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

A new ADAMTS13 missense mutation (D1362V) in thrombotic thrombocytopenic purpura diagnosed during pregnancy.

Thrombosis and haemostasis - 1 Aug 2012

Calderazzo Julio C, Kempfer Ana, Powazniak Yanina, López Ileana R, Sánchez-Luceros Analía, Woods Adriana I, Lazzari Maria A

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to ADAM Proteins
Share to ADAMTS13 Protein
Share to HEK293 Cells
Share to Introns

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation, Missense

Share to Pregnancy

Share to Pregnancy Complications, Hematologic

Share to Purpura, Thrombotic Thrombocytopenic

Source

Identifiers

PMID: 22627385
DOI: 10.1160/TH11-11-0783

Genes

ADAMTS13

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A new ADAMTS13 missense mutation (D1362V) in thrombotic thrombocytopenic purpura diagnosed during pregnancy.PMID 22627385Read ↗

Congenital thrombotic thrombocytopenic purpura related to a novel mutation in ADAMTS13 gene and management during pregnancy.Semantic proximity Read ↗

Hereditary thrombotic thrombocytopenic purpura mimicking immune thrombocytopenia was revealed by miscarriage-novel compound heterozygous mutations in hTTP.Semantic proximity Read ↗

Congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome) caused by novel ADAMTS13 mutations.Semantic proximity Read ↗

Inherited ADAMTS13 mutations associated with Thrombotic Thrombocytopenic Purpura: a short review and update.Semantic proximity Read ↗

Hereditary thrombotic thrombocytopenic purpura mimicking idiopathic thrombocytopenic purpura was revealed by miscarriage——Novel Compound Heterozygous Mutations in hTTPSemantic proximity Read ↗

A novel mutation in ADAMTS13 of a child with Upshaw-Schulman Syndrome.Semantic proximity Read ↗

ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura.Semantic proximity Read ↗

New missense mutation p.Trp387Ser affecting the functionally important TrpXXTrp motif in the TSR1 repeat of ADAMTS13 metalloproteinase: Case report.Semantic proximity Read ↗

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: key findings at enrollment until 2017Semantic proximity Read ↗

ADAMTS 13 genotype and vWF protease activity in an Italian family with TTP.Semantic proximity Read ↗

Hereditary Thrombotic Thrombocytopenic Purpura in a 9-Month-old: Diagnosing and Managing an Ultra-rare Disorder.Semantic proximity Read ↗

Congenital thrombotic thrombocytopenic purpura caused by new compound heterozygous mutations of the ADAMTS13 gene.Semantic proximity Read ↗

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