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authFullName_s : Samuel Deshayes

Quality of life assessment by SF-36 in elderly patients with familial Mediterranean fever: a comparative cross-sectional study from the Juvenile Inflammatory Rheumatism cohort

Audrey Rouet , Samuel Deshayes , Léa Savey , Gilles Grateau , Sophie Georgin-Lavialle
Other publications inserm-04050068v1
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Specific changes in faecal microbiota are associated with familial Mediterranean fever

Samuel Deshayes , Soraya Fellahi , Jean-Philippe Bastard , Jean-Marie Launay , Jacques Callebert , et al.
Annals of the Rheumatic Diseases, 2019, 78 (10), pp.1398-1404. ⟨10.1136/annrheumdis-2019-215258⟩
Journal articles hal-02291701v1

In familial Mediterranean fever, soluble TREM-1 plasma level is higher in case of amyloidosis

Clémence Gorlier , Jérémie Sellam , Ludivine Laurans , Tabassome Simon , Irina Giurgea , et al.
Innate Immunity, 2019, 25 (8), pp.487-490. ⟨10.1177/1753425919870847⟩
Journal articles hal-04001161v1
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A critical region of A20 unveiled by missense TNFAIP3 variations that lead to autoinflammation

Elma El Khouri , Farah Diab , Camille Louvrier , Eman Assrawi , Aphrodite Daskalopoulou , et al.
eLife, 2023, 12, pp.e81280. ⟨10.7554/eLife.81280⟩
Journal articles inserm-04148971v1
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An overview of the perspectives on experimental models and new therapeutic targets in giant cell arteritis

Samuel Deshayes , Hubert de Boysson , Anaël Dumont , Denis Vivien , Alain Manrique , et al.
Autoimmunity Reviews, 2020, 19, pp.102636 -. ⟨10.1016/j.autrev.2020.102636⟩
Journal articles hal-03491650v1

Typical Familial Mediterranean Fever associated with the heterozygous missense sequence p.T577N variant of the MEFV gene: Report on two Northern European Caucasians relatives in France

Ines Elhani , Anael Dumont , Samuel Deshayes , Sophie Georgin-Lavialle , Irina Giurgea , et al.
Joint Bone Spine, 2020, 87 (3), pp.251-255. ⟨10.1016/j.jbspin.2020.01.005⟩
Journal articles inserm-03798471v1

Response to Letter to the Editor

Clémence Gorlier , Jérémie Sellam , Ludivine Laurans , Tabassome Simon , Irina Giurgea , et al.
Other publications inserm-04050672v1

Cause of death and risk factors for mortality in AA amyloidosis: A French retrospective study

Alexandre Terré , Samuel Deshayes , Léa Savey , Gilles Grateau , Sophie Georgin-Lavialle
Other publications inserm-04050698v1
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Role of non-invasive methods in detecting liver impairment in familial Mediterranean fever adult patients with persistent hepatic cytolysis

Samuel Deshayes , Thibault Fraisse , Soraya Fellahi , Olivier Steichen , Léa Savey , et al.
Scientific Reports, 2022, 12 (1), pp.16644. ⟨10.1038/s41598-022-17358-x⟩
Journal articles inserm-03874714v1

AA amyloidosis associated with Fabry disease

Alexandre Terré , Bertrand Knebelmann , David Buob , Marion Rabant , Olivier Lidove , et al.
International Journal of Clinical Practice, 2020, 74 (10), ⟨10.1111/ijcp.13577⟩
Journal articles inserm-04050836v1
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Tumour necrosis factor receptor-1 associated periodic syndrome (TRAPS)-related AA amyloidosis: a national case series and systematic review

Jérémie Delaleu , Samuel Deshayes , Francois Rodrigues , Lea Savey , Etienne Rivière , et al.
Rheumatology, 2021, 60 (12), pp.5775-5784. ⟨10.1093/rheumatology/keab252⟩
Journal articles inserm-03790429v1
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Chronic hepatic involvement in the clinical spectrum of A20 haploinsufficiency

Samuel Deshayes , Céline Bazille , Elma El Khouri , Isabelle Kone-Paut , Irina Giurgea , et al.
Liver International, 2021, 41 (8), pp.1894-1900. ⟨10.1111/liv.14935⟩
Journal articles inserm-03798525v1

Abnormal electrochemical skin conductance values in patients with AA amyloidosis

Samuel Deshayes , Rim Bourguiba , Jean-Philippe Haymann , Léa Savey , Achille Aouba , et al.
Other publications inserm-04050434v1