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kw.\*:("Mevalonate kinase deficiencies")

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The inhibition of mevalonate pathway induces upregulation of NALP3 expression: new insight in the pathogenesis of mevalonate kinase deficiencyPONTILLO, Alessandra; PAOLUZZI, Elisa; CROVELLA, Sergio et al.European journal of human genetics. 2010, Vol 18, Num 7, pp 844-847, issn 1018-4813, 4 p.Article

Efficacy of interleukin-1-targeting drugs in mevalonate kinase deficiencyGALEOTTI, Caroline; MEINZER, Ulrich; QUARTIER, Pierre et al.Rheumatology (Oxford. Print). 2012, Vol 51, Num 10, pp 1855-1859, issn 1462-0324, 5 p.Article

A Clinical Criterion to Exclude the Hyperimmunoglobulin D Syndrome (Mild Mevalonate Kinase Deficiency) in Patients with Recurrent FeverSTEICHEN, Olivier; VAN DER HILST, Jeroen; SIMON, Anna et al.Journal of rheumatology. 2009, Vol 36, Num 8, pp 1677-1681, issn 0315-162X, 5 p.Article

PFAPA syndrome in siblings. Is there a genetic background?ANTON-MARTIN, Pilar; ORTIZ MOVILLA, Roberto; GUILLEN MARTIN, Sara et al.European journal of pediatrics. 2011, Vol 170, Num 12, pp 1563-1568, issn 0340-6199, 6 p.Article

Autoinflammatory syndromes and infections : pathogenetic and clinical implicationsEFTHIMIOU, P; FLAVELL, R. A; DORIA, A et al.Clinical and experimental rheumatology (Testo stampato). 2008, Vol 26, Num 1, issn 0392-856X, S53-S61, SUP48Conference Paper

Klinik der autoinflammatorischen Erkrankungen im Kindesalter : Autoinflammation = Autoinflammatory diseases in childhood : AutoinflammationFOELDVARI, I; KÜMMERLE-DESCHNER, J.Zeitschrift für Rheumatologie (Print). 2009, Vol 68, Num 9, issn 0340-1855, 726-732 [6 p.]Article

MVK mutations and associated clinical features in Italian patients affected with autoinflammatory disorders and recurrent feverD'OSUALDO, Andrea; PICCO, Paolo; OBICI, Laura et al.European journal of human genetics. 2005, Vol 13, Num 3, pp 314-320, issn 1018-4813, 7 p.Article

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