Cutaneous small‐vessel vasculitis associated with paediatric ulcerative colitis: A case study and literature review
- 期刊名称Journal of Paediatrics and Child Health
- 作者Romano, Claudio; Valenti, Simona; Pidone, Caterina; Spina, Massimo; Caruso, Rosario A; Gallizzi, Romina; Dipasquale, Valeria
- 印刷ISSN1034-4810
- 电子ISSN1440-1754
- 文件大小266.77KB
- 发表时间2019-03-20
- DOI10.1111/jpc.14440
A Novel RNA Splice Site Mutation in the C1 Inhibitor Gene of a Patient with Type I Hereditary AngioedemaSEKIJIMA, Yoshiki; HASHIMOTO, Takao; KAWACHI, Yasuhiro; KOSHIHARA, Hiroshi; OTSUKA, Fujio; IKEDA, Shu-ichi · Internal Medicine · 2004
A Novel Donor Splice Site Mutation in the C1 Inhibitor Gene of a Patient With Type I Hereditary Angioneurotic EdemaKawachi, Yasuhiro; Hibi, Takenobu; Yamazaki, Soji; Otsuka, Fujio · Journal of Investigative Dermatology · 1998
A novel donor splice site mutation in the C1-inhibitor gene of a patient with type I hereditary angioneurotic edemaKawachi, Yasuhiro; Hibi, Takenobu; Yamazaki, Soji; Otsuka, Fujio · Journal of Dermatological Science · 1998
A Novel Splice Acceptor Site Mutation of Protein S Gene in Affected Individuals with Type I Protein S Deficiency: Allelic Exclusion of the Mutant GeneMutsuko Nakahara; Hiroko Iida; Michiyo Urata; Masako Fujise; Machiko Wakiyama; Sachiko Kinoshita; Hiroko Tsuda; Takashi Okamura; Kenshi Yao; Tsuneyoshi Yao; Naotaka Hamasaki · 2001
Moderated Poster Session - Heart245The involvement of TWEAK and FN14 in murine autoimmune myocarditis246Sympathetic neurons that innervate the heart locally modulate cardiomyocyte trophic and electrophysiological properties247W4R variant of CSRP3 leads to the expression of a novel alternate reading frame protein due to alternative splicing248Glucocorticoid intervention prenatally: effects on fetal heart maturation249Uncoupling of myofilament Ca2+-sensitivity from troponin I phosphorylation by hypertrophic and dilated cardiomyopathy mutations can be reversed by EGCG and related Hsp90 inhibitors250Investigating inherited HCM caused by SCO2 and PRKAG2 mutations using the patients' induced pluripotent stem cell-derived cardiomyocytesFischer, A; Pianca, N; Azzimato, V; Batchen, E J; Messer, A E; Ben Jehuda, R; Mueller, A-M; Bangert, A; Bockstahler, M; Oettl, R; Katus, HA; Kaya, Z; Prando, V; Franzoso, M; Di Bona, A; Campione, M; Sandri, M; Zaglia, T; Mongillo, M; Tabish, AM; Buyandelger, B; Enesa, KN; Hunt, J; Milner, R; Wiseman, JW; Wahlgren, J; Bohlooly, M; Knoell, R; Richardson, R V; Thomson, A J W; Moran, C M; Gray, G A; Chapman, K E; Papadaki, M; Vikhorev, PG; Sheehan, A; Marston, SB; Hallas, T; Haykain, T; Eisen, B; Schick, R; Gherghiceanu, M; Mandel, H; Arad, M; Binah, O · Cardiovascular Research · 2016
Issue InformationJournal of Cellular and Molecular Medicine · 2012
Issue InformationJournal of Cellular and Molecular Medicine · 2012
Issue InformationJournal of Cellular and Molecular Medicine · 2013
Issue InformationJournal of Cellular and Molecular Medicine · 2014
ErratumJournal of Cellular and Molecular Medicine · 2014
Issue InformationJournal of Cellular and Molecular Medicine · 2014
Issue InformationJournal of Cellular and Molecular Medicine · 2014
CorrigendumJournal of Cellular and Molecular Medicine · 2014