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diaphysitis相关文献:
Hyperphosphatemic Tumoral Calcinosis: Pathogenesis, Clinical Presentation, and Challenges in Management.
Boyce AM, Lee AE, Roszko KL, Gafni RI.
Front Endocrinol (Lausanne). 2020 May 8;11:293. doi: 10.3389/fendo.2020.00293. eCollection 2020.
PMID:32457699
Tumoral calcinosis, diaphysitis, and hyperphosphatemia.
Clarke E, Swischuk LE, Hayden CK Jr.
Radiology. 1984 Jun;151(3):643-6. doi: 10.1148/radiology.151.3.6718723.
PMID:6718723
Diaphysitis in tumoral calcinosis syndrome.
Ballina-García FJ, Queiro-Silva R, Fernández-Vega F, Fernández-Sánchez JA, Weruaga-Rey A, Pérez-Del Rio MJ, Rodríguez-Pérez A.
J Rheumatol. 1996 Dec;23(12):2148-51.
PMID:8970054
Tuberculous diaphysitis of long bones.
Khanna U, Choudhury B, Roy D.
J Indian Med Assoc. 1980 Aug 16;75(4):71-2.
PMID:7217689
[Destructive diaphysitis in early congenital syphilis].
De Nichilo MA, Balsa RE, Florián A, Yarza C, Ceccón AM.
Med Cutan Ibero Lat Am. 1979;7(1-3):9-12.
PMID:398938
Topical Sodium Thiosulfate: A Treatment for Calcifications in Hyperphosphatemic Familial Tumoral Calcinosis?
Jost J, Bahans C, Courbebaisse M, Tran TA, Linglart A, Benistan K, Lienhardt A, Mutar H, Pfender E, Ratsimbazafy V, Guigonis V.
J Clin Endocrinol Metab. 2016 Jul;101(7):2810-5. doi: 10.1210/jc.2016-1087. Epub 2016 May 10.
PMID:27163355
[Pan-diaphysitis of the tibia; resection; pseudarthrosis; the Hahn-Hutington operation].
SALMON M, HENRY, BELLON.
Mars Chir. 1950 Nov-Dec;2(5):756-60.
PMID:14842244
Newly discovered mutations in the GALNT3 gene causing autosomal recessive hyperostosis-hyperphosphatemia syndrome.
Gok F, Chefetz I, Indelman M, Kocaoglu M, Sprecher E.
Acta Orthop. 2009 Feb;80(1):131-4. doi: 10.1080/17453670902807482.
PMID:19297793
Hyperphosphatemic familial tumoral calcinosis mimicking a cystic hemo-lymphangioma on MRI.
Houss SE, LRhorfi N, Yousfi ZE, Haddad SE, Chat L, Allali N, Rguieg N, Lamalmi N.
Radiol Case Rep. 2022 Sep 28;17(12):4603-4607. doi: 10.1016/j.radcr.2022.08.071. eCollection 2022 Dec.
PMID:36193273
Long-term clinical outcome and phenotypic variability in hyperphosphatemic familial tumoral calcinosis and hyperphosphatemic hyperostosis syndrome caused by a novel GALNT3 mutation; case report and review of the literature.
Rafaelsen S, Johansson S, Ræder H, Bjerknes R.
BMC Genet. 2014 Sep 24;15:98. doi: 10.1186/s12863-014-0098-3.
PMID:25249269
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