These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
135 related items for PubMed ID: 22959745
1. [Fanconi anemia in 2012: diagnosis, pediatric follow-up and treatment]. Lanneaux J, Poidvin A, Soole F, Leclerc G, Grimaud M, Dalle JH. Arch Pediatr; 2012 Oct; 19(10):1100-9. PubMed ID: 22959745 [Abstract] [Full Text] [Related]
8. Hematological consequences of a FANCG founder mutation in Black South African patients with Fanconi anemia. Feben C, Kromberg J, Wainwright R, Stones D, Poole J, Haw T, Krause A. Blood Cells Mol Dis; 2015 Mar; 54(3):270-4. PubMed ID: 25477267 [Abstract] [Full Text] [Related]
9. Gene transfer for the eventual treatment of Fanconi's anemia. Liu JM. Semin Hematol; 1998 Apr; 35(2):168-79. PubMed ID: 9565158 [Abstract] [Full Text] [Related]
10. Physician Education: Myelodysplastic Syndrome. Yoshida Y. Oncologist; 1996 Apr; 1(4):284-287. PubMed ID: 10388004 [Abstract] [Full Text] [Related]
11. Kidney complications in 107 Fanconi anemia patients submitted to hematopoietic cell transplantation. da Cunha MM, Barreto FC, Nichele S, Trennepohl J, Ribeiro L, Loth G, Koliski A, de Almeida Pinto Jardim T, Mello A, Pasquini R, de Castro Sylvestre L, Bonfim C. Eur J Pediatr; 2022 Feb; 181(2):715-723. PubMed ID: 34553252 [Abstract] [Full Text] [Related]
17. Successful umbilical cord blood transplantation for Fanconi anemia using preimplantation genetic diagnosis for HLA-matched donor. Bielorai B, Hughes MR, Auerbach AD, Nagler A, Loewenthal R, Rechavi G, Toren A. Am J Hematol; 2004 Dec; 77(4):397-9. PubMed ID: 15551406 [Abstract] [Full Text] [Related]
18. The need for more accurate and timely diagnosis in Fanconi anemia: a report from the International Fanconi Anemia Registry. Giampietro PF, Adler-Brecher B, Verlander PC, Pavlakis SG, Davis JG, Auerbach AD. Pediatrics; 1993 Jun; 91(6):1116-20. PubMed ID: 8502512 [Abstract] [Full Text] [Related]
20. A case of congenital pigmented dermatofibrosarcoma protuberans (Bednar tumor) in a patient with Fanconi anemia. Lee DW, Yang JH, Won CH, Chang SE, Lee MW, Choi JH, Moon KC. Pediatr Dermatol; 2011 Jun; 28(5):583-5. PubMed ID: 21438918 [Abstract] [Full Text] [Related] Page: [Next] [New Search]