Справка
x
Поиск
Закладки
Озвучить книгу
Изменить режим чтения
Изменить размер шрифта
Оглавление
Для озвучивания и цитирования книги перейдите в режим постраничного просмотра.
Наследственный ангиоотёк
Список литературы
Поставить закладку
Maurer M. et al. The international WAO/EAACI guideline for the management of hereditary angioedema-The 2017 revision and update // Allergy. 2018. Vol. 73, № 8. P. 1575–1596.
Caballero T. et al. Consensus statement on the diagnosis, management, and treatment of angioedema mediated by bradykinin. Part II. Treatment, follow-up, and special situations. // J. Investig. Allergol. Clin. Immunol. 2011. Vol. 21, № 6. P. 422–441.
Cicardi M. et al. Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working Group // Allergy. 2014. Vol. 69, № 5. P. 602–616.
Obtułowicz K. Bradykinin-mediated angioedema // Polish Arch. Intern. Med. 2016. Vol. 126, № 1–2. P. 76–85.
Picard C. et al. Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015 // J. Clin. Immunol. 2015. Vol. 35, № 8. P. 696–726.
Germenis A.E., Speletas M. The Genetics of Hereditary Angioedema the Iceberg Slowly Emerges // J. Angioedema. 2016. Vol. 2, № 1. P. 8–17.
Germenis A.E., Speletas M. Genetics of Hereditary Angioedema Revisited // Clin. Rev. Allergy Immunol. Clinical Reviews in Allergy & Immunology, 2016. Vol. 51, № 2. P. 170–182.
Davis A., Lu F., Mejia P. C1 inhibitor, a multi-functional serine protease inhibitor // Thromb. Haemost. 2010. Vol. 104, № 11. P. 886–893.
Bork K. Pasteurized and nanofiltered, plasma-derived C1 esterase inhibitor concentrate for the treatment of hereditary angioedema // Immunotherapy. 2014. Vol. 6, № 5. P. 533–551.
Kaplan A.P., Joseph K. Pathogenesis of Hereditary Angioedema: The Role of the Bradykinin- Forming Cascade // Immunol. Allergy Clin. North Am. Elsevier Inc, 2017. Vol. 37, № 3. P. 513–525.
Caccia S., Suffritti C., Cicardi M. Pathophysiology of Hereditary Angioedema // Pediatr. Allergy. Immunol. Pulmonol. 2014. Vol. 27, № 4. P. 159–163.
Bas M. et al. Nonallergic angioedema: role of bradykinin. // Allergy. 2007. Vol. 62, № 8. P. 842–856.
Levi M., Cohn D.M., Zeerleder S. Hereditary angioedema: Linking complement regulation to the coagulation system // Res. Pract. Thromb. Haemost. 2019. Vol. 3, № 1. P. 38–43.
van Geffen M. et al. Alterations of coagulation and fibrinolysis in patients with angioedema due to C1-inhibitor deficiency // Clin. Exp. Immunol. 2012. Vol. 167, № 3. P. 472–478.
Cicardi M. et al. Novelties in the diagnosis and treatment of angioedema // J. Investig. Allergol. Clin. Immunol. 2016. Vol. 26, № 4. P. 212–221.
Bafunno V. et al. Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema // J. Allergy Clin. Immunol. 2018. Vol. 141, № 3. P. 1009–1017.
Bork K. et al. Hereditary angioedema with a mutation in the plasminogen gene // Allergy. 2018. Vol. 73, № 2. P. 442–450.
Veronez C.L. et al. Genetic Variation of Kallikrein-Kinin System and Related Genes in Patients With Hereditary Angioedema // Front. Med. 2019. Vol. 6, № February. P. 1–6.
Bork K. et al. Guideline: Hereditary angioedema due to C1 inhibitor deficiency: S1 Guideline of the German Society for Angioedema (Deutsche Gesellschaft für Angioödeme, DGA), German Society for Internal Medicine (Deutsche Gesellschaft für Innere Medizin, DGIM), German S // Allergo J. Int. 2019. Vol. 28, № 1. P. 16–29.
