The Mortality from Hereditary Angioedema Worldwide: a Review of the Real-World Data Literature
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[1] T. Machnig,et al. Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence , 2020, Orphanet Journal of Rare Diseases.
[2] A. Rawat,et al. Novel SERPING1 gene mutations and clinical experience of type 1 hereditary angioedema from North India , 2020, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.
[3] Y. Zhi,et al. The natural course of hereditary angioedema in a Chinese cohort , 2020, Orphanet Journal of Rare Diseases.
[4] A. Grumach,et al. Assessment on hereditary angioedema burden of illness in Brazil: A patient perspective. , 2019, Allergy and asthma proceedings.
[5] Gabriella Gábos,et al. Consequences of Misdiagnosed and Mismanaged Hereditary Angioedema Laryngeal Attacks: An Overview of Cases from the Romanian Registry , 2018, Case reports in emergency medicine.
[6] D. Solé,et al. Brazilian Guidelines for Hereditary Angioedema Management - 2017 Update Part 1: Definition, Classification and Diagnosis , 2018, Clinics.
[7] R. Lockey,et al. The international WAO/EAACI guideline for the management of hereditary angioedema—The 2017 revision and update , 2018, Allergy.
[8] J. Peter,et al. Hereditary angio-oedema in the Western Cape Province, South Africa. , 2018, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.
[9] K. Bork. A Decade of Change: Recent Developments in Pharmacotherapy of Hereditary Angioedema (HAE) , 2016, Clinical Reviews in Allergy & Immunology.
[10] P. Arkuszewski,et al. Death due to obstruction of the upper airways caused by edema of the laryngeal mucosa in the course of hereditary angioedema. , 2015, Forensic science international.
[11] Z. Pourpak,et al. Type I and Type II Hereditary Angioedema: Clinical and Laboratory Findings in Iranian Patients. , 2015, Archives of Iranian medicine.
[12] J. Sheikh,et al. Angioedema deaths in the United States, 1979-2010. , 2014, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.
[13] N. Takahashi,et al. Hereditary angioedema as the cause of death from asphyxia: postmortem computed tomography study. , 2014, Allergology international : official journal of the Japanese Society of Allergology.
[14] K. Bork,et al. Fatal laryngeal attacks and mortality in hereditary angioedema due to C1-INH deficiency. , 2012, The Journal of allergy and clinical immunology.
[15] S. Shyur,et al. Type I hereditary angioedema in Taiwan -- clinical, biological features and genetic study. , 2011, Asian Pacific journal of allergy and immunology.
[16] B. Nathanson,et al. Descriptive epidemiology of hereditary angioedema hospitalizations in the United States, 2004-2007. , 2011, Allergy and asthma proceedings.
[17] A. Bygum,et al. Hereditary angio‐oedema in Denmark: a nationwide survey , 2009, The British journal of dermatology.
[18] K. Bork,et al. Hereditary angioedema: new findings concerning symptoms, affected organs, and course. , 2006, The American journal of medicine.
[19] F. Huang,et al. Hereditary angioedema: a family study. , 2005, Asian Pacific journal of allergy and immunology.
[20] A. Tordai,et al. Hereditary and acquired angioedema: Problems and progress: Proceedings of the third C1 esterase inhibitor deficiency workshop and beyond , 2004, Journal of Allergy and Clinical Immunology.
[21] K. Bork,et al. Sudden upper airway obstruction in patients with hereditary angioedema. , 2003, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.
[22] K. Bork,et al. Laryngeal edema and death from asphyxiation after tooth extraction in four patients with hereditary angioedema. , 2003, Journal of the American Dental Association.
[23] K. Bork,et al. Clinical studies of sudden upper airway obstruction in patients with hereditary angioedema due to C1 esterase inhibitor deficiency. , 2003, Archives of internal medicine.
[24] K. Bork,et al. Treatment of 193 episodes of laryngeal edema with C1 inhibitor concentrate in patients with hereditary angioedema. , 2001, Archives of internal medicine.
[25] M. Yılmaz,et al. Hereditary angioedema: case report of a family. , 2000, The Turkish journal of pediatrics.
[26] K. Bork,et al. Asphyxiation by laryngeal edema in patients with hereditary angioedema. , 2000, Mayo Clinic proceedings.
[27] H. Bürgi,et al. Type I hereditary angio‐oedema. Variability of clinical presentation and course within two large kindreds , 1997, Journal of internal medicine.
[28] M. Cicardi,et al. Hereditary and Acquired C1‐Inhibitor Deficiency: Biological and Clinical Characteristics in 235 Patients , 1992, Medicine.
[29] P. Blok,et al. Hereditary Angio-Edema (HAE) , 1984, The Journal of Laryngology & Otology.
[30] M. Cicardi,et al. Hereditary Angioedema: An Appraisal of 104 Cases , 1982, The American journal of the medical sciences.
[31] J. Kodama,et al. [Hereditary angioneurotic edema]. , 1982, Nihon rinsho. Japanese journal of clinical medicine.
[32] K. Ohela. Hereditary angioneurotic oedema in Finland. Clinical, immunological and genealogical studies. , 2009, Acta medica Scandinavica.
[33] A. Johnston,et al. Hereditary angioneurotic oedema. , 1973, The Lancet.
[34] N. S. Landerman. Hereditary angioneurotic edema. I. Case reports and review of the literature. , 1962, The Journal of allergy.
[35] W. Osler. HEREDITARY ANGIO‐NEUROTIC ŒDEMA , 1888 .