An analysis of the sensitivity and specificity of MHC-I and MHC-II immunohistochemical staining in muscle biopsies for the diagnosis of inflammatory myopathies by Rodríguez Cruz, Pedro M, Luo, Yue-Bei, Miller, James, Junckerstorff, Reimar C, Mastaglia, Frank L, Fabian, Victoria

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Childhood craniopharyngioma: 20-year institutional experience in Western Australia by Rath, Shoshana R, Lee, Sharon, Kotecha, Rishi S, Taylor, Mandy, Junckerstorff, Reimar C, Choong, Catherine SY

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Chemotherapy Increases Amenability of Surgical Resection in Congenital Glioblastoma by Kotecha, Rishi S., Burley, Katy, Junckerstorff, Reimar C., Lee, Sharon, Phillips, Marianne B., Cole, Catherine H., Gottardo, Nicholas G.

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Pediatric meningioma: current approaches and future direction by Kotecha, Rishi S., Junckerstorff, Reimar C., Lee, Sharon, Cole, Catherine H., Gottardo, Nicholas G.

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Novel CHKB mutation expands the megaconial muscular dystrophy phenotype by Cabrera‐Serrano, Macarena, Junckerstorff, Reimar C., Atkinson, Vanessa, Sivadorai, Padma, Allcock, Richard J., Lamont, Phillipa, Laing, Nigel G.

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Cystinosis distal myopathy, novel clinical, pathological and genetic features by Cabrera-Serrano, Macarena, Junckerstorff, Reimar C, Alisheri, Ali, Pestronk, Alan, Laing, Nigel G, Weihl, Conrad C, Lamont, Phillipa J

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The case for DNA methylation based molecular profiling to improve diagnostic accuracy for central nervous system embryonal tumors (not otherwise specified) in adults by Halliday, Gail C., Junckerstorff, Reimar C., Bentel, Jacqueline M., Miles, Andrew, Jones, David T.W., Hovestadt, Volker, Capper, David, Endersby, Raelene, Cole, Catherine H., van Hagen, Tom, Gottardo, Nicholas G.

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Childhood craniopharyngioma: 20‐year institutional experience in W estern A ustralia by Rath, Shoshana R, Lee, Sharon, Kotecha, Rishi S, Taylor, Mandy, Junckerstorff, Reimar C, Choong, Catherine SY

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Novel CHKB mutation expands the megaconial muscular dystrophy phenotype by Cabrera-Serrano, Macarena, Junckerstorff, Reimar C., Atkinson, Vanessa, Sivadorai, Padma, Allcock, Richard J., Lamont, Phillipa, Laing, Nigel G.

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SMARCA4-mutated atypical teratoid/rhabdoid tumors are associated with inherited germline alterations and poor prognosis by Hasselblatt, Martin, Nagel, Inga, Oyen, Florian, Bartelheim, Kerstin, Russell, Robert B., Schüller, Ulrich, Junckerstorff, Reimar, Rosenblum, Marc, Alassiri, Ali H., Rossi, Sabrina, Schmid, Irene, Gottardo, Nicholas G., Toledano, Helen, Viscardi, Elisabetta, Balbin, Milagros, Witkowski, Leora, Lu, Qianhao, Betts, Matthew J., Foulkes, William D., Siebert, Reiner, Frühwald, Michael C., Schneppenheim, Reinhard

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EPG5-Related Vici Syndrome: A Primary Defect of Autophagic Regulation with an Emerging Phenotype Overlapping with Mitochondrial Disorders by Balasubramaniam, Shanti, Riley, Lisa G., Vasudevan, Anand, Cowley, Mark J., Gayevskiy, Velimir, Sue, Carolyn M., Edwards, Caitlin, Edkins, Edward, Junckerstorff, Reimar, Kiraly-Borri, C., Rowe, P., Christodoulou, J.

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