[Contribution to the knowledge of spotted dystrophy of the corneal parenchyma. (Speckled dystrophy of François and Neetens)].
作者信息
Toselli C, Volpi U, Pirodda A
出版信息
Ann Ottalmol Clin Ocul. 1966 Sep;92(9):770-4.
PMID:5300513
Abstract
摘要
相似文献
1
[Contribution to the knowledge of spotted dystrophy of the corneal parenchyma. (Speckled dystrophy of François and Neetens)].[对角膜实质斑点状营养不良（弗朗索瓦和内滕斯斑点状营养不良）认识的贡献]
Ann Ottalmol Clin Ocul. 1966 Sep;92(9):770-4.
2
A clinical and histopathological study of François-Neetens speckled corneal dystrophy.
Am J Ophthalmol. 1977 Apr;83(4):554-60. doi: 10.1016/0002-9394(77)90566-9.
3
[Familial dermo-chondro-corneal dystrophy (François' syndrome)].[家族性皮肤-软骨-角膜营养不良（弗朗索瓦综合征）]
Ann Dermatol Venereol. 1977 Jun-Jul;104(6-7):475-8.
4
[Familial dermo-chondro-corneal dystrophy (François' syndrome) (author's transl)].[家族性皮肤-软骨-角膜营养不良（弗朗索瓦综合征）（作者译）]
Ann Dermatol Venereol. 1977 Jun-Jul;104(6-7):475-8.
5
[A hitherto unknown subepithelial hereditary corneal dystrophy].
Klin Monbl Augenheilkd. 1967;150(6):862-74.
6
Analysis of human transforming growth factor beta-induced gene mutation in corneal dystrophy.角膜营养不良中人类转化生长因子β诱导基因突变的分析。
Chin Med J (Engl). 2004 Sep;117(9):1418-21.
7
Genetic linkage of Francois-Neetens fleck (mouchetée) corneal dystrophy to chromosome 2q35.弗朗索瓦 - 内滕斯斑点状（穆谢泰）角膜营养不良与2号染色体q35区域的基因连锁关系。
Hum Genet. 2003 May;112(5-6):593-9. doi: 10.1007/s00439-002-0905-1. Epub 2003 Feb 27.
8
[Contribution to the knowledge of Schnyder's crystalline corneal dystrophy].[对施奈德结晶状角膜营养不良认识的贡献]
Ann Ottalmol Clin Ocul. 1967 Nov;93(11):1219-25.
9
Congenital hereditary endothelial dystrophy.先天性遗传性内皮营养不良
Bull Soc Belge Ophtalmol. 1984;211:1-5.
10
A new, X-linked endothelial corneal dystrophy.一种新的X连锁内皮性角膜营养不良。
Am J Ophthalmol. 2006 Mar;141(3):478-487. doi: 10.1016/j.ajo.2005.10.020.
Zotero 插件