Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Inga Melbārde-Gorkuša"'
Autor:
Ella R. Thompson, Michelle Wong-Brown, Simone M. Rowley, Susan Dooley, Na Lil, Michael Hipwell, Simone McInerny, Cliff Meldrum, Lisa Devereux, David Mossman, Alison H. Trainer, Briar-Rose Millar, Gillian Mitchell, Cate Smith, Paul A. James, Ian G. Campbell, Rodney J. Scott, Katarzyna Klonowska, Anna Jakubowska, Jelena Maksimenko, Arvids Irmejs, Miki Nakazawa-Miklasevica, Inga Melbarde-Gorkusa, Genadijs Trofimovics, Janis Gardovskis, Edvins Miklasevics, Karolina Tęcza, Jolanta Pamuła-Piłat, Joanna Łanuszewska, Ewa Grzybowska, M. Szwiec, J. Tomiczek-Szwiec, M. Gełej, C. Cybulski, T. Huzarski, E. Kilar, Małgorzata Oczko-Wojciechowska, Michał Świerniak, Jolanta Krajewska, Małgorzata Kowalska, Tomasz Tyszkiewicz, Agnieszka Pawlaczek, Michał Jarząb, Monika Kowal, Dagmara Rusinek, Jadwiga Zebracka-Gala, Agnieszka Czarniecka, Barbara Jarzab, Andrzej Plawski, Paweł Borun, Joanna Szczepinska, Monika Siolek, Beata Kozak-Klonowska, Katarzyna Kaczmarek, Magdalena Muszyńska, Wojciech Marciniak, Grzegorz Sukiennicki, Marcin Lener, Katarzyna Durda, Katarzyna Jaworska-Bieniek, Tomasz Gromowski, Tomasz Huzarski, Tomasz Byrski, Jacek Gronwald, Oleg Oszurek, Cezary Cybulski, Tadeusz Dębniak, Antoni Morawski, Jan Lubiński, Michał Post
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 15, Iss S1, Pp 1-5 (2017)
Externí odkaz:
https://doaj.org/article/959ca802658e4fe59a0522035180cc7e
Autor:
Liāna Švampāne, Viesturs Boka, Jānis Gardovskis, Viktors Borosenko, Arvīds Irmejs, Edvīns Miklaševičs, Ilze Strumfa, Signe Subatniece, Inga Melbārde-Gorkuša, Aldis Puķītis, Genādijs Trofimovičs, Jekaterina Žestkova, Andrejs Vanags, Andris Ābele, Aiga Stāka, Karina Aksenoka, Marianna Bitiņa, Andris Gardovskis, Laima Tihomirova, Dace Bērziņa, E. Vjaters
Publikováno v:
Proceedings of the Latvian Academy of Sciences. Section B, Natural Sciences, Vol 63, Iss 4-5, Pp 131-140 (2009)
Epidemiological, Clinical, Molecular Features and Early Detection Strategy of Most Frequent Hereditary Cancers in Latvia The aim of the study was to determine epidemiological, clinical and molecular features of hereditary breast-ovarian, colorectal,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f6b829f350569129fc381610fdcf184
https://doaj.org/article/2a64b55a02be47728699ec900f3cc520
https://doaj.org/article/2a64b55a02be47728699ec900f3cc520
Autor:
Genādijs Trofimovičs, Jānis Gardovskis, Dace Bērziņa, Andris Gardovskis, Edvīns Miklaševičs, Signe Subatniece, Arvīds Irmejs, Arnis Āboliņš, Ilze Strumfa, Inga Melbārde-Gorkuša
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 10, Iss 1, p 5 (2012)
Hereditary Cancer in Clinical Practice
Hereditary Cancer in Clinical Practice
We would like to present a patient with a classical phenotype of a rare disorder - Cowden syndrome, its diagnostics and management challenges. A breast surgeon has to be aware of this rare condition when treating a patient with breast manifestations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3624e918b100be87ea7e2fc1fad48e4e
http://www.hccpjournal.com/content/10/1/5
http://www.hccpjournal.com/content/10/1/5