174 related articles for article (PubMed ID: 19530235)
1. Fanconi anemia and biallelic BRCA2 mutation diagnosed in a young child with an embryonal CNS tumor.
Dewire MD; Ellison DW; Patay Z; McKinnon PJ; Sanders RP; Gajjar A
Pediatr Blood Cancer; 2009 Dec; 53(6):1140-2. PubMed ID: 19530235
[TBL] [Abstract][Full Text] [Related]
2. Genotype-cancer association in patients with Fanconi anemia due to pathogenic variants in FANCD1 (BRCA2) or FANCN (PALB2).
McReynolds LJ; Biswas K; Giri N; Sharan SK; Alter BP
Cancer Genet; 2021 Nov; 258-259():101-109. PubMed ID: 34687993
[TBL] [Abstract][Full Text] [Related]
3. Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemia.
Offit K; Levran O; Mullaney B; Mah K; Nafa K; Batish SD; Diotti R; Schneider H; Deffenbaugh A; Scholl T; Proud VK; Robson M; Norton L; Ellis N; Hanenberg H; Auerbach AD
J Natl Cancer Inst; 2003 Oct; 95(20):1548-51. PubMed ID: 14559878
[TBL] [Abstract][Full Text] [Related]
4. The clinical phenotype of children with Fanconi anemia caused by biallelic FANCD1/BRCA2 mutations.
Myers K; Davies SM; Harris RE; Spunt SL; Smolarek T; Zimmerman S; McMasters R; Wagner L; Mueller R; Auerbach AD; Mehta PA
Pediatr Blood Cancer; 2012 Mar; 58(3):462-5. PubMed ID: 21548014
[TBL] [Abstract][Full Text] [Related]
5. Fanconi anemia with biallelic FANCD1/BRCA2 mutations - Case report of a family with three affected children.
Svojgr K; Sumerauer D; Puchmajerova A; Vicha A; Hrusak O; Michalova K; Malis J; Smisek P; Kyncl M; Novotna D; Machackova E; Jencik J; Pycha K; Vaculik M; Kodet R; Stary J
Eur J Med Genet; 2016 Mar; 59(3):152-7. PubMed ID: 26657402
[TBL] [Abstract][Full Text] [Related]
6. Primitive neuroectodermal tumors of the central nervous system associated with genetic and metabolic defects.
Varan A; Yazici N; Akalan N; Yalcin B; Akyüz C; Kutluk T; Büyükpamukçu M
J Neurosurg Sci; 2012 Mar; 56(1):49-53. PubMed ID: 22415382
[TBL] [Abstract][Full Text] [Related]
7. Multiple synchronous malignancies in an infant with concomitant homozygous
Alghanim HM; Eltawel M; Alhaidari AI; Alobaid MM; Moghairi AM; Sufiani F; Ahmad N
Pediatr Hematol Oncol; 2023; 40(6):587-594. PubMed ID: 36731423
[TBL] [Abstract][Full Text] [Related]
8. [Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene--Case Report].
Puchmajerová A; Švojgr K; Novotná D; Macháčková E; Sumerauer D; Smíšek P; Kodet R; Kynčl M; Křepelová A; Foretová L
Klin Onkol; 2016; 29 Suppl 1():S89-92. PubMed ID: 26691948
[TBL] [Abstract][Full Text] [Related]
9. Treatment With Azacitidine in the Context of Palliative Care for a Patient With Acute Myeloid Leukemia Complicating Fanconi Anemia With Biallelic FANCD1/BRCA 2 Mutations.
