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2015年1月9日
総説一般「International consensus on hereditary and acquired angioedema.
2015年1月9日
臨床「Clinical and laboratory characteristics that differentiate hereditary angioedema in 72 patients with angioedema.
2015年1月9日
臨床「Perioperative management of tooth extractions for a patient with hereditary angioedema.
2015年1月9日
臨床「Risk of angioedema following invasive or surgical procedures in HAE type I and II--the natural history.
2015年1月9日
臨床「Leukocytosis and high hematocrit levels during abdominal attacks of hereditary angioedema.
2014年2月25日
総説一般「Hereditary Angioedema with Normal C1 Inhibitor.
2014年2月25日
病態解明「Less severe clinical manifestations in patients with hereditary angioedema with missense C1INH gene mutations.
2014年2月25日
病態解明「Antihistamine-resistant Angioedema in Women with Negative Family History: Estrogens and F12 Gene Mutations.
2014年2月25日
病態解明「Hereditary angioedemacaused by the p.Thr309-Lys mutation in the F12 gene: A multifactorial disease.
2014年2月25日
病態解明「Disease-modifying factors in hereditary angioedema: an RNA expression-based screening.
2013年6月7日
総説一般「Hereditary angioedema with normal C1 inhibitor function: consensus of an international expert panel.
2013年3月15日
総説一般「WAO guideline for the management of hereditary angioedema
2013年3月15日
総説一般「TGuideline for Hereditary Angioedema (HAE) 2010 by the Japanese Association for Complement Research - Secondary Publication
2013年3月15日
総説一般「Hereditary angioedema (HAE) in children and adolescents—a consensus on therapeutic strategies
2013年3月15日
臨床「Preprocedural administration of nanofiltered C1 esterase inhibitor to prevent hereditary angioedema attacks.
2013年3月15日
臨床「C1-inhibitor (C1-INH) autoantibodies in hereditary angioedema. Strong correlation with the severity of disease in C1-INH concentrate naïve patients.
2013年3月15日
病態解明「The role of ficolins and MASPs in hereditary angioedema due to C1-inhibitor deficiency
2013年3月15日
病態解明「The autoreactivity of B cells in hereditary angioedema due to C1 inhibitor deficiency
2013年3月15日
病態解明「Treatment with C1-inhibitor concentrate does not induce IgM type anti-C1 inhibitor antibodies in patients with hereditary angioedema
2012年6月13日
総説治療「Target levels of functional C1-inhibitor in hereditary angioedema.
2012年6月13日
臨床「C1 esterase inhibitor concentrate in 1085 Hereditary Angioedema attacks – final results of the I.M.P.A.C.T.2 study.
2012年6月13日
病態解明「Ca(2+) signalling and PKCalpha activate increased endothelial permeability by disassembly of VE-cadherin junctions.
2012年6月13日
総説治療「International consensus and practical guidelines on the gynecologic and obstetric management of female patients with hereditary angioedema caused by C1 inhibitor deficiency.
2012年2月13日
総説治療「Prospective, double-blind, placebo-controlled trials of ecallantide for acute attacks of hereditary angioedema.
2012年2月13日
総説治療「rhC1INH: a new drug for the treatment of attacks in hereditary angioedema caused by C1-inhibitor deficiency.
2012年2月13日
総説治療「New treatment options for acute edema attacks caused by hereditary angioedema.
2012年2月13日
総説治療「Human pasteurized C1-inhibitor concentrate for the treatment of hereditary angioedema due to C1-inhibitor deficiency.
2012年2月13日
臨床「Hereditary Angioedema in Japan: Genetic Analysis of 13 Unrelated Cases.
2012年2月13日
臨床「A Case of Hereditary Angioedema Involving Recurrent Abdominal Attacks.
2012年2月13日
病態解明「Endothelial Cell Function in Patients with Hereditary Angioedema: Elevated Soluble E-selectin Level During Inter-attack Periods.
