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Akademický článek

Expression patterns and clinical implications of PDL1 and DLL3 biomarkers in small cell lung cancer retrospectively studied: Insights for therapeutic strategies and survival prediction

Autor: Kalliopi Domvri, Alexey V. Yaremenko, Apostolos Apostolopoulos, Savvas Petanidis, Sofia Karachrysafi, Nikoleta Pastelli, Theodora Papamitsou, Styliani Papaemmanouil, Sofia Lampaki, Konstantinos Porpodis

Publikováno v: Heliyon, Vol 10, Iss 5, Pp e27208- (2024)

Lung cancer is a leading cause of cancer-related deaths globally, includes small cell lung cancer (SCLC), characterized by its aggressive nature and advanced disease at diagnosis. However, the identification of reliable biomarkers for SCLC has proven

Externí odkaz: https://doaj.org/article/f9d8f32ee6e946239b98fbc6f2a726f2

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Akademický článek

Lung cancer as a predominant feature in a patient with Peutz–Jeghers syndrome: Case report

Autor: Florentia Fostira, Elena Fountzilas, Kyriaki Papadopoulou, Theodoros Karaiskos, Ourania Mpatsi, Nikoleta Pastelli, Giannis Mountzios, Irene Konstantopoulou, George Fountzilas

Publikováno v: Thoracic Cancer, Vol 13, Iss 12, Pp 1862-1865 (2022)

Abstract Peutz–Jeghers syndrome (PJS) is characterized by mucocutaneous pigmentation and gastrointestinal hamartomatous polyposis, which can lead to intussusception. PJS patients face high lifetime risks for various cancer types, with the majority

Externí odkaz: https://doaj.org/article/69142dbae79042e9a9b4308f11c0ab9e

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Akademický článek

An Observational Study to Assess the Molecular Epidemiology and Direct Medical Costs of Epidermal Growth Factor Receptor (EGFR) Mutations in Patients with Advanced EGFR Mutation-Positive Non-Small Cell Lung Cancer Treated with Afatinib in Real-World Clinical Settings in Greece

Publikováno v: Lung Cancer: Targets and Therapy, Vol Volume 12, Pp 93-102 (2021)

Giannis Mountzios,1 Sofia Lampaki,2 Georgia-Angeliki Koliou,3 Athanassios Vozikis,4 Ioannis Kontogiorgos,4 Panagiotis Papantoniou,4 Margarita-Ioanna Koufaki,4 Eleni Res,5 Anastasios Boutis,6 Athina Christopoulou,7 Nicoleta Pastelli,8 Anastasios Griva

Externí odkaz: https://doaj.org/article/6a71618649294982a297524620b76668

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Akademický článek

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Akademický článek

COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect?

Autor: Konstantinos Voskarides, Gregory Papagregoriou, Despina Hadjipanagi, Ioanelli Petrou, Isavella Savva, Avraam Elia, Yiannis Athanasiou, Androulla Pastelli, Maria Kkolou, Michalis Hadjigavriel, Christoforos Stavrou, Alkis Pierides, Constantinos Deltas

Publikováno v: BMC Nephrology, Vol 19, Iss 1, Pp 1-8 (2018)

Abstract Background About 40–50% of patients with familial microscopic hematuria (FMH) caused by thin basement membrane nephropathy (TBMN) inherit heterozygous mutations in collagen IV genes (COL4A3, COL4A4). On long follow-up, the full phenotypic

Externí odkaz: https://doaj.org/article/60ea5110388c4002b20d58a5ee9ce72a

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Thyroglossal duct cysts: experience from a series of cases treated in the Oral and Maxillofacial Surgery Clinic of General Hospital 'G.Papanikolaou’’ in Thessaloniki, Greece

Autor: Theodoros Grivas, Ioannis Pappas, Nikoleta Pastelli, James Philip Skliris, Konstantinos Paraskevopoulos, Konstantinos Vaxtsevanos

Publikováno v: Hellenic Archives of Oral & Maxillofacial Surgery. 24

SUMMARY: Thyroglossal duct cyst is the most common swelling of fetal origin in the cervix, located predominantly in the frontal neck area. The prevalence of the disease is 7%, while in bibliography there is some controversy regarding the age of diagn

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4e314f47f204bb492389ff500974e1cc
https://doi.org/10.54936/haoms2411524

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