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authFullName_s : Linda Rossi-Semerano
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PW02-012 - First clinical description of an infant with DITRA

Linda Rossi-Semerano , Maryam Piram , Christine Chiaverini , Dominique de Ricaud , Asma Smahi , et al.
Pediatric Rheumatology, 2013, 11 (Suppl 1), pp.A152
Journal articles inserm-00881679v1
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The expanding spectrum of rare monogenic autoinflammatory diseases.

Isabelle Touitou , Caroline Galeotti , Linda Rossi-Semerano , Véronique Hentgen , Maryam Piram , et al.
Orphanet Journal of Rare Diseases, 2013, 8 (1), pp.162. ⟨10.1186/1750-1172-8-162⟩
Journal articles inserm-00878791v1
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Conventional radiography in juvenile idiopathic arthritis: Joint recommendations from the French societies for rheumatology, radiology and paediatric rheumatology

Pauline Marteau , Catherine Adamsbaum , Linda Rossi-Semerano , Michel de Bandt , Irène Lemelle , et al.
European Radiology, 2018, ⟨10.1007/s00330-018-5304-7⟩
Journal articles hal-01795616v1
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A survey of resistance to colchicine treatment for French patients with familial Mediterranean fever

Alice Corsia , Sophie Georgin-Lavialle , Véronique Hentgen , Eric Hachulla , Gilles Grateau , et al.
Orphanet Journal of Rare Diseases, 2017, 12 (1), pp.54. ⟨10.1186/s13023-017-0609-1⟩
Journal articles inserm-04051765v1
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Non‐amyloid liver involvement in familial Mediterranean fever: A systematic literature review

Thibault Fraisse , Léa Savey , Véronique Hentgen , Linda Rossi-Semerano , Isabelle Koné-Paut , et al.
Liver International, 2020, 40 (6), pp.1269-1277. ⟨10.1111/liv.14445⟩
Journal articles inserm-04050639v1
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The French Gaucher's disease registry: clinical characteristics, complications and treatment of 562 patients.

Jérôme Stirnemann , Marie Vigan , Dalil Hamroun , Djazia Heraoui , Linda Rossi-Semerano , et al.
Orphanet Journal of Rare Diseases, 2012, 7 (1), pp.77. ⟨10.1186/1750-1172-7-77⟩
Journal articles inserm-00767459v1
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Tolerance and efficacy of off-label anti-interleukin-1 treatments in France: a nationwide survey

Linda Rossi-Semerano , Bruno Fautrel , Daniel Wendling , Eric Hachulla , Caroline Galeotti , et al.
Orphanet Journal of Rare Diseases, 2015, 10, pp.19. ⟨10.1186/s13023-015-0228-7⟩
Journal articles hal-01275718v1