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Article

[Sporadic infantile myofibromatosis: Mutations with PDGFRB gain-of-function].

Annales de dermatologie et de venereologie - 1 Jan 2000

Dereure O

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 28756885
DOI: 10.1016/j.annder.2017.05.010

Genes

PDGFRB

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Sporadic infantile myofibromatosis: Mutations with PDGFRB gain-of-function].PMID 28756885Read ↗

Heterozygous PDGFRB Mutation in a Three-generation Family with Autosomal Dominant Infantile Myofibromatosis.Semantic proximity Read ↗

PDGFRB gain-of-function mutations in sporadic infantile myofibromatosis.Semantic proximity Read ↗

Association of PDGFRB Mutations With Pediatric Myofibroma and MyofibromatosisSemantic proximity Read ↗

Modulation of expressivity in PDGFRB-related infantile myofibromatosis: a role for PTPRG?Semantic proximity Read ↗

Genetic testing and surveillance in infantile myofibromatosis: a report from the SIOPE Host Genome Working GroupSemantic proximity Read ↗

Late Relapse in Genetically Determined Infantile Myofibromatosis. A Case Report and Brief Focus on Recurrences.Semantic proximity Read ↗

Case report: rapid and durable response to PDGFR targeted therapy in a child with refractory multiple infantile myofibromatosis and a heterozygous germline mutation of the PDGFRB geneSemantic proximity Read ↗

PDGFRB mutants found in patients with familial infantile myofibromatosis or overgrowth syndrome are oncogenic and sensitive to imatinib.Semantic proximity Read ↗

Recurrent Somatic PDGFRB Mutations in Sporadic Infantile/Solitary Adult Myofibromas But Not in Angioleiomyomas and MyopericytomasSemantic proximity Read ↗

Activating variants in PDGFRB result in a spectrum of disorders responsive to imatinib monotherapySemantic proximity Read ↗

Expansion of the phenotype of Kosaki overgrowth syndrome.Semantic proximity Read ↗

Infantile myofibromatosis: report on a family with autosomal dominant inheritance and variable penetrance.Semantic proximity Read ↗

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