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congenital myelodysplasia相关文献:
Congenital neutropenia syndromes.
Boztug K, Welte K, Zeidler C, Klein C.
Immunol Allergy Clin North Am. 2008 May;28(2):259-75, vii-viii. doi: 10.1016/j.iac.2008.01.007.
PMID:18424332
Congenital X-linked neutropenia with myelodysplasia and somatic tetraploidy due to a germline mutation in SEPT6.
Renella R, Gagne K, Beauchamp E, Fogel J, Perlov A, Sola M, Schlaeger T, Hofmann I, Shimamura A, Ebert BL, Schmitz-Abe K, Markianos K, Murphy K, Sun L, Rockowitz S, Sliz P, Campagna DR, Springer TA, Bahl C, Agarwal S, Fleming MD, Williams DA.
Am J Hematol. 2022 Jan 1;97(1):18-29. doi: 10.1002/ajh.26382. Epub 2021 Nov 3.
PMID:34677878
Congenital erythropoietic porphyria associated with myelodysplasia presenting in a 72-year-old man: report of a case and review of the literature.
Kontos AP, Ozog D, Bichakjian C, Lim HW.
Br J Dermatol. 2003 Jan;148(1):160-4. doi: 10.1046/j.1365-2133.2003.05040.x.
PMID:12534613
ELANE-Related Neutropenia.
Dale DC, Makaryan V.
2002 Jun 17 [updated 2018 Aug 23]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
PMID:20301705
Severe congenital neutropenia.
Welte K, Zeidler C, Dale DC.
Semin Hematol. 2006 Jul;43(3):189-95. doi: 10.1053/j.seminhematol.2006.04.004.
PMID:16822461
Congenital dyserythropoietic anemia type I mimicking myelodysplasia syndrome with a novel CDAN1 mutation.
Lv X, Dong S, Lan F, Zhang B, Chen H, Jin R.
Ann Hematol. 2020 Jan;99(1):197-199. doi: 10.1007/s00277-019-03848-y. Epub 2019 Nov 23.
PMID:31760486
WAS-Related Disorders.
Chandra S, Nagaraj CB, Sun M, Chandrakasan S, Zhang K.
2004 Sep 30 [updated 2024 Aug 15]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
PMID:20301357
Comparison of a restrictive versus liberal red cell transfusion policy for patients with myelodysplasia, aplastic anaemia, and other congenital bone marrow failure disorders.
Gu Y, Estcourt LJ, Doree C, Hopewell S, Vyas P.
Cochrane Database Syst Rev. 2015 Oct 5;2015(10):CD011577. doi: 10.1002/14651858.CD011577.pub2.
PMID:26436602
Hereditary myeloid malignancies.
Rafei H, DiNardo CD.
Best Pract Res Clin Haematol. 2019 Jun;32(2):163-176. doi: 10.1016/j.beha.2019.05.001. Epub 2019 May 3.
PMID:31203998
GATA2 deficiency.
Hsu AP, McReynolds LJ, Holland SM.
Curr Opin Allergy Clin Immunol. 2015 Feb;15(1):104-9. doi: 10.1097/ACI.0000000000000126.
PMID:25397911
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