نتایج جستجو برای: روش HAE

تعداد نتایج: 370459  

Asghar Aghamohammadi Hassan Abolhass ani Marzieh Tavakol Masoud Movahedi Payam Mohammadinejad Saba Arshi Shervin Shahinpour

Background: Hereditary angioedema (HAE) is a rare autosomal dominant primary immunodeficiency with complement system defect characterized by recurrent episodes of angioedema involving the skin or mucosa of the upper respiratory and gastrointestinal tracts. Objective: To characterize the clinical and laboratory data of hereditary angioedema in Iran. Methods: Patients with probable diagnosis of a...

2017
Laurence Bouillet Isabelle Boccon‐Gibod David Launay Anne Gompel Gisele Kanny Vincent Fabien Oliver Fain

INTRODUCTION The clinical characteristics and icatibant-treatment outcomes of patients with hereditary angioedema with normal C1 inhibitor (HAE-nC1 INH) are limited. METHODS We retrospectively analyzed data from French HAE patients enrolled in the Icatibant Outcome Survey registry (from July 2009 to September 2013) to compare disease characteristics and the effectiveness and safety of acute i...

2015
Nicola Bonner Linda Abetz-Webb Lydie Renault Teresa Caballero Hilary Longhurst Marcus Maurer Sandra Christiansen Bruce Zuraw

BACKGROUND Hereditary Angioedema (HAE), a rare genetic disease, manifests as intermittent, painful attacks of angioedema. Attacks vary in frequency and severity and include skin, abdominal and life-threatening laryngeal swellings. This study aimed to develop a patient reported outcome (PRO) tool for the assessment of HAE attacks, including their management and impact on patients' lives, for use...

Journal: :iranian journal of immunology 0
shervin shahinpour research center for immunod eficiencies, pediatrics ce nter of excel lence, children's medical c enter, tehran university of medical sciences, tehran marzieh tavakol department of allergy and clinical immunology, shahid bahonar hospital, alborz u niversity of medical sciences, karaj, iran hassan abolhass ani research center for immunod eficiencies, pediatrics ce nter of excel lence, children's medical c enter, tehran university of medical sciences, tehran payam mohammadinejad research center for immunod eficiencies, pediatrics ce nter of excel lence, children's medical c enter, tehran university of medical sciences, tehran masoud movahedi research center for immunod eficiencies, pediatrics ce nter of excel lence, children's medical c enter, tehran university of medical sciences, tehran saba arshi allergy and clinical immunology department of rasole-akram hospital, iran university of medical sciences, tehran, iran asghar aghamohammadi

background: hereditary angioedema (hae) is a rare autosomal dominant primary immunodeficiency with complement system defect characterized by recurrent episodes of angioedema involving the skin or mucosa of the upper respiratory and gastrointestinal tracts. objective: to characterize the clinical and laboratory data of hereditary angioedema in iran. methods: patients with probable diagnosis of a...

Journal: :The journal of allergy and clinical immunology. In practice 2017
Iris M Otani Sandra C Christiansen Paula Busse Carlos A Camargo Bruce L Zuraw Marc A Riedl Aleena Banerji

BACKGROUND Emergency department (ED) management of hereditary angioedema (HAE) has been hindered by misdiagnosis and limited treatment options. Food and Drug Administration approval of 4 on-demand HAE therapies starting in 2009 and the publication of ED guidelines for angioedema management in 2014 should facilitate improvement of HAE management in the ED. OBJECTIVE The objective of this study...

2014
Stephen Betschel

Hereditary angioedema (HAE) is a condition that results in recurrent and often unpredictable attacks of angioedema, which is associated with significant morbidity and can be fatal. The majority of literature related to management of HAE has focused on the adult patient. There is limited information on treatment and management strategies for the pediatric HAE population. Comprehensive care has b...

2010
Bruce L Zuraw

1 H ereditary angioedema (HAE) is a relatively rare disease, with an estimated prevalence of approximately 1 per 50,000 in the general population. Despite its rarity, HAE has become an area of intense interest within the medical community. This interest likely reflects several different aspects of HAE, including: the high potential for significant morbidity and mortality associated with attacks...

Traditionally, Lactuca sativa (lettuce) has been recommended for its hypnotic property.The present study was planned to investigate sleep-prolonging effect of this plant. The hydroalcoholicextract (HAE) of lettuce and its water fraction (WF), ethyl acetate fraction (EAF),and n-butanol fraction (NBF) were administrated (IP) to mice 30 min before the pentobarbitalinjection. Moreover, both in-vivo...

Journal: :Allergy 2018
M Maurer M Magerl I Ansotegui E Aygören-Pürsün S Betschel K Bork T Bowen H Balle Boysen H Farkas A S Grumach M Hide C Katelaris R Lockey H Longhurst W R Lumry I Martinez-Saguer D Moldovan A Nast R Pawankar P Potter M Riedl B Ritchie L Rosenwasser M Sánchez-Borges Y Zhi B Zuraw T Craig

Hereditary Angioedema (HAE) is a rare and disabling disease. Early diagnosis and appropriate therapy are essential. This update and revision of the global guideline for HAE provides up-to-date consensus recommendations for the management of HAE. In the development of this update and revision of the guideline, an international expert panel reviewed the existing evidence and developed 20 recommen...

Journal: :Journal of the Formosan Medical Association = Taiwan yi zhi 2015
Chia-Ti Wang Hung-Jung Lin Bor-Chih Cheng Mao-Tsun Lin Ching-Ping Chang

BACKGROUND/PURPOSE The primary goal of this study was to test whether high-altitude exposure (HAE: 0.9% O(2) at 0.47 ATA for 24 hours) was capable of increasing the systemic inflammatory markers as well as the toxic organ injury indicators in rats, with a secondary goal to test whether preinduction of heat shock protein (HSP) 70 by hypobaric hypoxia preconditioning (HHP: 18.3% O(2) at 0.66 ATA ...

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