Alonso M.L.O. et al. Hereditary angioedema: a prospective study of a Brazilian single‐center cohort // Int. J. Dermatol. 2019. P. ijd.14676.
Deroux A. et al. Hereditary angioedema with normal C1 inhibitor and factor XII mutation: a series of 57 patients from the French National Center of Reference for Angioedema // Clin. Exp. Immunol. 2016. Vol. 185, № 3. P. 332–337.
F12-related hereditary angioedema with normal C1Inh.
Zuraw B.L. Hereditary angioedema with normal C1 inhibitor: Four types and counting // J. Allergy Clin. Immunol. 2018. Vol. 141, № 3. P. 884–885.
Marcelino-Rodriguez I. et al. Bradykinin-Mediated Angioedema: An Update of the Genetic Causes and the Impact of Genomics // Front. Genet. 2019. Vol. 10.
Steiner U.C. et al. Hereditary angioedema due to C1 - inhibitor deficiency in Switzerland: clinical characteristics and therapeutic modalities within a cohort study // Orphanet J. Rare Dis. 2016. Vol. 11, № 1. P. 43.
Bouillet L. et al. Hereditary angioedema with C1 inhibitor deficiency: clinical presentation and quality of life of 193 French patients // Ann. Allergy, Asthma Immunol. American College of Allergy, Asthma & Immunology, 2013. Vol. 111, № 4. P. 290–294.
Bork K. et al. Hereditary angioedema: new findings concerning symptoms, affected organs, and course. // Am. J. Med. 2006. Vol. 119, № 3. P. 267–274.
Bork K., Hardt J., Witzke G. Fatal laryngeal attacks and mortality in hereditary angioedema due to C1-INH deficiency // J. Allergy Clin. Immunol. 2012. Vol. 130, № 3. P. 692–697.
Xu Y.-Y. et al. Upper airway edema in 43 patients with hereditary angioedema // Ann. Allergy, Asthma Immunol. 2014. Vol. 112, № 6. P. 539-544.e1.
Martinez-Saguer I., Farkas H. Erythema Marginatum as an Early Symptom of Hereditary Angioedema: Case Report of 2 Newborns // Pediatrics. 2016. Vol. 137, № 2. P. e20152411– e20152411.
Zotter Z. et al. The influence of trigger factors on hereditary angioedema due to C1-inhibitor deficiency. // Orphanet J. Rare Dis. 2014. Vol. 9, № 44. P. 1–6.
Hahn J. et al. Angioedema // Dtsch. Aerzteblatt Online. 2017. Vol. 114, № 29–30. P. 489–496.
Weldon D. Differential Diagnosis of Angioedema // Immunol. Allergy Clin. North Am. 2006. Vol. 26, № 4. P. 603–613.
Farkas H. Management of upper airway edema caused by hereditary angioedema // Allergy, Asthma Clin. Immunol. 2010. Vol. 6, № 19. P. 1–8.
Misra L., Khurmi N., Trentman T. Angioedema: Classification, management and emerging therapies for the perioperative physician // Indian J. Anaesth. 2016. Vol. 60, № 8. P. 534–541.
Giavina-Bianchi P. et al. Brazilian Guidelines for Hereditary Angioedema Management - 2017 Update Part 1: Definition, Classification and Diagnosis // Clinics. 2018. Vol. 73.
Bowen T. et al. 2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema // Allergy, Asthma Clin. Immunol. 2010. Vol. 6, № 24. P. 1– 13.
Caballero T. et al. Consensus statement on the diagnosis, management, and treatment of angioedema mediated by bradykinin. Part I. Classification, epidemiology, pathophysiology, genetics, clinical symptoms, and diagnosis. // J. Investig. Allergol. Clin. Immunol. 2011. Vol. 21, № 5. P. 333–347.
AGOSTONI A. et al. Hereditary and acquired angioedema: Problems and progress: Proceedings of the third C1 esterase inhibitor deficiency workshop and beyond // J. Allergy Clin. Immunol. 2004. Vol. 114, № 3. P. S51–S131.
