Young-Shin Ra
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Explore the profile of Young-Shin Ra including associated specialties, affiliations and a list of published articles.
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Articles
36
Citations
1038
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Recent Articles
11.
Jeong Nam S, Kim Y, Park J, Ra Y, Khang S, Cho Y, et al.
Cancer Immunol Immunother
. 2018 Nov;
68(2):305-318.
PMID: 30483834
Ependymomas are biologically and clinically heterogeneous tumors of the central nervous system that have variable clinical outcomes. The status of the tumor immune microenvironment in ependymoma remains unclear. Immune cell...
12.
Waszak S, Northcott P, Buchhalter I, Robinson G, Sutter C, Groebner S, et al.
Lancet Oncol
. 2018 May;
19(6):785-798.
PMID: 29753700
Background: Medulloblastoma is associated with rare hereditary cancer predisposition syndromes; however, consensus medulloblastoma predisposition genes have not been defined and screening guidelines for genetic counselling and testing for paediatric patients...
13.
Park E, Park J, Ra Y
J Korean Neurosurg Soc
. 2018 May;
61(3):352-362.
PMID: 29742884
Gliomas are the most common pediatric tumors of the central nervous system. In this review, we discuss the clinical features, treatment paradigms, and evolving concepts related to two types of...
14.
Hyun S, Kim J, Kim K, Jahng T, Roh S, Ra Y, et al.
Oper Neurosurg (Hagerstown)
. 2017 Sep;
14(2):112-120.
PMID: 28962021
Background: Since chordoma is refractory to chemotherapy and conventional radiotherapy, radical surgical resection is mandatory. However, it is surgically demanding in the craniocervical junction (CCJ) and upper cervical spine. Objective:...
15.
Goo H, Ra Y
Korean J Radiol
. 2017 Jan;
18(1):194-207.
PMID: 28096729
Conventional anatomic brain MRI is often limited in evaluating pediatric brain tumors, the most common solid tumors and a leading cause of death in children. Advanced brain MRI techniques have...
16.
Torchia J, Golbourn B, Feng S, Ho K, Sin-Chan P, Vasiljevic A, et al.
Cancer Cell
. 2016 Dec;
30(6):891-908.
PMID: 27960086
We recently reported that atypical teratoid rhabdoid tumors (ATRTs) comprise at least two transcriptional subtypes with different clinical outcomes; however, the mechanisms underlying therapeutic heterogeneity remained unclear. In this study,...
17.
Kim E, Yum M, Ra Y, Park J, Ahn J, Kim G, et al.
J Neurosurg
. 2015 Oct;
124(5):1221-7.
PMID: 26430847
OBJECT Moyamoya disease (MMD) is an idiopathic cerebrovascular occlusive disorder prevalent in East Asia. In the pathogenesis of MMD, the important role of genetic factors is being elucidated, and RNF213...
18.
Goo H, Ra Y
J Neurosurg Pediatr
. 2015 Apr;
16(1):50-3.
PMID: 25885801
Medullary hemangioblastoma is very rare in children. Based on small nodular enhancement with peritumoral edema and without dilated feeding arteries on conventional MRI, hemangioblastoma, pilocytic astrocytoma, oligodendroglioma, and ganglioglioma were...
19.
Torchia J, Picard D, Lafay-Cousin L, Hawkins C, Kim S, Letourneau L, et al.
Lancet Oncol
. 2015 Apr;
16(5):569-82.
PMID: 25882982
Background: Rhabdoid brain tumours, also called atypical teratoid rhabdoid tumours, are lethal childhood cancers with characteristic genetic alterations of SMARCB1/hSNF5. Lack of biological understanding of the substantial clinical heterogeneity of...
20.
Jung T, Lee J, Kim D, Park H, Kim C, Ra Y, et al.
J Neurooncol
. 2014 Nov;
121(2):413-9.
PMID: 25366367
We analyzed the prognostic factors of Korean pediatric patients with supratentorial high-grade glioma (HGG). Between 1997 and 2011, 62 patients with 34 glioblastomas and 28 anaplastic gliomas were surgically operated...