Terms: = Leukemia AND FANCA, MGC75158, 2175, ENSG00000187741, FA-H, FA, FAA, FANCH, FA1, FACA AND Diagnosis
67 results:
1. Germline biallelic BRCA2 pathogenic variants and medulloblastoma: an international cohort study.
Kastellan S; Kalb R; Sajjad B; McReynolds LJ; Giri N; Samuel D; Milde T; Elbracht M; Holzhauer S; Niewisch MR; Kratz CP
J Hematol Oncol; 2024 Apr; 17(1):26. PubMed ID: 38685107
[TBL] [Abstract] [Full Text] [Related]
2. Investigation of fatty acid metabolism in chronic lymphocytic leukemia to guide clinical outcome and therapy.
Pan B; Xu Z; Du K; Gao R; Zhang J; Yin H; Shen H; Liang J; Li Y; Wang L; Li J; Xu W; Wu J
Ann Hematol; 2024 Apr; 103(4):1241-1254. PubMed ID: 38150112
[TBL] [Abstract] [Full Text] [Related]
3. T-cell depleted allogeneic hematopoietic stem cell transplant for the treatment of Fanconi anemia and MDS/AML.
Satty AM; Klein E; Mauguen A; Kunvarjee B; Boelens JJ; Cancio M; Curran KJ; Kernan NA; Prockop SE; Scaradavou A; Spitzer B; Tamari R; Ruggiero J; Torok-Castanza J; Mehta PA; O'Reilly RJ; Boulad F
Bone Marrow Transplant; 2024 Jan; 59(1):23-33. PubMed ID: 37773270
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4. Modern management of Fanconi anemia.
Dufour C; Pierri F
Hematology Am Soc Hematol Educ Program; 2022 Dec; 2022(1):649-657. PubMed ID: 36485157
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5. Cytogenetics in Fanconi Anemia: The Importance of Follow-Up and the Search for New Biomarkers of Genomic Instability.
Merfort LW; Lisboa MO; Cavalli LR; Bonfim CMS
Int J Mol Sci; 2022 Nov; 23(22):. PubMed ID: 36430597
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6. Genetic analysis of a Fanconi anemia case revealed the presence of FANCF mutation (exon 1;469>C-T) with implications to develop acute myeloid leukemia.
Behera CK; Gyandeep G; Mishra R; Mohanty RP; Pal A; Behera J; Samal S; Das B
Mol Biol Rep; 2023 Jan; 50(1):931-936. PubMed ID: 36369330
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7. Fanconi anaemia: A syndrome with distinct subgroups.
Alter BP; Giri N; McReynolds LJ; Altintas B
Br J Haematol; 2022 May; 197(4):467-474. PubMed ID: 35191533
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8. Effects of cyclophosphamide related genetic variants on clinical outcomes of adult hematopoietic cell transplant patients.
Takahashi T; Pearson R; Cao Q; Scheibner A; Sanghavi K; Weisdorf D; Brunstein C; Rogosheske J; Bachanova V; Warlick ED; Wiseman A; Jacobson PA
Cancer Chemother Pharmacol; 2022 Apr; 89(4):543-549. PubMed ID: 35083501
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9. Fanconi-like anemia related to a FANCM mutation.
Encarnación JA; Cerezuela P; Español I; García MR; Manso C; De la Fuente I; Garrigós N; Viney A; Minguillon J; Surrallés J
Eur J Med Genet; 2022 Jan; 65(1):104399. PubMed ID: 34793962
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10. Fanconi Anemia Gene Variants in Patients with Gonadal Dysfunction.
Daum H; Zlotogora J
Reprod Sci; 2022 May; 29(5):1408-1413. PubMed ID: 33977503
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11. Outcome of patients with Fanconi anemia developing myelodysplasia and acute leukemia who received allogeneic hematopoietic stem cell transplantation: A retrospective analysis on behalf of EBMT group.
Giardino S; de Latour RP; Aljurf M; Eikema DJ; Bosman P; Bertrand Y; Tbakhi A; Holter W; Bornhäuser M; Rössig C; Burkhardt B; Zecca M; Afanasyev B; Michel G; Ganser A; Alseraihy A; Ayas M; Uckan-Cetinkaya D; Bruno B; Patrick K; Bader P; Itälä-Remes M; Rocha V; Jubert C; Diaz MA; Shaw PJ; Junior LGD; Locatelli F; Kröger N; Faraci M; Pierri F; Lanino E; Miano M; Risitano A; Robin M; Dufour C;
Am J Hematol; 2020 Jul; 95(7):809-816. PubMed ID: 32267023
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12. Fanconi anemia: a single center experience of a large cohort.
Kesici S; Ünal Ş; Kuşkonmaz B; Aytaç S; Çetin M; Gümrük F
Turk J Pediatr; 2019; 61(4):477-484. PubMed ID: 31990462
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13. Bone Marrow Failure in Fanconi Anemia: Clinical and Genetic Spectrum in a Cohort of 20 Pediatric Patients.
Kelaidi C; Makis A; Petrikkos L; Antoniadi K; Selenti N; Tzotzola V; Ioannidou ED; Tsitsikas K; Kitra V; Kalpini-Mavrou A; Fryssira H; Polychronopoulou S
J Pediatr Hematol Oncol; 2019 Nov; 41(8):612-617. PubMed ID: 31259830
[TBL] [Abstract] [Full Text] [Related]
14. Cancer patients as frequent attenders in emergency departments: A national cohort study.
Wong TH; Lau ZY; Ong WS; Tan KB; Wong YJ; Farid M; Teo MCC; Yee ACP; Nguyen HV; Ong MEH; Iyer NG
Cancer Med; 2018 Sep; 7(9):4434-4446. PubMed ID: 30117313
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15. Chronic neutrophilic leukemia, an extremely rare cause of neutrophilia in childhood: Cure with hematopoietic stem cell transplantation.
Uygun V; Daloğlu H; Öztürkmen S; Karasu G; Avcı Z; Yeşilipek A
Pediatr Transplant; 2018 Aug; 22(5):e13199. PubMed ID: 29676020
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16. A Rare Case of Pediatric Chronic Myelogenous leukemia Presenting With Severe Thrombocytosis Without Leukocytosis.
Huho AN; Issaq N; Iacobas I; Elghetany TM; López-Terrada D; Fisher KE; Punia JN
Pediatr Dev Pathol; 2018; 21(1):100-104. PubMed ID: 29187020
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17. Transplant results in adults with Fanconi anaemia.
Bierings M; Bonfim C; Peffault De Latour R; Aljurf M; Mehta PA; Knol C; Boulad F; Tbakhi A; Esquirol A; McQuaker G; Sucak GA; Othman TB; Halkes CJM; Carpenter B; Niederwieser D; Zecca M; Kröger N; Michallet M; Risitano AM; Ehninger G; Porcher R; Dufour C;
Br J Haematol; 2018 Jan; 180(1):100-109. PubMed ID: 29094350
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18. 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
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19. Structural brain alteration in survivors of acute lymphoblastic leukemia with chemotherapy treatment: A voxel-based morphometry and diffusion tensor imaging study.
Zou L; Su L; Xu J; Xiang L; Wang L; Zhai Z; Zheng S
Brain Res; 2017 Mar; 1658():68-72. PubMed ID: 28109978
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20. Acute myeloid leukemia in Baraitser-Winter cerebrofrontofacial syndrome.
Cianci P; Fazio G; Casagranda S; Spinelli M; Rizzari C; Cazzaniga G; Selicorni A
Am J Med Genet A; 2017 Feb; 173(2):546-549. PubMed ID: 27868373
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