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Neonatal neuroblastoma.
Fisher JPH, Tweddle DA. Fisher JPH, et al. Semin Fetal Neonatal Med. 2012 Aug;17(4):207-215. doi: 10.1016/j.siny.2012.05.002. Epub 2012 Jun 4. Semin Fetal Neonatal Med. 2012. PMID: 22673527 Review.
Universal mass screening for neuroblastoma is not indicated but targeted screening of infants at risk of hereditary neuroblastoma with germline ALK or PHOX2B mutations is appropriate. ...
Universal mass screening for neuroblastoma is not indicated but targeted screening of infants at risk of hereditary neuroblastoma …
Advances in the understanding of constitutional and somatic genomic alterations in neuroblastoma.
Deyell RJ, Attiyeh EF. Deyell RJ, et al. Cancer Genet. 2011 Mar;204(3):113-21. doi: 10.1016/j.cancergen.2011.03.001. Cancer Genet. 2011. PMID: 21504710 Review.
Neuroblastoma is the most common extracranial solid tumor of childhood and is responsible for 10% of childhood cancer related mortality. The genetic etiology of rare families with hereditary neuroblastoma is now largely understood, with the majority having activatin …
Neuroblastoma is the most common extracranial solid tumor of childhood and is responsible for 10% of childhood cancer related mortality. The …
Familial neuroblastoma - different histological manifestations in a family with three affected individuals.
Zimling ZG, Rechnitzer C, Rasmussen M, Petersen BL. Zimling ZG, et al. APMIS. 2004 Feb;112(2):153-8. doi: 10.1111/j.1600-0463.2004.apm1120211.x. APMIS. 2004. PMID: 15056233
The two daughters both developed malignant abdominal neuroblastomas, at the age of 2 and 8 years, respectively. Both died in spite of intensive therapy. Hereditary neuroblastoma appears to be as heterogeneous as the sporadic form of the disease. ...
The two daughters both developed malignant abdominal neuroblastomas, at the age of 2 and 8 years, respectively. Both died in spite of intens …