Výsledky vyhledávání - "Vaidas Dirsė"

Akademický článek

Case Report: Specific ABL-Inhibitor Imatinib Is an Effective Targeted Agent as the First Line Therapy to Treat B-Cell Acute Lymphoblastic Leukemia With a Cryptic NUP214::ABL1 Gene Fusion

Autor: Egle Stukaite-Ruibiene, Rimvydas Norvilas, Vaidas Dirse, Sigita Stankeviciene, Goda Elizabeta Vaitkeviciene

Publikováno v: Pathology and Oncology Research, Vol 28 (2022)

Acute lymphoblastic leukemia (ALL) with recurrent genetic lesions, affecting a series of kinase genes, is associated with unfavorable prognosis, however, it could benefit from treatment with tyrosine kinase inhibitors (TKI). NUP214::ABL1 fusion is de

Externí odkaz: https://doaj.org/article/00a6120b7306425192ee15a1d80d6ea6

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Akademický článek

Transient abnormal myelopoiesis without constitutional Down syndrome

Autor: Igne Kairiene, Vaidas Dirse, Ugnius Mickys, Audrone Muleviciene, Paresh Vyas, Jelena Rascon

Publikováno v: Journal of Pediatric and Neonatal Individualized Medicine, Vol 9, Iss 1, Pp e090104-e090104 (2019)

Transient abnormal myelopoiesis (TAM) is a unique entity that usually occurs in children with Down syndrome (DS) or with trisomy 21 mosaicism. The somatic GATA1 mutation is a distinct feature of TAM. At presentation, TAM can resemble congenital leuke

Externí odkaz: https://doaj.org/article/6f1934676fe04acbbe7e36199287627e

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Akademický článek

A De Novo 8q22.2q22.3 Interstitial Microdeletion in a Girl with Developmental Delay and Congenital Defects

Autor: Ruta Kalinauskiene, Deimante Brazdziunaite, Neringa Burokiene, Vaidas Dirsė, Ausra Morkuniene, Algirdas Utkus, Egle Preiksaitiene

Publikováno v: Medicina, Vol 59, Iss 6, p 1156 (2023)

Background and Objectives: Only nine patients with interstitial de novo 8q22.2q22.3 microdeletions have been reported to date. The objective of this report is to present clinical features of a new patient with an 8q22.2q22.3 microdeletion, to compare

Externí odkaz: https://doaj.org/article/9936e2dd6d854ace8ef28e27b9c30d37

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Akademický článek

Multiple Myeloma Immunophenotype Related to Chromosomal Abnormalities Used in Risk Assessment

Autor: Mantas Radzevičius, Vaidas Dirsė, Indrė Klimienė, Rėda Matuzevičienė, Zita Aušrelė Kučinskienė, Valdas Pečeliūnas

Publikováno v: Diagnostics, Vol 12, Iss 9, p 2049 (2022)

(1) Background: At diagnosis, multiplemyeloma risk estimation includes disease burden, end-organ damage, and biomarkers, with increasing emphasis on genetic abnormalities. Multicolor flow cytometry (MFC) is not always considered in risk estimation. W

Externí odkaz: https://doaj.org/article/6fc3aa19b06c41fa86670c3872aaea2d

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Akademický článek

Report of Jacobsen syndrome with a mild facial dysmorphism, severe hearing impairment and thrombocytopenia

Autor: Vaidas DIRSĖ, Loreta CIMBALISTIENĖ, Jūratė KASNAUSKIENĖ, Vaidutis KUČINSKAS

Publikováno v: Acta Medica Lituanica, Vol 19, Iss 1 (2012)

Background. Jacobsen syndrome is a rare syndrome with variable phenotypic expression depending on the breakpoints and the size of 11q deletion. There is presented a wide range of phenotypes of varying severity. Detailed molecular cytogenetic analysis

Externí odkaz: https://doaj.org/article/67ffe38349c54c5bba04e9760a58a9e6

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Opposite chromosome constitutions due to a familial translocation t(1;21)(q43;q22) in 2 cousins with development delay and congenital anomalies: a case report

Autor: Vaidas Dirsė, Violeta Mikštienė, Birutė Burnytė, Beata Aleksiūnienė, Aušra Matulevičienė, Vaidutis Kučinskas, Natalija Krasovskaja, Laima Ambrozaitytė, Algirdas Utkus, Rugilė Matulevičiūtė

Publikováno v: Medicine (Baltimore), Philadelphia : Lippincott Williams & Wilkins, 2017, Vol. 96, no 16, Art. no e6521 [p. 1-6]
Medicine

Supplemental Digital Content is available in the text
Rationale: Chromosomal rearrangements are the major cause of multiple congenital abnormalities and intellectual disability. Patient concerns and diagnosis: We report 2 first cousins with unba

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b00cc883e0ac490aeb54581274199ae1
https://repository.vu.lt/VU:ELABAPDB23024010&prefLang=en_US