Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Ricki S Carroll"'
Autor:
Ophélie Gourgas, Gabrielle Lemire, Alison J. Eaton, Sultanah Alshahrani, Angela L. Duker, Jingjing Li, Ricki S. Carroll, Stuart Mackenzie, Sarah M. Nikkel, Care4Rare Canada Consortium, Michael B. Bober, Kym M. Boycott, Monzur Murshed
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-20 (2023)
Abstract Matrix Gla protein (MGP) is a vitamin K-dependent post-translationally modified protein, highly expressed in vascular and cartilaginous tissues. It is a potent inhibitor of extracellular matrix mineralization. Biallelic loss-of-function vari
Externí odkaz:
https://doaj.org/article/da25b033c7fc4486b1e0a997e6fbb6d0
Autor:
David A. O'Connell, Ricki S. Carroll, Angela L. Duker, Andrea J. Schelhaas, Marjorie M. Postell, Paul T. Fawcett, Michael B. Bober
Publikováno v:
JBMR Plus, Vol 7, Iss 12, Pp n/a-n/a (2023)
Abstract The skeletal dysplasias are a heterogeneous group of genetic conditions caused by abnormalities of growth, development, and maintenance of bone and cartilage. Little is known about the roles that cytokines play in the inflammatory and non‐
Externí odkaz:
https://doaj.org/article/04a2a32850bd40e3bb3e1d75a8cde6fe
Autor:
Ophélie Gourgas, Gabrielle Lemire, Alison J. Eaton, Sultanah Alshahrani, Angela L. Duker, Jingjing Li, Ricki S. Carroll, Stuart Mackenzie, Sarah M. Nikkel, Care4Rare Canada Consortium, Michael B. Bober, Kym M. Boycott, Monzur Murshed
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-1 (2024)
Externí odkaz:
https://doaj.org/article/baf17e51d8864a008f9a109bd76b1197
Autor:
Ricki S. Carroll, Perri Donenfeld, Cristina McGreal, Jeanne M. Franzone, Richard W. Kruse, Catherine Preedy, Joanna Costa, Daniel R. Dirnberger, Michael B. Bober
Publikováno v:
Paediatric & Neonatal Pain, Vol 3, Iss 4, Pp 156-162 (2021)
Abstract Osteogenesis imperfecta (OI) is a rare genetic heterogeneous disorder that causes increased bone fragility and recurrent fractures. For infants with OI and diffuse fractures, pain management, which is nuanced and specific for this population
Externí odkaz:
https://doaj.org/article/96ef8613f7bb49e3800cf20617c37ae7
Microcephalic osteodysplastic primordial dwarfism type II is associated with global vascular disease
Autor:
Angela L. Duker, Dagmar Kinderman, Christy Jordan, Tim Niiler, Carissa M. Baker-Smith, Louise Thompson, David A. Parry, Ricki S. Carroll, Michael B. Bober
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-15 (2021)
Abstract Background Microcephalic osteodysplastic primordial dwarfism type II (MOPDII) is the most common form of primordial dwarfism, caused by bialleic mutations in the pericentrin gene (PCNT). Aside from its classic features, there are multiple as
Externí odkaz:
https://doaj.org/article/192b518261284b67aa8698531fe44ec0
Autor:
Ricki S. Carroll, Angela L. Duker, Andrea J. Schelhaas, Mary Ellen Little, Elissa G. Miller, Michael B. Bober
Publikováno v:
Palliative Medicine Reports, Vol 1, Iss 1, Pp 32-39 (2020)
Thanatophoric dysplasia (TD) is a rare skeletal dysplasia commonly thought to be lethal. In this case report, we discuss a nine-year-old male with TD and review his parents' decision making shortly after their son was born, the technology needed to s
Externí odkaz:
https://doaj.org/article/96adb5c51d0e429fb6410cc46ef36f92
Autor:
Ricki S. Carroll, Robert C. Olney, Angela L. Duker, Ryan F. Coghlan, William G. Mackenzie, Colleen P. Ditro, Cassondra J. Brown, David A. O’Connell, William A. Horton, Brian Johnstone, Eric A. Espiner, Timothy C. R. Prickett, Michael B. Bober
Publikováno v:
Calcified Tissue International. 111:66-72
This is the accepted manuscript version of the work published in its final form as Carroll, R. S., Olney, R. C., Duker, A. L., Coghlan, R. F., Mackenzie, W. G., Ditro, C. P., Brown, C. J., O’Connell, D. A., Horton, W. A., Johnstone, B., Espiner, E.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::746f9839b6a293968f4b85ea6b425fc4
https://doi.org/10.1007/s00223-022-00966-0
https://doi.org/10.1007/s00223-022-00966-0
Autor:
Jonathan M. Miller, Ricki S. Carroll
Publikováno v:
Delaware journal of public health. 8(1)
The tremendous success of vaccination programs worldwide over the past two centuries has produced a paradoxical effect whereby a lack of exposure to the devastating consequences of vaccine-preventable diseases has created an environment in which fear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3508d524aa0b0a7bf8b5641d936be02c
https://pubmed.ncbi.nlm.nih.gov/35402930
https://pubmed.ncbi.nlm.nih.gov/35402930
Autor:
Elissa G. Miller, Mary Ellen Little, Angela L. Duker, Ricki S Carroll, Michael B. Bober, Andrea J Schelhaas
Publikováno v:
Palliative Medicine Reports
Thanatophoric dysplasia (TD) is a rare skeletal dysplasia commonly thought to be lethal. In this case report, we discuss a nine-year-old male with TD and review his parents' decision making shortly after their son was born, the technology needed to s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fd84050a68bcf1dae31cf47eb706a30
http://europepmc.org/articles/PMC8241327
http://europepmc.org/articles/PMC8241327
Autor:
Ricki S, Carroll, Robert C, Olney, Angela L, Duker, Ryan F, Coghlan, William G, Mackenzie, Colleen P, Ditro, Cassondra J, Brown, David A, O'Connell, William A, Horton, Brian, Johnstone, Eric A, Espiner, Timothy C R, Prickett, Michael B, Bober
Publikováno v:
Calcified tissue international. 111(1)
Collagen X marker (CXM) is a degradation fragment of collagen type X. It is a real-time biomarker of height velocity with established norms. Plasma C-type natriuretic peptide (CNP) and NTproCNP levels have also been found to correlate with growth vel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d0bfdee41fbbb64f61e65ff8b84bcb60
https://pubmed.ncbi.nlm.nih.gov/35275235
https://pubmed.ncbi.nlm.nih.gov/35275235