Terms: = Germ cell tumor AND SMARCE1, ENSG00000073584, 6605, BAF57, Q969G3 AND Diagnosis
6 results:
1. Multiple Meningiomas as a Criterion for the diagnosis of Neurofibromatosis Type 2 and Other tumor Predisposition Syndromes.
Hannan CJ; Hammerbeck-Ward C; Pathmanaban ON; Smith MJ; Rutherford SA; Lloyd SK; Mackenzie Freeman SR; Wallace AJ; King AT; Richard Evans DG
Neurosurgery; 2022 Jun; 90(6):793-799. PubMed ID: 35343466
[TBL] [Abstract] [Full Text] [Related]
2. Identification of a glioma functional network from gene fitness data using machine learning.
Xiang CX; Liu XG; Zhou DQ; Zhou Y; Wang X; Chen F
J Cell Mol Med; 2022 Feb; 26(4):1253-1263. PubMed ID: 35044082
[TBL] [Abstract] [Full Text] [Related]
3. Whole Exome Sequencing Identifies Candidate Genes Associated with Hereditary Predisposition to Uveal Melanoma.
Abdel-Rahman MH; Sample KM; Pilarski R; Walsh T; Grosel T; Kinnamon D; Boru G; Massengill JB; Schoenfield L; Kelly B; Gordon D; Johansson P; DeBenedictis MJ; Singh A; Casadei S; Davidorf FH; White P; Stacey AW; Scarth J; Fewings E; Tischkowitz M; King MC; Hayward NK; Cebulla CM
Ophthalmology; 2020 May; 127(5):668-678. PubMed ID: 32081490
[TBL] [Abstract] [Full Text] [Related]
4. Targeted next-generation sequencing for differential diagnosis of neurofibromatosis type 2, schwannomatosis, and meningiomatosis.
Louvrier C; Pasmant E; Briand-Suleau A; Cohen J; Nitschké P; Nectoux J; Orhant L; Zordan C; Goizet C; Goutagny S; Lallemand D; Vidaud M; Vidaud D; Kalamarides M; Parfait B
Neuro Oncol; 2018 Jun; 20(7):917-929. PubMed ID: 29409008
[TBL] [Abstract] [Full Text] [Related]
5. Cancer and Central Nervous System tumor Surveillance in Pediatric Neurofibromatosis 2 and Related Disorders.
Evans DGR; Salvador H; Chang VY; Erez A; Voss SD; Druker H; Scott HS; Tabori U
Clin Cancer Res; 2017 Jun; 23(12):e54-e61. PubMed ID: 28620005
[TBL] [Abstract] [Full Text] [Related]
6. A heritable form of smarce1-related meningiomas with important implications for follow-up and family screening.
Gerkes EH; Fock JM; den Dunnen WF; van Belzen MJ; van der Lans CA; Hoving EW; Fakkert IE; Smith MJ; Evans DG; Olderode-Berends MJ
Neurogenetics; 2016 Apr; 17(2):83-9. PubMed ID: 26803492
[TBL] [Abstract] [Full Text] [Related]
