Zobrazeno 1 - 10
of 300
pro vyhledávání: '"Bone Dysplasias"'
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
National Journal of Medical Research, Vol 10, Iss 02 (2020)
Sclerosing bone dysplasias are skeletal abnormalities of varying severity with a wide range of radiologic, clinical, and genetic features. It is divided into Hereditary and Non-hereditary. Types of hereditary sclerosing bone dysplasia include osteope
Externí odkaz:
https://doaj.org/article/48c747bf8d5c470485713e6a0b3852d3
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
MaryAnn Weis, Nadja Fratzl-Zelman, Paul Roschger, Joseph E. Perosky, Sergey Leikin, Wayne A. Cabral, David R. Eyre, Kenneth M. Kozloff, Heeseog Kang, Peter S. Backlund, Elena Makareeva, Antonella Forlino, Joan C. Marini, Adrienne Alimasa, Rachel Harris, Klaus Klaushofer, Aileen M. Barnes
Publikováno v:
Matrix Biol
Null mutations in CRTAP or P3H1, encoding cartilage-associated protein and prolyl 3-hydroxylase 1, cause the severe bone dysplasias, types VII and VIII osteogenesis imperfecta. Lack of either protein prevents formation of the ER prolyl 3-hydroxylatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8a617e2ff3015475deb503107c513a3
https://doi.org/10.1016/j.matbio.2020.02.003
https://doi.org/10.1016/j.matbio.2020.02.003
Autor:
Christie-Lee Wall, Lara E Graves, Ella Onikul, Andrew Biggin, Bruce Bennetts, Karen Wong, Craig F Munns, Julie Briody
Publikováno v:
Hormone Research in Paediatrics. 93:263-271
Osteogenesis imperfecta (OI) is a heterogenous group of heritable bone dysplasias characterized by bone fragility, typically low bone mass, joint laxity, easy bruising, and variable short stature. Classical OI is caused by autosomal dominant pathogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::700bcecdad6e39d4f777d5bd8e28043b
https://doi.org/10.1159/000510463
https://doi.org/10.1159/000510463
Publikováno v:
Volume: 13, Issue: 1 61-65
Anatomy
Anatomy
Using standard search engines PubMed, Scopus, Scielo, Cochrane, Science Direct and Medline, 433 articles were found to evaluate the information about sutural bones. Thirty-six articles that match our stated objectives about sutural bones were analyze
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90afac2b8f23be5a2015f10bee9bb646
https://doi.org/10.2399/ana.18.062
https://doi.org/10.2399/ana.18.062
Autor:
Abdelhakim Kherfani, Hachem Mahjoub
Publikováno v:
The Pan African Medical Journal, Vol 18, Iss 251 (2014)
Melorheostosis is a rare entity belonging to the group of sclerotic bone dysplasias. Described for the first time in 1922 by Leri, it remains imperfectly known as clinical presentations are highly variable, and the etiological diagnosis is not fully
Externí odkaz:
https://doaj.org/article/7019b1b23f31433b8b5103604ea4012a
Autor:
N. Paylar, Isıl Ozkaynak, Osman Demirhan, Idris Emir, C. Sagliker, Yahya Sagliker, Piril Sagliker Ozkaynak, Hasan Sabit Sagliker
Publikováno v:
Nephrology Dialysis Transplantation. 35
Background and Aims Sagliker Syndrome seems to be related to CKD and the consequent SH.SS starts and develops particularly before puberty while CKD reaches stage III level with overt SH. Since it occurs in some patients, it is plausible to think SS i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf7f95aec9413d91811bbe17c533201b
https://doi.org/10.1093/ndt/gfaa142.p0907
https://doi.org/10.1093/ndt/gfaa142.p0907
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Indian Journal of Orthopaedics, Vol 49, Iss 4, Pp 418-424 (2015)
Indian Journal of Orthopaedics
Indian Journal of Orthopaedics
Background: Treatment for developmental dysplasia of the hip (DDH) varies according to the age of the patient. For children under 3 months, the preferred treatment is Pavlik bandaging and/or dynamic hip orthosis;for children of 3-18 months (with/with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1f2f70818e2b569751ab98d4e0a6ec3
https://doi.org/10.4103/0019-5413.159627
https://doi.org/10.4103/0019-5413.159627