Jonas Wixner

Kontakt

090-785 00 00

Verksam som

Läkare vid Institutionen för folkhälsa och klinisk medicin Enhet: Gastroenterologi

Byggnad 1A, plan 4, målpunkt B41, Norrlands universitetssjukhus

Five-year results with patisiran for hereditary transthyretin amyloidosis with polyneuropathy: a randomized clinical trial with open-label extension

JAMA Neurology, American Medical Association (AMA) 2025, Vol. 82, (3) : 228-236

Adams, David; Wixner, Jonas; Polydefkis, Michael; et al.

Estimating meaningful differences in measures of neuropathic impairment, health-related quality of life, and nutritional status in patients with hereditary transthyretin amyloidosis

Muscle and Nerve, John Wiley & Sons 2025, Vol. 71, (1) : 96-107

Folkvaljon, Folke; Gertz, Morie; Gillmore, Julian D.; et al.

Cognitive manifestations and brain integrity in hereditary transthyretin amyloidosis: a systematic review

Journal of Neurology, Springer Nature 2025, Vol. 272, (6)

Senem, Iara; Conde, Rodrigo Melo; Foss, Maria Paula; et al.

Exploring cognitive functions and brain structure in hereditary transthyretin amyloidosis using brain MRI and neuropsychological assessment

Neurological Sciences, Springer Nature 2025, Vol. 46 : 1349-1358

Senem, Iara; Foss, Maria Paula; Lavigne-Moreira, Carolina; et al.

Sixty years of experience with hereditary transthyretin amyloidosis: insights from the Swedish transthyretin amyloidosis registry

Journal of Internal Medicine, John Wiley & Sons 2025, Vol. 298 : 478-488

Stenberg, Lotta; Pilebro, Björn; Anan, Intissar; et al.

Effects of eplontersen on symptoms of autonomic neuropathy in hereditary transthyretin-mediated amyloidosis: secondary analysis from the NEURO-TTRansform trial

Amyloid: Journal of Protein Folding Disorders, Taylor & Francis 2025, Vol. 32, (1) : 29-38

Wixner, Jonas; Berk, John L.; Adams, David; et al.

Neuropathy impairment and nutritional status with eplontersen in patients with hereditary transthyretin-mediated amyloidosis

Amyloid: Journal of Protein Folding Disorders

Wixner, Jonas; Conceição, Isabel; Berk, John L.; et al.

Survival in a contemporary, real-world cohort of patients with mixed-phenotype transthyretin amyloid cardiomyopathy treated with tafamidis: an analysis from THAOS

Cardiology and therapy

Wixner, Jonas; Dispenzieri, Angela; Amass, Leslie; et al.

Introducing a revised version of the Kumamoto scale as an easy-to-use clinical tool for monitoring multisystemic changes in hereditary transthyretin amyloidosis

Orphanet Journal of Rare Diseases, BioMed Central (BMC) 2025, Vol. 20, (1)

Wixner, Jonas; Pilebro, Björn; Wien, Tale N.; et al.

Clinical and genotype characteristics and symptom migration in patients with mixed phenotype transthyretin amyloidosis from the transthyretin amyloidosis outcomes survey

Cardiology and Therapy, Springer Nature 2024, Vol. 13 : 117-135

González-Moreno, Juan; Dispenzieri, Angela; Grogan, Martha; et al.

Anti-PEG antibodies associated with reduced therapeutic effect of patisiran in patients with hereditary transthyretin amyloidosis

Amyloid: Journal of Protein Folding Disorders, Taylor & Francis 2024, Vol. 31, (4) : 342-343

Pilebro, Björn; Wixner, Jonas; Anan, Intissar

Patients with transthyretin amyloidosis enrolled in THAOS between 2018 and 2021 continue to experience substantial diagnostic delay

Amyloid: Journal of Protein Folding Disorders, Taylor & Francis 2023, Vol. 30, (4) : 445-448

Coelho, Teresa; Dispenzieri, Angela; Grogan, Martha; et al.

