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Avoiding misdiagnosis: expert consensus recommendations for the suspicion and diagnosis of transthyretin amyloidosis for the general practitioner

BMC family practice, 2020-09, Vol.21 (1), p.198, Article 198

2020

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Spectrum of clinical features in Muckle‐Wells syndrome and response to anakinra

Arthritis and rheumatism, 2004-02, Vol.50 (2), p.607-612

2004

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The emerging role of interleukin‐1β in autoinflammatory diseases

Arthritis and rheumatism, 2011-02, Vol.63 (2), p.314-324

2011

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AA amyloidosis complicating the hereditary periodic fever syndromes

Arthritis and rheumatism, 2013-04, Vol.65 (4), p.1116-1121

2013

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Phenotype, genotype, and sustained response to anakinra in 22 patients with autoinflammatory disease associated with CIAS-1/NALP3 mutations

Archives of dermatology (1960), 2006-12, Vol.142 (12), p.1591

2006

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Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis

Arthritis and rheumatism, 2002-09, Vol.46 (9), p.2445-2452

2002

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Abnormal tumor necrosis factor receptor I cell surface expression and NF‐κB activation in tumor necrosis factor receptor–associated periodic syndrome

Arthritis and rheumatism, 2008-01, Vol.58 (1), p.273-283

2008

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Rapid and complete resolution of proteinuria due to renal amyloidosis in a patient with rheumatoid arthritis treated with infliximab

Arthritis and rheumatism, 2002-10, Vol.46 (10), p.2571-2573

2002

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Response to anakinra in a de novo case of neonatal‐onset multisystem inflammatory disease

Arthritis and rheumatism, 2004-08, Vol.50 (8), p.2708-2709

2004

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Amyloidosis

Textbook of Hepatology, 2007, p.1702-1708

2007

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Amyloidosis

Postgraduate Haematology, 2015, p.562-574

2015

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Systemic Amyloidosis

Textbook of Clinical Gastroenterology and Hepatology, 2012, p.886-892

2012

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Abstract 14123: Assessment of Treatment Response in Cardiac AL Amyloidosis Using CMR Mapping - Results at 3 Months, 6 Months and 1 Year Post-Chemotherapy

Circulation (New York, N.Y.), 2018-11, Vol.138 (Suppl_1 Suppl 1), p.A14123-A14123

2018

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AA amyloidosis complicating hyperimmunoglobulinemia D with periodic fever syndrome: A report of two cases

Arthritis and rheumatism, 2006-06, Vol.54 (6), p.2010-2014

2006

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Systemic Amyloidosis

Textbook of Autoinflammation, 2019, p.267-289

2019

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Amyloidosis

Postgraduate Haematology, 2011, p.599-613

2011

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Abstract 14407: Regression of Cardiac AL Amyloid by Cardiovascular Magnetic Resonance

Circulation (New York, N.Y.), 2016-11, Vol.134 (Suppl_1 Suppl 1), p.A14407-A14407

2016

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An autosomal dominant periodic fever associated with AA amyloidosis in a North Indian family maps to distal chromosome 1q

Arthritis and rheumatism, 2000-09, Vol.43 (9), p.2034-2040

2000

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Amyloidosis

Postgraduate Haematology, 2005, p.703-713

2005

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An Israeli Arab patient with a de novo TNFRSF1A mutation causing tumor necrosis factor receptor‐associated periodic syndrome

Arthritis and rheumatism, 2002-01, Vol.46 (1), p.245-249

2002

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Two types of systemic amyloidosis in a single patient

Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 2020, Vol.27 (4), p.275-276

2020

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Hyperimmunoglobulin D syndrome in an Indian family undiagnosed for 11 years

International journal of rheumatic diseases, 2017, Vol.20 (12), p.2236-2237

2017

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Autoinflammatory Disorders

Primary Immunodeficiency Diseases, 2016, p.393-435

2016

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Novel pharmacological strategies in amyloidosis

Nephron, 2003-08, Vol.94 (4), p.c85-c88

2003

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Avoiding misdiagnosis: expert consensus recommendations for the suspicion and diagnosis of transthyretin amyloidosis for the general practitioner

Spectrum of clinical features in Muckle‐Wells syndrome and response to anakinra

The emerging role of interleukin‐1β in autoinflammatory diseases

AA amyloidosis complicating the hereditary periodic fever syndromes

Phenotype, genotype, and sustained response to anakinra in 22 patients with autoinflammatory disease associated with CIAS-1/NALP3 mutations

Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis

Abnormal tumor necrosis factor receptor I cell surface expression and NF‐κB activation in tumor necrosis factor receptor–associated periodic syndrome

Rapid and complete resolution of proteinuria due to renal amyloidosis in a patient with rheumatoid arthritis treated with infliximab

Heterogeneity among patients with tumor necrosis factor receptor–associated periodic syndrome phenotypes

Response to anakinra in a de novo case of neonatal‐onset multisystem inflammatory disease

Amyloidosis

Amyloidosis

Systemic Amyloidosis

Abstract 14123: Assessment of Treatment Response in Cardiac AL Amyloidosis Using CMR Mapping - Results at 3 Months, 6 Months and 1 Year Post-Chemotherapy

AA amyloidosis complicating hyperimmunoglobulinemia D with periodic fever syndrome: A report of two cases

Systemic Amyloidosis

Amyloidosis

Abstract 14407: Regression of Cardiac AL Amyloid by Cardiovascular Magnetic Resonance

An autosomal dominant periodic fever associated with AA amyloidosis in a North Indian family maps to distal chromosome 1q

Amyloidosis

An Israeli Arab patient with a de novo TNFRSF1A mutation causing tumor necrosis factor receptor‐associated periodic syndrome

Two types of systemic amyloidosis in a single patient

Hyperimmunoglobulin D syndrome in an Indian family undiagnosed for 11 years

Autoinflammatory Disorders

Novel pharmacological strategies in amyloidosis

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