Neuroblastoma and cutaneous angiosarcoma in a child with PTEN hamartoma tumor syndrome-Reference-Cited by-同舟云学术

Neuroblastoma and cutaneous angiosarcoma in a child with PTEN hamartoma tumor syndrome

Published:2022-03-12 Issue:10 Volume:69 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Leibowitz Michael S.¹,Zelley Kristin¹,Adams Denise¹²,Brodeur Garrett M.¹²,Fox Elizabeth³,Li Marilyn M.²⁴,Mattei Peter²⁵,Pogoriler Jennifer²⁴,MacFarland Suzanne P.¹²

Affiliation:

1. Division of Oncology, Department of Pediatrics Children's Hospital of Phialdelphia Philadelphia Pennsylvania USA

2. Department of Pediatrics University of Pennsylvania Perelman School of Medicine Philadelphia Pennsylvania USA

3. Department of Oncology St. Jude's Children's Research Hospital Memphis Tennessee USA

4. Department of Pathology and Laboratory Medicine Children's Hospital of Philadelpiha Philadelphia Pennsylvania USA

5. Department of Surgery Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.29656

Reference18 articles.

1. The Tumor Suppressor, PTEN/MMAC1, Dephosphorylates the Lipid Second Messenger, Phosphatidylinositol 3,4,5-Trisphosphate

2. PTEN hamartoma tumor syndrome: An overview

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1. Pediatric Angiosarcoma with Novel Phenotypic and Genotypic Profile in Chinese Children;Fetal and Pediatric Pathology;2024-09-13

2. A Bi-Institutional Study of Gastrointestinal and Hepatic Manifestations in Children With PTEN Hamartoma Tumor Syndrome;Gastro Hep Advances;2024