Showing results (1-10 of 9) with videos related to
Sort By:
Pageof 1
International Journal of Clinical and Experimental Pathology|July 28, 2010
Enchondromatosis: insights on the different subtypesTwinkal C Pansuriya, Herman M Kroon, Judith V M G BovéeGenes, Chromosomes & Cancer|June 8, 2012
Genetic characterization of mesenchymal, clear cell, and dedifferentiated chondrosarcomaDanielle Meijer, Danielle de Jong, Twinkal C Pansuriya, et al.Plant Physiology|February 29, 2012
Subclassification and biochemical analysis of plant papain-like cysteine proteases displays subfamily-specific characteristicsKerstin H Richau, Farnusch Kaschani, Martijn Verdoes, et al.Genes, Chromosomes & Cancer|May 18, 2011
Maffucci syndrome: a genome-wide analysis using high resolution single nucleotide polymorphism and expression arrays on four casesTwinkal C Pansuriya, Jan Oosting, Suzan H M Verdegaal, et al.Orphanet Journal of Rare Diseases|January 18, 2011
Genome-wide analysis of Ollier disease: Is it all in the genes?Twinkal C Pansuriya, Jan Oosting, Tibor Krenács, et al.The American Journal of Pathology|March 15, 2013
R132C IDH1 mutations are found in spindle cell hemangiomas and not in other vascular tumors or malformationsKyle C Kurek, Twinkal C Pansuriya, Maayke A J H van Ruler, et al.The Oncologist|December 8, 2011
Incidence, predictive factors, and prognosis of chondrosarcoma in patients with Ollier disease and Maffucci syndrome: an international multicenter study of 161 patientsSuzan H M Verdegaal, Judith V M G Bovée, Twinkal C Pansuriya, et al.Plos Genetics|May 3, 2011
Loss-of-function mutations in PTPN11 cause metachondromatosis, but not Ollier disease or Maffucci syndromeMargot E Bowen, Eric D Boyden, Ingrid A Holm, et al.Nature Genetics|November 8, 2011
Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndromeTwinkal C Pansuriya, Ronald van Eijk, Pio d'Adamo, et al.Pageof 1