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Annamari Immonen

folkhälsan research center

H指数:4

被引数:34

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A genetic and historical perspective on the origins of keratitis fugax hereditaria

从遗传学和历史学角度探讨遗传性暂时性角膜炎的起源

Acta Ophthalmologica

IF2.8

2026-09-200

OAAI

Genetic risk factors in Finnish patients with Fuchs endothelial corneal dystrophy

芬兰费舍尔内皮角膜营养不良患者的遗传风险因素

Acta Ophthalmologica

IF2.8

2026-04-200

OAAI

Prospective In Vivo Confocal Microscopy of the Central Cornea in Terrien Marginal Degeneration

特伦恩边缘性角膜病变中央角膜的活体共焦显微镜前瞻性研究

IF2.1

2025-10-012

PRE

Progression and topographic subtypes of Terrien marginal degeneration

Terrien边缘角膜营养不良的进展和地形亚型

ACTA OPHTHALMOLOGICA

IF2.8

2025-05-190

PRE

Diagnostic errors and delay of keratitis fugax hereditaria

ACTA OPHTHALMOLOGICA

IF2.8

2024-01-180

OA

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

ACTA OPHTHALMOLOGICA

IF2.8

2023-06-084

OA

Keratitis fugax hereditaria - useful to consider when you have a child with non-specific corneal findings and symptoms

ACTA OPHTHALMOLOGICA

IF2.8

2022-12-200

PRE

Pathogenic variant c.61G > C in NLRP3 lowers NLRP3 inflammasome activation threshold in patients with keratitis Fugax Hereditaria

ACTA OPHTHALMOLOGICA

IF2.8

2022-12-200

PRE

TCF4 trinucleotide repeat expansion in Finnish patients with Fuchs' endothelial corneal dystrophy

ACTA OPHTHALMOLOGICA

IF2.8

2022-12-200

PRE

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

BRITISH JOURNAL OF OPHTHALMOLOGY

IF3.5

2022-11-163

PRE

Letter to the editor: Keratitis fugax hereditaria is an eye-specific cryopyrin-associated periodic syndrome

AUTOIMMUNITY REVIEWS

IF8.3

2022-07-010

PRE

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

AMERICAN JOURNAL OF OPHTHALMOLOGY

IF4.2

2022-04-013

OAAI

Clinical spectrum and geographic distribution of keratitis fugax hereditaria caused by the pathogenic variant c.61G>C in NLRP3

ACTA OPHTHALMOLOGICA

IF2.8

2022-01-030

OA

The functional consequence of the pathogenic variant in the inflammasome component NLRP3 as the underlying cause of keratitis fugax hereditaria

ACTA OPHTHALMOLOGICA

IF2.8

2022-01-030

PRE

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

AMERICAN JOURNAL OF OPHTHALMOLOGY

IF4.2

2020-05-019

OAAI