Literature DB >> 18170832

X-LINKED HEREDITARY RETINOSCHISIS.

H Forsius1, B Vainio-Mattila, A Eriksson.   

Abstract

Entities:  

Mesh：

Year:  1962        PMID： 18170832      PMCID： PMC510266          DOI： 10.1136/bjo.46.11.678

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN： 0007-1161            Impact factor:   4.638


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  5 in total

1.  Hereditary retinoschisis.

Authors:  E P GIESER; H F FALLS
Journal:  Am J Ophthalmol       Date:  1961-06       Impact factor: 5.258

2.  Congenital vascular veils in the vitreous; hereditary retinoschisis.

Authors:  J V BALIAN; H F FALLS
Journal:  Arch Ophthalmol       Date:  1960-01

3.  [Two cases of hyaloid-retinal degeneration].

Authors:  M FAVRE
Journal:  Ophthalmologica       Date:  1958 May-Jun       Impact factor: 3.250

4.  Inherited retinal detachment.

Authors:  J LEVY
Journal:  Br J Ophthalmol       Date:  1952-11       Impact factor: 4.638

5.  Unusual retinal detachment possibly sex-linked.

Authors:  A SORSBY; M KLEIN; J H GANN; G SIGGINS
Journal:  Br J Ophthalmol       Date:  1951-01       Impact factor: 4.638
  5 in total
  9 in total

Review 1.  The Finnish Disease Heritage III: the individual diseases.

Authors:  Reijo Norio
Journal:  Hum Genet       Date:  2003-03-08       Impact factor: 4.132

2.  Retinoshchisis--retinal cysts.

Authors:  P A Cibis
Journal:  Trans Am Ophthalmol Soc       Date:  1965

Review 3.  X linked retinoschisis.

Authors:  N D George; J R Yates; A T Moore
Journal:  Br J Ophthalmol       Date:  1995-07       Impact factor: 4.638

4.  X-chromosomal-linked diseases affecting the eye: status of the heterozygote female.

Authors:  A E Krill
Journal:  Trans Am Ophthalmol Soc       Date:  1969

5.  Familial retinoschisis in female patients.

Authors:  J Shimazaki; M Matsuhashi
Journal:  Doc Ophthalmol       Date:  1987-03       Impact factor: 2.379

6.  Autosomal dominant juvenile vitreoretinal degeneration and retinal detachment.

Authors:  K M Saari
Journal:  Int Ophthalmol       Date:  1986-04       Impact factor: 2.031

7.  Retinal Structure and Gene Therapy Outcome in Retinoschisin-Deficient Mice Assessed by Spectral-Domain Optical Coherence Tomography.

Authors:  Yong Zeng; Ronald S Petralia; Camasamudram Vijayasarathy; Zhijian Wu; Suja Hiriyanna; Hongman Song; Ya-Xian Wang; Paul A Sieving; Ronald A Bush
Journal:  Invest Ophthalmol Vis Sci       Date:  2016-07-01       Impact factor: 4.799

Review 8.  Macular dystrophies: clinical and imaging features, molecular genetics and therapeutic options.

Authors:  Najiha Rahman; Michalis Georgiou; Kamron N Khan; Michel Michaelides
Journal:  Br J Ophthalmol       Date:  2019-11-08       Impact factor: 4.638

9.  Impact of Next Generation Sequencing in Unraveling the Genetics of 1036 Spanish Families With Inherited Macular Dystrophies.

Authors:  Marta Del Pozo-Valero; Rosa Riveiro-Alvarez; Inmaculada Martin-Merida; Fiona Blanco-Kelly; Saoud Swafiri; Isabel Lorda-Sanchez; Maria José Trujillo-Tiebas; Ester Carreño; Belen Jimenez-Rolando; Blanca Garcia-Sandoval; Marta Corton; Almudena Avila-Fernandez; Carmen Ayuso
Journal:  Invest Ophthalmol Vis Sci       Date:  2022-02-01       Impact factor: 4.799
  9 in total

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