2012年2月13日
病態解明「Case Report: Obstetrical Complications and Outcome in Two Families with Hereditary Angioedema due toMutation in the F12 Gene.
2012年2月13日
病態解明「Enzymatic pathways in the pathogenesis of hereditary angioedema: the role of C1 inhibitor therapy.
2012年2月13日
その他「A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1-inhibitor.
2011年10月1日
総説治療「Hereditary angioedema: a clinical review for the otolaryngologist
1.
HAE患者では、C1-inhibitorを投与する以前から抗C1-inhibitor IgM抗体が高率に陽性で、IgMの濃度と重症度が一致する。このため抗C1-inhibitor IgM抗体の測定が、HAEの活動性の指標になる可能性があるとしている。
C1-inhibitor (C1-INH) autoantibodies in hereditary angioedema. Strong correlation with the severity of disease in C1-INH concentrate naïve patients.
Varga L, Széplaki G, Visy B, Füst G, Harmat G, Miklós K, Németh J, Cervenak L, Karádi I, Farkas H.
Mol Immunol. 2007 Feb;44(6):1454-60
2.
Successful management with C1-inhibitor concentrate of hereditary angioedema attacks during two successive pregnancies: a case report.
Hermans C.
Arch Gynecol Obstet. 2007 Sep;276(3):271-6.
3.
Hereditary angio-oedema with normal C1 inhibitor in a family with affected women and men.
Bork K, Gül D, Dewald G.
Br J Dermatol. 2006 Mar;154(3):542-5.
4.
Massive mesenteric edema in a patient with type I hereditary angioedema.
Sekijima Y et al.
Mod Rheumatol. 2005;15(5):361-3.
5.
Worsening fluid retention in a patient with hereditary angioedema and end-stage renal disease.
Ohsawa et al.
Intern Med. 2004 Aug;43(8):708-12.
6.
Laryngeal edema and death from asphyxiation after tooth extraction in four patients with hereditary angioedema.
Bork K, Barnstedt SE.
J Am Dent Assoc. 2003 Aug;134(8):1088-94.
7.
Lupus erythematosus associated with C1 inhibitor deficiency.
Koide M et al.
J Dermatol. 2002 Aug;29(8):503-7.
8.
Autoimmune acquired form of angioedema that responded to danazol therapy.
Higa S et al.
Intern Med. 2002 May;41(5):398-402.
9.
Treatment of 193 episodes of laryngeal edema with C1 inhibitor concentrate in patients with hereditary angioedema.
Bork K, Barnstedt SE.
Arch Intern Med. 2001 Mar 12;161(5):714-8.
10.
Hereditary angioneurotic edema and thromboembolic diseases: I: How symptoms of acute attacks change with aging.
Kodama J et al.
Intern Med. 1998 May;37(5):440-3.
11.
Association of Sjögren's syndrome with hereditary angioneurotic edema: report of a case.
Suzuki Y et al.
Clin Immunol Immunopathol. 1997 Jul;84(1):95-7.
12.
Hereditary angioedema caused by a point mutation of exon 7 in the C1 inhibitor gene.
Ishii N et al.
Br J Dermatol. 1996 Apr;134(4):731-3.
13.
A point mutation in exon 7 of the C1-inhibitor gene causing type I hereditary angioedema.
Ono H et al.
Hum Genet. 1996 Oct;98(4):452-3.
14.
C1 inhibitor deficiency simulating systemic lupus erythematosus.
Shiraishi S et al.
Br J Dermatol. 1982 Apr;106(4):455-60.
15.
[Studies of a Japanese family with hereditary angioneurotic edema (HANE) with special reference to mechanisms involved in formation of edema (author's transl)].
Kodama J et al.
Nihon Naika Gakkai Zasshi. 1977 Sep 10;66(9):1277-85.
16.
Treatment of hereditary angioedema with danazol. Reversal of clinical and biochemical abnormalities
Gelfand JA et al.
N Engl J Med. 1976 Dec 23;295(26):1444-8.
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