Hereditary angioedema (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hereditary angioedema" in English language version.

refsWebsite

Global rank English rank

38nih.gov

4^th place

29doi.org

2^nd place

10web.archive.org

1^st place

7semanticscholar.org

11^th place

8^th place

5worldcat.org

5^th place

3nejm.org

2,374^th place

6,027^th place

2wiley.com

222^nd place

297^th place

2europa.eu

68^th place

117^th place

2fda.gov

447^th place

338^th place

1orpha.net

3,537^th place

7,177^th place

1elsevier.com

610^th place

704^th place

1rarediseases.org

5,181^st place

3,260^th place

1books.google.com

3^rd place

1bravecommunity.com

low place

1caep.ca

low place

1harvard.edu

18^th place

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1drugs.com

399^th place

333^rd place

1medscape.com

719^th place

636^th place

1takeda.com

low place

1haei.org

low place

1angioedemanews.com

low place

1congress.gov

730^th place

468^th place

1jerini.com

low place

1reuters.com

49^th place

47^th place

angioedemanews.com

Chapman M (5 May 2022). "HAE Awareness Day 'Stepping Up' With Activity Challenges, Storytelling". Retrieved 23 May 2022.

books.google.com

Levin AV, Enzenauer RW (2017). The Eye in Pediatric Systemic Disease. Springer. p. 71. ISBN 9783319183893. Archived from the original on 10 September 2017.

bravecommunity.com

"Inheritance of Hereditary Angioedema - Patient Information - Shire's Brave Community". Archived from the original on 6 May 2014. Retrieved 5 May 2014.

caep.ca

"Management of angioedema in the ER" (PDF). Archived from the original (PDF) on 3 November 2014. Retrieved 3 November 2014.

congress.gov

Inouye DK (31 January 2012). "S.Res.286 - 112th Congress (2011-2012): A resolution recognizing May 16, 2012, as Hereditary Angioedema Awareness Day and expressing the sense of the Senate that more research and treatments are needed for Hereditary Angioedema". www.congress.gov. Retrieved 23 May 2022.