Martinez-Saguer I. et al. Pharmacokinetics of plasma-derived C1-esterase inhibitor after subcutaneous versus intravenous administration in subjects with mild or moderate hereditary angioedema: the PASSION study // Transfusion. 2014. Vol. 54, № 6. P. 1552–1561.
Richards S. et al. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology // Genet. Med. 2015. Vol. 17, № 5. P. 405–423.
Farkas H. et al. International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency // Allergy Eur. J. Allergy Clin. Immunol. 2017. Vol. 72, № 2. P. 300–313.
Aabom A. et al. Clinical characteristics and real-life diagnostic approaches in all Danish children with hereditary angioedema // Orphanet J. Rare Dis. 2017. Vol. 12, № 1. P. 55.
Craig T. et al. WAO Guideline for the Management of Hereditary Angioedema // World Allergy Organ. J. 2012. Vol. 5, № 12. P. 182–199.
Tarzi M.D. et al. An evaluation of tests used for the diagnosis and monitoring of C1 inhibitor deficiency: normal serum C4 does not exclude hereditary angio-oedema // Clin. Exp. Immunol. 2007. Vol. 149, № 3. P. 513–516.
Pedrosa M. et al. Complement Study Versus CINH Gene Testing for the Diagnosis of Type I Hereditary Angioedema in Children // J. Clin. Immunol. 2016. Vol. 36, № 1. P. 16–18.
Karim Y. Normal complement C4 values do not exclude hereditary angioedema // J. Clin. Pathol. 2004. Vol. 57, № 2. P. 213–214.
Nielsen E. et al. Activation of the Complement, Coagulation, Fibrinolytic and Kallikrein- Kinin Systems During Attacks of Hereditary Angioedema // Scand. J. Immunol. 1996. Vol. 44, № 2. P. 185–192.
Zanichelli A. et al. Diagnosis, Course, and Management of Angioedema in Patients With Acquired C1-Inhibitor Deficiency // J. Allergy Clin. Immunol. Pract. 2017. Vol. 5, № 5. P. 1307–1313.
Riedl M.A. et al. Safety and Usage of C1-Inhibitor in Hereditary Angioedema: Berinert Registry Data // J. Allergy Clin. Immunol. Pract. Elsevier, 2016. Vol. 4, № 5. P. 963–971.
O’Shaughnessy D.F. et al. Guidelines for the use of fresh-frozen plasma, cryoprecipitate and cryosupernatant // Br. J. Haematol. 2004. Vol. 126, № 1. P. 11–28.
Moreno A.S. et al. Coagulation Factor XII Gene Mutation in Brazilian Families with Hereditary Angioedema with Normal C1 Inhibitor // Int. Arch. Allergy Immunol. 2015. Vol. 166, № 2. P. 114–120.
Firinu D. et al. Characterization of patients with angioedema without wheals: The importance of F12 gene screening // Clin. Immunol. 2015. Vol. 157, № 2. P. 239–248.
Germenis A.E. et al. International Consensus on the Use of Genetics in the Management of Hereditary Angioedema // J. Allergy Clin. Immunol. Pract. 2019.
Aygören-Pürsün E., Bork K. Hereditäres Angioödem // Internist (Berl). 2019. Vol. 60, № 9. P. 987–995.
Bork K. et al. Hereditary angioedema cosegregating with a novel kininogen 1 gene mutation changing the N‐terminal cleavage site of bradykinin // Allergy. 2019. Vol. 74, № 12. P. 2479–2481.
Patel N. et al. Hereditary Angioedema and Gastrointestinal Complications: An Extensive Review of the Literature // Case Reports Immunol. 2015. Vol. 2015. P. 1–8.
Riguzzi C. et al. Gastrointestinal Manifestations of Hereditary Angioedema Diagnosed by Ultrasound in the Emergency Department // West. J. Emerg. Med. 2014. Vol. 15, № 7. P. 816–818.
Farkas H. et al. Ultrasonography in the diagnosis and monitoring of ascites in acute abdominal attacks of hereditary angioneurotic oedema // Eur. J. Gastroenterol. Hepatol. 2001. Vol. 13, № 10. P. 1225–1230.
