Results 91 to 100 of about 3,934 (208)
Neuroblastoma and nephroblastoma: a radiological review. [PDF]
, 2015 Neuroblastoma (NBL) is the most common extra-cranial tumour in childhood. It can present as an abdominal mass, but is usually metastatic at diagnosis so the symptomatology can be varied.
Dumba, Maureen +2 more
core +2 more sources
Metastatic ganglioneuroma: A misnomer
Indian Journal of Pathology and Microbiology, 2014 Neuroblastoma, ganglioneuroblastoma and ganglioneuroma atumors arising from the neural crest cells. Ganglioneuroma is considered as the most mature amongst the three and usually has no metastatic potential.
Shatavisha DasGupta +4 more
doaj +1 more source
MANAGEMENT OF ADRENAL INCIDENTALOMA: THE POSITION STATEMENT OF THE CROATIAN REFERRAL CENTER FOR ADRENAL GLAND DISORDERS [PDF]
, 2010 Incidentalomi nadbubrežne žlijezde jesu tumori otkriveni tijekom dijagnostičke evaluacije nekoga drugog kliničkog stanja. Tehnološki napredak radioloških uređaja i njihova sve veća upotreba u svakodnevnoj kliničkoj praksi doveli su do češćeg otkrivanja ...
DARKO KAŠTELAN +15 more
core +2 more sources
Exploring the interdependencies of research funders in the UK [PDF]
, 2014 Investment in medical research is vital to the continuing improvement of the UK's health and wealth. It is through research that we expand our understanding of disease and develop new treatments for patients.
Crane, P +13 more
core +1 more source
Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma [PDF]
, 1996 Background. Neuroblastoma is a childhood tumor derived from cells of the neural crest, with a widely variable outcome. Differences in the behavior and prognosis of the tumor suggest that neuroblastoma can be divided into several biologic subgroups.
Bökkerink, J.P. (Jos) +9 more
core +1 more source
Clinical Case Reports, 2017 Key Clinical Message Survival of stage 4 ganglioneuroblastoma (GNB) patients is poor; no reports exist of patients surviving up to 5 years (1, 2). We report the clinical and therapeutic course of a patient with stage 4 GNB surviving beyond expectations ...
Signe Risum +2 more
doaj +1 more source
DNA copy number alterations in central primitive neuroectodermal tumors and tumors of the pineal region: an international individual patient data meta-analysis [PDF]
, 2018 Little is known about frequency, association with clinical characteristics, and prognostic impact of DNA copy number alterations (CNA) on survival in central primitive neuroectodermal tumors (CNS-PNET) and tumors of the pineal region. Searches of MEDLINE,
Baudis, Michael +12 more
core
Importance of Magnetic Resonance Imaging With Diffusion-weighted Imaging in Guiding Biopsy of Nodular Ganglioneuroblastoma: A Case Report [PDF]
, 2021 BACKGROUND: Nodular ganglioneuroblastoma is a rare peripheral neuroblastic tumor of variable prognosis. Accurate diagnosis, staging, and risk categorization can be particularly challenging in patients with nodular ganglioneuroblastoma due to the inherent
Anderson, J +7 more
core
Undifferentiated Ganglioneuroblastoma in a Sheep
Journal of Comparative Pathology, 2002 Ganglioneuroblastoma, presumably originating from the adrenal medulla, was found in an 18-month-old sheep. Histologically, the tumour was mainly composed of undifferentiated neuroblasts with neuropil and occasional ganglion cells. The morphological and immunohistochemical features with respect to intermediate filament proteins and the neuroendocrine ...
Yener, Zabit, Kıran, Metin Münir
openaire +4 more sources
Acta Neurológica Colombiana, 2015 El síndrome opsoclonus mioclonus (SOM) es una entidad poco frecuente en pediatría que por consenso de expertos se define como aquel que cumple tres de cuatro criterios: opsoclonus, ataxia, mioclonus, alteraciones de la conducta o del sueño y diagnóstico
Diego Andrés Rodríguez Rangel +1 more
doaj +1 more source