doi.org

Smith TD, Riedl MA (October 2024). "The future of therapeutic options for hereditary angioedema". Annals of Allergy, Asthma & Immunology. 133 (4): 380–390. doi:10.1016/j.anai.2024.04.029.
Busse PJ, Christiansen SC (2020). "Hereditary Angioedema". N Engl J Med. 382 (12): 1136–1148. doi:10.1056/NEJMra1808012. PMID 32187470. S2CID 214584080.
Nzeako UC, Frigas E, Tremaine WJ (November 2001). "Hereditary angioedema: a broad review for clinicians". Arch Intern Med. 161 (20): 2417–29. doi:10.1001/archinte.161.20.2417. PMID 11700154.
Ferraro MF, Moreno AS, Castelli EC, Donadi EA, Palma MS, Arcuri HA, et al. (October 2011). "A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family". Allergy. 66 (10): 1384–90. doi:10.1111/j.1398-9995.2011.02658.x. PMID 21623829. S2CID 23036731.
Bafunno V, Bova M, Loffredo S, Divella C, Petraroli A, Marone G, et al. (March 2014). "Mutational spectrum of the c1 inhibitor gene in a cohort of Italian patients with hereditary angioedema: description of nine novel mutations". Ann Hum Genet. 78 (2): 73–82. doi:10.1111/ahg.12052. PMID 24456027.
Weiler CR, van Dellen RG (July 2006). "Genetic test indications and interpretations in patients with hereditary angioedema". Mayo Clin Proc. 81 (7): 958–72. doi:10.4065/81.7.958. PMID 16835976.
Donaldson VH, Evans RR (July 1963). "A biochemical abnormality in hereditary angioneurotic edema: Absence of serum inhibitor of C' 1-esterase". Am. J. Med. 35 (1). The American Journal of Medicine: 37–44. doi:10.1016/0002-9343(63)90162-1. PMID 14046003.
Rosen FS, Pensky J, Donaldson V, Charache P (14 May 1965). "Hereditary angioneurotic edema: Two genetic variants". Science. 148 (3672): 957–958. Bibcode:1965Sci...148..957R. doi:10.1126/science.148.3672.957. PMID 14277836. S2CID 32776518.
Carugati A, Pappalardo E, Zingale LC, Cicardi M (August 2001). "C1-inhibitor deficiency and angioedema". Mol. Immunol. 38 (2–3). Molecular Immunology: 161–173. doi:10.1016/s0161-5890(01)00040-2. PMID 11532278.
Ponard D, Gaboriaud C, Charignon D, Ghannam A, Wagenaar-Bos IGA, Roem D, et al. (January 2020). "SERPING1 mutation update: Mutation spectrum and C1 Inhibitor phenotypes". Hum. Mutat. 41 (1). Human Mutation: 38–57. doi:10.1002/humu.23917. PMID 31517426.
Pappalardo E, Cicardi M, Duponchel C, Carugati A, Choquet S, Agostoni A, et al. (December 2000). "Frequent de novo mutations and exon deletions in the C1inhibitor gene of patients with angioedema". J. Allergy Clin. Immunol. 106 (6). The Journal of Allergy and Clinical Immunology: 1147–1154. doi:10.1067/mai.2000.110471. PMID 11112899.
Bork K, Barnstedt SE, Koch P, Traupe H (15 July 2000). "Hereditary angioedema with normal C1-inhibitor activity in women". Lancet. 356 (9225). The Lancet: 213–217. doi:10.1016/S0140-6736(00)02483-1. PMID 10963200. S2CID 30105665.
Banday AZ, Kaur A, Jindal AK, Rawat A, Singh S (March 2020). "An update on the genetics and pathogenesis of hereditary angioedema". Genes Dis. 7 (1). Genes & Diseases: 75–83. doi:10.1016/j.gendis.2019.07.002. PMC 7063419. PMID 32181278.
Jones D, Zafra H, Anderson J (22 April 2023). "Managing Diagnosis, Treatment, and Burden of Disease in Hereditary Angioedema Patients with Normal C1-Esterase Inhibitor". J Asthma Allergy. 16. Journal of Asthma and Allergy: 447–460. doi:10.2147/JAA.S398333. PMC 10132308. PMID 37124440.
Dewald G, Bork K (19 May 2006). "Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor". Biochem. Biophys. Res. Commun. 343 (4). Biochemical-and-Biophysical-Research-Communications: 1286–1289. doi:10.1016/j.bbrc.2006.03.092. PMID 16638441.
