelle C; Shriners Hospitals for Children, Montreal, Quebec, Canada., Pauyo T; Shriners Hospitals for Children, Montreal, Quebec, Canada.
Publikováno v:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2022 Jan; Vol. 10 (1), pp. e1773. Date of Electronic Publication: 2021 Dec 10.