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Approximately 17% of these patients were children and adolescents, and the median age at diagnosis was 34 years.[4] In addition, in the Children's Oncology Group (COG) ARST0332 (NCT00346164) and European paediatric Soft Tissue Sarcoma Study Group (EpSSG) 2005 protocols, synovial sarcoma was the single most common histological subtype.[5] Clinical presentation The most common primary tumor location is the extremities, followed by trunk and head and neck.[4] Rarely, a synovial sarcoma may arise in the heart or pericardium or appear with a pleuropulmonary presentation.[6-9] The most common site of metastasis is the lung.[10,11] The risk of metastases is highly influenced by tumor size

Merceron TK, Burt M, Seol Y-J, Kang H-W, Lee SJ, Yoo JJ, Atala A (2015) A 3D bioprinted complex structure for engineering the muscletendon unit

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A summary of their properties is presented in Table 26.1 (located at the end of the chapter)

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J Nutr 121 : 12431249 Whitin JC, Tham DM, Bhamre S, Ornt DB, Scandling JD, Tune BM, Salvatierra O, Avissar N, Cohen HJ 1998 Plasma glutathione peroxidase and its relationship to renal proximal tubule function