6533b82dfe1ef96bd12915ee
RESEARCH PRODUCT
Genetic features of neuroblastic tumors associated with opsoclonus-myoclonus syndrome opens up the possibility for detection in peripheral blood
Ricardo López-almarazAna P. BerbegallRosa NogueraSamuel Navarrosubject
congenital hereditary and neonatal diseases and abnormalitiesPathologymedicine.medical_specialtyGeneral NeuroscienceBiologymedicine.diseaseNeuroblastic TumorPeripheral bloodnervous system diseases03 medical and health sciences0302 clinical medicineCirculating tumor DNA030220 oncology & carcinogenesisOpsoclonus myoclonus syndromeImmunologymedicineNeurological syndromePharmacology (medical)Neurology (clinical)030217 neurology & neurosurgerydescription
Opsoclonus–myoclonus syndrome (OMS) is a rare paraneoplastic, postinfectious, or parainfectious or idiopathic acute neurological syndrome in children and adults. OMS is characterized by involuntary...
year | journal | country | edition | language |
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2016-03-08 | Expert Review of Neurotherapeutics |