Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Lucia, Fröhlichová"'
Autor:
Ivana Večurkovská, Jana Mašlanková, Vladimíra Tomečková, Jana Kaťuchová, Terézia Kisková, Lucia Fröhlichová, Mária Mareková, Marek Stupák
Publikováno v:
Biomedicines, Vol 11, Iss 7, p 1839 (2023)
Purpose: The development of sensitive and non-invasive biomarkers for the early detection of CRC and determination of their role in the individual stages of CRC. Methods: MMP-9 expression in serum and tissue, and BDNF expression in plasma were detect
Externí odkaz:
https://doaj.org/article/c95a586be40b4b33bbad1aa6fa7b6b20
Autor:
Stupák, Ivana Večurkovská, Jana Mašlanková, Vladimíra Tomečková, Jana Kaťuchová, Terézia Kisková, Lucia Fröhlichová, Mária Mareková, Marek
Publikováno v:
Biomedicines; Volume 11; Issue 7; Pages: 1839
Purpose: The development of sensitive and non-invasive biomarkers for the early detection of CRC and determination of their role in the individual stages of CRC. Methods: MMP-9 expression in serum and tissue, and BDNF expression in plasma were detect
Autor:
Daniel Farkaš, Mária Pisarčíková, Peter Vasovčák, Anna Crhová, Alžbeta Ginelliová, Lucia Mistríková, Lucia Fröhlichová, Silvia Farkašová Iannaccone
Publikováno v:
Rechtsmedizin.
Autor:
Reinhard B. Dettmeyer, Jana Šprláková, Dorota Sopková, Lucia Fröhlichová, Radoslav Matěj, Silvia Farkašová Iannaccone, Daniel Farkaš, Alžbeta Ginelliová
Publikováno v:
Rechtsmedizin. 30:190-193
Congenital lobar emphysema (CLE) is a rare congenital lung disorder characterized by hyperinflation and alveolar distention, mostly associated with bronchial cartilage deficiency. This article describes the case of a 5.5-week-old infant with postnata
Autor:
Daniel, Farkaš, Anna, Kružlíková, Jana, Němcová, Vladimír, Hrabovský, Silvia Farkašová, Iannaccone, Alžbeta, Ginelliová, Lucia, Fröhlichová, Marián, Švajdler
Publikováno v:
Ceskoslovenska patologie. 57(3)
In this article, we report the autopsy findings of a 50-year-old immunocompetent woman, who was hospitalized with an altered state of consciousness. Examinations, including cerebrospinal fluid analysis, carried out during hospitalization failed to id
Autor:
Monika Sedivcova, Radim Brabec, Petr Steiner, Tomas Jirasek, Marián Švajdler ml., Petr Grossmann, Jana Engelová, Renata Emmerová, Vladimír Beneš, Lucia Fröhlichová, Tomáš Vaněček
Publikováno v:
Onkologie. 13:87-91
Předkladame připad nasi dlouhodobě sledovane pacientky s radikalně resekovaným, IDH mutovaným glioblastomem s primitivnineuronalni komponentou, ktera s pouze mirnými neurologickými komplikacemi žije již 9 let od stanoveni diagnozy, se zacho
Autor:
Silvia Farkašová, Iannaccone, Peter, Švajdler, Marián, Švajdler, Dorota, Sopková, Ažbeta, Ginelliová, Jana, Šprláková, Miroslava, Petrášová, Lucia, Fröhlichová, Daniel, Farkaš
Publikováno v:
Ceskoslovenska patologie. 57(1)
In this paper, we report autopsy findings of a 1-day old full-term mature female neonate with pulmonary hypoplasia diagnosed postnatally. Death was attributed to acute respiratory failure due to hyaline membrane disease. We describe pathological feat
Autor:
Dorota Sopková, Daniel Farkaš, Lucia Fröhlichová, Silvia Farkašová Iannaccone, Lucia Mistríková, Reinhard B. Dettmeyer, Alžbeta Ginelliová
Publikováno v:
The American journal of forensic medicine and pathology. 42(1)
In this article, we report the autopsy findings of a 48-year-old man who sustained blunt trauma to the thorax. A medical record review revealed no history of cardiac disease. He presented to the hospital with a computed tomography-verified fracture o
Autor:
Silvia Farkašová, Iannaccone, Peter, Švajdler, Dorota, Sopková, Lucia, Fröhlichová, Daniel, Farkaš
Publikováno v:
Ceskoslovenska patologie. 55(4)
Sclerosing mesenteritis is a rare non-cancerous disease affecting the small bowel mesentery, which occurs predominantly in older age. The exact etiology is not known. Clinical symptoms are very variable and they include abdominal pain and distention,
Autor:
Silvia, Iannaccone Farkašová, Peter, Vasovčák, Dorota, Sopková, Mária, Pisarčíková, Marián, Švajdler, Lucia, Fröhlichová, Lucia, Mistríková, Daniel, Farkaš
Publikováno v:
Ceskoslovenska patologie. 55(3)
Neuronal ceroid lipofuscinoses (NCLs) are a group of inherited neurodegenerative disorders with clinical presentation predominantly in the childhood. The NCLs represent lysosomal storage disorders characterized by the accumulation of autofluorescent