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Page 1
Cutaneous manifestations of HAV, HBV, HCV.
Cozzani E, Herzum A, Burlando M, Parodi A. Cozzani E, et al. Ital J Dermatol Venerol. 2021 Feb;156(1):5-12. doi: 10.23736/S2784-8671.19.06488-5. Epub 2019 Dec 4. Ital J Dermatol Venerol. 2021. PMID: 31804053 Free article. Review.
Cutaneous manifestations are rare in HAV infections: these include urticaria, panniculitis, scarlatiniform eruption, evanescent skin rash, maculopapular prolonged rash, serum sickness-like illness rash, cutaneous vasculitis, cryoglobulinemia. ...In children, HBV infection …
Cutaneous manifestations are rare in HAV infections: these include urticaria, panniculitis, scarlatiniform eruption, evanescent skin …
[Angioedema: differential diagnosis].
Launay D. Launay D. Presse Med. 2015 Jan;44(1):30-6. doi: 10.1016/j.lpm.2014.06.016. Epub 2014 Dec 18. Presse Med. 2015. PMID: 25535161 Review. French.
Angioedema (AO) is a clinical syndrome defined by a local swelling of the deep dermis or subcutaneous/submucosal tissues. AO is of rapid installation, non-pruritic, always circumscribed and transitory without any sequellae. ...
Angioedema (AO) is a clinical syndrome defined by a local swelling of the deep dermis or subcutaneous/submucosal tissues. AO is of rapid ins …
Angioedema due to C1 inhibitor deficiency in 2010.
Cicardi M, Zanichelli A. Cicardi M, et al. Intern Emerg Med. 2010 Dec;5(6):481-6. doi: 10.1007/s11739-010-0408-3. Epub 2010 May 22. Intern Emerg Med. 2010. PMID: 20496014 Review.
Angioedema is a recurrent, non-pitting, non-pruritic, self-limiting swelling due to transient increase of endothelial permeability in the capillaries of the deep cutaneous and mucosal layers. ...
Angioedema is a recurrent, non-pitting, non-pruritic, self-limiting swelling due to transient increase of endothelial permeabi …
Diagnosis and treatment of hereditary angioedema.
Canonica GW, Rossi O. Canonica GW, et al. Panminerva Med. 2012 Sep;54(3):241-53. Panminerva Med. 2012. PMID: 22801442 Review.
Hereditary angioedema (HAE) is a rare autosomal dominant disorder affecting approximately 1 in 50000 persons. It causes frequent attacks of non-pitting, non-pruritic edema without urticaria, usually of the skin of the extremities, gastrointestinal tract, and …
Hereditary angioedema (HAE) is a rare autosomal dominant disorder affecting approximately 1 in 50000 persons. It causes frequent attacks of …
Hereditary angioedema in childhood: an approach to management.
Ebo DG, Verweij MM, De Knop KJ, Hagendorens MM, Bridts CH, De Clerck LS, Stevens WJ. Ebo DG, et al. Paediatr Drugs. 2010 Aug 1;12(4):257-68. doi: 10.2165/11532590-000000000-00000. Paediatr Drugs. 2010. PMID: 20593909 Review.
Hereditary angioedema (HAE) is an inherited disorder characterized by recurrent, circumscribed, non-pitting, non-pruritic, and rather painful subepithelial swelling of sudden onset, which fades during the course of 48-72 hours, but can persist for up to 1 week. ...T …
Hereditary angioedema (HAE) is an inherited disorder characterized by recurrent, circumscribed, non-pitting, non-pruritic, and …
Hereditary angioneurotic edema: review of the literature.
Ebo DG, Stevens WJ. Ebo DG, et al. Acta Clin Belg. 2000 Jan-Feb;55(1):22-9. doi: 10.1080/17843286.2000.11754268. Acta Clin Belg. 2000. PMID: 10783504 Review.
The disease is characterised by recurrent, circumscribed, non-pitting, and non-pruritic subepithelial swellings of sudden onset, which fade during the course of 48-72 hours, but can persist up to 1 week. ...The diagnosis is suggested by family history, the lack of a …
The disease is characterised by recurrent, circumscribed, non-pitting, and non-pruritic subepithelial swellings of sudden onse …
Therapeutic options for patients with angioedema due to C1-inhibitor deficiencies: from pathophysiology to the clinic.
Castelli R, Zanichelli A, Cugno M. Castelli R, et al. Immunopharmacol Immunotoxicol. 2013 Feb;35(1):181-90. doi: 10.3109/08923973.2012.726627. Immunopharmacol Immunotoxicol. 2013. PMID: 23137231 Review.
The clinical features of C1-INH deficiencies are the same in both forms of angioedema, and include subcutaneous non-pruritic swelling, the involvement of the upper respiratory tract, and abdominal pain due to partial obstruction of the gastrointestinal tract; howeve …
The clinical features of C1-INH deficiencies are the same in both forms of angioedema, and include subcutaneous non-pruritic s …
Angioedema due to acquired C1-inhibitor deficiency: a bridging condition between autoimmunity and lymphoproliferation.
Cugno M, Castelli R, Cicardi M. Cugno M, et al. Autoimmun Rev. 2008 Dec;8(2):156-9. doi: 10.1016/j.autrev.2008.05.003. Epub 2008 Jun 12. Autoimmun Rev. 2008. PMID: 19014872 Review.
The clinical features of C1-INH deficiency, which may also be of genetic origin (hereditary angioedema, HAE), include subcutaneous, non-pruritic swelling, involvement of the upper respiratory tract, and abdominal pain due to partial obstruction of the gastrointestin …
The clinical features of C1-INH deficiency, which may also be of genetic origin (hereditary angioedema, HAE), include subcutaneous, non …
The dermatology view of hereditary angio-oedema: practical diagnostic and management considerations.
Maurer M, Parish LC. Maurer M, et al. J Eur Acad Dermatol Venereol. 2013 Feb;27(2):133-41. doi: 10.1111/j.1468-3083.2012.04562.x. Epub 2012 May 8. J Eur Acad Dermatol Venereol. 2013. PMID: 22568407 Review.
Hereditary angio-oedema (HAE) is characterized by recurrent, localized, non-pitting, non-pruritic, non-urticarial oedema. Nearly all patients experience skin swelling as a feature of HAE. ...
Hereditary angio-oedema (HAE) is characterized by recurrent, localized, non-pitting, non-pruritic, non-urticarial oedema. Near …
Diagnosis and management of hereditary angioedema: an emergency medicine perspective.
Moellman JJ, Bernstein JA. Moellman JJ, et al. J Emerg Med. 2012 Aug;43(2):391-400. doi: 10.1016/j.jemermed.2011.06.125. Epub 2012 Jan 27. J Emerg Med. 2012. PMID: 22285754 Review.
The clinical consequence is a pattern of recurring attacks of non-pitting, non-pruritic edema, the urgency of which varies by the affected site. ...
The clinical consequence is a pattern of recurring attacks of non-pitting, non-pruritic edema, the urgency of which varies by …
13 results