Eplontersen for Hereditary Transthyretin Amyloidosis with Polyneuropathy

Journal of the American Medical Association (JAMA), American Medical Association (AMA) 2023, Vol. 330, (15) : 1448-1458

Coelho, Teresa; Marques, Wilson; Dasgupta, Noel R.; et al.

Characteristics of Patients with Hereditary Transthyretin Amyloidosis-Polyneuropathy (ATTRv-PN) in NEURO-TTRansform, an Open-label Phase 3 Study of Eplontersen

Neurology and Therapy, Springer Nature 2023, Vol. 12 : 267-287

Coelho, Teresa; Waddington Cruz, Márcia; Chao, Chi-Chao; et al.

A 15-year consolidated overview of data in over 6000 patients from the Transthyretin Amyloidosis Outcomes Survey (THAOS)

Orphanet Journal of Rare Diseases, BioMed Central (BMC) 2023, Vol. 18, (1)

Gentile, Luca; Coelho, Teresa; Dispenzieri, Angela; et al.

Defunctioning loop ileostomy in anterior resection for rectal cancer and subsequent renal failure: nationwide population-based study

BJS Open, Oxford University Press 2023, Vol. 7, (3)

Rutegård, Martin; Häggström, Jenny; Back, Erik; et al.

Improved survival in at-risk patients undergoing surveillance for hepatocellular carcinoma: a nationwide Swedish register-based study

Journal of Hepatocellular Carcinoma, Dove Medical Press 2023, Vol. 10 : 1573-1586

Thörn, Richard; Hemmingsson, Oskar; Danielsson Borssén, Åsa; et al.

Amyloid fibril composition type is consistent over time in patients with Val30Met (p. Val50Met) transthyretin amyloidosis

PLOS ONE, Public Library of Science 2022, Vol. 17, (3)

Anan, Intissar; Suhr, Ole B.; Liszewska, Katarzyna; et al.

Characteristics of patients with autonomic dysfunction in the Transthyretin Amyloidosis Outcomes Survey (THAOS)

Amyloid: Journal of Protein Folding Disorders, Taylor & Francis 2022, Vol. 29, (3) : 175-183

Barroso, Fabio A.; Coelho, Teresa; Dispenzieri, Angela; et al.

Clinical and genetic profile of patients enrolled in the Transthyretin Amyloidosis Outcomes Survey (THAOS): 14-year update

Orphanet Journal of Rare Diseases, BioMed Central (BMC) 2022, Vol. 17, (1)

Dispenzieri, Angela; Coelho, Teresa; Conceição, Isabel; et al.

Epidemiology of hereditary transthyretin amyloidosis in the northernmost region of Sweden: a retrospective cohort study

Amyloid: Journal of Protein Folding Disorders, Taylor & Francis 2022, Vol. 29, (2) : 120-127

Mejia Baranda, Jorge; Ljungberg, Jenny; Wixner, Jonas; et al.

Hereditary transthyretin amyloidosis in Sweden: Comparisons between a non-endemic and an endemic region

Amyloid: Journal of Protein Folding Disorders, Taylor & Francis 2022, Vol. 29, (4) : 220-227

Samuelsson, Kristin; Jovanovic, Ana; Egervall, Karl; et al.

Patisiran treatment in patients with hereditary transthyretin-mediated amyloidosis with polyneuropathy after liver transplantation

American Journal of Transplantation, John Wiley & Sons 2022, Vol. 22, (6) : 1646-1657

Schmidt, Hartmut H.; Wixner, Jonas; Planté-Bordeneuve, Violaine; et al.

Survival after first diagnosis of oesophageal or gastric varices in a single centre in northern Sweden: a retrospective study

Clinical and Experimental Hepatology, Vol. 8, (2) : 103-110

Thörn, Richard; Christensen, Evelina; Wixner, Jonas; et al.

