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pro vyhledávání: '"Anastasiadou, Violetta C."'
Akademický článek
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Akademický článek
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Autor:
Hendricks, Linda A J, Hoogerbrugge, Nicoline, Mensenkamp, Arjen R, Brunet, Joan, Lleuger-Pujol, Roser, Høberg-Vetti, Hildegunn, Haavind, Marianne Tveit, Innella, Giovanni, Turchetti, Daniela, Aretz, Stefan, Spier, Isabel, Tischkowitz, Marc, Jahn, Arne, Links, Thera P, Olderode-Berends, Maran J W, Blatnik, Ana, Leter, Edward M, Evans, D Gareth, Woodward, Emma R, Steinke-Lange, Verena, Anastasiadou, Violetta C, Colas, Chrystelle, Villy, Marie-Charlotte, Benusiglio, Patrick R, Gerasimenko, Anna, Barili, Valeria, Branchaud, Maud, Houdayer, Claude, Tesi, Bianca, Yazicioglu, M Omer, van der Post, Rachel S, Schuurs-Hoeijmakers, Janneke H M, Vos, Janet R
Publikováno v:
Journal of the National Cancer Institute. Oxford University Press
Journal of the National Cancer Institute, 115(1), 93-103. Oxford University Press
Journal of the National Cancer Institute, 115, 93-103
Journal of the National Cancer Institute, 115, 1, pp. 93-103
PTEN Study Group 2023, ' Cancer risks by sex and variant type in PTEN hamartoma tumor syndrome ', Journal of the National Cancer Institute, vol. 115, no. 1, pp. 93-103 . https://doi.org/10.1093/jnci/djac188
Journal of the National Cancer Institute, 115(1), 93-103. Oxford University Press
Journal of the National Cancer Institute, 115, 93-103
Journal of the National Cancer Institute, 115, 1, pp. 93-103
PTEN Study Group 2023, ' Cancer risks by sex and variant type in PTEN hamartoma tumor syndrome ', Journal of the National Cancer Institute, vol. 115, no. 1, pp. 93-103 . https://doi.org/10.1093/jnci/djac188
Background PTEN Hamartoma Tumor Syndrome (PHTS) is a rare syndrome with a broad phenotypic spectrum, including increased risks of breast (BC, 67%-78% at age 60 years), endometrial (EC, 19%-28%), and thyroid cancer (TC, 6%-38%). Current risks are like
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15488006c0a9820b2ccee609e3f8a26c
https://cris.maastrichtuniversity.nl/en/publications/f3630f3a-f3af-4c92-9bd4-b59efd9de145
https://cris.maastrichtuniversity.nl/en/publications/f3630f3a-f3af-4c92-9bd4-b59efd9de145
Autor:
Hendricks, Linda AJ, Hoogerbrugge, Nicoline, Mensenkamp, Arjen R, Brunet, Joan, Lleuger-Pujol, Roser, Høberg-Vetti, Hildegunn, Tveit Haavind, Marianne, Innella, Giovanni, Turchetti, Daniela, Aretz, Stefan, Spier, Isabel, Tischkowitz, Marc, Jahn, Arne, Links, Thera P, Olderode-Berends, Maran JW, Blatnik, Ana, Leter, Edward M, Evans, D Gareth, Woodward, Emma R, Steinke-Lange, Verena, Anastasiadou, Violetta C, Colas, Chrystelle, Villy, Marie-Charlotte, Benusiglio, Patrick R, Gerasimenko, Anna, Barili, Valeria, Branchaud, Maud, Houdayer, Claude, Tesi, Bianca, Yazicioglu, M Omer, Van Der Post, Rachel S, Schuurs-Hoeijmakers, Janneke HM, PTEN Study Group, Vos, Janet R
BACKGROUND: PTEN Hamartoma Tumor Syndrome (PHTS) is a rare syndrome with a broad phenotypic spectrum, including increased risks of breast (BC, 67%-78% at age 60 years), endometrial (EC, 19%-28%), and thyroid cancer (TC, 6%-38%). Current risks are lik
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03ef2fcf51863a4dd3f21bc8fa1ac7b2
Akademický článek
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Autor:
Neocleous, Vassos, Skordis, Nicos A., Portides, George, Efstathiou, Elisavet, Costi, Constantina Eleni, Ioannou, N., Pantzaris, Marios C., Anastasiadou, Violetta C., Constantinou-Deltas, Constantinos D., Phylactou, Leonidas A.
Publikováno v:
Journal of endocrinological investigation
J.Endocrinol.Invest.
J.Endocrinol.Invest.
Background: RET germline mutations predispose to the development of inherited cancer syndrome multiple endocrine neoplasia type 2 (MEN2). Several variants of the RET proto-oncogene including G691S and S904S have been suggested to act as genetic modif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4485::9d0934d8e60ed8fe874c05d5d00fa872
http://gnosis.library.ucy.ac.cy/handle/7/53268
http://gnosis.library.ucy.ac.cy/handle/7/53268
Autor:
Patsalis, Philippos C., Sismani, Carolina, Hadjimarcou, Michael I., Rose, Nancy C., Stylianidou, Goula, Koukoulli, R., Anastasiadou, Violetta C., Constantinou-Deltas, Constantinos D., Middleton, Lefkos T.
Publikováno v:
Genetic Counseling
Genet.Couns.
Genet.Couns.
The aim of this program was to investigate the patients with Mental Retardation Of Unknown Etiology (MROUE), on the island of Cyprus. The MROUE patients were examined cytogenetically for gross chromosomal abnormalities, and by molecular methods for t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4485::c0aef8c535bd5671beaec837b88b7a61
http://gnosis.library.ucy.ac.cy/handle/7/53294
http://gnosis.library.ucy.ac.cy/handle/7/53294
Autor:
Koufaris, Costas, Papagregoriou, Gregory N., Kousoulidou, Ludmila, Moutafi, Maria, Tauber, Maïthé Thérèse, Jouret, Béatrice, Kieffer, Isabelle, Constantinou-Deltas, Constantinos D., Tanteles, George A., Anastasiadou, Violetta C., Patsalis, Philippos C., Sismani, Carolina
Publikováno v:
Gene
MicroRNA haploinsufficiency has been associated with developmental defects in only a limited number of cases. Here we report a de novo genomic microdeletion that includes the LINGO2 gene as well as two microRNA genes, MIR873 and MIR876, in a patient