[HTML][HTML] Hereditary angioedema (HAE) in children and adolescents—a consensus on therapeutic strategies
P Späth - European journal of pediatrics, 2012 - Springer
Hereditary angioedema due to C1 inhibitor (C1 esterase inhibitor) deficiency (types I and II
HAE-C1-INH) is a rare disease that usually presents during childhood or adolescence with …
HAE-C1-INH) is a rare disease that usually presents during childhood or adolescence with …
Hereditary angioedema (HAE) in children and adolescents-a consensus on therapeutic strategies.
V Wahn, W Aberer, W Eberl… - European Journal …, 2012 - search.ebscohost.com
Hereditary angioedema due to C1 inhibitor (C1 esterase inhibitor) deficiency (types I and II
HAE-C1-INH) is a rare disease that usually presents during childhood or adolescence with …
HAE-C1-INH) is a rare disease that usually presents during childhood or adolescence with …
[引用][C] Hereditary angioedema (HAE) in children and adolescents—a consensus on therapeutic strategies
V Wahn, W Aberer, W Eberl, M Faßhauer… - European Journal of …, 2012 - cir.nii.ac.jp
Hereditary angioedema (HAE) in children and adolescents—a consensus on therapeutic
strategies | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 検索 …
strategies | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 検索 …
Hereditary angioedema (HAE) in children and adolescents: a consensus on therapeutic strategies
V Wahn, W Aberer, W Eberl… - European …, 2012 - publikationen.ub.uni-frankfurt.de
Hereditary angioedema due to C1 inhibitor (C1 esterase inhibitor) deficiency (types I and II
HAE-C1-INH) is a rare disease that usually presents during childhood or adolescence with …
HAE-C1-INH) is a rare disease that usually presents during childhood or adolescence with …
[PDF][PDF] Hereditary angioedema (HAE) in children and adolescents—a consensus on therapeutic strategies
V Wahn, W Aberer, W Eberl, M Faßhauer, T Kühne… - Eur J Pediatr, 2012 - core.ac.uk
Hereditary angioedema due to C1 inhibitor (C1 esterase inhibitor) deficiency (types I and II
HAE-C1-INH) is a rare disease that usually presents during childhood or adolescence with …
HAE-C1-INH) is a rare disease that usually presents during childhood or adolescence with …
[引用][C] Hereditary angioedema (HAE) in children and adolescents: a consensus on therapeutic strategies
V WAHN, W ABERER… - European journal of …, 2012 - pascal-francis.inist.fr
Hereditary angioedema (HAE) in children and adolescents: a consensus on therapeutic
strategies CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases …
strategies CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases …
Hereditary angioedema (HAE) in children and adolescents--a consensus on therapeutic strategies
V Wahn, W Aberer, W Eberl, M Faßhauer… - European journal of …, 2012 - boris.unibe.ch
Hereditary angioedema due to C1 inhibitor (C1 esterase inhibitor) deficiency (types I and II
HAE-C1-INH) is a rare disease that usually presents during childhood or adolescence with …
HAE-C1-INH) is a rare disease that usually presents during childhood or adolescence with …
[PDF][PDF] Hereditary angioedema (HAE) in children and adolescents—a consensus on therapeutic strategies
V Wahn, W Aberer, W Eberl, M Faßhauer, T Kühne… - Eur J Pediatr, 2012 - Citeseer
Hereditary angioedema due to C1 inhibitor (C1 esterase inhibitor) deficiency (types I and II
HAE-C1-INH) is a rare disease that usually presents during childhood or adolescence with …
HAE-C1-INH) is a rare disease that usually presents during childhood or adolescence with …
[引用][C] Hereditary angioedema (HAE) in children and adolescents—a consensus on therapeutic strategies
V Wahn, W Aberer, W Eberl, M Faßhauer… - European Journal of …, 2012 - folia.unifr.ch
Hereditary angioedema (HAE) in children and adolescents—a consensus on therapeutic strategies
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[PDF][PDF] Hereditary angioedema (HAE) in children and adolescents—a consensus on therapeutic strategies
V Wahn, W Aberer, W Eberl, M Faßhauer, T Kühne… - Eur J Pediatr, 2012 - researchgate.net
Hereditary angioedema due to C1 inhibitor (C1 esterase inhibitor) deficiency (types I and II
HAE-C1-INH) is a rare disease that usually presents during childhood or adolescence with …
HAE-C1-INH) is a rare disease that usually presents during childhood or adolescence with …