Association of PDGFRB Mutations With Pediatric Myofibroma and Myofibromatosis-Reference-Cited by-同舟云学术

Association of PDGFRB Mutations With Pediatric Myofibroma and Myofibromatosis

Published:2019-08-01 Issue:8 Volume:155 Page:946
ISSN:2168-6068
Container-title:JAMA Dermatology
language:en
Short-container-title:JAMA Dermatol

Author:

Dachy Guillaume¹,de Krijger Ronald R.²,Fraitag Sylvie³,Théate Ivan⁴,Brichard Bénédicte⁵,Hoffman Suma B.⁶,Libbrecht Louis⁷,Arts Florence A.¹,Brouillard Pascal⁸,Vikkula Miikka⁸⁹,Limaye Nisha¹⁰,Demoulin Jean-Baptiste¹

Affiliation:

1. Experimental Medicine Unit, de Duve Institute, Université Catholique de Louvain, Brussels, Belgium

2. Department of Pathology, Princess Maxima Centre for Pediatric Oncology and University Medical Centre, Utrecht, Netherlands

3. Department of Pathology, Hôpital Necker-Enfants Malades, Assistance Publique–Hôpitaux de Paris, Paris, France

4. Department of Pathology, Institut de Pathologie et de Génétique, Gosselies, Belgium

5. Department of Pediatric Hematology and Oncology, Cliniques Universitaires Saint-Luc, Université catholique de Louvain, Brussels, Belgium

6. Department of Pediatrics, University of Maryland School of Medicine, Baltimore

7. Department of Pathology, Cliniques Universitaires Saint-Luc, Université catholique de Louvain, Brussels, Belgium

8. Human Molecular Genetics, de Duve Institute, Université Catholique de Louvain, Brussels, Belgium

9. Walloon Excellence in Lifesciences and Biotechnology, Wallonia, Belgium

10. Genetics of Autoimmune Disease and Cancer, de Duve Institute, Université catholique de Louvain, Brussels, Belgium

Publisher

American Medical Association (AMA)

Subject

Dermatology

Link

https://jamanetwork.com/journals/jamadermatology/article-pdf/155/8/946/17752664/jamadermatology_dachy_2019_br_190001.pdf

Reference15 articles.

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2. Solitary, multifocal and generalized myofibromas: clinicopathological and immunohistochemical features of 114 cases.;Oudijk;Histopathology,2012

3. WHO classification of soft tissue tumours: an update based on the 2013 (4th) edition.;Jo;Pathology,2014

4. A recurrent PDGFRB mutation causes familial infantile myofibromatosis.;Cheung;Am J Hum Genet,2013

5. PDGFRB mutants found in patients with familial infantile myofibromatosis or overgrowth syndrome are oncogenic and sensitive to imatinib.;Arts;Oncogene,2016

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