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Progressive diaphyseal dysplasia (Engelmann's disease). Report of a sporadic case of the mild form.

作者信息

Fallon M D, Whyte M P, Murphy W A

出版信息

J Bone Joint Surg Am. 1980 Apr;62(3):465-72.

PMID:7364820
Abstract
摘要

相似文献

1
Progressive diaphyseal dysplasia (Engelmann's disease). Report of a sporadic case of the mild form.
J Bone Joint Surg Am. 1980 Apr;62(3):465-72.
2
Progressive diaphyseal dysplasia--Engelmann's disease.
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[Observations on Camurati-Engelmann's disease (author's transl)].
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[Familial progressive diaphyseal dysplasia (Engelmann's disease)].
Zhonghua Fang She Xue Za Zhi. 1985 Feb;19(1):25-7.
5
Clinical and biochemical studies in Engelmann's disease (progressive diaphyseal dysplasia).
Q J Med. 1977 Apr;46(182):273-94.
6
Progressive diaphyseal dysplasia: genetics and clinical and radiologic manifestations.进行性骨干发育不良:遗传学及临床和影像学表现
Pediatrics. 1984 Sep;74(3):399-405.
7
[Camurati-Engelmann disease: description of a case in a child].[卡姆拉蒂-恩格尔曼病:一例儿童病例描述]
Radiol Med. 1980 Oct;66(10):711-2.
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Progressive diaphyseal dysplasia (Camurati-Engelmann's disease).进行性骨干发育异常(卡穆拉蒂-恩格尔曼病)。
Indian Pediatr. 1984 Aug;21(8):653-5.
9
[Progressive diaphyseal dysplasia (report of 4 cases)].
Zhonghua Fang She Xue Za Zhi. 1982 Aug;16(3):175-7.
10
[Course of diaphyseal dysplasia. Camurati-Engelmann disease followed for 14 years].[骨干发育异常病程。随访14年的卡姆拉蒂-恩格尔曼病]
J Radiol. 1983 Dec;64(12):675-9.

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Camurati-Engelmann disease: unique variant featuring a novel mutation in TGFβ1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligand.卡姆鲁蒂-恩格尔曼病:一种独特的变异型,其特征在于 TGFβ1 编码转化生长因子β 1 的新突变和 TNFSF11 编码 RANK 配体的错义变化。
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Papilloedema, a complication of progressive diaphyseal dysplasia: a series of three case reports.视乳头水肿,进行性骨干发育异常的一种并发症:三例病例报告系列
Br J Ophthalmol. 1998 Sep;82(9):1042-8. doi: 10.1136/bjo.82.9.1042.
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Craniotubular bone disorders.颅骨管状骨疾病。
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