[关于遗传性玻璃体视网膜变性（瓦格纳病）的临床表现和病理学] - Suppr

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[On the clinical manifestation and pathology of degeneratio hyaloideoretinalis hereditaria (Wagner)].

作者信息

BOEHRINGER H R, DIETERLE P, LANDOLT E

出版信息

Ophthalmologica. 1960 Mar-Apr;139:330-8. doi: 10.1159/000303718.

DOI:10.1159/000303718

PMID:13802004

Abstract

摘要

相似文献

[On the clinical manifestation and pathology of degeneratio hyaloideoretinalis hereditaria (Wagner)].

Ophthalmologica. 1960 Mar-Apr;139:330-8. doi: 10.1159/000303718.

ERYTHROCYTIC ANOMALIES IN HEREDITARY VITREO-RETINAL DEGENERATION (DEGENERATIO HYALOIDEORETINALIS).

Br J Ophthalmol. 1963 Oct;47(10):620-31. doi: 10.1136/bjo.47.10.620.

[Degeneratio hyaloideo-retinalis hereditaria Wagner (author's transl)].

Klin Monbl Augenheilkd. 1978 Dec;173(6):774-85.

Retina and vitreous pathology after LASIK.

Ophthalmology. 2001 Dec;108(12):2157. doi: 10.1016/s0161-6420(01)00872-7.

Concerning the pathogenesis of retinal holes.

Am J Ophthalmol. 1955 Oct;40(4):515-22. doi: 10.1016/0002-9394(55)90554-7.

Congenital vascular veils in the vitreous; hereditary retinoschisis.

Arch Ophthalmol. 1960 Jan;63:92-101. doi: 10.1001/archopht.1960.00950020094014.

Hereditary retinoschisis.

Am J Ophthalmol. 1961 Jun;51:1193-200. doi: 10.1016/0002-9394(61)92457-6.

A review of vitreoretinal interface pathology.

Int Ophthalmol Clin. 2009 Winter;49(1):133-43. doi: 10.1097/IIO.0b013e3181924b3e.

[Retinovitreous hemorrhages and their association with thrombopenia].

Sem Hop. 1961 May 2;37:1536-9.

Anatomy and pathology of the vitreo-retinal interface.

Eye (Lond). 1992;6 ( Pt 6):541-52. doi: 10.1038/eye.1992.119.

引用本文的文献

Wagner's syndrome.

Doc Ophthalmol. 1974 Nov;37(2):245-59. doi: 10.1007/BF00147261.

ERYTHROCYTIC ANOMALIES IN HEREDITARY VITREO-RETINAL DEGENERATION (DEGENERATIO HYALOIDEORETINALIS).

Br J Ophthalmol. 1963 Oct;47(10):620-31. doi: 10.1136/bjo.47.10.620.

COL2A1 exon 2 mutations: relevance to the Stickler and Wagner syndromes.

Br J Ophthalmol. 2000 Apr;84(4):364-71. doi: 10.1136/bjo.84.4.364.

Hereditary vitreoretinal dystrophy associated with peripheral neuropathy.

Graefes Arch Clin Exp Ophthalmol. 1994 Jun;232(6):330-6. doi: 10.1007/BF00175984.

Chorioretinal dysplasia in young subjects with Wagner's hereditary vitreoretinal degeneration.

Int Ophthalmol. 1981 Mar;3(2):67-77. doi: 10.1007/BF00133417.

The Wagner syndrome versus hereditary arthroophthalmopathy.

Trans Am Ophthalmol Soc. 1982;80:349-65.

The Wagner-Stickler syndrome complex.

Doc Ophthalmol. 1981 Dec 16;52(2):179-88. doi: 10.1007/BF01675204.

[On the clinical aspects, pathogenesis and differential diagnosis of peripheral uveitis].

Albrecht Von Graefes Arch Klin Exp Ophthalmol. 1967;174(1):9-33. doi: 10.1007/BF00406583.

Inherited hyaloideoretinopathy and skeletal dysplasia.

