Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Response to DDAVP in children with von Willebrand disease type 2.

Hamostaseologie - 1 May 2009

Schneppenheim Reinhard, Budde U, Beutel Karin, Hassenpflug W-A, Hauch H, Obser T, Oyen F, Schneppenheim S, Schrum J

Abstract excerpt

UNLABELLED: We have prospectively evaluated the biologic response to desmopressin (DDAVP) in 28 children with type 2 von Willebrand disease (VWD) in correlation with the phenotype and the molecular defect of VWF. The diagnosis of VWD type 2 was mainly based on VWF functional parameters and/or an aberrant VWF multimer pattern. Seventeen different mutations were identified (6 of them novel). No response with...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Child
Share to Deamino Arginine Vasopressin
Share to VWF gene

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Hemostatics

Share to Mutation

Share to Phenotype

Share to von Willebrand Diseases

Share to von Willebrand Factor

Source

Identifiers

PMID: 19404524

Genes

VWF

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Response to DDAVP in children with von Willebrand disease type 2.PMID 19404524Read ↗

Biologic response to desmopressin in patients with severe type 1 and type 2 von Willebrand disease: results of a multicenter European study.Semantic proximity Read ↗

Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD): results from the European Study MCMDM-1VWD.Semantic proximity Read ↗

Von Willebrand disease in children: diagnosis and management of a pediatric cohort in one single center in Argentina.Semantic proximity Read ↗

Clinical features and laboratory patterns in a cohort of consecutive Argentinian patients with von Willebrand's disease.Semantic proximity Read ↗

Type 2N von Willebrand disease: genotype drives different bleeding phenotypes and treatment needs.Semantic proximity Read ↗

Biological effect of desmopressin in eight patients with type 2N ('Normandy') von Willebrand disease. Collaborative Group.Semantic proximity Read ↗

How I treat type 2 variant forms of von Willebrand disease.Semantic proximity Read ↗

Factor VIII:C increases after desmopressin in a subgroup of patients with autosomal recessive severe von Willebrand disease.Semantic proximity Read ↗

Management of inherited von Willebrand disease in Italy: results from the retrospective study on 1234 patients.Semantic proximity Read ↗

Diagnosis and management of von Willebrand disease in a single institution of Argentina.Semantic proximity Read ↗

Advances in the genetics and treatment of von Willebrand disease.Semantic proximity Read ↗

Autosomal dominant von Willebrand disease type 2M.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.