L'angolo dell'immunologo
Febbri ricorrenti con alti indici di flogosi
ALBERTO TOMMASINI1, LOREDANA LEPORE2
1Laboratorio Immunologico, 2Istituto di Clinica Pediatrica, IRCCS “Burlo Garofolo”, Trieste
Ottobre 1999 - pagg. 506 -510
Parole chiave
Suggerite dall'AI
Classificazione MeSH
Bibliografia
1. Marshall GS, Edwards KM, Butler J, Lawton
AR: Syndrome of periodic fever, pharyngitis,
and aphthous stomatitis. J Pediatr 110, 43-
6, 1987.
2. Padeh S, Brezniak N, Zemer D, Pras E, Livneh A, et al: Periodic fever, aphthous stomatitis, pharyngitis, and adenopathy syndrome: clinical characteristics and outcome. J Pediatr 135, 98-101, 1999.
3. Thomas KT, Feder HM Jr, Lawton AR, Edwards KM: Periodic fever syndrome in children. J Pediatr 135, 15-21, 1999.
4. Long SS: Syndrome of periodic fever, aphtous stomatitis, pharyngitis, and adenitis (PFAPA) - What it isn’t. What is it? J Pediatr 135, 1-5, 1999.
5. Not T, Buratti E, Berti I, et al: L’apoptosi nella fisiologia e nella patologia umana. Medico e Bambino 4, 251-4, 1998.
6. McDermott MF, Aksentijevich I, Galon J, McDermott EM, Ogunkolade BW: Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes. Cell 2, 97,133-44, 1999.
7. The French FMF Consortium: A candidate gene for familial Mediterranean fever. Nat Genet Sep 17(1), 25-31, 1997.
8. Babior B, Matzner Y: The familial Mediterranean fever gene-cloned at least. N Engl J Med 337, 1548-9, 1997.
9. Drenth JPH, Haagsma CJ, van der Meer JWM: The International Hyper-IgD Study Group: Hyperimmunoglobulinemia D and periodic fever syndrome: the clinical spectrum in a series of 50 patients. Medicine 73, 133-44, 1994.
10. Drenth JP, Cuisset L, Grateau G, Vasseur C, van de Velde-Visser SD, et al: Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. International Hyper-IgD Study Group. Nat Genet 22, 178-81, 1999.
11. Houten SM, Kuis W, Duran M, de Koning TJ, van Royen-Kerkhof A, et al: Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinemia D and periodic fever syndrome. Nat Genet 22, 175-7, 1999.
12. Hoffmann G, Gibson KM, Brandt IK, Bader PI, Wappner RS, Sweetman L, et al: Mevalonic aciduria - an inborn error of cholesterol and nonsterol isoprene biosynthesis. N Engl J Med 19, 314, 1610-4, 1986.
13. Valle D: You give me fever. Nat Genet 22, 121-3, 1999.
14. Livneh A, Drenth JP, Klasen IS, Langevitz P, George J, et al: Familial Mediterranean fever and hyperimmunoglobulinemia D syndrome: two diseases with distinct clinical, serologic, and genetic features. J Rheumatol 24, 1558-63, 1997.
2. Padeh S, Brezniak N, Zemer D, Pras E, Livneh A, et al: Periodic fever, aphthous stomatitis, pharyngitis, and adenopathy syndrome: clinical characteristics and outcome. J Pediatr 135, 98-101, 1999.
3. Thomas KT, Feder HM Jr, Lawton AR, Edwards KM: Periodic fever syndrome in children. J Pediatr 135, 15-21, 1999.
4. Long SS: Syndrome of periodic fever, aphtous stomatitis, pharyngitis, and adenitis (PFAPA) - What it isn’t. What is it? J Pediatr 135, 1-5, 1999.
5. Not T, Buratti E, Berti I, et al: L’apoptosi nella fisiologia e nella patologia umana. Medico e Bambino 4, 251-4, 1998.
6. McDermott MF, Aksentijevich I, Galon J, McDermott EM, Ogunkolade BW: Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes. Cell 2, 97,133-44, 1999.
7. The French FMF Consortium: A candidate gene for familial Mediterranean fever. Nat Genet Sep 17(1), 25-31, 1997.
8. Babior B, Matzner Y: The familial Mediterranean fever gene-cloned at least. N Engl J Med 337, 1548-9, 1997.
9. Drenth JPH, Haagsma CJ, van der Meer JWM: The International Hyper-IgD Study Group: Hyperimmunoglobulinemia D and periodic fever syndrome: the clinical spectrum in a series of 50 patients. Medicine 73, 133-44, 1994.
10. Drenth JP, Cuisset L, Grateau G, Vasseur C, van de Velde-Visser SD, et al: Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. International Hyper-IgD Study Group. Nat Genet 22, 178-81, 1999.
11. Houten SM, Kuis W, Duran M, de Koning TJ, van Royen-Kerkhof A, et al: Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinemia D and periodic fever syndrome. Nat Genet 22, 175-7, 1999.
12. Hoffmann G, Gibson KM, Brandt IK, Bader PI, Wappner RS, Sweetman L, et al: Mevalonic aciduria - an inborn error of cholesterol and nonsterol isoprene biosynthesis. N Engl J Med 19, 314, 1610-4, 1986.
13. Valle D: You give me fever. Nat Genet 22, 121-3, 1999.
14. Livneh A, Drenth JP, Klasen IS, Langevitz P, George J, et al: Familial Mediterranean fever and hyperimmunoglobulinemia D syndrome: two diseases with distinct clinical, serologic, and genetic features. J Rheumatol 24, 1558-63, 1997.