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Literature DB >> 6846740

C1 INH concentrate in the therapy of hereditary angioedema.

L Bergamaschini, M Cicardi, A Tucci, M Gardinali, D Frangi, C Valle, A Agostoni.

Abstract

Entities: Disease Gene

Mesh：

Substances：

Year: 1983 PMID： 6846740 DOI： 10.1111/j.1398-9995.1983.tb01590.x

Source DB: PubMed Journal: Allergy ISSN： 0105-4538 Impact factor: 13.146

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8 in total

1. Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyond.

Authors: Angelo Agostoni; Emel Aygören-Pürsün; Karen E Binkley; Alvaro Blanch; Konrad Bork; Laurence Bouillet; Christoph Bucher; Anthony J Castaldo; Marco Cicardi; Alvin E Davis; Caterina De Carolis; Christian Drouet; Christiane Duponchel; Henriette Farkas; Kálmán Fáy; Béla Fekete; Bettina Fischer; Luigi Fontana; George Füst; Roberto Giacomelli; Albrecht Gröner; C Erik Hack; George Harmat; John Jakenfelds; Mathias Juers; Lajos Kalmár; Pál N Kaposi; István Karádi; Arianna Kitzinger; Tímea Kollár; Wolfhart Kreuz; Peter Lakatos; Hilary J Longhurst; Margarita Lopez-Trascasa; Inmaculada Martinez-Saguer; Nicole Monnier; István Nagy; Eva Németh; Erik Waage Nielsen; Jan H Nuijens; Caroline O'grady; Emanuela Pappalardo; Vincenzo Penna; Carlo Perricone; Roberto Perricone; Ursula Rauch; Olga Roche; Eva Rusicke; Peter J Späth; George Szendei; Edit Takács; Attila Tordai; Lennart Truedsson; Lilian Varga; Beáta Visy; Kayla Williams; Andrea Zanichelli; Lorenza Zingale
Journal: J Allergy Clin Immunol Date: 2004-09 Impact factor: 10.793

Review 2. FXII.

Authors: G Fuhrer; M J Gallimore; W Heller; H E Hoffmeister
Journal: Blut Date: 1990-11

Review 3. Current management of hereditary angio-oedema (C'1 esterase inhibitor deficiency).

Authors: A Fay; M Abinun
Journal: J Clin Pathol Date: 2002-04 Impact factor: 3.411

4. Acquired C1 inhibitor (C1-INH) deficiency type II. Replacement therapy with C1-INH and analysis of patients' C1-INH and anti-C1-INH autoantibodies.

Authors: J Alsenz; J D Lambris; K Bork; M Loos
Journal: J Clin Invest Date: 1989-06 Impact factor: 14.808

C1 INH concentrate in the therapy of hereditary angioedema.

1. Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyond.

Review 2. FXII.

Review 3. Current management of hereditary angio-oedema (C'1 esterase inhibitor deficiency).

4. Acquired C1 inhibitor (C1-INH) deficiency type II. Replacement therapy with C1-INH and analysis of patients' C1-INH and anti-C1-INH autoantibodies.

5. Nonsense mutations affect C1 inhibitor messenger RNA levels in patients with type I hereditary angioneurotic edema.

6. Restriction fragment length polymorphism of the C1 inhibitor gene in hereditary angioneurotic edema.

7. Effects of C1-esterase inhibitor in three models of acute pancreatitis.

8. HAE therapies: past present and future.