Santacroce R, D'Andrea G, Maffione AB, Margaglione M, d'Apolito M (9 May 2021). "The Genetics of Hereditary Angioedema: A Review". J. Clin. Med. 10 (9). Journal of Clinical Medicine: 2023. doi:10.3390/jcm10092023. PMC 8125999. PMID 34065094.
Shamanaev A, Dickeson SK, Ivanov I, Litvak M, Sun MF, Kumar S, et al. (23 May 2023). "Mechanisms involved in hereditary angioedema with normal C1-inhibitor activity". Front. Physiol. 14. Frontiers in Physiology: 1146834. doi:10.3389/fphys.2023.1146834. PMC 10242079. PMID 37288434.
Deroux A, Boccon-Gibod I, Fain O, Pralong P, Ollivier Y, Pagnier A, et al. (September 2016). "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. 185 (3). Clinical & Experimental Immunology: 332–337. doi:10.1111/cei.12820. PMC 4991515. PMID 27271546.
Dewald G (25 March 2018). "A missense mutation in the plasminogen gene, within the plasminogen kringle 3 domain, in hereditary angioedema with normal C1 inhibitor". Biochem Biophys Res Commun. 498 (1). Biochemical-and-Biophysical-Research-Communications: 193–198. doi:10.1016/j.bbrc.2017.12.060. PMID 29548426.
Dickeson SK, Kumar S, Sun MF, Mohammed BM, Phillips DR, Whisstock JC, et al. (5 May 2022). "A mechanism for hereditary angioedema caused by a lysine 311-to-glutamic acid substitution in plasminogen". Blood. 139 (18). Blood: 2816–2829. doi:10.1182/blood.2021012945. PMC 9074402. PMID 35100351.
Dendorfer A, Wolfrum S, Wagemann M, Qadri F, Dominiak P (May 2001). "Pathways of bradykinin degradation in blood and plasma of normotensive and hypertensive rats". Am. J. Physiol. Heart Circ. Physiol. 280 (5): H2182–8. doi:10.1152/ajpheart.2001.280.5.H2182. PMID 11299220. S2CID 5898184.
Kuoppala A, Lindstedt KA, Saarinen J, Kovanen PT, Kokkonen JO (April 2000). "Inactivation of bradykinin by angiotensin-converting enzyme and by carboxypeptidase N in human plasma". Am. J. Physiol. Heart Circ. Physiol. 278 (4): H1069–74. doi:10.1152/ajpheart.2000.278.4.H1069. PMID 10749699. S2CID 10371501.
Xu YY, Buyantseva LV, Agarwal NS, Olivieri K, Zhi YX, Craig TJ (April 2013). "Update on treatment of hereditary angioedema". Clinical & Experimental Allergy. 43 (4): 395–405. doi:10.1111/cea.12080. ISSN 0954-7894. PMID 23517035.
Xu YY, Buyantseva LV, Agarwal NS, Olivieri K, Zhi YX, Craig TJ (April 2013). "Update on treatment of hereditary angioedema". Clinical & Experimental Allergy. 43 (4): 395–405. doi:10.1111/cea.12080. ISSN 0954-7894. PMID 23517035.
Varga L, Farkas H (1 November 2008). "Treatment of type I and II hereditary angioedema with Rhucin, a recombinant human C1 inhibitor". Expert Review of Clinical Immunology. 4 (6): 653–661. doi:10.1586/1744666X.4.6.653. ISSN 1744-666X. PMID 20477114. S2CID 11656834.
Bernstein JA (January 2008). "Hereditary angioedema: a current state-of-the-art review, VIII: current status of emerging therapies". Ann. Allergy Asthma Immunol. 100 (1 Suppl 2): S41–6. doi:10.1016/S1081-1206(10)60585-6. PMID 18220151.
Riedl MA, Farkas H, Aygören-Pürsün E, Psarros F, Soteres DF, Staevska M, et al. (4 July 2024). "Oral Sebetralstat for On-Demand Treatment of Hereditary Angioedema Attacks". New England Journal of Medicine. 391 (1): 32–43. doi:10.1056/NEJMoa2314192. ISSN 0028-4793. PMID 38819658.
Riedl MA, Tachdjian R, Lumry WR, Craig T, Karakaya G, Gelincik A, et al. (31 May 2024). "Efficacy and Safety of Donidalorsen for Hereditary Angioedema". New England Journal of Medicine. 391 (1): 21–31. doi:10.1056/NEJMoa2402478. ISSN 0028-4793. PMID 38819395.
Longhurst HJ, Lindsay K, Petersen RS, Fijen LM, Gurugama P, Maag D, et al. (2024). "CRISPR-Cas9 in Vivo Gene Editing of KLKB1 for Hereditary Angioedema". New England Journal of Medicine. 390 (5): 432–441. doi:10.1056/NEJMoa2309149. PMID 38294975.

