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congenital megakaryocyte dysplasia 相关文献:
[Megakaryocyte dysplasia in congenital thrombocytopenia].
BECKER H.
Zentralbl Allg Pathol. 1962 May 30;103:375-84.
PMID:13866333
A Child With Dyserythropoietic Anemia and Megakaryocyte Dysplasia Due to a Novel 5'UTR GATA1s Splice Mutation.
Zucker J, Temm C, Czader M, Nalepa G.
Pediatr Blood Cancer. 2016 May;63(5):917-21. doi: 10.1002/pbc.25871. Epub 2015 Dec 29.
PMID:26713410
Phf6-null hematopoietic stem cells have enhanced self-renewal capacity and oncogenic potentials.
Hsu YC, Chen TC, Lin CC, Yuan CT, Hsu CL, Hou HA, Kao CJ, Chuang PH, Chen YR, Chou WC, Tien HF.
Blood Adv. 2019 Aug 13;3(15):2355-2367. doi: 10.1182/bloodadvances.2019000391.
PMID:31395598
Bone marrow morphology and disease progression in congenital thrombocytopenia: a detailed clinicopathologic and genetic study of eight cases.
Tsang HC, Bussel JB, Mathew S, Liu YC, Imahiyerobo AA, Orazi A, Geyer JT.
Mod Pathol. 2017 Apr;30(4):486-498. doi: 10.1038/modpathol.2016.218. Epub 2017 Jan 6.
PMID:28059092
GATA2 deficiency-associated bone marrow disorder differs from idiopathic aplastic anemia.
Ganapathi KA, Townsley DM, Hsu AP, Arthur DC, Zerbe CS, Cuellar-Rodriguez J, Hickstein DD, Rosenzweig SD, Braylan RC, Young NS, Holland SM, Calvo KR.
Blood. 2015 Jan 1;125(1):56-70. doi: 10.1182/blood-2014-06-580340. Epub 2014 Oct 30.
PMID:25359990
Spectrum of Myelodysplastic Syndrome in Patients Evaluated for Cytopenia(s). A Report from a Reference Centre in Saudi Arabia.
AlMozain N, Mashi A, Alneami Q, Al-Omran A, Bakshi N, Owaidah T, Khalil S, Khogeer H, Hashmi S, Al-Sweedan S, Morris T, AlNounou R.
Hematol Oncol Stem Cell Ther. 2022 Jun 1;15(2):39-44. doi: 10.1016/j.hemonc.2020.11.001.
PMID:33227261
An uncommon t(9;11)(p24;q22) with monoallelic loss of ATMKMT2A genes in a child with myelodysplastic syndrome/acute myeloid leukemia who evolved from Fanconi anemia.
Lovatel VL, de Souza DC, Alvarenga TF, Capela de Matos RR, Diniz C, Schramm MT, Llerena Júnior JC, Silva MLM, Abdelhay E, de Souza Fernandez T.
Mol Cytogenet. 2018 Jul 11;11:40. doi: 10.1186/s13039-018-0389-x. eCollection 2018.
PMID:30008805
A lethal osteochondrodysplasia with mesomelic brachymelia, round pelvis, and congenital hepatic fibrosis: two siblings born to consanguineous parents.
Nishimura G, Nakayama M, Fuke Y, Suehara N.
Pediatr Radiol. 1998 Jan;28(1):43-7. doi: 10.1007/s002470050289.
PMID:9426272
Nuclear bridging of erythroblasts in acquired dyserythropoiesis: an early and transient preleukemic marker.
Bethlenfalvay NC, Phaure TA, Phyliky RL, Bowman RP.
Am J Hematol. 1986 Mar;21(3):315-22. doi: 10.1002/ajh.2830210311.
PMID:3946411
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