Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Congenital hereditary corneal dystrophy.

Literature DB >> 13768390

Congenital hereditary corneal dystrophy.

A E MAUMENEE.

Abstract

Entities: Disease

Keywords: CORNEA/diseases

Mesh：

Year: 1960 PMID： 13768390 DOI： 10.1016/0002-9394(60)90998-3

Source DB: PubMed Journal: Am J Ophthalmol ISSN： 0002-9394 Impact factor: 5.258

Keyword Cloud
Cited

× No keyword cloud information.

14 in total

1. Successful Descemet's stripping automated endothelial keratoplasty for congenital hereditary endothelial dystrophy in a pediatric patient.

Authors: Jeffrey M Goshe; Jennifer Y Li; Mark A Terry
Journal: Int Ophthalmol Date: 2012-01-25 Impact factor: 2.031

2. Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy.

Authors: Julie Desir; Graciela Moya; Orit Reish; Nicole Van Regemorter; Hilde Deconinck; Karen L David; Françoise M Meire; Marc J Abramowicz
Journal: J Med Genet Date: 2007-01-12 Impact factor: 6.318

3. [New international classification of corneal dystrophies (CD)].

Authors: W Lisch; B Seitz
Journal: Ophthalmologe Date: 2011-09 Impact factor: 1.059

4. Reis-Bücklers' dystrophy. A clinico-pathological study.

Authors: N S Rice; N Ashton; B Jay; R K Blach
Journal: Br J Ophthalmol Date: 1968-08 Impact factor: 4.638

5. Homozygosity mapping and linkage analysis demonstrate that autosomal recessive congenital hereditary endothelial dystrophy (CHED) and autosomal dominant CHED are genetically distinct.

Authors: M Callaghan; C K Hand; S M Kennedy; J S FitzSimon; L M Collum; N A Parfrey
Journal: Br J Ophthalmol Date: 1999-01 Impact factor: 4.638

10. Amyloid corneal deposition in corneal buttons of congenital hereditary endothelial dystrophy (CHED) - A clinical and histopathological case series.

Authors: Abdulmajid Al-Shehah; Ali Al-Rajhi; Hind Alkatan
Journal: Saudi J Ophthalmol Date: 2010-10-06

Congenital hereditary corneal dystrophy.

1. Successful Descemet's stripping automated endothelial keratoplasty for congenital hereditary endothelial dystrophy in a pediatric patient.

2. Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy.

3. [New international classification of corneal dystrophies (CD)].

4. Reis-Bücklers' dystrophy. A clinico-pathological study.

5. Homozygosity mapping and linkage analysis demonstrate that autosomal recessive congenital hereditary endothelial dystrophy (CHED) and autosomal dominant CHED are genetically distinct.

6. Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11.

7. Congenital hereditary endothelial dystrophy associated with nail hypoplasia.

8. Immuno-electron labelling of matrix components in congenital hereditary endothelial dystrophy.

9. Congenital hereditary corneal oedema of Maumenee: its clinical features, management, and pathology.

10. Amyloid corneal deposition in corneal buttons of congenital hereditary endothelial dystrophy (CHED) - A clinical and histopathological case series.