Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Barbara Kocsis-Deák"'
Autor:
András Kiss, Balázs Szili, Bence Bakos, Richárd Ármós, Zsuzsanna Putz, Kristóf Árvai, Barbara Kocsis-Deák, Bálint Tobiás, Bernadett Balla, Henriett Pikó, Magdolna Dank, János Pál Kósa, István Takács, Péter Lakatos
Publikováno v:
BMC Endocrine Disorders, Vol 23, Iss 1, Pp 1-7 (2023)
Abstract Context Increasing diagnostic sensitivity in the detection of thyroid cancer has led to uncertainties in the optimal surgical approach of the smaller, low risk tumors. Current ATA guidelines consider lobectomy safe between 1 and 4 cm, while
Externí odkaz:
https://doaj.org/article/57d40bdc27c541269c8ce4d36df9c8ef
Autor:
Bernadett Balla, János P. Kósa, Gabriella Győri, Balázs Járay, Eszter Székely, Peter L. Lakatos, Barbara Kocsis-Deák, Kristóf Árvai, Bálint Tobiás, János Podani
Publikováno v:
Orvosi Hetilap. 160:1417-1425
Abstract: Introduction: Twenty-five percent of fine-needle aspiration biopsy samples of thyroid nodules produce indeterminate cytological results. Genetic testing of nodules can contribute to accurate diagnosis. Aim: Developing the first gene panel i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2bd51ea5b05011776faa3bb46667e37d
https://doi.org/10.1556/650.2019.31492
https://doi.org/10.1556/650.2019.31492
Autor:
Barbara, Kocsis-Deák, Bernadett, Balla, Kristóf, Árvai, Bálint, Tobiás, Gabriella, Győri, Balázs, Járay, Eszter, Székely, János, Podani, János, Kósa, Péter, Lakatos
Publikováno v:
Orvosi hetilap. 160(36)
Absztrakt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::65458a42bd9161bebf7e1725f4d90606
https://pubmed.ncbi.nlm.nih.gov/31492087
https://pubmed.ncbi.nlm.nih.gov/31492087
Autor:
János Podani, Andrea Kohánka, Bálint Tobiás, Balázs Járay, Bernadett Balla, Zsuzsanna Putz, István Takács, Peter L. Lakatos, Kristóf Árvai, János P. Kósa, János Horányi, Barbara Kocsis-Deák
Publikováno v:
Pathology Oncology Research
Nowadays, the complementary diagnostics based on the suspicious thyroid lesion specific mutational state analysis is indispensable in the clinical practice. We aimed to test and validate our novel 568-mutational hotspot panel (23 cancer-related genes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f007e9d94ad9c6d3022db5af68e93ac4
https://pubmed.ncbi.nlm.nih.gov/31758407
https://pubmed.ncbi.nlm.nih.gov/31758407
Autor:
Peter L. Lakatos, Bernadett Balla, János P. Kósa, István Takács, Kristóf Árvai, Barbara Kocsis-Deák, Bálint Tobiás
Publikováno v:
Magyar Tudomány.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84eb7a00438fdf9bfa3d54cc411902c1
https://doi.org/10.1556/2065.180.2019.5.4
https://doi.org/10.1556/2065.180.2019.5.4
Autor:
Peter L. Lakatos, István Takács, Bernadett Balla, Kristóf Árvai, Bálint Tobiás, János P. Kósa, Barbara Kocsis-Deák
Publikováno v:
Magyar Tudomány.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42c2cbae5c0cb69fa00ee595ec9be8e3
https://doi.org/10.1556/2065.180.2019.5.6
https://doi.org/10.1556/2065.180.2019.5.6
Autor:
Zsolt Liposits, Miklós Sárvári, Bernadett Balla, Peter L. Lakatos, Barbara Kocsis-Deák, János P. Kósa, Bálint Tobiás, István Takács, Kristóf Árvai, János Podani
Publikováno v:
The Journal of steroid biochemistry and molecular biology. 188
Gonadal hormones including 17β-estradiol exert important protective functions in skeletal homeostasis. However, numerous details of ovarian hormone deficiency in the common bone marrow microenvironment have not yet been revealed and little informati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92e7e93ce1366b4ca23828864d5506d9
https://pubmed.ncbi.nlm.nih.gov/30685384
https://pubmed.ncbi.nlm.nih.gov/30685384
Autor:
Barbara Kocsis-Deák, Edina Nemes, Adrienn Sulák, Piroska Dósa, Nikoletta Nagy, Andrea Drubi, Márta Széll, Katalin Farkas, Lakatos Ferenc, Kornélia Tripolszki
Publikováno v:
Archives of Dermatological Research. 307:891-895
LEOPARD syndrome (LS, OMIM 151100) is a rare monogenic disorder. The name is an acronym of its major features such as multiple lentigines, electrocardiographic conduction defects, ocular hypertelorism, pulmonary stenosis, abnormalities of genitalia,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7f2e44ebbd651f81e8f837a5c195b83
https://doi.org/10.1007/s00403-015-1597-4
https://doi.org/10.1007/s00403-015-1597-4
Autor:
Péter Lakatos, Bernadett Balla, Bálint Tobiás, Balázs Járay, János P. Kósa, Tamás Székely, Andrea Kövesdi, Barbara Kocsis-Deák, János Horányi, Kristóf Árvai
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33687ccadc1666b38033296c5faf208d
https://doi.org/10.1530/endoabs.49.ep1434
https://doi.org/10.1530/endoabs.49.ep1434
Autor:
Barbara Kocsis Deák, Juan José Vilata Corell, Alfredo Montoro Botella, Katalin Farkas, Raquel Rodriguez Lopez, Goitzane Marcaida Benito, Joan N.R. Kromosoeto, Ans M.W. van den Ouweland, Tomas Vanecek, Ana Mercedes Victoria Martínez, Nikoletta Nagy, Márta Széll, Laura Cubells Sánchez, Dmitry V. Kazakov, János Varga
Publikováno v:
BMC Genetics
BMC Genetics, 17:36. BioMed Central Ltd.
BMC Genetics, 17:36. BioMed Central Ltd.
Background Multiple familial trichoepithelioma type 1 (MFT1; MIM 601606), a rare monogenic skin disease with autosomal dominant inheritance, is characterized by the development of multiple skin-colored papules on the central area of the face, frequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b9b261edf57f643665b7528c551a51f
https://pubmed.ncbi.nlm.nih.gov/26861065
https://pubmed.ncbi.nlm.nih.gov/26861065