[HTML][HTML] Overview of SERPING1 variations identified in Hungarian patients with hereditary angioedema
E Szabó, D Csuka, N Andrási, L Varga, H Farkas… - Frontiers in …, 2022 - frontiersin.org
Background Hereditary angioedema (HAE) due to C1-inhibitor (C1-INH) deficiency (C1-INH-
HAE) is a rare autosomal dominant disorder, characterized by recurrent, unpredictable …
HAE) is a rare autosomal dominant disorder, characterized by recurrent, unpredictable …
Overview of SERPING1 Variations Identified in Hungarian Patients With Hereditary Angioedema
E Szabó, D Csuka, N Andrási, L Varga… - C1 Inhibitor …, 2022 - books.google.com
Background: Hereditary angioedema (HAE) due to C1-inhibitor (C1-INH) deficiency (C1-INH-
HAE) is a rare autosomal dominant disorder, characterized by recurrent, unpredictable …
HAE) is a rare autosomal dominant disorder, characterized by recurrent, unpredictable …
Overview of SERPING1 Variations Identified in Hungarian Patients With Hereditary Angioedema
E Szabó, D Csuka, N Andrási, L Varga… - Frontiers in …, 2022 - pubmed.ncbi.nlm.nih.gov
Background Hereditary angioedema (HAE) due to C1-inhibitor (C1-INH) deficiency (C1-INH-
HAE) is a rare autosomal dominant disorder, characterized by recurrent, unpredictable …
HAE) is a rare autosomal dominant disorder, characterized by recurrent, unpredictable …
Overview of SERPING1 Variations Identified in Hungarian Patients With Hereditary Angioedema.
E Szabó, D Csuka, N Andrási, L Varga, H Farkas… - Frontiers in …, 2022 - europepmc.org
Background Hereditary angioedema (HAE) due to C1-inhibitor (C1-INH) deficiency (C1-INH-
HAE) is a rare autosomal dominant disorder, characterized by recurrent, unpredictable …
HAE) is a rare autosomal dominant disorder, characterized by recurrent, unpredictable …
[PDF][PDF] Parlament
Z Szabó - Internetes Jogtudományi Enciklopédia, 2022 - real.mtak.hu
A parlament története, fejlődése minden nemzet sajátos, egyedi történetének része, ezekből
közös fejlődési tendenciák rajzolódnak ki, párhuzamos spontán és kölcsönhatásból adódó …
közös fejlődési tendenciák rajzolódnak ki, párhuzamos spontán és kölcsönhatásból adódó …
[HTML][HTML] Overview of SERPING1 Variations Identified in Hungarian Patients With Hereditary Angioedema
E Szabó, D Csuka, N Andrási, L Varga… - Frontiers in …, 2022 - ncbi.nlm.nih.gov
Background Hereditary angioedema (HAE) due to C1-inhibitor (C1-INH) deficiency (C1-INH-
HAE) is a rare autosomal dominant disorder, characterized by recurrent, unpredictable …
HAE) is a rare autosomal dominant disorder, characterized by recurrent, unpredictable …
Overview of SERPING1 Variations Identified in Hungarian Patients With Hereditary Angioedema.
E Szabó, D Csuka, N Andrási, L Varga, H Farkas… - Frontiers in …, 2022 - europepmc.org
Background Hereditary angioedema (HAE) due to C1-inhibitor (C1-INH) deficiency (C1-INH-
HAE) is a rare autosomal dominant disorder, characterized by recurrent, unpredictable …
HAE) is a rare autosomal dominant disorder, characterized by recurrent, unpredictable …