Zobrazeno 1 - 6
of 6
pro vyhledávání: '"LSC, Least significant change"'
Publikováno v:
Journal of Clinical & Translational Endocrinology
Journal of Clinical & Translational Endocrinology, Vol 27, Iss, Pp 100281-(2022)
Journal of Clinical & Translational Endocrinology, Vol 27, Iss, Pp 100281-(2022)
Highlights • CF bone disease is prevalent in children and adults despite recent advances in care. • DXA is the current gold standard in the evaluation of bone strength. • Limited evidence exists for the use of MRI or HRpQCT in the assessment of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b26146e68fffbe85e5b871272ac8fd2
https://pubmed.ncbi.nlm.nih.gov/34984171
https://pubmed.ncbi.nlm.nih.gov/34984171
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 24, Iss, Pp 100606-(2020)
Molecular Genetics and Metabolism Reports, Vol 24, Iss, Pp 100606-(2020)
Gaucher disease (GD; OMIM 230800 ) is a lysosomal storage disorder caused by a deficiency in acid beta-glucosidase as a result of mutation in the GBA gene. Type 1 GD (GD1) is the most common form and its clinical manifestations include severe hematol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bad142e2badcc8ef79097b4cc1ba28ed
http://europepmc.org/articles/PMC7264072
http://europepmc.org/articles/PMC7264072
Akademický článek
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Akademický článek
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Autor:
Williams KM; Division of Pediatric Endocrinology, Diabetes, and Metabolism, Columbia University Irving Medical Center, 1150 St Nicholas Avenue, New York, NY, USA., Darukhanavala A; Division of Pediatric Endocrinology, University of Massachusetts Medical Center, 55 Lake Ave North, Worcester, MA, USA., Hicks R; Division of Pediatric Endocrinology, David Geffen School of Medicine, UCLA, 10833 Le Conte Ave, MDCC 22-315, Los Angeles, CA, USA., Kelly A; Division of Endocrinology and Diabetes, The Children's Hospital of Philadelphia, 2716 South Street, Philadelphia, PA, USA.
Publikováno v:
Journal of clinical & translational endocrinology [J Clin Transl Endocrinol] 2021 Dec 06; Vol. 27, pp. 100281. Date of Electronic Publication: 2021 Dec 06 (Print Publication: 2022).
Autor:
Sidhu K; McCaig Institute for Bone and Joint Health, Cumming School of Medicine, University of Calgary, 3280 Hospital Drive NW, Calgary, Alberta T2N 4Z6, Canada.; Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, 28 Oki Drive NW, Calgary, Alberta T3B 6A8, Canada., Boyd SK; McCaig Institute for Bone and Joint Health, Cumming School of Medicine, University of Calgary, 3280 Hospital Drive NW, Calgary, Alberta T2N 4Z6, Canada., Khan A; Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, 28 Oki Drive NW, Calgary, Alberta T3B 6A8, Canada.; Medical Genetics and Pediatrics, Cumming School of Medicine, University of Calgary, 28 Oki Drive NW, Calgary, Alberta T3B 6A8, Canada.
Publikováno v:
Molecular genetics and metabolism reports [Mol Genet Metab Rep] 2020 May 30; Vol. 24, pp. 100606. Date of Electronic Publication: 2020 May 30 (Print Publication: 2020).