Amyloid in parenchymal organs in gelsolin (AGel) amyloidosis-Reference-Cited by-同舟云学术

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Amyloid in parenchymal organs in gelsolin (AGel) amyloidosis

Published:2019-05-23 Issue:3 Volume:26 Page:118-124
ISSN:1350-6129
Container-title:Amyloid
language:en
Short-container-title:Amyloid

Author:

Schmidt Eeva-Kaisa¹,Kiuru-Enari Sari¹,Atula Sari¹²,Tanskanen Maarit³⁴

Affiliation:

1. Department of Neurosciences, Faculty of Medicine, University of Helsinki, Helsinki, Finland;

2. Department of Neurology, Helsinki University Hospital, Helsinki, Finland;

3. Department of Pathology, HUSLAB, Helsinki University Hospital, Helsinki, Finland;

4. Department of Pathology, Faculty of Medicine, University of Helsinki, Helsinki, Finland

Publisher

Informa UK Limited

Subject

Internal Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/13506129.2019.1604336

Reference38 articles.

1. Gelsolin gene mutation—at codon 187—in familial amyloidosis, Finnish: DNA-diagnostic assay

2. Hereditary gelsolin amyloidosis

3. The First Korean Family With Hereditary Gelsolin Amyloidosis Caused by p.D214Y Mutation in the GSN Gene

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1. 2024 Update on Classification, Etiology, and Typing of Renal Amyloidosis: A Review;American Journal of Kidney Diseases;2024-09

2. Advancing Renal Amyloidosis Care: The Role of Modern Diagnostic Techniques with the Potential of Enhancing Patient Outcomes;International Journal of Molecular Sciences;2024-05-28

3. Transthyretin cardiac amyloidosis: particularities in North-Eastern Romania;Revista Medico-Chirurgicala;2023-12-30

4. Hereditary gelsolin amyloidosis: a rare cause of cranial, peripheral and autonomic neuropathies linked to D187N and Y447H substitutions;Amyloid;2023-05-04

5. Role of Diphosphonates Bone Scintigraphy in Correlation with Biomarkers for a Personalized Approach to ATTR Cardiac Amyloidosis in North-Eastern Romania;Diagnostics;2022-12-28

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