Berot A; Pluchart C
J Pediatr Hematol Oncol; 2018 Apr; 40(3):247-248. PubMed ID: 29389832
[No Abstract] [Full Text] [Related]
10. Fanconi anemia caused by biallelic inactivation of BRCA2 can present with an atypical cancer phenotype in adulthood.
Maxwell KN; Patel V; Nead KT; Merrill S; Clark D; Jiang Q; Wubbenhorst B; D'Andrea K; Cohen RB; Domchek SM; Morrissette JJD; Greenberg RA; Babushok DV; Nathanson KL
Clin Genet; 2023 Jan; 103(1):119-124. PubMed ID: 36089892
[TBL] [Abstract][Full Text] [Related]
11. A homozygous nonsense mutation early in exon 5 of BRCA2 is associated with very severe Fanconi anemia.
Radulovic I; Kuechler A; Schündeln MM; Paulussen M; von Neuhoff N; Reinhardt D; Hanenberg H
Eur J Med Genet; 2021 Aug; 64(8):104260. PubMed ID: 34118472
[TBL] [Abstract][Full Text] [Related]
12. The association between FANCD1/BRCA2 mutations and leukaemia.
Alter BP
Br J Haematol; 2006 May; 133(4):446-8; author reply 448. PubMed ID: 16643458
[No Abstract] [Full Text] [Related]
13. Fanconi anemia: correlating central nervous system malformations and genetic complementation groups.
Johnson-Tesch BA; Gawande RS; Zhang L; MacMillan ML; Nascene DR
Pediatr Radiol; 2017 Jun; 47(7):868-876. PubMed ID: 28283722
[TBL] [Abstract][Full Text] [Related]
14. Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2.
Alter BP; Rosenberg PS; Brody LC
J Med Genet; 2007 Jan; 44(1):1-9. PubMed ID: 16825431
[TBL] [Abstract][Full Text] [Related]
15. A novel cancer risk prediction score for the natural course of FA patients with biallelic BRCA2/FANCD1 mutations.
Radulovic I; Schündeln MM; Müller L; Ptok J; Honisch E; Niederacher D; Wiek C; Scheckenbach K; Leblanc T; Larcher L; Soulier J; Reinhardt D; Schaal H; Andreassen PR; Hanenberg H
Hum Mol Genet; 2023 May; 32(11):1836-1849. PubMed ID: 36721989
[TBL] [Abstract][Full Text] [Related]
16. Biallelic BRCA2 mutations in two black South African children with Fanconi anaemia.
Feben C; Spencer C; Lochan A; Laing N; Fieggen K; Honey E; Wainstein T; Krause A
Fam Cancer; 2017 Jul; 16(3):441-446. PubMed ID: 28185119
[TBL] [Abstract][Full Text] [Related]
17. Central nervous system primitive neuroectodermal tumors: a clinicopathologic and genetic study of 33 cases.
Behdad A; Perry A
Brain Pathol; 2010 Mar; 20(2):441-50. PubMed ID: 19725831
[TBL] [Abstract][Full Text] [Related]
18. Association of biallelic BRCA2/FANCD1 mutations with spontaneous chromosomal instability and solid tumors of childhood.
Hirsch B; Shimamura A; Moreau L; Baldinger S; Hag-alshiekh M; Bostrom B; Sencer S; D'Andrea AD
Blood; 2004 Apr; 103(7):2554-9. PubMed ID: 14670928
[TBL] [Abstract][Full Text] [Related]
19. Hepatoblastoma in a 4-year-old girl with Fanconi anaemia.
Kopic S; Eirich K; Schuster B; Hanenberg H; Varon-Mateeva R; Rittinger O; Schimpl G; Schindler D; Jones N
Acta Paediatr; 2011 May; 100(5):780-3. PubMed ID: 21138478
[TBL] [Abstract][Full Text] [Related]
20. Mutational analysis of FANCL, FANCM and the recently identified FANCI suggests that among the 13 known Fanconi Anemia genes, only FANCD1/BRCA2 plays a major role in high-risk breast cancer predisposition.
García MJ; Fernández V; Osorio A; Barroso A; Fernández F; Urioste M; Benítez J
Carcinogenesis; 2009 Nov; 30(11):1898-902. PubMed ID: 19737859
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