drugs.com

"FDA Approves Takhzyro (lanadelumab-flyo) for Hereditary Angioedema". Drugs.com.

elsevier.com

linkinghub.elsevier.com

Smith TD, Riedl MA (October 2024). "The future of therapeutic options for hereditary angioedema". Annals of Allergy, Asthma & Immunology. 133 (4): 380–390. doi:10.1016/j.anai.2024.04.029.

europa.eu

ema.europa.eu

"Ruconest EPAR". European Medicines Agency (EMA). 28 October 2010. Retrieved 24 September 2024.
"Firazyr EPAR". European Medicines Agency (EMA). 17 February 2003. Retrieved 24 September 2024.

fda.gov

"Drug Trials Snapshot: Orladeyo". U.S. Food and Drug Administration. 3 December 2020. Retrieved 25 December 2020. This article incorporates text from this source, which is in the public domain.

accessdata.fda.gov

"Orladeyo: FDA-Approved Drugs". U.S. Food and Drug Administration (FDA). Retrieved 25 December 2020.

haei.org

"HAEi website". Archived from the original on 8 September 2017. Retrieved 10 September 2017.

harvard.edu

ui.adsabs.harvard.edu

Rosen FS, Pensky J, Donaldson V, Charache P (14 May 1965). "Hereditary angioneurotic edema: Two genetic variants". Science. 148 (3672): 957–958. Bibcode:1965Sci...148..957R. doi:10.1126/science.148.3672.957. PMID 14277836. S2CID 32776518.

jerini.com

Jerini AG (15 July 2008). "Jerini Receives European Commission Approval for Firazyr (Icatibant) in the Treatment of HAE - Press release". Archived from the original on 29 September 2018. Retrieved 28 July 2008.

medscape.com

"FDA OKs New Prophylactic Drug for Rare Hereditary Angioedema". Medscape.

nejm.org

Riedl MA, Farkas H, Aygören-Pürsün E, Psarros F, Soteres DF, Staevska M, et al. (4 July 2024). "Oral Sebetralstat for On-Demand Treatment of Hereditary Angioedema Attacks". New England Journal of Medicine. 391 (1): 32–43. doi:10.1056/NEJMoa2314192. ISSN 0028-4793. PMID 38819658.
Riedl MA, Tachdjian R, Lumry WR, Craig T, Karakaya G, Gelincik A, et al. (31 May 2024). "Efficacy and Safety of Donidalorsen for Hereditary Angioedema". New England Journal of Medicine. 391 (1): 21–31. doi:10.1056/NEJMoa2402478. ISSN 0028-4793. PMID 38819395.
Longhurst HJ, Lindsay K, Petersen RS, Fijen LM, Gurugama P, Maag D, et al. (2024). "CRISPR-Cas9 in Vivo Gene Editing of KLKB1 for Hereditary Angioedema". New England Journal of Medicine. 390 (5): 432–441. doi:10.1056/NEJMoa2309149. PMID 38294975.