Dinkel H.-P., Maroske J., Schrod L. Sonographic appearances of the abdominal manifestations of hereditary angioedema // Pediatr. Radiol. 2001. Vol. 31, № 4. P. 296–298.
Borum M.L., Ali M.A. Hereditary angioedema: what the gastroenterologist needs to know // Clin. Exp. Gastroenterol. 2014. Vol. 20, № 7. P. 435–445.
Farkas H. et al. Treatment Effect and Safety of Icatibant in Pediatric Patients with Hereditary Angioedema // J. Allergy Clin. Immunol. Pract. Elsevier Inc, 2017. Vol. 5, № 6. P. 1671–1678.
Farkas H. et al. Safety Of Plasma-derived C1-inhibitor Treatment In Pediatric Patients With Hereditary Angioedema Due To C1-inhibitor Deficiency – A Long-term Survey // J. Allergy Clin. Immunol. 2017. Vol. 139, № 2. P. AB236.
Lumry W.R. et al. Randomized placebo-controlled trial of the bradykinin B2 receptor antagonist icatibant for the treatment of acute attacks of hereditary angioedema: the FAST-3 trial // Ann. Allergy, Asthma Immunol. 2011. Vol. 107, № 6. P. 529-537.e2.
Cicardi M. et al. Icatibant, a new bradykinin-receptor antagonist, in hereditary angioedema. // N. Engl. J. Med. 2010. Vol. 363, № 6. P. 532–541.
Craig T.J. et al. Efficacy of human C1 esterase inhibitor concentrate compared with placebo in acute hereditary angioedema attacks // J. Allergy Clin. Immunol. 2009. Vol. 124, № 4. P. 801–808.
Lumry W.R. et al. Icatibant for Multiple Hereditary Angioedema Attacks across the Controlled and Open-Label Extension Phases of FAST-3 // Int. Arch. Allergy Immunol. 2015. Vol. 168, № 1. P. 44–55.
Craig T.J. et al. Effect of time to treatment on response to C1 esterase inhibitor concentrate for hereditary angioedema attacks // Ann. Allergy, Asthma Immunol. 2013. Vol. 111, № 3. P. 211– 215.
Maurer M. et al. Hereditary Angioedema Attacks Resolve Faster and Are Shorter after Early Icatibant Treatment // PLoS One / ed. Stover C.M. 2013. Vol. 8, № 2. P. e53773.
Hernández Fernandez de Rojas D. et al. Treatment of HAE Attacks in the Icatibant Outcome Survey: An Analysis of Icatibant Self-Administration versus Administration by Health Care Professionals // Int. Arch. Allergy Immunol. 2015. Vol. 167, № 1. P. 21–28.
Kawalec P. et al. Administration of conestat alfa, human C1 esterase inhibitor and icatibant in the treatment of acute angioedema attacks in adults with hereditary angioedema due to C1 esterase inhibitor deficiency. Treatment comparison based on systematic review results // Pneumonol. Alergol. Pol. 2013. Vol. 81, № 2. P. 95–104.
Farkas H., Kőhalmi K.V. Icatibant for the treatment of hereditary angioedema with C1- inhibitor deficiency in adolescents and in children aged over 2 years // Expert Rev. Clin. Immunol. 2018. Vol. 14, № 6. P. 447–460.
Busse P. et al. Safety of C1-inhibitor concentrate use for hereditary angioedema in pediatric patients // J. Allergy Clin. Immunol. Pract. American Academy of Allergy, Asthma & Immunology, 2017. Vol. 5, № 4. P. 1142–1145.
Инструкция по медицинскому применению лекарственного препарата фиразир®.
Mühlberg H., Ettl N., Magerl M. An analysis of the teaching of intravenous self- administration in patients with hereditary angio-oedema // Clin. Exp. Dermatol. 2016. Vol. 41, № 4. P. 366–371.
Cicardi M. et al. Review of Recent Guidelines and Consensus Statements on Hereditary Angioedema Therapy with Focus on Self-Administration // Int. Arch. Allergy Immunol. 2013. Vol. 161, № s1. P. 3–9.
Aygören-Pürsün E. et al. On demand treatment and home therapy of hereditary angioedema in Germany - the Frankfurt experience // Allergy, Asthma Clin. Immunol. 2010. Vol. 6, № 21. P. 1–4.
