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Systemic amyloidosis

The Lancet (British edition), 2016-06, Vol.387 (10038), p.2641-2654

2016

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Native T1 and Extracellular Volume in Transthyretin Amyloidosis

JACC. Cardiovascular imaging, 2019-05, Vol.12 (5), p.810-819

2019

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Online Registry for Mutations in Hereditary Amyloidosis Including Nomenclature Recommendations

Human mutation, 2014-09, Vol.35 (9), p.E2403-E2412

2014

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Safety and Efficacy of RNAi Therapy for Transthyretin Amyloidosis

The New England journal of medicine, 2013-08, Vol.369 (9), p.819-829

2013

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Use of Canakinumab in the Cryopyrin-Associated Periodic Syndrome

The New England journal of medicine, 2009-06, Vol.360 (23), p.2416-2425

2009

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Clinical impact of a targeted next-generation sequencing gene panel for autoinflammation and vasculitis

PloS one, 2017-07, Vol.12 (7), p.e0181874-e0181874

2017

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Association of the transthyretin variant V122I with polyneuropathy among individuals of African ancestry

Scientific reports, 2021-06, Vol.11 (1), p.11645-10, Article 11645

2021

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Misdiagnosis of Hereditary Amyloidosis as AL (Primary) Amyloidosis

The New England journal of medicine, 2002-06, Vol.346 (23), p.1786-1791

2002

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Diagnostic imaging of cardiac amyloidosis

Nature reviews cardiology, 2020-07, Vol.17 (7), p.413

2020

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Magnetic Resonance in Transthyretin Cardiac Amyloidosis

Journal of the American College of Cardiology, 2017-07, Vol.70 (4), p.466-477

2017

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Myocardial Edema and Prognosis in Amyloidosis

Journal of the American College of Cardiology, 2018-06, Vol.71 (25), p.2919-2931

2018

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Long-term safety and effectiveness of canakinumab therapy in patients with cryopyrin-associated periodic syndrome: results from the β-Confident Registry

Rheumatic & musculoskeletal diseases open, 2021-05, Vol.7 (2), p.e001663

2021

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The electrocardiographic features associated with cardiac amyloidosis of variant transthyretin isoleucine 122 type in Afro-Caribbean patients

The American heart journal, 2012-07, Vol.164 (1), p.72-79

2012

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Retrospective case series describing the efficacy, safety and cost-effectiveness of a vial-sharing programme for canakinumab treatment for paediatric patients with cryopyrin-associated periodic syndrome

Pediatric rheumatology online journal, 2019-07, Vol.17 (1), p.36-7, Article 36

2019

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Occult Transthyretin Cardiac Amyloid in Severe Calcific Aortic Stenosis: Prevalence and Prognosis in Patients Undergoing Surgical Aortic Valve Replacement

Circulation. Cardiovascular imaging, 2016-08, Vol.9 (8)

2016

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Cardiac transthyretin amyloidosis

Heart (British Cardiac Society), 2012-11, Vol.98 (21), p.1546-1554

2012

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Exploratory Study of MYD88 L265P, Rare NLRP3 Variants, and Clonal Hematopoiesis Prevalence in Patients With Schnitzler Syndrome

Arthritis & rheumatology (Hoboken, N.J.), 2019-12, Vol.71 (12), p.2121-2125

2019

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A novel mechano‐enzymatic cleavage mechanism underlies transthyretin amyloidogenesis

EMBO molecular medicine, 2015-10, Vol.7 (10), p.1337-1349

2015

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Cardiac phenotype and clinical outcome of familial amyloid polyneuropathy associated with transthyretin alanine 60 variant

European heart journal, 2012-05, Vol.33 (9), p.1120-1127

2012

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Afro-Caribbean Heart Failure in the United Kingdom: Cause, Outcomes, and ATTR V122I Cardiac Amyloidosis

Circulation. Heart failure, 2016-09, Vol.9 (9)

