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pro vyhledávání: '"rhabdoid tumour predisposition syndrome"'
Akademický článek
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Autor:
J. L. J. M. Teepen, Cees C. Tijssen, M P W A Houben, A. C. J. Ammerlaan, Theo J. M. Hulsebos, Pieter Wesseling, A Ararou, Frank Baas
Publikováno v:
British journal of cancer, 98(2), 474-479. Nature Publishing Group
British Journal of Cancer, 98, 2, pp. 474-9
British Journal of Cancer, 98, 474-9
British Journal of Cancer
British Journal of Cancer, 98, 2, pp. 474-9
British Journal of Cancer, 98, 474-9
British Journal of Cancer
Item does not contain fulltext Rhabdoid tumour predisposition syndrome (RTPS) is a rare syndrome caused by inheritance of a mutated INI1 gene for which only two multigeneration families have been reported. To further characterise the genotype and phe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39feb5f246e8a963472f7a03c4dd451e
https://pure.amc.nl/en/publications/longterm-survival-and-transmission-of-ini1mutation-via-nonpenetrant-males-in-a-family-with-rhabdoid-tumour-predisposition-syndrome(37a4697b-80eb-4be4-a195-e7844d47744f).html
https://pure.amc.nl/en/publications/longterm-survival-and-transmission-of-ini1mutation-via-nonpenetrant-males-in-a-family-with-rhabdoid-tumour-predisposition-syndrome(37a4697b-80eb-4be4-a195-e7844d47744f).html
Rhabdoid tumour predisposition syndrome (RTPS) is a rare syndrome caused by inheritance of a mutated INI1 gene for which only two multigeneration families have been reported. To further characterise the genotype and phenotype of RTPS, we present a th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dris___00902::50cfa31fa5bfcb3eecb18f885e4d1ed1
Publikováno v:
WHO/IARC Classification of Tumours; 2021, Vol. 6, p460-461, 2p
Autor:
Biswas, Ahitagni1 (AUTHOR) dr_ahitagni@yahoo.co.in, Ramdulari, Anjali V.1 (AUTHOR), Thakur, Alok1 (AUTHOR), Kumar, Amandeep2 (AUTHOR), G. S., Anju3 (AUTHOR), Jana, Manisha4 (AUTHOR), Suri, Vaishali3 (AUTHOR)
Publikováno v:
British Journal of Neurosurgery. Aug2024, Vol. 38 Issue 4, p978-982. 5p.
Autor:
Marques, Thamires Coutinho, Costa, Rangel de Sousa, de Souza, Simone Rachid, Corrêa, Diogo Goulart
Publikováno v:
Child's Nervous System; Aug2022, Vol. 38 Issue 8, p1429-1432, 4p
Autor:
Witkowski, Leora, Lalonde, Emilie, Zhang, Jian, Albrecht, Steffen, Hamel, Nancy, Cavallone, Luca, May, Sandra Thompson, Nicholson, James C, Coleman, Nicholas, Murray, Matthew J, Tauber, Peter F, Huntsman, David G, Schönberger, Stefan, Yandell, David, Hasselblatt, Martin, Tischkowitz, Marc D, Majewski, Jacek, Foulkes, William D
Publikováno v:
Journal of Pathology; Sep2013, Vol. 231 Issue 1, p35-43, 9p
Autor:
Piccardo, Arnoldo1 (AUTHOR), Albert, Nathalie L.2 (AUTHOR), Borgwardt, Lise3 (AUTHOR), Fahey, Frederic H.4 (AUTHOR), Hargrave, Darren5 (AUTHOR), Galldiks, Norbert6,7 (AUTHOR), Jehanno, Nina8 (AUTHOR), Kurch, Lars9 (AUTHOR) lars.kurch@medizin.uni-leipzig.de, Law, Ian3 (AUTHOR), Lim, Ruth10 (AUTHOR), Lopci, Egesta11 (AUTHOR), Marner, Lisbeth12 (AUTHOR), Morana, Giovanni13 (AUTHOR), Young Poussaint, Tina4 (AUTHOR), Seghers, Victor J.14,15 (AUTHOR), Shulkin, Barry L.16 (AUTHOR), Warren, Katherine E.17 (AUTHOR), Traub-Weidinger, Tatjana18 (AUTHOR), Zucchetta, Pietro19 (AUTHOR)
Publikováno v:
European Journal of Nuclear Medicine & Molecular Imaging. Sep2022, Vol. 49 Issue 11, p3852-3869. 18p. 4 Charts.
Autor:
SOYLEMEZOGLU, Figen1, OZ, Buge2, EGILMEZ, Reyhan3, PEKMEZCI, Melike4, BOZKURT, Suheyla5, ERSEN DANYELI, Ayca6, ONGURU, Onder7, KULAC, Ibrahim8, TIHAN, Tarik4,8
Publikováno v:
Turkish Journal of Pathology. Sep2022, Vol. 38 Issue 3, p185-204. 20p.
Autor:
Katsumi, Yoshiki1,2 (AUTHOR), Iehara, Tomoko1 (AUTHOR), Kuwahara, Yasumichi3 (AUTHOR), Tsuchiya, Kunihiko1 (AUTHOR), Konishi, Eiichi4 (AUTHOR), Hosoi, Hajime1,5 (AUTHOR)
Publikováno v:
Pediatric Hematology & Oncology. Apr2022, Vol. 39 Issue 3, p278-285. 8p.