Betschel S. et al. Canadian hereditary angioedema guideline // Allergy, Asthma Clin. Immunol. 2014. Vol. 10, № 50. P. 1–18.
Zuraw B.L. et al. Hereditary angioedema with normal C1 inhibitor function: Consensus of an international expert panel // Allergy Asthma Proc. 2012. Vol. 33, № 6. P. 145–156.
Bork K. et al. Hereditary angioedema caused by missense mutations in the factor XII gene: Clinical features, trigger factors, and therapy // J. Allergy Clin. Immunol. 2009. Vol. 124, № 1. P. 129–134.
Bouillet L. et al. Bradykinin receptor 2 antagonist (icatibant) for hereditary angioedema type III attacks. // Ann. Allergy, Asthma Immunol. 2009. Vol. 103, № 5. P. 448.
Boccon-Gibod I., Bouillet L. Safety and efficacy of icatibant self-administration for acute hereditary angioedema // Clin. Exp. Immunol. 2012. Vol. 168, № 3. P. 303–307.
Piñero-Saavedra M. et al. Hereditary angioedema with F12 mutation // Ann. Allergy, Asthma Immunol. 2016. Vol. 117, № 5. P. 520–526.
Bouillet L. et al. Hereditary angioedema with normal C1 inhibitor in a French cohort: Clinical characteristics and response to treatment with icatibant // Immunity, Inflamm. Dis. 2017. Vol. 5, № 1. P. 29–36.
Ohsawa I. et al. Clinical and laboratory characteristics that differentiate hereditary angioedema in 72 patients with angioedema // Allergol. Int. Elsevier Masson SAS, 2014. Vol. 63, № 4. P. 595–602.
Betschel S. et al. The International/Canadian Hereditary Angioedema Guideline // Allergy, Asthma Clin. Immunol. 2019. Vol. 15, № 1. P. 72.
Bouillet L. et al. Hereditary angioedema with normal C1 inhibitor: clinical characteristics and treatment response with plasma-derived human C1 inhibitor concentrate (Berinert®) in a French cohort // Eur. J. Dermatology. 2017. Vol. 27, № 2. P. 155–159.
Craig T.J. et al. Treatment response after repeated administration of C1 esterase inhibitor for successive acute hereditary angioedema attacks // Allergy Asthma Proc. 2012. Vol. 33, № 4. P. 354– 361.
Pekdemir M. et al. Effective Treatment of Hereditary Angioedema with Fresh Frozen Plasma in an Emergency Department // J. Emerg. Med. 2007. Vol. 33, № 2. P. 137–139.
Prematta M. et al. Fresh frozen plasma for the treatment of hereditary angioedema // Ann. Allergy, Asthma Immunol. 2007. Vol. 98, № 4. P. 383–388.
Pickering R.J. et al. REPLACEMENT THERAPY IN HEREDITARY ANGIOEDEMA // Lancet. 1969. Vol. 293, № 7590. P. 326–330.
Magerl M. et al. Hereditary Angioedema with Normal C1 Inhibitor // Immunol. Allergy Clin. North Am. 2017. Vol. 37, № 3. P. 571–584.
Wilkerson R.G. Angioedema in the emergency department: an evidence-based review. // Emerg. Med. Pract. 2012. Vol. 14, № 11. P. 1–21.
Betschel S. et al. Development of the Hereditary Angioedema Rapid Triage Tool // J. Allergy Clin. Immunol. Pract. 2020. Vol. 8, № 1. P. 310-317.e3.
Zanichelli A. et al. Standard care impact on angioedema because of hereditary C1 inhibitor deficiency: a 21-month prospective study in a cohort of 103 patients // Allergy. 2011. Vol. 66, № 2. P. 192–196.
Bork K. et al. Risk of laryngeal edema and facial swellings after tooth extraction in patients with hereditary angioedema with and without prophylaxis with C1 inhibitor concentrate: a retrospective study // Oral Surgery, Oral Med. Oral Pathol. Oral Radiol. Endodontology. 2011. Vol. 112, № 1. P. 58–64.