2016

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Involvement of X-box binding protein 1 and reactive oxygen species pathways in the pathogenesis of tumour necrosis factor receptor-associated periodic syndrome

Annals of the rheumatic diseases, 2012-12, Vol.71 (12), p.2035-2043

2012

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Autosomal dominant familial Mediterranean fever in Northern European Caucasians associated with deletion of p.M694 residue-a case series and genetic exploration

Rheumatology (Oxford, England), 2017-02, Vol.56 (2), p.209-213

2017

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Diagnosis, Pathogenesis, Treatment, and Prognosis of Hereditary Fibrinogen Aα-Chain Amyloidosis

Journal of the American Society of Nephrology, 2009-02, Vol.20 (2), p.444-451

2009

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Clinical characteristics in subjects with NLRP3 V198M diagnosed at a single UK center and a review of the literature

Arthritis research & therapy, 2013-02, Vol.15 (1), p.R30-R30

2013

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INSAID Variant Classification and Eurofever Criteria Guide Optimal Treatment Strategy in Patients with TRAPS: Data from the Eurofever Registry

The journal of allergy and clinical immunology in practice (Cambridge, MA), 2021-02, Vol.9 (2), p.783-791.e4

2021

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Systemic amyloidosis

Native T1 and Extracellular Volume in Transthyretin Amyloidosis

Online Registry for Mutations in Hereditary Amyloidosis Including Nomenclature Recommendations

Safety and Efficacy of RNAi Therapy for Transthyretin Amyloidosis

Use of Canakinumab in the Cryopyrin-Associated Periodic Syndrome

Clinical impact of a targeted next-generation sequencing gene panel for autoinflammation and vasculitis

Association of the transthyretin variant V122I with polyneuropathy among individuals of African ancestry

Misdiagnosis of Hereditary Amyloidosis as AL (Primary) Amyloidosis

Diagnostic imaging of cardiac amyloidosis

Magnetic Resonance in Transthyretin Cardiac Amyloidosis

Myocardial Edema and Prognosis in Amyloidosis

Long-term safety and effectiveness of canakinumab therapy in patients with cryopyrin-associated periodic syndrome: results from the β-Confident Registry

The electrocardiographic features associated with cardiac amyloidosis of variant transthyretin isoleucine 122 type in Afro-Caribbean patients

Retrospective case series describing the efficacy, safety and cost-effectiveness of a vial-sharing programme for canakinumab treatment for paediatric patients with cryopyrin-associated periodic syndrome

Occult Transthyretin Cardiac Amyloid in Severe Calcific Aortic Stenosis: Prevalence and Prognosis in Patients Undergoing Surgical Aortic Valve Replacement

Cardiac transthyretin amyloidosis

Exploratory Study of MYD88 L265P, Rare NLRP3 Variants, and Clonal Hematopoiesis Prevalence in Patients With Schnitzler Syndrome

A novel mechano‐enzymatic cleavage mechanism underlies transthyretin amyloidogenesis

Cardiac phenotype and clinical outcome of familial amyloid polyneuropathy associated with transthyretin alanine 60 variant

Afro-Caribbean Heart Failure in the United Kingdom: Cause, Outcomes, and ATTR V122I Cardiac Amyloidosis

Involvement of X-box binding protein 1 and reactive oxygen species pathways in the pathogenesis of tumour necrosis factor receptor-associated periodic syndrome

Autosomal dominant familial Mediterranean fever in Northern European Caucasians associated with deletion of p.M694 residue-a case series and genetic exploration

Diagnosis, Pathogenesis, Treatment, and Prognosis of Hereditary Fibrinogen Aα-Chain Amyloidosis

Clinical characteristics in subjects with NLRP3 V198M diagnosed at a single UK center and a review of the literature

INSAID Variant Classification and Eurofever Criteria Guide Optimal Treatment Strategy in Patients with TRAPS: Data from the Eurofever Registry

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