Poorly differentiated chordoma with SMARCB1/INI1 loss: a distinct molecular entity with dismal prognosis-Reference-Cited by-同舟云学术

Poorly differentiated chordoma with SMARCB1/INI1 loss: a distinct molecular entity with dismal prognosis

Published:2016-04-11 Issue:1 Volume:132 Page:149-151
ISSN:0001-6322
Container-title:Acta Neuropathologica
language:en
Short-container-title:Acta Neuropathol

Author:

Hasselblatt Martin,Thomas Christian,Hovestadt Volker,Schrimpf Daniel,Johann Pascal,Bens Susanne,Oyen Florian,Peetz-Dienhart Susanne,Crede Yvonne,Wefers Annika,Vogel Hannes,Riemenschneider Markus J.,Antonelli Manila,Giangaspero Felice,Bernardo Marie Christine,Giannini Caterina,Ud Din Nasir,Perry Arie,Keyvani Kathy,van Landeghem Frank,Sumerauer David,Hauser Peter,Capper David,Korshunov Andrey,Jones David T. W.,Pfister Stefan M.,Schneppenheim Reinhard,Siebert Reiner,Frühwald Michael C.,Kool Marcel

Funder

IZKF Münster

KinderKrebsInitiative Buchholz Holm-Seppensen.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Clinical Neurology,Pathology and Forensic Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00401-016-1574-9.pdf

Reference10 articles.

1. Chavez JA, Din NU, Memon A et al (2014) Anaplastic chordoma with loss of INI1 and brachyury expression in a 2-year-old girl. Clin Neuropathol 33:418–420

2. Hoch BL, Nielsen GP, Liebsch NJ et al (2006) Base of skull chordomas in children and adolescents: a clinicopathologic study of 73 cases. Am J Surg Pathol 30:811–818