Literature DB >> 31850186

Dominant cystoid macular dystrophy associated with mutations in the RP1L1 gene.

Yan Fu1, Tian-Hao Xie2, Yue-Ling Zhang1, Na Yang1, Xiao-Nan Shi1, Zhao-Hui Gu1.   

Abstract

Entities:  

Year:  2019        PMID： 31850186      PMCID： PMC6901896          DOI： 10.18240/ijo.2019.12.23

Source DB:  PubMed          Journal:  Int J Ophthalmol        ISSN： 2222-3959            Impact factor:   1.779


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  16 in total

1.  Isolation and mapping of novel candidate genes for retinal disorders using suppression subtractive hybridization.

Authors:  A I den Hollander; M A van Driel; Y J de Kok; D J van de Pol; C B Hoyng; H G Brunner; A F Deutman; F P Cremers
Journal:  Genomics       Date:  1999-06-15       Impact factor: 5.736

2.  Occult macular dystrophy in an Italian family carrying a mutation in the RP1L1 gene.

Authors:  Stefano Piermarocchi; Tatiana Segato; Alberta Leon; Davide Colavito; Stefania Miotto
Journal:  Mol Med Rep       Date:  2016-01-14       Impact factor: 2.952

3.  Clinical and genetic characteristics of Korean occult macular dystrophy patients.

Authors:  Seong Joon Ahn; Sung Im Cho; Jeeyun Ahn; Sung Sup Park; Kyu Hyung Park; Se Joon Woo
Journal:  Invest Ophthalmol Vis Sci       Date:  2013-07-18       Impact factor: 4.799

4.  Therapies for Macular Edema Associated with Branch Retinal Vein Occlusion: A Report by the American Academy of Ophthalmology.

Authors:  Justis P Ehlers; Stephen J Kim; Steven Yeh; Jennifer E Thorne; Prithvi Mruthyunjaya; Scott D Schoenberger; Sophie J Bakri
Journal:  Ophthalmology       Date:  2017-05-24       Impact factor: 12.079

5.  Retinitis Pigmentosa and Other Dystrophies.

Authors:  Sarah Mrejen; Isabelle Audo; Sébastien Bonnel; José-Alain Sahel
Journal:  Dev Ophthalmol       Date:  2017-03-28

6.  Octreotide acetate in dominant cystoid macular dystrophy.

Authors:  B F Hogewind; G Pieters; C B Hoyng
Journal:  Eur J Ophthalmol       Date:  2008 Jan-Feb       Impact factor: 2.597

7.  Novel RP1L1 Variants and Genotype-Photoreceptor Microstructural Phenotype Associations in Cohort of Japanese Patients With Occult Macular Dystrophy.

Authors:  Kaoru Fujinami; Shuhei Kameya; Sachiko Kikuchi; Shinji Ueno; Mineo Kondo; Takaaki Hayashi; Kei Shinoda; Shigeki Machida; Kazuki Kuniyoshi; Yuichi Kawamura; Masakazu Akahori; Kazutoshi Yoshitake; Satoshi Katagiri; Ayami Nakanishi; Hiroyuki Sakuramoto; Yoko Ozawa; Kazuo Tsubota; Kunihiko Yamaki; Atsushi Mizota; Hiroko Terasaki; Yozo Miyake; Takeshi Iwata; Kazushige Tsunoda
Journal:  Invest Ophthalmol Vis Sci       Date:  2016-09-01       Impact factor: 4.799

8.  A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p.

Authors:  C F Inglehearn; S A Carter; T J Keen; J Lindsey; A M Stephenson; R Bashir; M al-Maghtheh; A T Moore; M Jay; A C Bird
Journal:  Nat Genet       Date:  1993-05       Impact factor: 38.330

9.  Localization of the gene for dominant cystoid macular dystrophy on chromosome 7p.

Authors:  H Kremer; A Pinckers; B van den Helm; A F Deutman; H H Ropers; E C Mariman
Journal:  Hum Mol Genet       Date:  1994-02       Impact factor: 6.150

10.  Multimodal imaging in dominant cystoid macular dystrophy.

Authors:  Rupak Roy; Kumar Saurabh; Sourav Bhattacharyya; Nicey Roy Thomas; Kaustav Datta
Journal:  Indian J Ophthalmol       Date:  2017-09       Impact factor: 1.848
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