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Amyloid
The Journal of Protein Folding Disorders
Volume 28, 2021 - Issue 2
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Articles

New data on the genetic profile and penetrance of hereditary Val30Met transthyretin amyloidosis in Sweden

Farida Gorrama Department of Neurology, Henri Mondor University Hospital, APHP, Créteil, France;b University Paris Est- Creteil, INSERM U955, Institut Mondor de Recherche Biomédicale(IMRB), Creteil, FranceView further author information
,
Malin Olssonc Department of Public Health and Clinical Medicine/Medicine, Umeå University, Umeå, Sweden;d Wallenberg Centre for Molecular Medicine, Umeå University, Umeå, Sweden;View further author information
,
Flora Alarcone Laboratory MAP5 UMR CNRS 8145, Paris Descartes University, Paris, FranceView further author information
,
Gregory Nuelf Stochastics and Biology Group, Department of Probability and Statistics (LPSM, CNRS 8001), Sorbonne University, Campus Pierre et Marie Curie, Paris, France View further author information
,
Intissar Ananc Department of Public Health and Clinical Medicine/Medicine, Umeå University, Umeå, Sweden;d Wallenberg Centre for Molecular Medicine, Umeå University, Umeå, Sweden;ORCID Iconhttps://orcid.org/0000-0003-2874-7643View further author information
ORCID Icon &
Violaine Planté-Bordeneuvea Department of Neurology, Henri Mondor University Hospital, APHP, Créteil, France;b University Paris Est- Creteil, INSERM U955, Institut Mondor de Recherche Biomédicale(IMRB), Creteil, FranceCorrespondence[email protected]
ORCID Iconhttps://orcid.org/0000-0002-7880-2316View further author information
ORCID Icon
Pages 84-90 | Received 12 May 2020, Accepted 20 Sep 2020, Published online: 04 Nov 2020

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Sandra Arvidsson, Robert Eriksson, Intissar Anan & Victoria Heldestad. (2023) Enlarged cross-sectional area in peripheral nerves in Swedish patients with hereditary V30M transthyretin amyloidosis. Annals of Medicine 55:2.
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Violaine Planté-Bordeneuve, Farida Gorram, Malin Olsson, Intissar Anan, Anna Mazzeo, Luca Gentile, Eugenia Cisneros-Barroso, Juan Gonzalez-Moreno, Ines Losada, Marcia Waddington-Cruz, Luiz Felipe Pinto, Yeşim Parman, Pascale Fanen, Flora Alarcon & Gregory Nuel. (2023) A multicentric study of the disease risks and first manifestations in hereditary transthyretin amyloidosis (ATTRv): insights for an earlier diagnosis. Amyloid 30:3, pages 313-320.
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Fernando de Frutos, Juan Pablo Ochoa, Cristina Gómez-González, David Reyes-Leiva, Juan I. Aróstegui, Carlos Casasnovas, Roberto Barriales-Villa, Teresa Sevilla, Esther Gonzalez-Lopez, Elvira Ramil, Lucia Galan, Jose González-Costello, Ana García-Álvarez, Ricard Rojas-Garcia, Maria Angeles Espinosa & Pablo Garcia-Pavia. (2023) Phenotype and clinical outcomes of Glu89Lys hereditary transthyretin amyloidosis: a new endemic variant in Spain. Amyloid 30:2, pages 199-207.
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Jorge Mejia Baranda, Jenny Ljungberg, Jonas Wixner, Intissar Anan & Viktor Oskarsson. (2022) Epidemiology of hereditary transthyretin amyloidosis in the northernmost region of Sweden: a retrospective cohort study. Amyloid 29:2, pages 120-127.
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