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Staff photo Jonas Wixner

Jonas Wixner

Contact

E-mail
jonas.wixner@umu.se
Phone
+46 90 785 00 00

Works as

Affiliation
Affiliated as physician at Department of Public Health and Clinical Medicine Section: Gastroenterology
Location
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.
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.
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.
Sex-Related Risk of Cardiac Involvement in Hereditary Transthyretin Amyloidosis: Insights From THAOS
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
THAOS: Gastrointestinal manifestations of transthyretin amyloidosis - common complications of a rare disease
Orphanet Journal of Rare Diseases, BioMed Central (BMC) 2014, Vol. 9, (1) : 61-
Wixner, Jonas; Mundayat, Rajiv; Karayal, Onur N; et al.
Loss of gastric interstitial cells of Cajal in patients with hereditary transthyretin amyloidosis
Amyloid: Journal of Protein Folding Disorders, Informa Healthcare 2013, Vol. 20, (2) : 99-106
Wixner, Jonas; Obayashi, Konen; Ando, Yukio; et al.
Gastric emptying in hereditary transthyretin amyloidosis: the impact of autonomic neuropathy
Neurogastroenterology and Motility, Wiley-Blackwell 2012, Vol. 24, (12) : 1111-e568
Wixner, Jonas; Karling, Pontus; Rydh, Anders; et al.
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