Search | TVST | ARVO Journals

tvst

Issues
Topics
For Authors
About
- Editorial Board

Journals Home

MANAGE ALERTS

Forgot password?

Create an Account

To View More...

Purchase this article with an account.

or

Subscribe Now

Issues
Topics
For Authors
About
- Editorial Board

Narrow View

NARROW

Content Type

Meeting Abstract (11)
Journal Articles (3)

Journal

Investigative Ophthalmology & Visual Science (12)
Journal of Vision (1)
Translational Vision Science & Technology (1)

Article Type

ARVO Annual Meeting Abstract (10)
Articles (1)
Biochemistry and Molecular Biology (1)
Cornea (1)
Vision Sciences Society Annual Meeting Abstract (1)

Topics

Genetics (3)
Eye Anatomy and Disorders (2)
Biochemistry and Molecular Biology (1)
Clinical and Epidemiologic Research (1)
Cornea (1)
Retina (1)
Translational Research (1)

Tags

autoimmune inner ear disease (1)
autosomal recessive inheritance (1)
cohort studies (1)
cornea (1)
exons (1)
eye diseases (1)
family (1)
language morphology (1)
microscopy, confocal (1)
morphology (1)

Specify Date Range

From: To: Apply

Showing 1 – 14 of 14

SORT: Best Match Most Recent Oldest

VIEW: Basic | Expanded

Articles January 2022

Prevalence of RPGR -Mediated Retinal Dystrophy in an Unselected Cohort of Over 5000 Patients

PDF

Sari Tuupanen; Kimberly Gall; Johanna Sistonen; Inka Saarinen; Kati Kämpjärvi; Kirsty Wells; Katja Merkkiniemi; Pernilla von Nandelstadh; Laura Sarantaus; Johanna Känsäkoski; Emma Mårtenson; Hanna Västinsalo; Jennifer Schleit; Eeva-Marja Sankila; Annakarin Kere; Heidi Junnila; Pauli Siivonen; Margarita Andreevskaya; Ville Kytölä; Mikko Muona; Pertteli Salmenperä; Samuel Myllykangas; Juha Koskenvuo; Tero-Pekka Alastalo
TAGS: cohort studies, prevalence, retinal dystrophies
Trans. Vis. Sci. Tech.. 2022; 11(1):6. doi: https://doi.org/10.1167/tvst.11.1.6

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2021

NIGHT study: natural progression of choroideremia

Byron L Lam; Robert E MacLaren; M. Dominik Fischer; Frank G Holz; Mark E Pennesi; David G Birch; Eeva-Marja Sankila; Isabelleanne Meunier; Kimberly E Stepien; Juliana M.F. Sallum; Cindy Lu; Jiajun Liu; Dan Yoon

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):34. doi:

ARVO Annual Meeting Abstract July 2019

RPGR ORF15 sequencing improves diagnostic yield in patients with inherited retinal dystrophies.

Sari Tuupanen; Johanna Sistonen; Kati Kämpjärvi; Pauli Siivonen; Miika Mehine; Johanna Känsäkoski; Kirsty Wells; Jennifer Schleit; Miko Valori; Pertteli Salmenperä; Eeva-Marja Sankila; Eveliina Salminen; Tero-Pekka Alastalo; Juha Koskenvuo; Samuel Myllykangas

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):2939. doi:

ARVO Annual Meeting Abstract July 2019

Characterization of copy number variants (CNVs) identified by genetic testing of inherited retinal disorders

Lucia Guidugli; Miika Mehine; Sari Tuupanen; Kati Kämpjärvi; Kirsty Wells; Johanna Känsäkoski; Miko Valori; Inka Saarinen; Mikko Muona; Eeva-Marja Kaarina Sankila; Samuel Myllykangas; Juha Koskenvuo; Tero-Pekka Alastalo

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):2944. doi:

ARVO Annual Meeting Abstract July 2019

Natural History of the Progression of RPGR-Associated X-Linked Retinitis Pigmentosa (XOLARIS) Study: Cross-Sectional Analysis of Baseline Characteristics

Moreno Menghini; David G Birch; Camiel Boon; Jacque L Duncan; M Dominik Fischer; Frank G Holz; Carel C B Hoyng; Kamron N Khan; Isabelle Anne Meunier; Mark E Pennesi; Eeva-Marja Kaarina Sankila; Robert E MacLaren

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):5168. doi:

ARVO Annual Meeting Abstract July 2019

Prevalence and genetic characteristics of RPE65 -associated retinal disease

Tero-Pekka Alastalo; Kati Kämpjärvi; Lucia Guidugli; Johanna Känsäkoski; Kirsty Wells; Hanna Västinsalo; Laura Sarantaus; Pertteli Salmenperä; Samuel Myllykangas; Eeva-Marja Kaarina Sankila; Juha Koskenvuo; Sari Tuupanen