nih.gov

pubmed.ncbi.nlm.nih.gov

Busse PJ, Christiansen SC (2020). "Hereditary Angioedema". N Engl J Med. 382 (12): 1136–1148. doi:10.1056/NEJMra1808012. PMID 32187470. S2CID 214584080.
Nzeako UC, Frigas E, Tremaine WJ (November 2001). "Hereditary angioedema: a broad review for clinicians". Arch Intern Med. 161 (20): 2417–29. doi:10.1001/archinte.161.20.2417. PMID 11700154.
Ferraro MF, Moreno AS, Castelli EC, Donadi EA, Palma MS, Arcuri HA, et al. (October 2011). "A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family". Allergy. 66 (10): 1384–90. doi:10.1111/j.1398-9995.2011.02658.x. PMID 21623829. S2CID 23036731.
Bafunno V, Bova M, Loffredo S, Divella C, Petraroli A, Marone G, et al. (March 2014). "Mutational spectrum of the c1 inhibitor gene in a cohort of Italian patients with hereditary angioedema: description of nine novel mutations". Ann Hum Genet. 78 (2): 73–82. doi:10.1111/ahg.12052. PMID 24456027.
Weiler CR, van Dellen RG (July 2006). "Genetic test indications and interpretations in patients with hereditary angioedema". Mayo Clin Proc. 81 (7): 958–72. doi:10.4065/81.7.958. PMID 16835976.
Donaldson VH, Evans RR (July 1963). "A biochemical abnormality in hereditary angioneurotic edema: Absence of serum inhibitor of C' 1-esterase". Am. J. Med. 35 (1). The American Journal of Medicine: 37–44. doi:10.1016/0002-9343(63)90162-1. PMID 14046003.
Rosen FS, Pensky J, Donaldson V, Charache P (14 May 1965). "Hereditary angioneurotic edema: Two genetic variants". Science. 148 (3672): 957–958. Bibcode:1965Sci...148..957R. doi:10.1126/science.148.3672.957. PMID 14277836. S2CID 32776518.
Carugati A, Pappalardo E, Zingale LC, Cicardi M (August 2001). "C1-inhibitor deficiency and angioedema". Mol. Immunol. 38 (2–3). Molecular Immunology: 161–173. doi:10.1016/s0161-5890(01)00040-2. PMID 11532278.
Ponard D, Gaboriaud C, Charignon D, Ghannam A, Wagenaar-Bos IGA, Roem D, et al. (January 2020). "SERPING1 mutation update: Mutation spectrum and C1 Inhibitor phenotypes". Hum. Mutat. 41 (1). Human Mutation: 38–57. doi:10.1002/humu.23917. PMID 31517426.
Pappalardo E, Cicardi M, Duponchel C, Carugati A, Choquet S, Agostoni A, et al. (December 2000). "Frequent de novo mutations and exon deletions in the C1inhibitor gene of patients with angioedema". J. Allergy Clin. Immunol. 106 (6). The Journal of Allergy and Clinical Immunology: 1147–1154. doi:10.1067/mai.2000.110471. PMID 11112899.
Bork K, Barnstedt SE, Koch P, Traupe H (15 July 2000). "Hereditary angioedema with normal C1-inhibitor activity in women". Lancet. 356 (9225). The Lancet: 213–217. doi:10.1016/S0140-6736(00)02483-1. PMID 10963200. S2CID 30105665.
Banday AZ, Kaur A, Jindal AK, Rawat A, Singh S (March 2020). "An update on the genetics and pathogenesis of hereditary angioedema". Genes Dis. 7 (1). Genes & Diseases: 75–83. doi:10.1016/j.gendis.2019.07.002. PMC 7063419. PMID 32181278.
Jones D, Zafra H, Anderson J (22 April 2023). "Managing Diagnosis, Treatment, and Burden of Disease in Hereditary Angioedema Patients with Normal C1-Esterase Inhibitor". J Asthma Allergy. 16. Journal of Asthma and Allergy: 447–460. doi:10.2147/JAA.S398333. PMC 10132308. PMID 37124440.
Dewald G, Bork K (19 May 2006). "Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor". Biochem. Biophys. Res. Commun. 343 (4). Biochemical-and-Biophysical-Research-Communications: 1286–1289. doi:10.1016/j.bbrc.2006.03.092. PMID 16638441.
Santacroce R, D'Andrea G, Maffione AB, Margaglione M, d'Apolito M (9 May 2021). "The Genetics of Hereditary Angioedema: A Review". J. Clin. Med. 10 (9). Journal of Clinical Medicine: 2023. doi:10.3390/jcm10092023. PMC 8125999. PMID 34065094.
Shamanaev A, Dickeson SK, Ivanov I, Litvak M, Sun MF, Kumar S, et al. (23 May 2023). "Mechanisms involved in hereditary angioedema with normal C1-inhibitor activity". Front. Physiol. 14. Frontiers in Physiology: 1146834. doi:10.3389/fphys.2023.1146834. PMC 10242079. PMID 37288434.
Deroux A, Boccon-Gibod I, Fain O, Pralong P, Ollivier Y, Pagnier A, et al. (September 2016). "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. 185 (3). Clinical & Experimental Immunology: 332–337. doi:10.1111/cei.12820. PMC 4991515. PMID 27271546.
Dewald G (25 March 2018). "A missense mutation in the plasminogen gene, within the plasminogen kringle 3 domain, in hereditary angioedema with normal C1 inhibitor". Biochem Biophys Res Commun. 498 (1). Biochemical-and-Biophysical-Research-Communications: 193–198. doi:10.1016/j.bbrc.2017.12.060. PMID 29548426.
Dickeson SK, Kumar S, Sun MF, Mohammed BM, Phillips DR, Whisstock JC, et al. (5 May 2022). "A mechanism for hereditary angioedema caused by a lysine 311-to-glutamic acid substitution in plasminogen". Blood. 139 (18). Blood: 2816–2829. doi:10.1182/blood.2021012945. PMC 9074402. PMID 35100351.
Dendorfer A, Wolfrum S, Wagemann M, Qadri F, Dominiak P (May 2001). "Pathways of bradykinin degradation in blood and plasma of normotensive and hypertensive rats". Am. J. Physiol. Heart Circ. Physiol. 280 (5): H2182–8. doi:10.1152/ajpheart.2001.280.5.H2182. PMID 11299220. S2CID 5898184.
Kuoppala A, Lindstedt KA, Saarinen J, Kovanen PT, Kokkonen JO (April 2000). "Inactivation of bradykinin by angiotensin-converting enzyme and by carboxypeptidase N in human plasma". Am. J. Physiol. Heart Circ. Physiol. 278 (4): H1069–74. doi:10.1152/ajpheart.2000.278.4.H1069. PMID 10749699. S2CID 10371501.
Xu YY, Buyantseva LV, Agarwal NS, Olivieri K, Zhi YX, Craig TJ (April 2013). "Update on treatment of hereditary angioedema". Clinical & Experimental Allergy. 43 (4): 395–405. doi:10.1111/cea.12080. ISSN 0954-7894. PMID 23517035.
Xu YY, Buyantseva LV, Agarwal NS, Olivieri K, Zhi YX, Craig TJ (April 2013). "Update on treatment of hereditary angioedema". Clinical & Experimental Allergy. 43 (4): 395–405. doi:10.1111/cea.12080. ISSN 0954-7894. PMID 23517035.
Varga L, Farkas H (1 November 2008). "Treatment of type I and II hereditary angioedema with Rhucin, a recombinant human C1 inhibitor". Expert Review of Clinical Immunology. 4 (6): 653–661. doi:10.1586/1744666X.4.6.653. ISSN 1744-666X. PMID 20477114. S2CID 11656834.
Bernstein JA (January 2008). "Hereditary angioedema: a current state-of-the-art review, VIII: current status of emerging therapies". Ann. Allergy Asthma Immunol. 100 (1 Suppl 2): S41–6. doi:10.1016/S1081-1206(10)60585-6. PMID 18220151.
Riedl MA, Farkas H, Aygören-Pürsün E, Psarros F, Soteres DF, Staevska M, et al. (4 July 2024). "Oral Sebetralstat for On-Demand Treatment of Hereditary Angioedema Attacks". New England Journal of Medicine. 391 (1): 32–43. doi:10.1056/NEJMoa2314192. ISSN 0028-4793. PMID 38819658.
Riedl MA, Tachdjian R, Lumry WR, Craig T, Karakaya G, Gelincik A, et al. (31 May 2024). "Efficacy and Safety of Donidalorsen for Hereditary Angioedema". New England Journal of Medicine. 391 (1): 21–31. doi:10.1056/NEJMoa2402478. ISSN 0028-4793. PMID 38819395.
Longhurst HJ, Lindsay K, Petersen RS, Fijen LM, Gurugama P, Maag D, et al. (2024). "CRISPR-Cas9 in Vivo Gene Editing of KLKB1 for Hereditary Angioedema". New England Journal of Medicine. 390 (5): 432–441. doi:10.1056/NEJMoa2309149. PMID 38294975.

