Working the endless puzzle of hereditary autoinflammatory disorders (Q33357128)

26 July 2017

title

Working the endless puzzle of hereditary autoinflammatory disorders (English)

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Luisa Costa

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Leonardo Punzi

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Leonardo Punzi

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Paolo Sfriso

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Paolo Sfriso

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Mauro Galeazzi

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object named as

Mauro Galeazzi

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Mariangela Atteno

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Bruno Frediani

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Donato Rigante

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Flora Magnotti

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Isabella Muscari

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Maria Fioretti

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Antonio Vitale

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26 July 2017

publication date

18 October 2013

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26 July 2017

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26 July 2017

volume

24

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26 July 2017

issue

3

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page(s)

381-389

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The fresco of autoinflammatory diseases from the pediatric perspective

26 July 2017

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Clinical significance of P46L and R92Q substitutions in the tumour necrosis factor superfamily 1A gene

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Tumour necrosis factor receptor trafficking dysfunction opens the TRAPS door to pro-inflammatory cytokine secretion.

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The enlarging clinical, genetic, and population spectrum of tumor necrosis factor receptor-associated periodic syndrome

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Autoinflammatory diseases and cardiovascular manifestations.

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Binding and Functional Comparisons of Two Types of Tumor Necrosis Factor Antagonists

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Persistent efficacy of anakinra in patients with tumor necrosis factor receptor-associated periodic syndrome

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Use of canakinumab in the cryopyrin-associated periodic syndrome

21 January 2018

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Identification and functional consequences of a recurrent NLRP12 missense mutation in periodic fever syndromes.

21 January 2018

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21 January 2018

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21 January 2018

Blau syndrome revisited.

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Thalidomide dramatically improves the symptoms of early-onset sarcoidosis/Blau syndrome: its possible action and mechanism

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The eye as a common site for the early clinical manifestation of sarcoidosis

21 January 2018

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Peculiarities of PAPA syndrome

21 January 2018

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Clinical, Molecular, and Genetic Characteristics of PAPA Syndrome: A Review

21 January 2018

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An autoinflammatory disease with deficiency of the interleukin-1-receptor antagonist

21 January 2018

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Homozygous mutations in LPIN2 are responsible for the syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia (Majeed syndrome).

21 January 2018

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Amyloidosis in autoinflammatory syndromes

21 January 2018

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Recent insights into the pathogenesis of type AA amyloidosis.

21 January 2018

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Favourable and sustained response to anakinra in tumour necrosis factor receptor-associated periodic syndrome (TRAPS) with or without AA amyloidosis

21 January 2018

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Successful Treatment of Tumor Necrosis Factor Receptor–Associated Periodic Syndrome With Canakinumab

21 January 2018

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10.3109/14397595.2013.843755

21 January 2018

Identifiers

DOI

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26 July 2017

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