Cerebellar and Cerebral Amyloid Visualized by [18F]flutemetamol PET in Long-Term Hereditary V30M (p.V50M) Transthyretin Amyloidosis Survivors

Frontiers in Neurology, Frontiers Media S.A. 2022, Vol. 13

Unéus, Erica Irene; Wilhelmsson, Christer; Bäckström, David; et al.

Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study

Lancet Neurology, Elsevier 2021, Vol. 20, (1) : 49-59

Adams, David; Polydefkis, Michael; Gonzalez-Duarte, Alejandra; et al.

JACC. Heart failure, Elsevier 2021, Vol. 9, (10) : 736-746

Caponetti, Angelo Giuseppe; Rapezzi, Claudio; Gagliardi, Christian; et al.

A simple core dataset and disease severity score for hereditary transthyretin (ATTRv) amyloidosis

Amyloid: Journal of Protein Folding Disorders, Taylor & Francis 2021, Vol. 28, (3) : 189-198

Damy, Thibaud; Conceição, Isabel; García-Pavía, Pablo; et al.

Combining ECG and echocardiography to identify transthyretin cardiac amyloidosis in heart failure

Clinical Physiology and Functional Imaging, John Wiley & Sons 2021, Vol. 41, (5) : 408-416

Löfbacka, Viktor; Suhr, Ole B.; Pilebro, Björn; et al.

Patisiran in patients with hATTR amyloidosis post-orthotopic liver transplant: 12-month results

Journal of the peripheral nervous system, Peripheral Nerve Society 2021, Vol. 26, (3) : 307-307

Muñoz-Beamud, Francisco; Coelho, Teresa; Gillmore, Julian D.; et al.

Recommendations for the diagnosis and management of transthyretin amyloidosis with gastrointestinal manifestations

European Journal of Gastroenterology and Hepathology, Lippincott Williams & Wilkins 2021, Vol. 33, (5) : 613-622

Nakov, Radislav; Suhr, Ole B.; Ianiro, Gianluca; et al.

Metabolomics analysis for diagnosis and biomarker discovery of transthyretin amyloidosis

Amyloid: Journal of Protein Folding Disorders, Taylor & Francis Group 2021, Vol. 28, (4) : 234-242

Olsson, Malin; Hellman, Urban; Wixner, Jonas; et al.

Characteristics of Patients with Late- vs. Early-Onset Val30Met Transthyretin Amyloidosis from the Transthyretin Amyloidosis Outcomes Survey (THAOS)

Neurology and Therapy, Springer London 2021, Vol. 10, (2) : 753-766

Waddington-Cruz, Márcia; Wixner, Jonas; Amass, Leslie; et al.

Abdominal fat pad biopsies exhibit good diagnostic accuracy in patients with suspected transthyretin amyloidosis

Orphanet Journal of Rare Diseases, BioMed Central (BMC) 2020, Vol. 15, (1)

Paulsson Rokke, Hedvig; Sadat Gousheh, Nima; Westermark, Per; et al.

Long-term safety and efficacy of Patisiran in patients with hATTR amyloidosis: Global OLE study

Journal of the peripheral nervous system, Vol. 25 : S13-S13

Polydefkis, Michael; Gonzalez-Duarte, Alejandra; Coelho, Teresa; et al.

Long-term Safety and Efficacy of Patisiran in Patients with hATTR Amyloidosis: Global OLE Study

Neurology, Lippincott Williams & Wilkins 2020, Vol. 94, (15)

Polydefkis, Michael; Gonzalez-Duarte, Alejandra; Coelho, Teresa; et al.

A case report of osteoarthritis associated with hereditary transthyretin amyloidosis ATTRV30M

Amyloid: Journal of Protein Folding Disorders, Taylor & Francis 2019, Vol. 26 : 29-30

Anan, Intissar; Bång, Joakim; Lundgren, Hans-Erik; et al.