ncbi.nlm.nih.gov

Banday AZ, Kaur A, Jindal AK, Rawat A, Singh S (March 2020). "An update on the genetics and pathogenesis of hereditary angioedema". Genes Dis. 7 (1). Genes & Diseases: 75–83. doi:10.1016/j.gendis.2019.07.002. PMC 7063419. PMID 32181278.
Jones D, Zafra H, Anderson J (22 April 2023). "Managing Diagnosis, Treatment, and Burden of Disease in Hereditary Angioedema Patients with Normal C1-Esterase Inhibitor". J Asthma Allergy. 16. Journal of Asthma and Allergy: 447–460. doi:10.2147/JAA.S398333. PMC 10132308. PMID 37124440.
Santacroce R, D'Andrea G, Maffione AB, Margaglione M, d'Apolito M (9 May 2021). "The Genetics of Hereditary Angioedema: A Review". J. Clin. Med. 10 (9). Journal of Clinical Medicine: 2023. doi:10.3390/jcm10092023. PMC 8125999. PMID 34065094.
Shamanaev A, Dickeson SK, Ivanov I, Litvak M, Sun MF, Kumar S, et al. (23 May 2023). "Mechanisms involved in hereditary angioedema with normal C1-inhibitor activity". Front. Physiol. 14. Frontiers in Physiology: 1146834. doi:10.3389/fphys.2023.1146834. PMC 10242079. PMID 37288434.
Deroux A, Boccon-Gibod I, Fain O, Pralong P, Ollivier Y, Pagnier A, et al. (September 2016). "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. 185 (3). Clinical & Experimental Immunology: 332–337. doi:10.1111/cei.12820. PMC 4991515. PMID 27271546.
Dickeson SK, Kumar S, Sun MF, Mohammed BM, Phillips DR, Whisstock JC, et al. (5 May 2022). "A mechanism for hereditary angioedema caused by a lysine 311-to-glutamic acid substitution in plasminogen". Blood. 139 (18). Blood: 2816–2829. doi:10.1182/blood.2021012945. PMC 9074402. PMID 35100351.

