Hereditary angioedema (HAE) is a rare autosomal dominant disease that results from mutations in the C1-esterase inhibitor (C1-INH) gene. HAE is characterized by recurrent episodes of angioedema of the skin (face, extremities, genitalia, trunk), the gastrointestinal tract, and respiratory tract. Symptoms experienced can be debilitating, may impact quality of life, and can be life threatening. Preventing attacks particularly for patients undergoing procedures is critical. Patients with HAE may now treat acute attacks or prevent attacks with medications that have recently become available in the United States; however, these same medications can be used for perioperative management for patients undergoing medical, surgical, and dental procedur...
Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...
Background: Hereditary angioedema (HAE), caused by deficiency in C1-inhibitor (C1-INH), leads to unp...
Hereditary angioedema (HAE) caused by C1-esterase inhibitor deficiency is an autosomal-dominant dise...
Hereditary angioedema (HAE) is a rare autosomal dominant disorder mostly due to the deficiency of C1...
Hereditary angioedema (HAE) is a disease which is associated with random and often unpredictable att...
Hereditary angioedema is a rare autosomal dominant disorder caused by reduced activity of the C1 est...
Hereditary angioedema (HAE) is a rare autosomal dominant disorder caused by reduced activity of the ...
AbstractHereditary angioedema (HAE), with an estimated prevalence of 1:50,000, is a rare but potenti...
Abstract This is an update to the 2014 Canadian Hereditary Angioedema Guideline with a...
Hereditary angioedema (HAE), with an estimated prevalence of 1:50,000, is a rare but potentially fat...
This is an update to the 2014 Canadian Hereditary Angioedema Guideline with an expanded scope to inc...
Hereditary angioedema (HAE) is a rare disease, little known to medical and dental practitioners, but...
Hereditary Angioedema (HAE) is a rare disease characterized by a deficiency or a reduced function of...
Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...
Hereditary angioedema (HAE) is a disease which is associated with random and often unpredictable att...
Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...
Background: Hereditary angioedema (HAE), caused by deficiency in C1-inhibitor (C1-INH), leads to unp...
Hereditary angioedema (HAE) caused by C1-esterase inhibitor deficiency is an autosomal-dominant dise...
Hereditary angioedema (HAE) is a rare autosomal dominant disorder mostly due to the deficiency of C1...
Hereditary angioedema (HAE) is a disease which is associated with random and often unpredictable att...
Hereditary angioedema is a rare autosomal dominant disorder caused by reduced activity of the C1 est...
Hereditary angioedema (HAE) is a rare autosomal dominant disorder caused by reduced activity of the ...
AbstractHereditary angioedema (HAE), with an estimated prevalence of 1:50,000, is a rare but potenti...
Abstract This is an update to the 2014 Canadian Hereditary Angioedema Guideline with a...
Hereditary angioedema (HAE), with an estimated prevalence of 1:50,000, is a rare but potentially fat...
This is an update to the 2014 Canadian Hereditary Angioedema Guideline with an expanded scope to inc...
Hereditary angioedema (HAE) is a rare disease, little known to medical and dental practitioners, but...
Hereditary Angioedema (HAE) is a rare disease characterized by a deficiency or a reduced function of...
Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...
Hereditary angioedema (HAE) is a disease which is associated with random and often unpredictable att...
Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...
Background: Hereditary angioedema (HAE), caused by deficiency in C1-inhibitor (C1-INH), leads to unp...
Hereditary angioedema (HAE) caused by C1-esterase inhibitor deficiency is an autosomal-dominant dise...