Asymptomatic incidental neuroblastoma in a patient with SH2D1A deficiency-Reference-Cited by-同舟云学术

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Asymptomatic incidental neuroblastoma in a patient with SH2D1A deficiency

Published:2021-08-29 Issue:1 Volume:69 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr Blood Cancer

Author:

Ghosh Taumoha¹²³^ORCID,Guerrero‐Pena Angela¹²,Kashyap Madhuri¹²,Saad Ali G.¹⁴,Thorson Chad M.¹⁵,Pillai Asha B.¹²⁶

Affiliation:

1. Holtz Children Hospital University of Miami‐Jackson Health System Miami Florida USA

2. Department of Pediatrics University of Miami Miami Florida USA

3. Sylvester Comprehensive Cancer Center University of Miami Miami Florida USA

4. Department of Pathology University of Miami Miami Florida USA

5. Department of Surgery University of Miami Miami Florida USA

6. Department of Microbiology & Immunology University of Miami Miami Florida USA

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.29314

Reference22 articles.

1. Correlation of mutations of the SH2D1A gene and Epstein–Barr virus infection with clinical phenotype and outcome in X‐linked lymphoproliferative disease;Sumegi J;Blood,2000

2. X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease

3. Molecular and cellular pathogenesis of X-linked lymphoproliferative disease

4. XLP: Clinical Features and Molecular Etiology due to Mutations in SH2D1A Encoding SAP

5. X-linked lymphoproliferative disease (XLP): a model of impaired anti-viral, anti-tumor and humoral immune responses

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