Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Angela Scalise"'
Autor:
Rose Khoobyar, Mikhail Roshal, Maria E. Arcila, Jinjuan Yao, Wenbin Xiao, Angela Scalise, Umut Aypar, Dory Londono, Yanming Zhang
Publikováno v:
Genes, Chromosomes and Cancer. 60:100-107
Chromosome translocations involving the RUNX1 gene at 21q22 are recurring abnormalities in acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS), that is, t(8;21) and t(3;21) and in B-cell acute lymphoblastic leukemia with t(12;21). These t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18b8ba2a1291b22ef2f191dfb9659851
https://doi.org/10.1002/gcc.22901
https://doi.org/10.1002/gcc.22901
Publikováno v:
Acta Haematologica. 133:1-5
We describe a patient with acute myeloid leukemia (AML) who had a normal karyotype at diagnosis and was negative for NPM1 and FLT3 mutations, but had a KIT G565V mutation in exon 11. This has not been described previously in AML. The patient received
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff46c5848771f233ef8d5053eb39a79a
https://doi.org/10.1159/000360389
https://doi.org/10.1159/000360389
Autor:
Amanda LeBlanc, Michael Mikulasovich, Angela Scalise, Deepa Manwani, Vesna Najfeld, Alla Keyzner
Publikováno v:
Cancer Genetics and Cytogenetics. 188:83-87
We report on two patients with complicons resulting in duplication der(21)t(8;21)(q22;q22), triplication in the form of isochromosome of der(21)t(8;21), and four copies of ETO-AML1 fusion. Duplication of der(21) was present at diagnosis as a minor ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aee39ee0ebdd999b222d781cdd834b37
https://doi.org/10.1016/j.cancergencyto.2008.10.004
https://doi.org/10.1016/j.cancergencyto.2008.10.004
Publikováno v:
British Journal of Haematology. 85:627-630
Summary. Patients with Fanconi's anaemia (FA) have aplastic anaemia, leukaemia, myelodysplasia and tumours. Since leukaemia has a very poor prognosis, it is desirable to identify high-risk patients. To determine the significance of clonal marrow chro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db2c1da456b9d0a6a98ef20fcbb9eed4
https://doi.org/10.1111/j.1365-2141.1993.tb03362.x
https://doi.org/10.1111/j.1365-2141.1993.tb03362.x
Publikováno v:
Cancer Genetics and Cytogenetics. 105:193-197
Dual-color interphase fluorescence in situ hybridization (I-FISH) for chromosomes 7 and 8 was studied retrospectively on 32 patients with suspected lymphoid disorders, and the results were compared with standard cytogenetics. One of 29 (3.4%) patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81ce5172156f599e352b177732fc4641
https://doi.org/10.1016/s0165-4608(98)00021-1
https://doi.org/10.1016/s0165-4608(98)00021-1
Publikováno v:
Acta haematologica. 133(1)
We describe a patient with acute myeloid leukemia (AML) who had a normal karyotype at diagnosis and was negative for NPM1 and FLT3 mutations, but had a KIT G565V mutation in exon 11. This has not been described previously in AML. The patient received
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ee3175718dae2aa46c3d5e0815f0ee27
https://pubmed.ncbi.nlm.nih.gov/24968822
https://pubmed.ncbi.nlm.nih.gov/24968822
Autor:
Edward P. Ambinder, Samuel Waxman, Angela Scalise, Gloria Fernandez, Alex Chen, Vesna Najfeld
Publikováno v:
Genes, Chromosomes and Cancer. 10:15-25
Variants of the t(15;17)(q22;q12-q21) chromosomal rearrangement associated with acute promyelocytic leukemia (APL) have been previously described and they frequently involve either chromosome 15 and/or 17. Previously we reported a rare variant t(11;1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0512fab9f77934fd6bf7f674cbc0b793
https://doi.org/10.1002/gcc.2870100104
https://doi.org/10.1002/gcc.2870100104
Autor:
Ronald Hoffman, Richard T. Silver, Steven M. Fruchtman, Vesna Najfeld, Joseph Tripodi, Angela Scalise, Lewis R. Silverman
Publikováno v:
British journal of haematology. 151(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbe58ee7bd89b1b9e9751e60c978ab98
https://pubmed.ncbi.nlm.nih.gov/20738298
https://pubmed.ncbi.nlm.nih.gov/20738298
Autor:
Debra Hoops, Martina Kautz, Anna Jones, Elizabeth Van Winkle, Sarah Jackson, Kelly Trauschke, Christina Roth, Leah Whaley, Deborah Cato, Angela Scalise, Susan DeGhelder, Nicole Mauton, Patrice Roberts
Publikováno v:
MCN. The American journal of maternal child nursing. 35(5)
PURPOSE To determine the (1) incidence of peripheral blood glucose (PBG < 40 mg/dL) in infants within 2 hours of birth and (2) validity of using maternal and infant risk factors and/or infant signs/symptoms of hypoglycemia as a screen for PBG < 40 mg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67bd3542cc52b1d85fe10d5e62e727a6
https://pubmed.ncbi.nlm.nih.gov/20737660
https://pubmed.ncbi.nlm.nih.gov/20737660
Autor:
Eva Perdahl-Wallace, Vesna Najfeld, Chris Theodossiou, Lewis B. Silverman, Angela Scalise, Kevin Troy
Publikováno v:
Cancer Genetics and Cytogenetics. 63:89-94
We report three patients with acute lymphoblastic leukemia with biphenotypic and early progenitor phenotype who had del(5q). In the first patient, the del(5q) was the sole abnormality; in the second patient, the del(5q) was interpreted as subclonal e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76aa46b689ed16bc184a062820edb0b3
https://doi.org/10.1016/0165-4608(92)90385-l
https://doi.org/10.1016/0165-4608(92)90385-l