Orphanet Journal of Rare Diseases | Supplements | First European Congress on Hereditary ATTR amyloidosis

Orphanet Journal of Rare Diseases | Supplements | First European Congress on Hereditary ATTR amyloidosis

The following new article has just been published in Orphanet Journal of Rare Diseases

Orphanet Journal of Rare Diseases publishes selected collections of research articles, conference proceedings, reviews and reports as supplements, which are free to access online. All articles published in supplements are subject to peer review; meeting abstracts undergo review and selection by the conference. Find out more about publishing a supplement with BioMed Central.

Volume 10 Supplement 1

First European Congress on Hereditary ATTR amyloidosis

Meeting abstracts

First European Congress on Hereditary ATTR amyloidosis

Paris, France

2-3 November 2015

Publication of this supplement was funded by the First European Congress on Hereditary ATTR amyloidosis.

Invited speaker presentation    Symptomatic therapy in ATTR amyloidosis: pain killers in TTR-FAP Nadine AttalOrphanet Journal of Rare Diseases 2015, 10(Suppl 1):I1 (2 November 2015) Full text | PDF

Invited speaker presentation    Neuropathic phenotypes and natural history of FAP David AdamsOrphanet Journal of Rare Diseases 2015, 10(Suppl 1):I2 (2 November 2015) Full text | PDF

Invited speaker presentation    Which assessment for the carriers: the cardiac view Arnt V KristenOrphanet Journal of Rare Diseases 2015, 10(Suppl 1):I3 (2 November 2015) Full text | PDF

Invited speaker presentation    When to decide to enroll a TTR-FAP patient in a Clinical Trial? Juan BuadesOrphanet Journal of Rare Diseases 2015, 10(Suppl 1):I4 (2 November 2015) Full text | PDF

Invited speaker presentation    Preimplantation genetic diagnosis for TTR-FAP in Portugal Filipa CarvalhoOrphanet Journal of Rare Diseases 2015, 10(Suppl 1):I5 (2 November 2015) Full text | PDF

Invited speaker presentation    TTR-FAP: liver transplant vs oral medication. How and when Teresa CoelhoOrphanet Journal of Rare Diseases 2015, 10(Suppl 1):I6 (2 November 2015) Full text | PDF

Invited speaker presentation    Which assessment for the carriers ? The point of view of the neurologist Isabel ConceicãoOrphanet Journal of Rare Diseases 2015, 10(Suppl 1):I7 (2 November 2015) Full text | PDF

Invited speaker presentation    ATTR-FAP: liver transplantation vs oral medication, how and when Bo ErikzonOrphanet Journal of Rare Diseases 2015, 10(Suppl 1):I8 (2 November 2015) Full text | PDF

Invited speaker presentation    Ophtalmologic changes in transthyretin familial amyloid polyneuropathy (ATTR-FAP) Natália FerreiraOrphanet Journal of Rare Diseases 2015, 10(Suppl 1):I9 (2 November 2015) Full text | PDF

Invited speaker presentation    Imaging cardiac ATTR amyloid Philip N HawkinsOrphanet Journal of Rare Diseases 2015, 10(Suppl 1):I10 (2 November 2015) Full text | PDF

Invited speaker presentation    Minimal assessment of index cases: the point of view of the neurologist Ernst HundOrphanet Journal of Rare Diseases 2015, 10(Suppl 1):I11 (2 November 2015) Full text | PDF

Invited speaker presentation    The landscape of treatment of chronic kidney disease in hereditary ATTR amyloidosis Luisa LobatoOrphanet Journal of Rare Diseases 2015, 10(Suppl 1):I12 (2 November 2015) Full text | PDF

Invited speaker presentation    Do we need to demonstrate Amyloid in tissue? Laurent MagyOrphanet Journal of Rare Diseases 2015, 10(Suppl 1):I13 (2 November 2015) Full text | PDF

Invited speaker presentation    Emerging CNS involvement in FAP-TTR long survival patients Luisa MaiaOrphanet Journal of Rare Diseases 2015, 10(Suppl 1):I14 (2 November 2015) Full text | PDF

Invited speaker presentation    Biopsy experience in a FAP endemic area Manuel PiresOrphanet Journal of Rare Diseases 2015, 10(Suppl 1):I15 (2 November 2015) Full text | PDF

Invited speaker presentation    New tools to diagnose and follow FAC patients: biomarkers Giampaolo MerliniOrphanet Journal of Rare Diseases 2015, 10(Suppl 1):I16 (2 November 2015) Full text | PDF

Invited speaker presentation    New therapeutic perspectives – amyloid removal Mark PepysOrphanet Journal of Rare Diseases 2015, 10(Suppl 1):I17 (2 November 2015) Full text | PDF

Invited speaker presentation    Cardiologic Phenotypes and Natural History of FAC Claudio RapezziOrphanet Journal of Rare Diseases 2015, 10(Suppl 1):I18 (2 November 2015) Full text | PDF

Invited speaker presentation    TTR amyloidosis: a scientific journey since Andrade Maria SaraivaOrphanet Journal of Rare Diseases 2015, 10(Suppl 1):I19 (2 November 2015) Full text | PDF

Invited speaker presentation    Guidelines for genetic counselling in ATTR amyloidosis Jorge SequeirosOrphanet Journal of Rare Diseases 2015, 10(Suppl 1):I20 (2 November 2015) Full text | PDF