Farkas H. et al. Short-term prophylaxis in hereditary angioedema due to deficiency of the C1-inhibitor--a long-term survey. // Allergy. 2012. Vol. 67, № 12. P. 1586–1593.
Aygören-Pürsün E. et al. Risk of angioedema following invasive or surgical procedures in HAE type I and II - the natural history // Allergy. 2013. Vol. 68, № 8. P. 1034–1039.
Jurado-Palomo J. et al. Management of dental-oral procedures in patients with hereditary angioedema due to C1 inhibitor deficiency. // J. Investig. Allergol. Clin. Immunol. 2013. Vol. 23, № 1. P. 1–6.
Magerl M. et al. Short-term prophylactic use of C1-inhibitor concentrate in hereditary angioedema: Findings from an international patient registry // Ann. Allergy, Asthma Immunol. The Authors, 2017. Vol. 118, № 1. P. 110–112.
Farkas H. et al. The efficacy of short-term danazol prophylaxis in hereditary angioedema patients undergoing maxillofacial and dental procedures // J. Oral Maxillofac. Surg. 1999. Vol. 57, № 4. P. 404–408.
Sabharwal G., Craig T. Pediatric hereditary angioedema: an update // F1000Research. 2017. Vol. 6, № 0. P. 1205.
Peled M. et al. Preoperative prophylaxis for C1 esterase-inhibitor deficiency in patients undergoing oral surgery: a report of three cases. // Quintessence Int. 1997. Vol. 28, № 3. P. 169– 171.
Atkinson J.C., Frank M.M. Oral manifestations and dental management of patients with hereditary angioedema. // J. Oral Pathol. Med. 1991. Vol. 20, № 3. P. 139–142.
Bouillet L. et al. Hereditary angioedema with normal C1 inhibitor: Clinical characteristics and treatment response with plasma-derived human C1 inhibitor concentrate (Berinert®) in a french cohort // Eur. J. Dermatology. 2017. Vol. 27, № 2. P. 155–159.
Bork K., Bygum A., Hardt J. Benefits and risks of danazol in hereditary angioedema: a long- term survey of 118 patients // Ann. Allergy, Asthma Immunol. 2008. Vol. 100, № 2. P. 153–161.
Füst G. et al. Long-term efficacy of danazol treatment in hereditary angioedema // Eur. J. Clin. Invest. 2011. Vol. 41, № 3. P. 256–262.
Gelfand J.A. et al. Treatment of Hereditary Angioedema with Danazol // N. Engl. J. Med. 1976. Vol. 295, № 26. P. 1444–1448.
Maurer M., Magerl M. Long-term prophylaxis of hereditary angioedema with androgen derivates: a critical appraisal and potential alternatives. // J. Dtsch. Dermatol. Ges. 2011. Vol. 9, № 2. P. 99–107.
Longhurst H. et al. Prevention of Hereditary Angioedema Attacks with a Subcutaneous C1 Inhibitor // N. Engl. J. Med. 2017. Vol. 376, № 12. P. 1131–1140.
Wintenberger C. et al. Tranexamic acid as maintenance treatment for non-histaminergic angioedema: analysis of efficacy and safety in 37 patients // Clin. Exp. Immunol. 2014. Vol. 178, № 1. P. 112–117.
Maurer M., Magerl M. Hereditary angioedema: an update on available therapeutic options // JDDG J. der Dtsch. Dermatologischen Gesellschaft. 2010. Vol. 8, № 9. P. 663–672.
Bork K., Hardt J. Hereditary Angioedema: Long-Term Treatment with One or More Injections of C1 Inhibitor Concentrate per Week // Int. Arch. Allergy Immunol. 2011. Vol. 154, № 1. P. 81–88.
Craig T. et al. Efficacy and safety of an intravenous C1-inhibitor concentrate for long-term prophylaxis in hereditary angioedema. // Allergy Rhinol. (Providence). 2017. Vol. 8, № 1. P. 13–19.
Fox J. et al. Safety of a C1-inhibitor concentrate in pregnant women with hereditary angioedema // Allergy Asthma Proc. 2017. Vol. 38, № 3. P. 216–221.
