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1987
2025

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1987 1
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2025 0

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Page 1
Exploring the molecular pathogenesis, diagnosis and treatment of fibrolamellar hepatocellular carcinoma: A state of art review of the current literature.
Alshareefy Y, Shen CY, Prekash RJ. Alshareefy Y, et al. Pathol Res Pract. 2023 Aug;248:154655. doi: 10.1016/j.prp.2023.154655. Epub 2023 Jun 26. Pathol Res Pract. 2023. PMID: 37429175 Free article. Review.
With this said, several unusual presentations have been documented such as Budd Chiari syndrome, severe anaemia, non-bacterial thrombotic endocarditis and many more. In regards to this tumour's genetic analysis, it is characterised by a 400 kb deletion on chromosome 19 lea …
With this said, several unusual presentations have been documented such as Budd Chiari syndrome, severe anaemia, non-bacterial thromb …
MCA/MR syndrome in a female infant with tetraploidy mosaicism: review of the human polyploid phenotype.
Wilson GN, Vekemans MJ, Kaplan P. Wilson GN, et al. Am J Med Genet. 1988 Aug;30(4):953-61. doi: 10.1002/ajmg.1320300413. Am J Med Genet. 1988. PMID: 3055989 Review.
Comparison with 11 previously reported cases with mosaic or complete tetraploidy does not establish an easily recognizable syndrome. However, a malformation pattern is apparent when tetraploidy patients are compared with 14 cases of triploid mosaicism and 44 …
Comparison with 11 previously reported cases with mosaic or complete tetraploidy does not establish an easily recognizable syndrom
Renal and urinary tract abnormalities associated with chromosome aberrations.
Barakat AY, Butler MG. Barakat AY, et al. Int J Pediatr Nephrol. 1987 Oct-Dec;8(4):215-26. Int J Pediatr Nephrol. 1987. PMID: 3329638 Free PMC article. Review.
The frequency of malformations of the kidney and urinary tract is much higher in patients with chromosome aberrations than in the general population. Sixty to 100% of "cat-eye" syndrome, 60 to 80% of Turner, 75% of trisomy 8, 33 to 70% of trisomy 18, 50 to 60% of trisomy 1 …
The frequency of malformations of the kidney and urinary tract is much higher in patients with chromosome aberrations than in the general po …
Rubella virus and birth defects: molecular insights into the viral teratogenesis at the cellular level.
Atreya CD, Mohan KV, Kulkarni S. Atreya CD, et al. Birth Defects Res A Clin Mol Teratol. 2004 Jul;70(7):431-7. doi: 10.1002/bdra.20045. Birth Defects Res A Clin Mol Teratol. 2004. PMID: 15259032 Review.
BACKGROUND: In utero rubella virus (RV) infection of a fetus can result in birth defects that are often collectively referred to as congenital rubella syndrome (CRS). In extreme cases, fetal death can occur. In spite of the availability of a safe and effective vaccine agai …
BACKGROUND: In utero rubella virus (RV) infection of a fetus can result in birth defects that are often collectively referred to as congenit …
Is 5q deletion in de novo Acute Myelogenous Leukemia (AML) with excess blasts a surrogate marker for the cryptic t(7;21)(p22;q22)? A case report and review of literature.
Johnston RD, Sayedian FH, Mendiola C, Ehman W Jr, Ortega V, Velagaleti GVN. Johnston RD, et al. Cancer Genet. 2022 Apr;262-263:30-34. doi: 10.1016/j.cancergen.2021.12.008. Epub 2021 Dec 24. Cancer Genet. 2022. PMID: 34974291 Review.
Although the 5q- syndrome is common in both de novo and treatment related myelodysplastic syndrome (MDS) and the World Health Organization defined 5q- syndrome as a specific type of MDS, it is less common in acute myelogenous leukemia (AML). Recently, it was …
Although the 5q- syndrome is common in both de novo and treatment related myelodysplastic syndrome (MDS) and the World Health …
Ornithine decarboxylase as a marker for colorectal polyps and cancer.
Luk GD, Moshier JA, Ehrinpreis MN. Luk GD, et al. Prog Clin Biol Res. 1988;279:227-39. Prog Clin Biol Res. 1988. PMID: 3054922 Review.
Tumor markers that have been studied include tetraploidy and increased colonic mucosal proliferation; and these markers have identified those patients that are at high risk for colon cancer. ...Ornithine decarboxylase needs to be studied in greater detail to determine its …
Tumor markers that have been studied include tetraploidy and increased colonic mucosal proliferation; and these markers have identifi …
Congenital genetic instability in colorectal carcinomas.
Svendsen LB. Svendsen LB. Dan Med Bull. 1993 Nov;40(5):546-56. Dan Med Bull. 1993. PMID: 8299399 Review.
It has been postulated, that inborn chromosomal instability is not limited to a few rare syndromes. Indeed, one of the common colorectal cancer (CRC) syndromes, familial adenomatous polyposis (FAP), is supposed to be a chromosomal instability syndrome. Also t …
It has been postulated, that inborn chromosomal instability is not limited to a few rare syndromes. Indeed, one of the common colorec …
[Acute megakaryoblastic leukemia developing 11 years after diagnosis of essential thrombocythemia].
Miyoshi Y, Okada S, Takizawa Y, Hagiwara S, Mori H, Niikura H, Terada H, Fujita K. Miyoshi Y, et al. Rinsho Ketsueki. 1991 Aug;32(8):868-73. Rinsho Ketsueki. 1991. PMID: 1942527 Review. Japanese.
Bone marrow aspiration revealed hypercellular marrow with 72.8% blasts. Chromosomal analysis showed tetraploidy with 7p+ and 19p+. Cytochemistry of blasts showed the positivity for platelet peroxidase and CDw 41. ...Since there was no evidence of myelodysplastic syndrom
Bone marrow aspiration revealed hypercellular marrow with 72.8% blasts. Chromosomal analysis showed tetraploidy with 7p+ and 19p+. Cy …