Results 151 to 160 of about 3,171 (206)
Hereditary angioedema revisited [PDF]
Allergy and Asthma Proceedings, 2018 Joseph A, Bellanti, Russell A, Settipane
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Hereditary angioedema in childhood [PDF]
Clinical and Experimental Pediatrics, 2020 openaire +3 more sources
Hereditary angioedema: An update
Indian Journal of Dermatology, Venereology, and Leprology, 2011 openaire +2 more sources
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Immunology and Allergy Clinics of North America, 2022
Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder that usual results from a decreased level of functional C1-INH and clinically manifests with intermittent attacks of swelling of the subcutaneous tissue or submucosal layers of the respiratory or gastrointestinal tracts.
R Gentry, Wilkerson, Joseph J, Moellman
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Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder that usual results from a decreased level of functional C1-INH and clinically manifests with intermittent attacks of swelling of the subcutaneous tissue or submucosal layers of the respiratory or gastrointestinal tracts.
R Gentry, Wilkerson, Joseph J, Moellman
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Hereditary Angioedema in Pregnancy
Obstetrical & Gynecological Survey, 2021Importance Hereditary angioedema is a rare disease of potentially life-threatening attacks of angioedema that can affect patients of all ages, including women of childbearing age. Pregnancy can affect the course of the disease and the choice of treatment used. It is important for the care providers to recognize this disease and
Irene I, Chair +2 more
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Annals of Emergency Medicine, 1988
Although the condition is rare, patients with hereditary angioedema often present because of abdominal pain or airway compromise. A 27-year-old woman presented to the emergency department in acute abdominal distress. Identification of the disease in this patient allowed for proper management and avoidance of invasive procedures.
G P, Moore, W T, Hurley, S A, Pace
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Although the condition is rare, patients with hereditary angioedema often present because of abdominal pain or airway compromise. A 27-year-old woman presented to the emergency department in acute abdominal distress. Identification of the disease in this patient allowed for proper management and avoidance of invasive procedures.
G P, Moore, W T, Hurley, S A, Pace
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Current Opinion in Pediatrics, 2005
Major advances have been made in understanding the clinical signs and symptoms, the pathophysiology and the treatment of hereditary angioedema. This disease that often begins in childhood is caused by partial absence of the plasma protein C1-inhibitor.
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Major advances have been made in understanding the clinical signs and symptoms, the pathophysiology and the treatment of hereditary angioedema. This disease that often begins in childhood is caused by partial absence of the plasma protein C1-inhibitor.
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Genetics of Hereditary Angioedema Revisited
Clinical Reviews in Allergy and Immunology, 2016 Contemporary genetic research has provided evidences that angioedema represents a diverse family of disorders related to kinin metabolism, with a much greater genetic complexity than was initially considered.
Anastasios E Germenis +2 more
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Hereditary Angioedema and Pregnancy
Obstetric Anesthesia Digest, 2009Background: Hereditary angioedema (HAE) is an autosomal dominant disease caused by a quantitative or functional defect in C1‐esterase inhibitor (C1‐INH). Patients with this deficiency present with episodes of angioedema which can be life‐threatening. Studies examining HAE and pregnancy are scarce with little known about the interrelationship between ...
Niranthari, Chinniah +1 more
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