Transthyretin Glu54Leu - an unknown mutation within the Swedish population associated with amyloid cardiomyopathy and a unique fibril type

Scandinavian Journal of Clinical and Laboratory Investigation, Taylor & Francis 2019, Vol. 79, (6) : 372-376

Hellman, Urban; Lång, Kenneth; Ihse, Elisabet; et al.

Prevalence of transthyretin cardiac amyloidosis in a community-based heart failure population

European Heart Journal, Oxford University Press 2019, Vol. 40 : 132-132

Lindmark, Krister; Pilebro, Björn; Solekrans, L.; et al.

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

Amyloid: Journal of Protein Folding Disorders, Taylor & Francis 2019, Vol. 26 : 47-48

Marberg, Therese; Karling, Pontus; Söderberg, Karin; et al.

Amyloid fibril composition within hereditary Val30Met (p. Val50Met) transthyretin amyloidosis families

PLOS ONE, Public Library Science 2019, Vol. 14, (2)

Suhr, Ole Bernt; Wixner, Jonas; Anan, Intissar; et al.

Visualisation of amyloid deposition within the brain of long-term hereditary transthyretin amyloidosis survivors by 18F-flutemetamol positron emission tomography

European Journal of Neurology, John Wiley & Sons 2019, Vol. 26, (S1) : 287-287

Unéus, Erica; Wilhelmsson, Christer; Suhr, Ole; et al.

The Swedish open-label diflunisal trial (DFNS01) on hereditary transthyretin amyloidosis and the impact of amyloid fibril composition

Amyloid: Journal of Protein Folding Disorders, Taylor & Francis Group 2019, Vol. 26 : 39-40

Wixner, Jonas; Westermark, Per; Ihse, Elisabet; et al.

Atrial Fibrillation and Central Nervous Complications in Liver Transplanted Hereditary Transthyretin Amyloidosis Patients

Transplantation, LIPPINCOTT WILLIAMS & WILKINS 2018, Vol. 102, (2) : e59-e66

Wange, Niklas; Anan, Intissar; Ericzon, Bo-Göran; et al.

Management of gastrointestinal complications in hereditary transthyretin amyloidosis: a single-center experience over 40 years

Expert Review of Gastroenterology & Hepatology, Taylor & Francis 2018, Vol. 12, (1) : 73-81

Wixner, Jonas; Suhr, Ole B.; Anan, Intissar

Abnormal small bowel motility in patients with hereditary transthyretin amyloidosis

Neurogastroenterology and Motility, Wiley-Blackwell 2018, Vol. 30, (9)

Wixner, Jonas; Törnblom, H.; Karling, Pontus; et al.

The Swedish landscape of hereditary ATTR amyloidosis

Amyloid: Journal of Protein Folding Disorders, Vol. 24, (1) : 93-94

Suhr, Ole B; Wixner, Jonas; Pilebro, Björn; et al.

Effect of doxycycline and ursodeoxycholic acid on transthyretin amyloidosis

Amyloid: Journal of Protein Folding Disorders, Vol. 24, (1) : 78-79

Wixner, Jonas; Pilebro, Bjorn; Lundgren, Hans-Erik; et al.

Outcome of gastric emptying and gastrointestinal symptoms after liver transplantation for hereditary transthyretin amyloidosis

BMC Gastroenterology, Vol. 15

Wixner, Jonas; Sundström, Torbjorn; Karling, Pontus; et al.

Gastrointestinal disturbances in hereditary transthyretin amyloidosis

Umeå University medical dissertations, 1633

Wixner, Jonas

Visa publikationer i DiVA

Forskargrupper

Gruppmedlem

Amyloidoscentrum

Mårten Werner - leverforskning

Forskningsprojekt

1 januari 2019

Patogenes, diagnostik och behandling av transtyretinamyloidos

1 januari 2016

Hjärtamyloidos och hjärtsvikt. Förbättrad diagnostik och optimerad behandling