Results 1 to 10 of about 12,349 (241)

Fulminant systemic capillary leak syndrome due to C1 inhibitor deficiency complicating acute dermatomyositis: a case report [PDF]

, 2014
INTRODUCTION: Dermatomyositis is a chronic inflammatory disorder characterized by muscular and dermatologic symptoms with variable internal organ involvement.
Andreas Brunauer, Daniel Neureiter, Hermann Salmhofer, Ilse Gradwohl-Matis, Martin W Dünser, Romana Illig   +5 more
core   +1 more source

Novel SERPING1 Genetic Variant in Two Family Members with Hereditary Angioedema

Acta Médica Portuguesa
Hereditary angioedema is a rare, autosomal dominant, genetic disorder characterized by recurrent episodes of angioedema. Over 800 SERPING1 gene variants have been reported, and their clinical profiles and causal genetic variants are highly heterogeneous.
Sofia Cosme Ferreira, Alexandra Rosa, Filipa Sousa, Alejandro Mendoza-Alvarez, Rafaela González-Montelongo, Ariel Callero, Carlos Flores, Rita Câmara   +7 more
doaj   +1 more source

Urticaria and angioedema

Allergy, Asthma & Clinical Immunology, 2018
Urticaria (hives) is a common disorder that often presents with angioedema (swelling that occurs beneath the skin). It is generally classified as acute or chronic.
Amin Kanani, Stephen D. Betschel, Richard Warrington   +2 more
doaj   +1 more source

Characteristics of Patients with Hereditary Angioedema Who Reduced Lanadelumab Treatment Administration Frequency: A Retrospective Observational Study of US Claims Data

Drugs - Real World Outcomes
Background Lanadelumab is the only long-term prophylaxis indicated for reduced administration frequency in patients with hereditary angioedema who have been well controlled for > 6 months.
Nicole Princic, Kristin A. Evans, Chintal H. Shah, Krystal Sing, Salomé Juethner, Bob G. Schultz   +5 more
doaj   +1 more source

Recurrent angioedema – a case report [PDF]

, 2014
Introduction: Hereditary angioedema (HA) is a rare cause of recurrent angioedema caused by a default in the gene that encodes the C1 esterase inhibitor (C1-INH). The oedema involves predominantly the face, limbs and genital and gastrointestinal tract.
Araújo, Rita, Martinho, Isabel, Martins, Sandrina, Pinto, Diana, Raposo, Filipa, Salgado, Miguel   +5 more
core  

International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1-Inhibitor deficiency [PDF]

, 2016
BACKGROUND: The consensus documents published to date on hereditary angioedema with C1-inhibitor deficiency (C1-INH-HAE) have focused on adult patients. Many of the previous recommendations have not been adapted to pediatric patients.
Agostoni, Agostoni, Agostoni, Altorjai, Andrew, Assadi, Aygoren-Pursun, Aygoren-Pursun, Bautista-Llacer, Bennett, Berkun, Betschel, Bork, Bork, Bork, Bork, Bork, Bouillet, Bouillet, Bouillet, Bowen, Bowen, Bowen, Bygum, Caballero, Caballero, Caballero, Caballero, Castelli, Chagas, Church, Cicardi, Cicardi, Cicardi, Cicardi, Cicardi, Craig, Craig, Craig, Craig, Craig, Csuka, Cugno, Czaller, Dinkel, Doherty, Ebo, El-Hachem, Fabiani, Farkas, Farkas, Farkas, Farkas, Farkas, Farkas, Farkas, Farkas, Farkas, Foix-L'Helias, Fouche, Gomez-Traseira, Gompels, Grumach, Grumach, Hogasen, Hubiche, Janardhanan, Kalmar, Kaplan, Kelemen, Kim, Kreuz, Kruger, Levy, Li, Lindecken, Longhurst, Lumry, MacGinnitie, Magerl, Martinez-Saguer, Martinez-Saguer, Martinez-Saguer, Martinez-Saguer, McCollough, Nanda, Nielsen, Nurnberger, O'Bier, Ohsawa, Pappalardo, Pappalardo, Pedrosa, Petraroli, Prior, Pritzker, Quintana, Rasmussen, Ren, Riedl, Riedl, Roach, Roche, Sanchez, Sanhueza, Shah, Speletas, Strawczynski, Tuong, Veszeli, Visy, Wahn, Wang, Wasserman, Wilson, Zanichelli, Zanichelli, Zilberberg, Zotter, Zotter, Zuraw, Zuraw, Zuraw   +122 more
core   +3 more sources

The diagnosis of hereditary angioedema: family caregivers’ experiences [PDF]

, 2018
The aim of this study was to understand the experiences of family caregivers in the process of diagnosing hereditary angioedema. An interpretive and qualitative research methodology based on Gadamer’s philosophical hermeneutics was carried out.
Cayetano Fernández-Sola, Francisco Sánchez-Hernández, Gadamer H. G., Green J., José Granero-Molina, José Manuel Hernández-Padilla, Laura Helena Antequera-Raynal, María del Mar Jiménez-Lasserrotte   +7 more
core   +1 more source

Value co-creation in healthcare: evidence from innovative therapeutic alternatives for hereditary angioedema [PDF]

, 2018
Background Our research focuses on the co-creation of value in healthcare with reference to a case of hereditary angioedema with C1 inhibitor deficiency (C1-INH-HAE). Our work is mainly based on the concept of value co-creation in healthcare.
Barbarino, Alessandro, Bova, Maria, Di Paola, Nadia, Spanò, Rosanna   +3 more
core   +1 more source

Hereditary angioedema: how to approach it at the emergency department?

Einstein (São Paulo)
Angioedema attacks are common causes of emergency care, and due to the potential for severity, it is important that professionals who work in these services know their causes and management.
Faradiba Sarquis Serpa, Eli Mansour, Marcelo Vivolo Aun, Pedro Giavina-Bianchi, Herberto José Chong Neto, Luisa Karla Arruda, Regis Albuquerque Campos, Antônio Abílio Motta, Eliana Toledo, Anete Sevciovic Grumach, Solange Oliveira Rodrigues Valle   +10 more
doaj   +2 more sources

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

, 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., Malbran, Eloisa, Malbrán, Alejandro, Menéndez, Alejandra   +3 more
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