Sabita Kawan

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University of Helsinki

Finland

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Understanding the role of a novel NLRP3 pathogenic variant c.61G>C in the pathogenesis of Keratitis Fugax Hereditaria

Open Date: 2023-01-01

Close Date: 2024-12-01

Articles (5)

Year:

2023

Year:

2022

Year:

2021

Year:

2020

Year:

2020

Collaborators (2)

Tero T. Kivelä

FINLAND

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Joni Turunen

University of Helsinki

FINLAND

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Sabita Kawan

Research Interests

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Recent Grants

Articles (5)

Epithelial recurrent erosion dystrophy (<scp>ERED</scp>) from the splice site altering <i>COL17A1</i> variant c.<scp>3156C>T</scp> in families of <scp>Finnish‐Swedish</scp> ancestry

Functional consequences of pathogenic variant c.61G>C in the inflammasome gene <i>NLRP3</i> underlying keratitis fugax hereditaria.

Clinical Spectrum and Geographic Distribution of Keratitis Fugax Hereditaria Caused by the Pathogenic Variant c.61G>C in NLRP3

Neuromuscular Diseases Due to Chaperone Mutations: A Review and Some New Results.

In Vivo Corneal Confocal Microscopy and Histopathology of Keratitis Fugax Hereditaria From a Pathogenic Variant in NLRP3.

Collaborators (2)

Tero T. Kivelä

Joni Turunen

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Sabita Kawan

Research Interests

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Recent Grants

Articles (5)

Epithelial recurrent erosion dystrophy (<scp>ERED</scp>) from the splice site altering <i>COL17A1</i> variant c.<scp>3156C&gt;T</scp> in families of <scp>Finnish‐Swedish</scp> ancestry

Functional consequences of pathogenic variant c.61G>C in the inflammasome gene <i>NLRP3</i> underlying keratitis fugax hereditaria.

Clinical Spectrum and Geographic Distribution of Keratitis Fugax Hereditaria Caused by the Pathogenic Variant c.61G>C in NLRP3

Neuromuscular Diseases Due to Chaperone Mutations: A Review and Some New Results.

In Vivo Corneal Confocal Microscopy and Histopathology of Keratitis Fugax Hereditaria From a Pathogenic Variant in NLRP3.

Collaborators (2)

Tero T. Kivelä

Joni Turunen

Make your next move.

Epithelial recurrent erosion dystrophy (<scp>ERED</scp>) from the splice site altering <i>COL17A1</i> variant c.<scp>3156C>T</scp> in families of <scp>Finnish‐Swedish</scp> ancestry