Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1954 1
1966 2
1967 1
1969 1
1971 1
1972 2
1973 2
1974 1
1975 4
1976 5
1977 7
1978 8
1979 5
1980 9
1981 8
1982 8
1983 7
1984 13
1985 11
1986 12
1987 9
1988 16
1989 21
1990 18
1991 9
1992 14
1993 15
1994 25
1995 15
1996 27
1997 25
1998 24
1999 28
2000 31
2001 38
2002 31
2003 34
2004 30
2005 30
2006 34
2007 37
2008 38
2009 38
2010 51
2011 50
2012 54
2013 66
2014 63
2015 63
2016 52
2017 59
2018 65
2019 64
2020 77
2021 89
2022 77
2023 62
2024 21

Text availability

Article attribute

Article type

Publication date

Search Results

1,445 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Bone marrow failure syndrome 5"
Page 1
Approach to the diagnosis of aplastic anemia.
DeZern AE, Churpek JE. DeZern AE, et al. Blood Adv. 2021 Jun 22;5(12):2660-2671. doi: 10.1182/bloodadvances.2021004345. Blood Adv. 2021. PMID: 34156438 Free PMC article. Review.
Childhood Myelodysplastic Syndrome.
Chisholm KM, Bohling SD. Chisholm KM, et al. Clin Lab Med. 2023 Dec;43(4):639-655. doi: 10.1016/j.cll.2023.06.005. Epub 2023 Aug 7. Clin Lab Med. 2023. PMID: 37865508 Review.

Myelodysplastic syndrome (MDS) in children is rare, accounting for < 5% of all childhood hematologic malignancies. ...Herein, cMDS classification schema, clinical presentation, laboratory values, bone marrow histology, differential diagnostic consid

Myelodysplastic syndrome (MDS) in children is rare, accounting for < 5% of all childhood hematologic malignancies. ...Herei

