Publications by authors named "Intissar Anan"

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Sixty years of experience with hereditary transthyretin amyloidosis: Insights from the Swedish transthyretin amyloidosis registry.
Lotta Stenberg, Björn Pilebro, Intissar Anan, Jorge Mejia Baranda, Kristin Samuelsson

J Intern Med· November 2025

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Advances in the treatment of transthyretin amyloidosis.
Intissar Anan

eGastroenterology· September 2025

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The other side of variant transthyretin amyloidosis with polyneuropathy: psychosocial experience of members of Portuguese families with late onset of the disease.
José D Pereira, Andreia Santos, Eugenia Cisneros-Barroso, Intissar Anan, Marina S Lemos

J Community Genet· June 2025

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Misfolding of transthyretin in vivo is controlled by the redox environment and macromolecular crowding.
Sanduni Wasana Jayaweera, Melisnur Sahin, Fabian Lundkvist, Alice Leven, Laura Tereenstra, Intissar Anan

J Biol Chem· January 2025

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Anti-PEG antibodies associated with reduced therapeutic effect of patisiran in patients with hereditary transthyretin amyloidosis.
Björn Pilebro, Jonas Wixner, Intissar Anan

Amyloid· December 2024

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Assessing left atrial dysfunction in cardiac amyloidosis using LA-LV strain slope.
Fredrik Edbom, Per Lindqvist, Urban Wiklund, Björn Pilebro, Intissar Anan

Eur Heart J Imaging Methods Pract· July 2024

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A multicentric study of the disease risks and first manifestations in hereditary transthyretin amyloidosis (ATTRv): insights for an earlier diagnosis.
Violaine Planté-Bordeneuve, Farida Gorram, Malin Olsson, Intissar Anan, Anna Mazzeo

Amyloid· September 2023

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Enlarged cross-sectional area in peripheral nerves in Swedish patients with hereditary V30M transthyretin amyloidosis.
Sandra Arvidsson, Robert Eriksson, Intissar Anan, Victoria Heldestad

Ann Med· September 2023

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Hereditary transthyretin amyloidosis in Sweden: Comparisons between a non-endemic and an endemic region.
Kristin Samuelsson, Ana Jovanovic, Karl Egervall, Intissar Anan, Jonas Wixner

Amyloid· December 2022

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Epidemiology of hereditary transthyretin amyloidosis in the northernmost region of Sweden: a retrospective cohort study.
Jorge Mejia Baranda, Jenny Ljungberg, Jonas Wixner, Intissar Anan, Viktor Oskarsson

Amyloid· June 2022

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[Hereditary transthyretin amyloidosis - from symptomatic to curative treatment?].
Jonas Wixner, Intissar Anan, Björn Pilebro, Erica Uneus, Jorge Mejia Baranda

Lakartidningen· June 2022

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Amyloid fibril composition type is consistent over time in patients with Val30Met (p.Val50Met) transthyretin amyloidosis.
Intissar Anan, Ole B Suhr, Katarzyna Liszewska, Jorge Mejia Baranda, Björn Pilebro

PLoS One· April 2022

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Cerebellar and Cerebral Amyloid Visualized by [F]flutemetamol PET in Long-Term Hereditary V30M () Transthyretin Amyloidosis Survivors.
Erica Irene Uneus, Christer Wilhelmsson, David Bäckström, Intissar Anan, Jonas Wixner

Front Neurol· March 2022

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Endogenous Human Proteins Interfering with Amyloid Formation.
Anna L Gharibyan, Sanduni Wasana Jayaweera, Manuela Lehmann, Intissar Anan, Anders Olofsson

Biomolecules· March 2022

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Metabolomics analysis for diagnosis and biomarker discovery of transthyretin amyloidosis.
Malin Olsson, Urban Hellman, Jonas Wixner, Intissar Anan

Amyloid· December 2021

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Structural basis for transthyretin amyloid formation in vitreous body of the eye.
Irina Iakovleva, Michael Hall, Melanie Oelker, Linda Sandblad, Intissar Anan

Nat Commun· December 2021

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Combining ECG and echocardiography to identify transthyretin cardiac amyloidosis in heart failure.
Viktor Löfbacka, Ole B Suhr, Bjorn Pilebro, Jonas Wixner, Torbjorn Sundström, Intissar Anan

Clin Physiol Funct Imaging· September 2021

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New data on the genetic profile and penetrance of hereditary Val30Met transthyretin amyloidosis in Sweden.
Farida Gorram, Malin Olsson, Flora Alarcon, Gregory Nuel, Intissar Anan

Amyloid· June 2021

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Mechanisms of Transthyretin Inhibition of IAPP Amyloid Formation.
Sanduni Wasana Jayaweera, Solmaz Surano, Nina Pettersson, Elvira Oskarsson, Lovisa Lettius, Intissar Anan

Biomolecules· March 2021

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Abdominal fat pad biopsies exhibit good diagnostic accuracy in patients with suspected transthyretin amyloidosis.
Hedvig Paulsson Rokke, Nima Sadat Gousheh, Per Westermark, Ole B Suhr, Intissar Anan

Orphanet J Rare Dis· October 2020

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Self-reported gastrointestinal symptoms are more common in liver transplanted transthyretin amyloidosis patients than in healthy controls and in patients transplanted for end-stage liver disease.
Therese Marberg, Pontus Karling, Karin Söderberg, Intissar Anan, Jonas Wixner

Amyloid· January 2020

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The Swedish open-label diflunisal trial (DFNS01) on hereditary transthyretin amyloidosis and the impact of amyloid fibril composition.
Jonas Wixner, Per Westermark, Elisabet Ihse, Björn Pilebro, Hans-Erik Lundgren, Intissar Anan

Amyloid· January 2020

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A case report of osteoarthritis associated with hereditary transthyretin amyloidosis ATTRV30M.
Intissar Anan, Joakim Bång, Hans-Erik Lundgren, Jonas Wixner, Per Westermark

Amyloid· January 2020

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Amyloid fibril composition within hereditary Val30Met (p. Val50Met) transthyretin amyloidosis families.
Ole Bernt Suhr, Jonas Wixner, Intissar Anan, Hans-Erik Lundgren, Priyantha Wijayatunga

PLoS One· November 2019

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Transthyretin Glu54Leu - an unknown mutation within the Swedish population associated with amyloid cardiomyopathy and a unique fibril type.
Urban Hellman, Kenneth Lång, Elisabet Ihse, Jenni Jonasson, Malin Olsson, Intissar Anan

Scand J Clin Lab Invest· October 2019

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