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

Year Number of Results
1967 6
1969 2
1970 1
1971 1
1972 1
1973 5
1974 5
1975 2
1976 7
1977 4
1978 3
1979 2
1980 3
1981 3
1982 3
1983 3
1984 4
1985 7
1986 6
1987 6
1988 2
1989 10
1990 12
1991 7
1992 8
1993 9
1994 5
1995 10
1996 10
1997 9
1998 7
1999 8
2000 14
2001 6
2002 18
2003 18
2004 9
2005 16
2006 9
2007 10
2008 13
2009 8
2010 15
2011 12
2012 12
2013 15
2014 13
2015 15
2016 12
2017 18
2018 28
2019 7
2020 15
2021 19
2022 10
2023 16
2024 6

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482 results

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Page 1
Osteopetrosis.
Stark Z, Savarirayan R. Stark Z, et al. Orphanet J Rare Dis. 2009 Feb 20;4:5. doi: 10.1186/1750-1172-4-5. Orphanet J Rare Dis. 2009. PMID: 19232111 Free PMC article. Review.
Osteopetrosis ("marble bone disease") is a descriptive term that refers to a group of rare, heritable disorders of the skeleton characterized by increased bone density on radiographs. ...Treatment of osteopetrotic conditions is largely symptomatic, although h …
Osteopetrosis ("marble bone disease") is a descriptive term that refers to a group of rare, heritable disorders of the skeleto …
Doxorubicin-Induced Cardiotoxicity: An Overview on Pre-clinical Therapeutic Approaches.
Sheibani M, Azizi Y, Shayan M, Nezamoleslami S, Eslami F, Farjoo MH, Dehpour AR. Sheibani M, et al. Cardiovasc Toxicol. 2022 Apr;22(4):292-310. doi: 10.1007/s12012-022-09721-1. Epub 2022 Jan 21. Cardiovasc Toxicol. 2022. PMID: 35061218 Review.
This anti-cancer drug has various side effects, such as allergic reactions, cardiac damage, hair loss, bone marrow suppression, vomiting, and bladder irritation. The most dangerous side effect of doxorubicin is cardiomyopathy, leading to congestive heart failure
This anti-cancer drug has various side effects, such as allergic reactions, cardiac damage, hair loss, bone marrow suppression …
The Pathophysiology of Acquired Aplastic Anemia: Current Concepts Revisited.
Schoettler ML, Nathan DG. Schoettler ML, et al. Hematol Oncol Clin North Am. 2018 Aug;32(4):581-594. doi: 10.1016/j.hoc.2018.03.001. Epub 2018 May 8. Hematol Oncol Clin North Am. 2018. PMID: 30047412 Free PMC article. Review.
Idiopathic acquired aplastic anemia is a rare, life-threatening bone marrow failure syndrome characterized by cytopenias and hypocellular bone marrow. ...The authors review the literature and propose that the major driver of acquired apla …
Idiopathic acquired aplastic anemia is a rare, life-threatening bone marrow failure syndrome characterized by cy …
Acute Liver Failure: An Update.
Squires JE, McKiernan P, Squires RH. Squires JE, et al. Clin Liver Dis. 2018 Nov;22(4):773-805. doi: 10.1016/j.cld.2018.06.009. Epub 2018 Aug 22. Clin Liver Dis. 2018. PMID: 30266162 Review.
Pediatric acute liver failure (PALF) is a dynamic, life-threatening condition of disparate etiology. ...Proper recognition and treatment of common complications of liver failure are critical to optimizing outcomes. In parallel, investigations to identify underlying …
Pediatric acute liver failure (PALF) is a dynamic, life-threatening condition of disparate etiology. ...Proper recognition and treatm …
How I treat myelodysplastic syndromes of childhood.
Locatelli F, Strahm B. Locatelli F, et al. Blood. 2018 Mar 29;131(13):1406-1414. doi: 10.1182/blood-2017-09-765214. Epub 2018 Feb 8. Blood. 2018. PMID: 29438960 Free article. Review.
Pediatric myelodysplastic syndromes (MDSs) are a heterogeneous group of clonal disorders with an annual incidence of 1 to 4 cases per million, accounting for less than 5% of childhood hematologic malignancies. MDSs in children often occur in the context of inherited …
Pediatric myelodysplastic syndromes (MDSs) are a heterogeneous group of clonal disorders with an annual incidence of 1 to 4 ca …
Severe aplastic anemia: allogeneic bone marrow transplantation as first-line treatment.
Georges GE, Doney K, Storb R. Georges GE, et al. Blood Adv. 2018 Aug 14;2(15):2020-2028. doi: 10.1182/bloodadvances.2018021162. Blood Adv. 2018. PMID: 30108110 Free PMC article. Review.
The priority order of donor source for bone marrow transplantation is: (1) HLA-identical sibling, (2) HLA-matched unrelated donor, and (3) HLA-haploidentical donor if an HLA-matched unrelated donor is not rapidly available. ...In contrast, marrow transplantat …
The priority order of donor source for bone marrow transplantation is: (1) HLA-identical sibling, (2) HLA-matched unrelated do …
Crises in Sickle Cell Disease.
Novelli EM, Gladwin MT. Novelli EM, et al. Chest. 2016 Apr;149(4):1082-93. doi: 10.1016/j.chest.2015.12.016. Epub 2015 Dec 28. Chest. 2016. PMID: 26836899 Free PMC article. Review.
These pathological changes can occur acutely and lead to a dramatic clinical presentation, but are frequently superimposed over a milieu of chronic vasculopathy, immune dysregulation, and decreased functional reserve. In the lungs, acute chest syndrome is a particularly om …
These pathological changes can occur acutely and lead to a dramatic clinical presentation, but are frequently superimposed over a milieu of …
Clonal expansion in non-cancer tissues.
Kakiuchi N, Ogawa S. Kakiuchi N, et al. Nat Rev Cancer. 2021 Apr;21(4):239-256. doi: 10.1038/s41568-021-00335-3. Epub 2021 Feb 24. Nat Rev Cancer. 2021. PMID: 33627798 Review.
Revesz syndrome revisited.
Karremann M, Neumaier-Probst E, Schlichtenbrede F, Beier F, Brümmendorf TH, Cremer FW, Bader P, Dürken M. Karremann M, et al. Orphanet J Rare Dis. 2020 Oct 23;15(1):299. doi: 10.1186/s13023-020-01553-y. Orphanet J Rare Dis. 2020. PMID: 33097095 Free PMC article. Review.
Clinical features are summarized, indicating a low prevalence of the classical DKC triad. All patients experienced early bone marrow failure, in most cases within the second year of life (median age 1.5 years; 95% CI 1.4-1.6). ...Stem cell transplantat …
Clinical features are summarized, indicating a low prevalence of the classical DKC triad. All patients experienced early bone marr
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 consideration

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

482 results