Hepatitis-Associated Aplastic Anemia.
Alshaibani A, Dufour C, Risitano A, de Latour R, Aljurf M. Alshaibani A, et al. Hematol Oncol Stem Cell Ther. 2022 Jun 1;15(2):8-12. doi: 10.1016/j.hemonc.2020.10.001. Hematol Oncol Stem Cell Ther. 2022. PMID: 33197413 Review.
Hepatitis-associated aplastic anemia (HAAA) is a rare illness, characterized by onset of pancytopenia with a hypoplastic bone marrow that traditionally occurs within 6 months of an increase in serum aminotransferases. HAAA is observed in 1% to 5% of all newly …
Hepatitis-associated aplastic anemia (HAAA) is a rare illness, characterized by onset of pancytopenia with a hypoplastic bone marr
Bone Marrow Failure and Immunodeficiency Associated with Human RAD50 Variants.
Takagi M, Hoshino A, Bousset K, Röddecke J, Martin HL, Folcut I, Tomomasa D, Yang X, Kobayashi J, Sakata N, Yoshida K, Miyano S, Ogawa S, Kojima S, Morio T, Dörk T, Kanegane H. Takagi M, et al. J Clin Immunol. 2023 Nov;43(8):2136-2145. doi: 10.1007/s10875-023-01591-8. Epub 2023 Oct 5. J Clin Immunol. 2023. PMID: 37794136
We aimed to characterize a newly identified RAD50 deficiency/NBS-like disorder (NBSLD) patient with bone marrow failure and immunodeficiency. METHODS: We report on a girl with microcephaly, mental retardation, bird-like face, short stature, bone mar
We aimed to characterize a newly identified RAD50 deficiency/NBS-like disorder (NBSLD) patient with bone marrow failure
The clinical picture of ERCC6L2 disease: from bone marrow failure to acute leukemia.
Hakkarainen M, Kaaja I, Douglas SPM, Vulliamy T, Dokal I, Soulier J, Larcher L, Peffault de Latour R, Leblanc T, Sicre de Fontbrune F, Siitonen T, Lohi O, Hellström-Lindberg E, Barbany G, Tesi B, Shimamura A, Beier F, Jackson S, Kuperman AA, Falik Zaccai T, Tamary H, Mecucci C, Capolsini I, Jahnukainen K, Salmenniemi U, Niinimäki R, Varilo T, Kilpivaara O, Wartiovaara-Kautto U. Hakkarainen M, et al. Blood. 2023 Jun 8;141(23):2853-2866. doi: 10.1182/blood.2022019425. Blood. 2023. PMID: 36952636
Biallelic germ line excision repair cross-complementing 6 like 2 (ERCC6L2) variants strongly predispose to bone marrow failure (BMF) and myeloid malignancies, characterized by somatic TP53-mutated clones and erythroid predominance. ...Changes in the complete …
Biallelic germ line excision repair cross-complementing 6 like 2 (ERCC6L2) variants strongly predispose to bone marrow fail
Childhood myelodysplastic syndrome.
Chatterjee T, Choudhry VP. Chatterjee T, et al. Indian J Pediatr. 2013 Sep;80(9):764-71. doi: 10.1007/s12098-013-1130-8. Epub 2013 Aug 3. Indian J Pediatr. 2013. PMID: 23912822 Review.
Myelodysplastic syndrome (MDS) comprises of a heterogeneous group of bone marrow disorders resulting from a clonal stem cell defect characterised by cytopenias despite a relatively hypercellular marrow, ineffective hematopoiesis, morphological d …
Myelodysplastic syndrome (MDS) comprises of a heterogeneous group of bone marrow disorders resulting from a clon …
Aplastic anemia.
Čermák J. Čermák J. Vnitr Lek. 2018 Summer;64(5):501-507. Vnitr Lek. 2018. PMID: 30193518 English.
Aplastic anemia - bone marrow failure (AA) is defined as pancytopenia with hypocellular bone marrow without signs of marrow fibrosis or of presence of abnormal cells. ...Toxic agent leads to expression of neoantigens or cryptic antigens o …
Aplastic anemia - bone marrow failure (AA) is defined as pancytopenia with hypocellular bone marrow witho …
How I investigate bone marrow necrosis.
Deucher A, Wool GD. Deucher A, et al. Int J Lab Hematol. 2019 Oct;41(5):585-592. doi: 10.1111/ijlh.13091. Epub 2019 Aug 19. Int J Lab Hematol. 2019. PMID: 31424633 Review.
While bone marrow necrosis is not uncommon in site-directed biopsy specimens or autopsy material, substantial necrosis is much less common in nondirected bone marrow biopsy specimens. ...Rarely, such as in fat embolization syndrome (FES), bon
While bone marrow necrosis is not uncommon in site-directed biopsy specimens or autopsy material, substantial necrosis is much …
Haploidentical bone marrow transplants with post transplant cyclophosphamide on day + 3 + 5: The Genova protocol.
Raiola AM, Angelucci E, Sica S, Bacigalupo A. Raiola AM, et al. Blood Rev. 2023 Nov;62:101031. doi: 10.1016/j.blre.2022.101031. Epub 2022 Nov 11. Blood Rev. 2023. PMID: 36435691 Review.
We report 634 patients who underwent unmanipulated haploidentical (HAPLO) bone marrow transplantation (BMT) in two Centers. The diagnosis was acute myeloid leukemia (AML) (n = 251), acute lymphoblastic leukemia (ALL)(n = 107), myelodysplastic syndrome and mye …
We report 634 patients who underwent unmanipulated haploidentical (HAPLO) bone marrow transplantation (BMT) in two Centers. Th …
Comprehensive laboratory diagnosis of Fanconi anaemia: comparison of cellular and molecular analysis.
Joshi G, Arthur NBJ, Geetha TS, Datari PVR, Modak K, Roy D, Chaudhury AD, Sundaraganesan P, Priyanka S, Na F, Ramprasad V, Abraham A, Srivastava VM, Srivastava A, Kulkarni UP, George B, Velayudhan SR. Joshi G, et al. J Med Genet. 2023 Aug;60(8):801-809. doi: 10.1136/jmg-2022-108714. Epub 2023 Mar 9. J Med Genet. 2023. PMID: 36894310 Free PMC article.
BACKGROUND: Fanconi anaemia (FA) is a rare inherited bone marrow failure disease caused by germline pathogenic variants in any of the 22 genes involved in the FA-DNA interstrand crosslink (ICL) repair pathway. ...RESULTS: Our study showed that FANCD2-Ub analy …
BACKGROUND: Fanconi anaemia (FA) is a rare inherited bone marrow failure disease caused by germline pathogenic variants …
1,445 results