Results 71 to 80 of about 43,363 (192)
Diagnóstico incidental tardio de teratoma intrapericárdico – relato de caso
Resumo: Descrevemos um caso de teratoma intrapericárdico, tumor cardíaco primário raro, usualmente encontrado em neonatos e lactentes. O teratoma pode causar insuficiência respiratória, grande acúmulo de líquido pericárdico e compressão cardíaca, levando
Annelisa Moura Garcia +3 more
doaj +1 more source
Co-expression networks in generation of induced pluripotent stem cells. [PDF]
We developed an adenoviral vector, in which Yamanaka's four reprogramming factors (RFs) were controlled by individual CMV promoters in a single cassette (Ad-SOcMK). This permitted coordinated expression of RFs (SOX2, OCT3/4, c-MYC and KLF4) in a cell for
Coppola, Giovanni +6 more
core +2 more sources
ABSTRACT Aim Screening criteria for retinopathy of prematurity (ROP) vary among countries. Early detection of ROP and minimising the burden of screening are important. Methods We analysed data from very preterm infants born in Switzerland between 2006 and 2022.
R. Gerull +31 more
wiley +1 more source
In vitro grown plantlets, tumour and teratoma tissues of horseradish (Armoracia lapathifolia Gilib.) were compared with regard to glucosinolate profiles.
Ivana Radojčić Redovniković +5 more
doaj
Anal canal duplication in an 11-year-old-child [PDF]
Anal canal duplication (ACD) is the least frequent digestive duplication. Symptoms are often absent but tend to increase with age. Recognition is, however, important as almost half of the patients with ACD have concomitant malformations.
De Bruyne, Ruth +8 more
core +3 more sources
Genomic Profiling of Pediatric Solid Tumors With a Dual DNA/RNA Panel: JCCG‐TOP2 Study
In the JCCG‐TOP2 nationwide pediatric cancer genomic profiling study, 204 patients' tumors and peripheral blood from 50 institutions across Japan were successfully analyzed using a dual DNA/RNA panel. A total of 147 (72%) had potentially actionable findings, including diagnostic, prognostic, and therapeutic findings in 111 (54%), 61 (30%), and 64 (31%),
Kayoko Tao +38 more
wiley +1 more source
Malignant ovarian germ cell tumor subtypes exhibit distinct tumor microenvironments. Dysgerminomas harbor abundant nonexhausted T cells, with progenitor exhausted T cells present in 60% of PD‐1–positive cases. However, MHC class I expression is lost across all analyzed subtypes, suggesting that restoring class I expression in dysgerminomas may enhance ...
Miya Nakashima +13 more
wiley +1 more source
Looks can be deceiving: adrenal Teratoma causing diagnostic difficulty [PDF]
Teratomas are unusual tumours that derived from totipotent cells with their origin from more than one or usually all three germ cells. Here authors are presenting a case of primary retroperitoneal tumour that is a rare clinical entity. A 19-year-old male
H, Ather M +3 more
core +4 more sources
Our findings indicate that a pediatric/AYA‐specific targeted panel deployed in a hospital can deliver rapid, clinically actionable molecular insights with high diagnostic and prognostic yield. This complements larger sequencing platforms by offering speed, focused content, and easier interpretation.
Masato Kojima +8 more
wiley +1 more source
Teratoma is a rare type of germ cell neoplasm (GCN) which has an incidence of 0.9/100,000. These tumours occur more frequently in girls than in boys, and they usually are diagnosed before four years of age, with a mean age of 18 months.
Yaying Eileen Xu +2 more
doaj +1 more source

