Results 161 to 170 of about 197,953 (330)

Five novel mutations in the C1 inhibitor gene (C1NH) leading to a premature stop codon in patients with type I hereditary angioedema [PDF]

open access: gold, 2002
Tomáš Freiberger   +5 more
openalex   +1 more source

Reconstructing Dermatology Education: The Backward Design and Curricular Content Expansion

open access: yesThe Clinical Teacher, Volume 22, Issue 5, October 2025.
ABSTRACT Background Despite the high prevalence of skin conditions, access to dermatologists remains limited, leaving patients to rely on primary care doctors, paediatricians or emergency medicine providers for diagnosis and treatment. Additionally, dermatology education in medical school is often insufficient, with limited hours dedicated to the ...
Ellen Overson, Aakanksha Angra
wiley   +1 more source

Hereditary angioedema.Treatment of acute attacks in Argentina [PDF]

open access: yes, 2014
En el mundo, el angioedema hereditario (HAE) afecta a 1 de cada 50 000 personas. Produceepisodios de angioedema cutáneo, abdominal y laríngeos que generan gran incapacidad. Lamortalidad por la enfermedad oscila entre 15 y 50%.
Fernández Romero, Diego S.   +3 more
core  

Normal complement C4 values do not exclude hereditary angioedema [PDF]

open access: bronze, 2004
Mohammed Yousuf Karim   +2 more
openalex   +1 more source

Hereditary and acquired angioedema: Problems and progress: Proceedings of the third C1 esterase inhibitor deficiency workshop and beyond [PDF]

open access: hybrid, 2004
A Agostoni   +9 more
openalex   +1 more source

Management of acute attacks of hereditary angioedema: potential role of icatibant

open access: yesVascular Health and Risk Management, 2010
Hilary J LonghurstDepartment of Immunology, Barts and The London NHS Trust, London, UKAbstract: Icatibant (Firazyr®) is a novel subcutaneous treatment recently licensed in the European Union for acute hereditary angioedema. Hereditary angioedema,
Hilary J Longhurst
doaj  

Personalized biological treatment with lanadelumab in a patient with recurrent attacks of hereditary angioedema

open access: yesAlergologia Polska
Hereditary angioedema (HAE) is an autosomal dominantly inherited disease caused by deficiency of C1 esterase inhibitor protein type 1 (about 85% of patients with HAE-C1-INH) or type 2 oedema (about 15% of patients with HAE-C1-INH) by C1 inhibitor ...
Artur Gęsicki   +6 more
doaj   +1 more source

Erythema marginatum preceding hereditary angioedema

open access: bronze, 1974
John C. Starr, George W. Brasher
openalex   +1 more source

Herpes zoster ophthalmicus with dependent contralateral edema

open access: yes
Journal of Hospital Medicine, Volume 20, Issue 10, Page 1147-1148, October 2025.
Tyler B. Larsen
wiley   +1 more source

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