Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Irina Kletskaya"'
Autor:
Tatiana Belysheva, Tatiana Nasedkina, Irina Kletskaya, Dana Volchek, Irina Barinova, Vera Semenova, Aida Gadzhigoroeva, Ekaterina Zelenova, Timur Valiev, Elena Sharapova, Anna Michenko, Anastasiia Allenova, Darya Ponomareva
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
Diagnosing skin diseases in children can be a complex interdisciplinary problem. Incontinentia pigmenti (IP), also known as Bloch-Sulzberger syndrome, is a rare hereditary genodermatosis related to a mutation in the IKBKG gene. We present a family ca
Externí odkaz:
https://doaj.org/article/9bbd02d73b2f4b84a40bcec5748a3af4
Autor:
Ekaterina Zelenova, Tatiana Belysheva, Denis Sofronov, Vera Semenova, Galimat Radjabova, Yana Vishnevskaya, Irina Kletskaya, Elena Sharapova, Ivan Karasev, Denis Romanov, Malika Denieva, Nikolay Petrochenko, Timur Valiev, Tatiana Nasedkina
Publikováno v:
Diagnostics, Vol 14, Iss 21, p 2420 (2024)
Background/Objectives: Metastatic colorectal cancer remains a fatal disease, with a 5-year survival rate lower than 15%. The most common metastatic sites are the lungs and the liver, while skin metastases are very rare and often indicate a poor progn
Externí odkaz:
https://doaj.org/article/ef296b6e0db84bb18871ccd3369d29cf
Autor:
Angelica Zin, Rita DeVito, Cláudia M. Salgado, Gianni Bisogno, Vittoria Donofrio, Irina Kletskaya, Rita Alaggio, Marta Garrido, Miguel Reyes-Múgica
Publikováno v:
Pediatric and Developmental Pathology. 23:424-430
Introduction Somatic internal tandem duplication of 3’ of BCOR ( BCOR ITD) has been found in clear cell sarcomas of the kidney (CCSK), soft tissue undifferentiated round cell sarcomas/primitive myxoid mesenchymal tumors of infancy (URCS/PMMTI), and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe88f15864b98783f696c033418c6b1f
https://doi.org/10.1177/1093526620945528
https://doi.org/10.1177/1093526620945528
Autor:
Diana Szilagyi, Petr Blasch, Antonina V. Kalmykova, Dmitry V. Kazakov, Martina Baneckova, Michal Michal, Petr Martinek, Petr Grossmann, Tomas Vanecek, Josef Feit, Irina Kletskaya, Pietro Donati, Isabel Kolm, Michele Donati, Paolo Persichetti, Liubov Kastnerova, Anna Crescenzi, Petr Steiner, Alfonso Baldi
BAP1-inactivated melanocytic tumor (BIMT) is a group of melanocytic neoplasms with epithelioid cell morphology molecularly characterized by the loss of function of BAP1, a tumor suppressor gene located on chromosome 3p21, and a mutually exclusive mit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf84b079bc9e85c59a8e00df1778e7bd
http://hdl.handle.net/11591/470348
http://hdl.handle.net/11591/470348