Bygum A. et al. Use of a C1 Inhibitor Concentrate in Adults ≥65 Years of Age with Hereditary Angioedema: Findings from the International Berinert® (C1-INH) Registry // Drugs and Aging. Springer International Publishing, 2016. Vol. 33, № 11. P. 819–827.
Saule C. et al. Benefits of progestin contraception in non-allergic angioedema // Clin. Exp. Allergy. 2013. Vol. 43, № 4. P. 475–482.
Bouillet L. et al. Disease expression in women with hereditary angioedema // Am. J. Obstet. Gynecol. 2008. Vol. 199, № 5. P. 484.e1-484.e4.
Ott H.W. et al. Treatment of hereditary angioneurotic oedema (HANE) with tibolone // Clin. Endocrinol. (Oxf). 2007. Vol. 66, № 2. P. 180–184.
Maitrot-Mantelet L. et al. Antigonadotropic progestogens as contraceptive agents in women with contraindication to combined pill // Horm. Mol. Biol. Clin. Investig. 2010. Vol. 3, № 3. P. 441– 447.
Bouillet L. et al. Traitements des angiœdèmes héréditaires: Recommandations du centre de référence national des angiœdèmes (consensus 2014de Bordeaux) // Press. Medicale. 2015. Vol. 44, № 5. P. 526–532.
Longhurst H.J. Hereditary and other orphan angioedemas: A new prophylactic option at last? // Clin. Exp. Allergy. 2013. Vol. 43, № 4. P. 380–382.
Craig T. et al. Long-term prophylaxis therapy in patients with hereditary angioedema with C1 inhibitor deficiency // Ann. Allergy, Asthma Immunol. Elsevier Inc., 2018. Vol. 121, № 6. P. 673– 679.
Латышева Т.В. et al. Долгосрочная профилактика ангиоотёков у пациентов с НАО // Российский аллергологический журнал. 2019. Vol. 16, № 3. P. 75–83.
Bork K. et al. Treatment for hereditary angioedema with normal C1-INH and specific mutations in the F12 gene (HAE-FXII) // Allergy. 2017. Vol. 72, № 2. P. 320–324.
Gower R.G. et al. Hereditary angioedema caused by c1-esterase inhibitor deficiency: a literature-based analysis and clinical commentary on prophylaxis treatment strategies. // World Allergy Organ. J. 2011. Vol. 4, № 2 Suppl. P. S9–S21.
Caballero T. et al. International consensus and practical guidelines on the gynecologic and obstetric management of female patients with hereditary angioedema caused by C1 inhibitor deficiency // J. Allergy Clin. Immunol. 2012. Vol. 129, № 2. P. 308–320.
Bork K., Fischer B., Dewald G. Recurrent episodes of skin angioedema and severe attacks of abdominal pain induced by oral contraceptives or hormone replacement therapy // Am. J. Med. 2003. Vol. 114, № 4. P. 294–298.
Banerji A., Riedl M. Managing the female patient with hereditary angioedema // Women’s Heal. 2016. Vol. 12, № 3. P. 351–361.
González-Quevedo T. et al. Management of Pregnancy and Delivery in Patients With Hereditary Angioedema Due to C1 Inhibitor Deficiency // J. Investig. Allergol. Clin. Immunol. 2016. Vol. 26, № 3. P. 161–167.
Milingos D.S. et al. Hereditary angioedema and pregnancy: successful management of recurrent and frequent attacks of angioedema with C1-inhibitor concentrate, danazol and tranexamic acid - a case report. // Obstet. Med. 2009. Vol. 2, № 3. P. 123–125.
Для продолжения работы требуется
Регистрация
Предыдущая страница
Следующая страница
Оглавление
Список сокращений
Термины и определения
Наследственный ангиоотёк
+
Список литературы
Приложение А1. Состав рабочей группы
Приложение А2. Методология разработки клинических рекомендаций
Приложение А3. Связанные документы
+
Приложение Б. Алгоритмы ведения пациента
+
Приложение В. Информация для пациентов
+
Данный блок поддерживает скрол*