267 related articles for article (PubMed ID: 32192808)
1. [Hereditary predisposition to tumors of the central and peripheral nervous systems].
Sourty B; Rousseau A
Ann Pathol; 2020 Apr; 40(2):168-179. PubMed ID: 32192808
[TBL] [Abstract][Full Text] [Related]
2. Tumors of central and peripheral nervous system associated with inherited genetic syndromes.
Stefanaki K; Alexiou GA; Stefanaki C; Prodromou N
Pediatr Neurosurg; 2012; 48(5):271-85. PubMed ID: 23796843
[TBL] [Abstract][Full Text] [Related]
3. Nervous system (NS) Tumors in Cancer Predisposition Syndromes.
Patil P; Pencheva BB; Patil VM; Fangusaro J
Neurotherapeutics; 2022 Oct; 19(6):1752-1771. PubMed ID: 36056180
[TBL] [Abstract][Full Text] [Related]
4. Update on the management of familial central nervous system tumor syndromes.
Hottinger AF; Khakoo Y
Curr Neurol Neurosci Rep; 2007 May; 7(3):200-7. PubMed ID: 17488585
[TBL] [Abstract][Full Text] [Related]
5. [Molecular genetics of familial tumour syndromes of the central nervous system].
Murnyák B; Szepesi R; Hortobágyi T
Orv Hetil; 2015 Feb; 156(5):171-7. PubMed ID: 25618858
[TBL] [Abstract][Full Text] [Related]
6. Neurooncology of familial cancer syndromes.
Hottinger AF; Khakoo Y
J Child Neurol; 2009 Dec; 24(12):1526-35. PubMed ID: 19955345
[TBL] [Abstract][Full Text] [Related]
7. [Hereditary tumor syndromes in neuropathology].
Mawrin C
Pathologe; 2017 May; 38(3):186-196. PubMed ID: 28474160
[TBL] [Abstract][Full Text] [Related]
8. Absence of expression of SMARCB1/INI1 in malignant rhabdoid tumors of the central nervous system, kidneys and soft tissue: an immunohistochemical study with implications for diagnosis.
Sigauke E; Rakheja D; Maddox DL; Hladik CL; White CL; Timmons CF; Raisanen J
Mod Pathol; 2006 May; 19(5):717-25. PubMed ID: 16528370
[TBL] [Abstract][Full Text] [Related]
9. Genetic causes of brain tumors: neurofibromatosis, tuberous sclerosis, von Hippel-Lindau, and other syndromes.
Farrell CJ; Plotkin SR
Neurol Clin; 2007 Nov; 25(4):925-46, viii. PubMed ID: 17964021
[TBL] [Abstract][Full Text] [Related]
10. [The role of diagnostic neuropathology in familial tumour syndromes].
Feiden S; Sartorius E; Feiden W
Pathologe; 2010 Oct; 31(6):464-70. PubMed ID: 20848106
[TBL] [Abstract][Full Text] [Related]
11. Recent developments in brain tumor predisposing syndromes.
Johansson G; Andersson U; Melin B
Acta Oncol; 2016; 55(4):401-11. PubMed ID: 26634384
[TBL] [Abstract][Full Text] [Related]
12. Tumor Syndromes: Neurosurgical Evaluation and Management.
Ganapathy A; Diaz EJ; Coleman JT; Mackey KA
Neurosurg Clin N Am; 2022 Jan; 33(1):91-104. PubMed ID: 34801146
[TBL] [Abstract][Full Text] [Related]
13. Genetic insights into familial tumors of the nervous system.
Melean G; Sestini R; Ammannati F; Papi L
Am J Med Genet C Semin Med Genet; 2004 Aug; 129C(1):74-84. PubMed ID: 15264275
[TBL] [Abstract][Full Text] [Related]
14. SMARCB1-deficient and SMARCA4-deficient Malignant Brain Tumors With Complex Copy Number Alterations and TP53 Mutations May Represent the First Clinical Manifestation of Li-Fraumeni Syndrome.
Hasselblatt M; Thomas C; Federico A; Nemes K; Johann PD; Bison B; Bens S; Dahlum S; Kordes U; Redlich A; Lessel L; Pajtler KW; Mawrin C; Schüller U; Nolte K; Kramm CM; Hinz F; Sahm F; Giannini C; Penkert J; Kratz CP; Pfister SM; Siebert R; Paulus W; Kool M; Frühwald MC
Am J Surg Pathol; 2022 Sep; 46(9):1277-1283. PubMed ID: 35446794
[TBL] [Abstract][Full Text] [Related]
15. SMARCB1 deficiency in tumors from the peripheral nervous system: a link between schwannomas and rhabdoid tumors?
Rizzo D; Fréneaux P; Brisse H; Louvrier C; Lequin D; Nicolas A; Ranchère D; Verkarre V; Jouvet A; Dufour C; Edan C; Stéphan JL; Orbach D; Sarnacki S; Pierron G; Parfait B; Peuchmaur M; Delattre O; Bourdeaut F
Am J Surg Pathol; 2012 Jul; 36(7):964-72. PubMed ID: 22614000
[TBL] [Abstract][Full Text] [Related]
16. Germline TP53 Mutations in Patients With Early-Onset Colorectal Cancer in the Colon Cancer Family Registry.
Yurgelun MB; Masciari S; Joshi VA; Mercado RC; Lindor NM; Gallinger S; Hopper JL; Jenkins MA; Buchanan DD; Newcomb PA; Potter JD; Haile RW; Kucherlapati R; Syngal S;
JAMA Oncol; 2015 May; 1(2):214-21. PubMed ID: 26086041
[TBL] [Abstract][Full Text] [Related]
17. Neurofibromatosis type 2 and von Hippel-Lindau disease: from gene cloning to function.
Kley N; Whaley J; Seizinger BR
Glia; 1995 Nov; 15(3):297-307. PubMed ID: 8586465
[TBL] [Abstract][Full Text] [Related]
18. Rhabdoid tumor predisposition syndrome.
Sredni ST; Tomita T
Pediatr Dev Pathol; 2015; 18(1):49-58. PubMed ID: 25494491
[TBL] [Abstract][Full Text] [Related]
19. Immunohistochemical analysis of INI1 protein in malignant pediatric CNS tumors: Lack of INI1 in atypical teratoid/rhabdoid tumors and in a fraction of primitive neuroectodermal tumors without rhabdoid phenotype.
Haberler C; Laggner U; Slavc I; Czech T; Ambros IM; Ambros PF; Budka H; Hainfellner JA
Am J Surg Pathol; 2006 Nov; 30(11):1462-8. PubMed ID: 17063089
[TBL] [Abstract][Full Text] [Related]
20. Genetic Syndromes Associated with Central Nervous System Tumors.
Vijapura C; Saad Aldin E; Capizzano AA; Policeni B; Sato Y; Moritani T
Radiographics; 2017; 37(1):258-280. PubMed ID: 27911673
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