dailymed.nlm.nih.gov

"Firazyr- icatibant acetate injection, solution". DailyMed. 19 January 2024. Retrieved 24 September 2024.
"Cinryze- human c1-esterase inhibitor injection, powder, lyophilized, for solution; Cinryze- human c1-esterase inhibitor kit". DailyMed. 23 February 2023. Retrieved 24 September 2024.

rarediseases.info.nih.gov

"Hereditary angioedema". GARD. 2017. Archived from the original on 4 July 2017. Retrieved 10 July 2017.

ghr.nlm.nih.gov

Reference GH (5 July 2017). "hereditary angioedema". Genetics Home Reference. Archived from the original on 10 July 2017. Retrieved 10 July 2017.

orpha.net

"Orphanet: Hereditary angioedema". www.orpha.net. August 2011. Archived from the original on 9 October 2015. Retrieved 10 July 2017.

rarediseases.org

"Hereditary Angioedema - NORD (National Organization for Rare Disorders)". NORD (National Organization for Rare Disorders). 2008. Archived from the original on 14 July 2017. Retrieved 10 July 2017.

reuters.com

Reuters: UPDATE 1-US clears Lev Pharma drug for rare swelling disease Archived 2009-09-09 at the Wayback Machine

semanticscholar.org

api.semanticscholar.org

Busse PJ, Christiansen SC (2020). "Hereditary Angioedema". N Engl J Med. 382 (12): 1136–1148. doi:10.1056/NEJMra1808012. PMID 32187470. S2CID 214584080.
Ferraro MF, Moreno AS, Castelli EC, Donadi EA, Palma MS, Arcuri HA, et al. (October 2011). "A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family". Allergy. 66 (10): 1384–90. doi:10.1111/j.1398-9995.2011.02658.x. PMID 21623829. S2CID 23036731.
Rosen FS, Pensky J, Donaldson V, Charache P (14 May 1965). "Hereditary angioneurotic edema: Two genetic variants". Science. 148 (3672): 957–958. Bibcode:1965Sci...148..957R. doi:10.1126/science.148.3672.957. PMID 14277836. S2CID 32776518.
Bork K, Barnstedt SE, Koch P, Traupe H (15 July 2000). "Hereditary angioedema with normal C1-inhibitor activity in women". Lancet. 356 (9225). The Lancet: 213–217. doi:10.1016/S0140-6736(00)02483-1. PMID 10963200. S2CID 30105665.
Dendorfer A, Wolfrum S, Wagemann M, Qadri F, Dominiak P (May 2001). "Pathways of bradykinin degradation in blood and plasma of normotensive and hypertensive rats". Am. J. Physiol. Heart Circ. Physiol. 280 (5): H2182–8. doi:10.1152/ajpheart.2001.280.5.H2182. PMID 11299220. S2CID 5898184.
Kuoppala A, Lindstedt KA, Saarinen J, Kovanen PT, Kokkonen JO (April 2000). "Inactivation of bradykinin by angiotensin-converting enzyme and by carboxypeptidase N in human plasma". Am. J. Physiol. Heart Circ. Physiol. 278 (4): H1069–74. doi:10.1152/ajpheart.2000.278.4.H1069. PMID 10749699. S2CID 10371501.
Varga L, Farkas H (1 November 2008). "Treatment of type I and II hereditary angioedema with Rhucin, a recombinant human C1 inhibitor". Expert Review of Clinical Immunology. 4 (6): 653–661. doi:10.1586/1744666X.4.6.653. ISSN 1744-666X. PMID 20477114. S2CID 11656834.

