Detalhe da pesquisa
1.
Germline predisposition to pediatric Ewing sarcoma is characterized by inherited pathogenic variants in DNA damage repair genes.
Am J Hum Genet
; 109(6): 1026-1037, 2022 06 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35512711
2.
Belzutifan, a Potent HIF2α Inhibitor, in the Pacak-Zhuang Syndrome.
N Engl J Med
; 385(22): 2059-2065, 2021 11 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-34818480
3.
Outcomes in ovarian Sertoli-Leydig cell tumor: A report from the International Pleuropulmonary Blastoma/DICER1 and Ovarian and Testicular Stromal Tumor Registries.
Gynecol Oncol
; 186: 117-125, 2024 Apr 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38657450
4.
Type I and Ir pleuropulmonary blastoma (PPB): A report from the International PPB/DICER1 Registry.
Cancer
; 129(4): 600-613, 2023 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36541021
5.
Loss of heterozygosity does not occur in BRCA1/2 mutant pediatric solid and central nervous system tumors.
Pediatr Blood Cancer
; 70(11): e30643, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37596911
6.
Thyroid Nodules in Children With Familial Adenomatous Polyposis.
Am J Gastroenterol
; 117(7): 1166-1168, 2022 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35333786
7.
DICER1 mutations in primary central nervous system tumors: new insights into histologies, mutations, and prognosis.
J Neurooncol
; 157(3): 499-510, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35384518
8.
68 Ga-DOTATATE PET and functional imaging in pediatric pheochromocytoma and paraganglioma.
Pediatr Blood Cancer
; 69(8): e29740, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35484995
9.
DICER1-associated central nervous system sarcoma in children: comprehensive clinicopathologic and genetic analysis of a newly described rare tumor.
Mod Pathol
; 33(10): 1910-1921, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32291395
10.
Genomic analysis reveals germline and somatic PDGFRB variants with clinical implications in familial infantile myofibromatosis.
Pediatr Blood Cancer
; 70(6): e30262, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36861440
11.
Screening with whole-body magnetic resonance imaging in pediatric subjects with Li-Fraumeni syndrome: A single institution pilot study.
Pediatr Blood Cancer
; 65(2)2018 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-29077256
12.
Socioeconomic status and global variations in the incidence of neuroblastoma: call for support of population-based cancer registries in low-middle-income countries.
Pediatr Blood Cancer
; 64(2): 321-323, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27734570
13.
Synchronous occurrence of acute lymphoblastic leukemia and wilms tumor in two patients: underlying etiology and combined treatment plan.
Pediatr Blood Cancer
; 64(5)2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27862952
14.
Germline TP53 mutations and the changing landscape of Li-Fraumeni syndrome.
Hum Mutat
; 35(6): 654-62, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24706533
15.
Update on cancer predisposition syndromes and surveillance guidelines for childhood brain tumors.
Clin Cancer Res
; 2024 Apr 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38573059
16.
Perspectives of Rare Disease Experts on Newborn Genome Sequencing.
JAMA Netw Open
; 6(5): e2312231, 2023 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37155167
17.
A single-institution pediatric and young adult interventional oncology collaborative: Novel therapeutic options for relapsed/refractory solid tumors.
Cancer Med
; 12(12): 13300-13308, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37264747
18.
Outcomes for Children With Type II and Type III Pleuropulmonary Blastoma Following Chemotherapy: A Report From the International PPB/DICER1 Registry.
J Clin Oncol
; 41(4): 778-789, 2023 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36137255
19.
Rare Tumors: Opportunities and challenges from the Children's Oncology Group perspective.
EJC Paediatr Oncol
; 22023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37829670
20.
Germline pathogenic variants in cancer risk genes among patients with thyroid cancer and suspected predisposition.
Cancer Med
; 11(8): 1745-1752, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35174967