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33 results
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Properdin deficiency in a large Swiss family: identification of a stop codon in the properdin gene, and association of meningococcal disease with lack of the IgG2 allotype marker G2m(n).
Späth PJ, Sjöholm AG, Fredrikson GN, Misiano G, Scherz R, Schaad UB, Uhring-Lambert B, Hauptmann G, Westberg J, Uhlén M, Wadelius C, Truedsson L. Späth PJ, et al. Among authors: misiano g. Clin Exp Immunol. 1999 Nov;118(2):278-84. doi: 10.1046/j.1365-2249.1999.01056.x. Clin Exp Immunol. 1999. PMID: 10540191 Free PMC article.
Single nucleotide polymorphisms (SNPs) of pro-inflammatory/anti-inflammatory and thrombotic/fibrinolytic genes in patients with acute ischemic stroke in relation to TOAST subtype.
Tuttolomondo A, Di Raimondo D, Forte GI, Casuccio A, Vaccarino L, Scola L, Pecoraro R, Serio A, Clemente G, Arnao V, Palmeri M, Misiano G, Lio D, Pinto A, Licata G. Tuttolomondo A, et al. Among authors: misiano g. Cytokine. 2012 Jun;58(3):398-405. doi: 10.1016/j.cyto.2012.02.012. Epub 2012 Mar 17. Cytokine. 2012. PMID: 22425140
Relevance of gamma interferon, tumor necrosis factor alpha, and interleukin-10 gene polymorphisms to susceptibility to Mediterranean spotted fever.
Forte GI, Scola L, Misiano G, Milano S, Mansueto P, Vitale G, Bellanca F, Sanacore M, Vaccarino L, Rini GB, Caruso C, Cillari E, Lio D, Mansueto S. Forte GI, et al. Among authors: misiano g. Clin Vaccine Immunol. 2009 Jun;16(6):811-5. doi: 10.1128/CVI.00121-09. Epub 2009 Apr 22. Clin Vaccine Immunol. 2009. PMID: 19386798 Free PMC article.
Genetic epidemiology of autosomal recessive hypercholesterolemia in Sicily: Identification by next-generation sequencing of a new kindred.
Spina R, Noto D, Barbagallo CM, Monastero R, Ingrassia V, Valenti V, Baschi R, Pipitone A, Giammanco A, La Spada MP, Misiano G, Scrimali C, Cefalù AB, Averna MR. Spina R, et al. Among authors: misiano g. J Clin Lipidol. 2018 Jan-Feb;12(1):145-151. doi: 10.1016/j.jacl.2017.10.014. Epub 2017 Oct 27. J Clin Lipidol. 2018. PMID: 29153781
Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing.
Cefalù AB, Spina R, Noto D, Ingrassia V, Valenti V, Giammanco A, Fayer F, Misiano G, Cocorullo G, Scrimali C, Palesano O, Altieri GI, Ganci A, Barbagallo CM, Averna MR. Cefalù AB, et al. Among authors: misiano g. J Clin Lipidol. 2017 Jan-Feb;11(1):272-281.e8. doi: 10.1016/j.jacl.2017.01.003. Epub 2017 Jan 11. J Clin Lipidol. 2017. PMID: 28391895
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