takeda.com

"U.S. FDA Approves Takeda's Takhzyro (lanadelumab-flyo) to Prevent Hereditary Angioedema (HAE) Attacks in Children 2 Years of Age and Older". Takeda (Press release). Retrieved 6 February 2023.

web.archive.org

"Hereditary angioedema". GARD. 2017. Archived from the original on 4 July 2017. Retrieved 10 July 2017.
"Orphanet: Hereditary angioedema". www.orpha.net. August 2011. Archived from the original on 9 October 2015. Retrieved 10 July 2017.
Reference GH (5 July 2017). "hereditary angioedema". Genetics Home Reference. Archived from the original on 10 July 2017. Retrieved 10 July 2017.
"Hereditary Angioedema - NORD (National Organization for Rare Disorders)". NORD (National Organization for Rare Disorders). 2008. Archived from the original on 14 July 2017. Retrieved 10 July 2017.
Levin AV, Enzenauer RW (2017). The Eye in Pediatric Systemic Disease. Springer. p. 71. ISBN 9783319183893. Archived from the original on 10 September 2017.
"Inheritance of Hereditary Angioedema - Patient Information - Shire's Brave Community". Archived from the original on 6 May 2014. Retrieved 5 May 2014.
"Management of angioedema in the ER" (PDF). Archived from the original (PDF) on 3 November 2014. Retrieved 3 November 2014.
"HAEi website". Archived from the original on 8 September 2017. Retrieved 10 September 2017.
Jerini AG (15 July 2008). "Jerini Receives European Commission Approval for Firazyr (Icatibant) in the Treatment of HAE - Press release". Archived from the original on 29 September 2018. Retrieved 28 July 2008.
Reuters: UPDATE 1-US clears Lev Pharma drug for rare swelling disease Archived 2009-09-09 at the Wayback Machine

wiley.com

onlinelibrary.wiley.com

Xu YY, Buyantseva LV, Agarwal NS, Olivieri K, Zhi YX, Craig TJ (April 2013). "Update on treatment of hereditary angioedema". Clinical & Experimental Allergy. 43 (4): 395–405. doi:10.1111/cea.12080. ISSN 0954-7894. PMID 23517035.
Xu YY, Buyantseva LV, Agarwal NS, Olivieri K, Zhi YX, Craig TJ (April 2013). "Update on treatment of hereditary angioedema". Clinical & Experimental Allergy. 43 (4): 395–405. doi:10.1111/cea.12080. ISSN 0954-7894. PMID 23517035.

worldcat.org

search.worldcat.org

Xu YY, Buyantseva LV, Agarwal NS, Olivieri K, Zhi YX, Craig TJ (April 2013). "Update on treatment of hereditary angioedema". Clinical & Experimental Allergy. 43 (4): 395–405. doi:10.1111/cea.12080. ISSN 0954-7894. PMID 23517035.
Xu YY, Buyantseva LV, Agarwal NS, Olivieri K, Zhi YX, Craig TJ (April 2013). "Update on treatment of hereditary angioedema". Clinical & Experimental Allergy. 43 (4): 395–405. doi:10.1111/cea.12080. ISSN 0954-7894. PMID 23517035.
Varga L, Farkas H (1 November 2008). "Treatment of type I and II hereditary angioedema with Rhucin, a recombinant human C1 inhibitor". Expert Review of Clinical Immunology. 4 (6): 653–661. doi:10.1586/1744666X.4.6.653. ISSN 1744-666X. PMID 20477114. S2CID 11656834.
Riedl MA, Farkas H, Aygören-Pürsün E, Psarros F, Soteres DF, Staevska M, et al. (4 July 2024). "Oral Sebetralstat for On-Demand Treatment of Hereditary Angioedema Attacks". New England Journal of Medicine. 391 (1): 32–43. doi:10.1056/NEJMoa2314192. ISSN 0028-4793. PMID 38819658.
Riedl MA, Tachdjian R, Lumry WR, Craig T, Karakaya G, Gelincik A, et al. (31 May 2024). "Efficacy and Safety of Donidalorsen for Hereditary Angioedema". New England Journal of Medicine. 391 (1): 21–31. doi:10.1056/NEJMoa2402478. ISSN 0028-4793. PMID 38819395.