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):400. doi:

ARVO Annual Meeting Abstract July 2018

Natural History of Progression of Choroideremia (NIGHT) Study: Cross-Sectional Analysis of Baseline Characteristics

Byron L Lam; M Dominik Fischer; Mark E Pennesi; Eeva-Marja Kaarina Sankila; Frank G. Holz; Robert E MacLaren; David G Birch; Ian M MacDonald; Carel C B Hoyng; Graeme Black; Neil M Bressler; Stephen H. Tsang; Kimberly E Stepien; Michael S Ip; Vedran Pavlovic; Aniz Girach

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):3899. doi:

ARVO Annual Meeting Abstract July 2018

The Natural History of the Progression of Choroideremia (NIGHT) Study: Longitudinal Changes in Visual Acuity over 12 Months

Mark E Pennesi; Byron L Lam; M Dominik Fischer; Eeva-Marja Kaarina Sankila; Frank G. Holz; Robert E MacLaren; David G Birch; Ian M MacDonald; Graeme Black; Carel C B Hoyng; Neil M Bressler; Stephen H. Tsang; Kimberly E Stepien; Michael S Ip; Vedran Pavlovic; Aniz Girach

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):3898. doi:

ARVO Annual Meeting Abstract July 2018

Spatial distribution of preserved autofluorescence in patients with choroideremia

Amir H Hariri; Aniz Girach; Michael S Ip; Byron L Lam; M Dominik Fischer; Eeva-Marja Kaarina Sankila; Mark E Pennesi; Frank G. Holz; David G Birch; Robert E MacLaren; Ian M MacDonald; Carel C B Hoyng; Graeme Black; Neil M Bressler; Stephen H. Tsang; Srinivas R. Sadda

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):4991. doi:

ARVO Annual Meeting Abstract April 2011

Clarin-1 Expression In The Retina Using AAV Mediated Gene Delivery

Astra Dinculescu; Yoshikazu Imanishi; Frank M. Dyka; Jianwen Liu; Issam McDoom; Xuan Liu; Hanna Västinsalo; Reetta Jalkanen; Eeva-Marja Sankila; William W. Hauswirth

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):3336. doi:

ARVO Annual Meeting Abstract April 2011

Cone Structure in Patients with Usher Syndrome III Caused by Mutations in the Clarin-1 Gene

Kavitha Ratnam; Hanna Vastinsalo; Sanna Sundquist; Austin Roorda; Eeva-Marja K. Sankila; Jacque L. Duncan

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):4975. doi:

Biochemistry and Molecular Biology June 2007

A Novel CACNA1F Gene Mutation Causes Åland Island Eye Disease

PDF

Reetta Jalkanen; N. Torben Bech-Hansen; Rose Tobias; Eeva-Marja Sankila; Maija Mäntyjärvi; Henrik Forsius; Albert de la Chapelle; Tiina Alitalo
TAGS: autoimmune inner ear disease, eye diseases, mutation, exons, family
Invest. Ophthalmol. Vis. Sci.. 2007; 48(6):2498-2502. doi: https://doi.org/10.1167/iovs.06-1103

Vision Sciences Society Annual Meeting Abstract August 2004

Multifocal Electroretinography (mERG): Normative values and a new clinical analysis procedure

Anu Holm; Juha Päällysaho; Mika Letonsaari; Eeva-Marja Sankila; Markku Sainio

Journal of Vision. 2004; 4(8):759. doi: https://doi.org/10.1167/4.8.759

Cornea July 2000

Autosomal Recessive Cornea Plana: In Vivo Corneal Morphology and Corneal Sensitivity

PDF

Minna H. Vesaluoma; Eeva–Marja Sankila; Juana Gallar; Linda J. Müller; W. Matthew Petroll; Jukka A. O. Moilanen; Henrik Forsius; Timo M. T. Tervo
TAGS: autosomal recessive inheritance, cornea, language morphology, morphology, sensory perception, microscopy, confocal
Invest. Ophthalmol. Vis. Sci.. 2000; 41(8):2120-2126. doi:

« Previous

Advertisement

Follow @ARVOtvst

TVST Home
Issues
Topics
For Authors

About
- Editorial Board

Online ISSN: 2164-2591

Investigative Ophthalmology & Visual Science
Journal of Vision
Translational Vision Science & Technology

JOURNALS HOME
TOPICS
ABOUT ARVO JOURNALS

Copyright © 2015 Association for Research in Vision and Ophthalmology.

Forgot password?

To View More...

Purchase this article with an account.

Create an Account

or

Subscribe Now

×

×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×

This site uses cookies. By continuing to use our website, you are agreeing to our privacy policy.Accept