Increasing amount of amyloid are associated with the severity of clinical features in hereditary gelsolin (AGel) amyloidosis-Reference-Cited by-同舟云学术

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Increasing amount of amyloid are associated with the severity of clinical features in hereditary gelsolin (AGel) amyloidosis

Published:2016-10-01 Issue:4 Volume:23 Page:225-233
ISSN:1350-6129
Container-title:Amyloid
language:en
Short-container-title:Amyloid

Author:

Pihlamaa Tiia¹,Suominen Sinikka¹,Kiuru-Enari Sari²,Tanskanen Maarit³

Affiliation:

1. Department of Plastic and Reconstructive Surgery, Helsinki University Hospital, Helsinki, Finland,

2. Department of Neurology, Clinical Neurosciences, University of Helsinki, Helsinki, Finland, and

3. Department of Pathology, University of Helsinki and HUSLAB, Helsinki, Finland

Publisher

Informa UK Limited

Subject

Internal Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/13506129.2016.1238355

Reference23 articles.

1. Hereditary gelsolin amyloidosis

2. Gelsolin Amyloidosis as a Cause of Early Aging and Progressive Bilateral Facial Paralysis

3. Gelsolin–derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187

4. The Complexity of Elastic Fiber Biogenesis: The Paradigm of Cutis Laxa

5. Cutis laxa in hereditary gelsolin amyloidosis

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1. Hereditary neuropathic itch caused by gelsolin mutation;Journal of the Neurological Sciences;2024-08

2. The first Chinese renal gelsolin amyloidosis with the p.Asp174Asn mutation in the GSN gene: Nephrology picture;Journal of Nephrology;2021-01-04

3. A novel hotspot of gelsolin instability triggers an alternative mechanism of amyloid aggregation;Computational and Structural Biotechnology Journal;2021

4. Kidney Transplantation in Systemic Amyloidosis;Transplantation;2020-02-11

5. Finnish gelsolin amyloidosis causes significant disease burden but does not affect survival: FIN-GAR phase II study;Orphanet Journal of Rare Diseases;2020-01-17

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