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Literature DB >> 27892982

Vision Loss in a Teenage Girl With Postconcussion Syndrome.

Hasenin Al-Khersan¹, Tim Hain², Michael A Grassi³.

Abstract

Entities: Chemical Disease Gene Species

Mesh：

Substances：

Year: 2017 PMID： 27892982 PMCID： PMC5195859 DOI： 10.1001/jamaophthalmol.2016.2830

Source DB: PubMed Journal: JAMA Ophthalmol ISSN： 2168-6165 Impact factor: 7.389

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References

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9 in total

1. Usher syndrome type III: revised genomic structure of the USH3 gene and identification of novel mutations.

Authors: Randall R Fields; Guimei Zhou; Dali Huang; Jack R Davis; Claes Möller; Samuel G Jacobson; William J Kimberling; Janos Sumegi
Journal: Am J Hum Genet Date: 2002-07-16 Impact factor: 11.025

2. Massive SCA7 expansion detected in a 7-month-old male with hypotonia, cardiomegaly, and renal compromise.

Authors: Andrea Whitney; Ming Lim; Dipak Kanabar; Jean-Pierre Lin
Journal: Dev Med Child Neurol Date: 2007-02 Impact factor: 5.449

Review 3. Ophthalmic manifestations of inherited neurodegenerative disorders.

Authors: Hannah M Kersten; Richard H Roxburgh; Helen V Danesh-Meyer
Journal: Nat Rev Neurol Date: 2014-05-20 Impact factor: 42.937

Review 4. Molecular pathogenesis of spinocerebellar ataxias.

Authors: Antoni Matilla Dueñas; Robert Goold; Paola Giunti
Journal: Brain Date: 2006-04-13 Impact factor: 13.501

5. Retinal disease in Usher syndrome III caused by mutations in the clarin-1 gene.

Authors: Waldo Herrera; Tomas S Aleman; Artur V Cideciyan; Alejandro J Roman; Eyal Banin; Tamar Ben-Yosef; Leigh M Gardner; Alexander Sumaroka; Elizabeth A M Windsor; Sharon B Schwartz; Edwin M Stone; Xue-Zhong Liu; William J Kimberling; Samuel G Jacobson
Journal: Invest Ophthalmol Vis Sci Date: 2008-02-15 Impact factor: 4.799

Vision Loss in a Teenage Girl With Postconcussion Syndrome.

1. Usher syndrome type III: revised genomic structure of the USH3 gene and identification of novel mutations.

2. Massive SCA7 expansion detected in a 7-month-old male with hypotonia, cardiomegaly, and renal compromise.

Review 3. Ophthalmic manifestations of inherited neurodegenerative disorders.

Review 4. Molecular pathogenesis of spinocerebellar ataxias.

5. Retinal disease in Usher syndrome III caused by mutations in the clarin-1 gene.

Review 6. Spinocerebellar ataxia type 7 associated with pigmentary retinal dystrophy.

7. Neuro-ophthalmologic features of spinocerebellar ataxia type 7.

8. Ophthalmic features of spinocerebellar ataxia type 7.

Review 9. Vision and vision-related outcome measures in multiple sclerosis.