Ganglioglioma
What's New
Last Posted: Dec 16, 2023
- A new subtype of diffuse midline glioma, H3 K27 and BRAF/FGFR1 co-altered: a clinico-radiological and histomolecular characterisation.
Lucie Auffret, et al. Acta neuropathologica 2023 0 (1) 2 - Epilepsy Outcome and Pathology Analysis for Ganglioglioma: A Series of 51 Pediatric Patients.
Qingzhu Liu, et al. Pediatric neurology 2023 0 127-133 - The clinicopathological features of ganglioglioma with CD34 expression and BRAF mutation in patients with epilepsy.
Xie Ming-Guo, et al. Frontiers in molecular neuroscience 2023 0 1022364 - Desmoplastic non-infantile astrocytoma/ganglioglioma: rare low-grade tumor with frequent BRAF V600E mutation.
Chatterjee Debajyoti, et al. Human pathology 2018 0 186-191 - Genome sequencing identifies somatic BRAF duplication c.1794_1796dupTAC;p.Thr599dup in pediatric patient with low-grade ganglioglioma.
Miller Katherine E, et al. Cold Spring Harbor molecular case studies 2018 0 (2) - MEK inhibition with trametinib is a successful therapy in ganglioglioma.
Daniel Eliza Baird, et al. Clinical case reports and reviews 2020 0 (2) - Somatostatin receptor expression and mTOR pathway activation in glioneuronal tumours of childhood.
Ehrstedt Christoffer, et al. Seizure 2020 0 123-130 - Integrated genotype-phenotype analysis of long-term epilepsy-associated ganglioglioma.
Wang Yujiao, et al. Brain pathology (Zurich, Switzerland) 2021 0 (1) e13011 - Low-grade epilepsy-associated neuroepithelial tumours with a prominent oligodendroglioma-like component: The diagnostic challenges.
Métais Alice, et al. Neuropathology and applied neurobiology 2021 0 (2) e12769 - Detection of Brain Somatic Mutations in Cerebrospinal Fluid from Refractory Epilepsy Patients.
Kim Seyeon, et al. Annals of neurology 2021 0 (6) 1248-1252
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Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 21, 2024
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