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Staff photo Jonas Wixner

Jonas Wixner

Contact

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

Works at

Affiliation
Affiliated as physician at Department of Public Health and Clinical Medicine
Location
Byggnad 1A, plan 4, målpunkt B41, Norrlands universitetssjukhus
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
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.
Prognostic value of pre-transplant cardiomyopathy in Swedish liver transplanted patients for familial amyloidotic polyneuropathy
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, Pearl River: Parthenon 2011, Vol. 18 Suppl 1 : 166-8
Okamoto, Sadahisa; Wixner, Jonas; Ericzon, B-G; et al.
Liver transplantation for familial amyloidotic polyneuropathy: impact on Swedish patients' survival
Liver transplantation, John Wiley & Sons 2009, Vol. 15, (10) : 1229-1235
Okamoto, Sadahisa; Wixner, Jonas; Obayashi, Konen; et al.
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