Trans Am Ophthalmol Soc. 1975;73:417-51.

Stickler's syndrome and neovascular glaucoma.

Br J Ophthalmol. 1979 Dec;63(12):826-31. doi: 10.1136/bjo.63.12.826.

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相似文献

[On the clinical manifestation and pathology of degeneratio hyaloideoretinalis hereditaria (Wagner)].

Ophthalmologica. 1960 Mar-Apr;139:330-8. doi: 10.1159/000303718.

ERYTHROCYTIC ANOMALIES IN HEREDITARY VITREO-RETINAL DEGENERATION (DEGENERATIO HYALOIDEORETINALIS).

Br J Ophthalmol. 1963 Oct;47(10):620-31. doi: 10.1136/bjo.47.10.620.

[Degeneratio hyaloideo-retinalis hereditaria Wagner (author's transl)].

Klin Monbl Augenheilkd. 1978 Dec;173(6):774-85.

Retina and vitreous pathology after LASIK.

Ophthalmology. 2001 Dec;108(12):2157. doi: 10.1016/s0161-6420(01)00872-7.

Concerning the pathogenesis of retinal holes.

Am J Ophthalmol. 1955 Oct;40(4):515-22. doi: 10.1016/0002-9394(55)90554-7.

Congenital vascular veils in the vitreous; hereditary retinoschisis.

Arch Ophthalmol. 1960 Jan;63:92-101. doi: 10.1001/archopht.1960.00950020094014.

Hereditary retinoschisis.

Am J Ophthalmol. 1961 Jun;51:1193-200. doi: 10.1016/0002-9394(61)92457-6.

A review of vitreoretinal interface pathology.

Int Ophthalmol Clin. 2009 Winter;49(1):133-43. doi: 10.1097/IIO.0b013e3181924b3e.

[Retinovitreous hemorrhages and their association with thrombopenia].

Sem Hop. 1961 May 2;37:1536-9.

Anatomy and pathology of the vitreo-retinal interface.

Eye (Lond). 1992;6 ( Pt 6):541-52. doi: 10.1038/eye.1992.119.

引用本文的文献

Wagner's syndrome.

Doc Ophthalmol. 1974 Nov;37(2):245-59. doi: 10.1007/BF00147261.

ERYTHROCYTIC ANOMALIES IN HEREDITARY VITREO-RETINAL DEGENERATION (DEGENERATIO HYALOIDEORETINALIS).

Br J Ophthalmol. 1963 Oct;47(10):620-31. doi: 10.1136/bjo.47.10.620.

COL2A1 exon 2 mutations: relevance to the Stickler and Wagner syndromes.

Br J Ophthalmol. 2000 Apr;84(4):364-71. doi: 10.1136/bjo.84.4.364.

Hereditary vitreoretinal dystrophy associated with peripheral neuropathy.

Graefes Arch Clin Exp Ophthalmol. 1994 Jun;232(6):330-6. doi: 10.1007/BF00175984.

Chorioretinal dysplasia in young subjects with Wagner's hereditary vitreoretinal degeneration.

Int Ophthalmol. 1981 Mar;3(2):67-77. doi: 10.1007/BF00133417.

The Wagner syndrome versus hereditary arthroophthalmopathy.

Trans Am Ophthalmol Soc. 1982;80:349-65.

The Wagner-Stickler syndrome complex.

Doc Ophthalmol. 1981 Dec 16;52(2):179-88. doi: 10.1007/BF01675204.

[On the clinical aspects, pathogenesis and differential diagnosis of peripheral uveitis].

Albrecht Von Graefes Arch Klin Exp Ophthalmol. 1967;174(1):9-33. doi: 10.1007/BF00406583.

Inherited hyaloideoretinopathy and skeletal dysplasia.

Trans Am Ophthalmol Soc. 1975;73:417-51.

Stickler's syndrome and neovascular glaucoma.

Br J Ophthalmol. 1979 Dec;63(12):826-31. doi: 10.1136/bjo.63.12.826.