Search Results - "Jacques, T S"

Brachyury, a crucial regulator of notochordal development, is a novel biomarker for chordomas by Vujovic, S, Henderson, S, Presneau, N, Odell, E, Jacques, TS, Tirabosco, R, Boshoff, C, Flanagan, AM

“…Chordomas are malignant tumours that occur along the spine and are thought to derive from notochordal remnants. There is significant morphological variability…”
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Expression of myxovirus‐resistance protein A: a possible marker of muscle disease activity and autoantibody specificities in juvenile dermatomyositis by Soponkanaporn, S., Deakin, C. T., Schutz, P. W., Marshall, L. R., Yasin, S. A., Johnson, C. M., Sag, E., Tansley, S. L., McHugh, N. J., Wedderburn, L. R., Jacques, T. S.

“…Aims To evaluate the relationship between expression of myxovirus‐resistance protein A (MxA) protein on muscle biopsies by immunohistochemistry and disease…”
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Effective induction therapy for anti-SRP associated myositis in childhood: A small case series and review of the literature by Binns, E L, Moraitis, E, Maillard, S, Tansley, S, McHugh, N, Jacques, T S, Wedderburn, L R, Pilkington, C, Yasin, S A, Nistala, K

“…Anti-Signal Recognition Particle associated myopathy is a clinically and histopathologically distinct subgroup of Juvenile Idiopathic Inflammatory Myositis,…”
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The neuropathological consequences of CDKL5 mutation by Paine, S. M. L., Munot, P., Carmichael, J., Das, K., Weber, M. A., Prabhakar, P., Jacques, T. S.

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Free virtual issue: novel paradigms for in inborn errors with muscular and central neuropathology by Morava, E., Jacques, T. S.

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Parallel changes in bladder suburothelial vanilloid receptor TRPV1 and pan‐neuronal marker PGP9.5 immunoreactivity in patients with neurogenic detrusor overactivity after intravesical resiniferatoxin treatment by Brady, C.M., Apostolidis, A.N., Harper, M., Yiangou, Y., Beckett, A., Jacques, T.S., Freeman, A., Scaravilli, F., Fowler, C.J., Anand, P.

“…OBJECTIVE To compare PGP9.5 and transient receptor potential vanilloid receptor (TRPV1) suburothelial immunoreactivity between controls and patients with…”
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Prospective parental consent for autopsy research following sudden unexpected childhood deaths: a successful model by Thayyil, S, Robertson, N J, Scales, A, Weber, M A, Jacques, T S, Sebire, N J, Taylor, A M

“…Background:Organ retention issues, recent changes in the Coroners’ (Amendment) Rules 2005 and the Human Tissue Act have resulted in pessimism regarding…”
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CNS embryonal tumours: WHO 2016 and beyond by Pickles, J. C., Hawkins, C., Pietsch, T., Jacques, T. S.

“…Embryonal tumours of the central nervous system (CNS) present a significant clinical challenge. Many of these neoplasms affect young children, have a very high…”
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Antenatal neurodevelopmental defects in ornithine transcarbamylase deficiency by Paine, S. M. L., Grünewald, S., Jacques, T. S.

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Taxonomy of CNS tumours; a series of three short reviews on the WHO 2016 classification and beyond by Wesseling, P., Jacques, T. S.

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Review: Challenges in the histopathological classification of ganglioglioma and DNT: microscopic agreement studies and a preliminary genotype‐phenotype analysis by Blümcke, I., Coras, R., Wefers, A. K., Capper, D., Aronica, E., Becker, A., Honavar, M., Stone, T. J., Jacques, T. S., Miyata, H., Mühlebner, A., Pimentel, J., Söylemezoğlu, F., Thom, M.

“…Low‐grade epilepsy‐associated brain tumours (LEAT) are the second most common cause for drug‐resistant, focal epilepsy, that is ganglioglioma (GG) and…”
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Novel therapeutic targets in epilepsy: oxidative stress and iron metabolism by Li, Y.‐F., Thom, M., Jacques, T. S.

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Mixed glioneuronal tumour of the fourth ventricle with prominent rosette formation by Jacques, T. S., Eldridge, C., Patel, A., Saleem, N. M., Powell, M., Kitchen, N. D., Thom, M., Revesz, T.

“…We describe three unusual tumours characterized by a mixture of glial and neuronal differentiation, involvement of the posterior fossa and formation of…”
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Impact of non-invasive post-mortem micro-CT imaging on a fetal autopsy service: a single centre retrospective study by Simcock, I.C., Arthurs, O.J., Hutchinson, J.C., Sebire, N.J., Jacques, T.S., Sekar, T., Shelmerdine, S.C., Alvarez, D., Lee, V., Yates, E., Smith, E., McMinn, L., Ward, L., Levine, S., Palm, L., Devdas, A., Kumar, A., Merve, A.

“…To evaluate the impact of a new, less-invasive micro-computed tomography (CT) service on autopsy service provision. We recorded parental consent, type of…”
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CTNNB1 mutations are clonal in adamantinomatous craniopharyngioma by Apps, J. R., Stache, C., Gonzalez‐Meljem, J. M., Gutteridge, A., Chalker, J., Jacques, T. S., Forshew, T., Hölsken, A., Martinez‐Barbera, J. P.

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A fatal case of cough by Bossley, C.J., Hogg, C., Stoneham, S., Jacques, T.S., Bush, A.

“…Dysfunctional swallowing is an uncommon, but important cause of bronchiectasis. We describe a child with a brainstem tumor, who developed bronchiectasis caused…”
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Review: Molecular characteristics of long‐term epilepsy‐associated tumours (LEATs) and mechanisms for tumour‐related epilepsy (TRE) by Stone, T. J., Rowell, R., Jayasekera, B. A. P., Cunningham, M. O., Jacques, T. S.

“…Brain tumours are the second most common cause of seizures identified in epilepsy surgical series. While any tumour involving the brain has the potential to…”
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A Diagnostic Algorithm for Posterior Fossa Tumors in Children: A Validation Study by Alves, C A P F, Löbel, U, Martin-Saavedra, J S, Toescu, S, Tsunemi, M H, Teixeira, S R, Mankad, K, Hargrave, D, Jacques, T S, da Costa Leite, C, Gonçalves, F G, Vossough, A, D'Arco, F

“…Primary posterior fossa tumors comprise a large group of neoplasias with variable aggressiveness and short and long-term outcomes. This study aimed to validate…”
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Histological heterogeneity in a large clinical cohort of juvenile idiopathic inflammatory myopathy: analysis by myositis autoantibody and pathological features by Yasin, S. A., Schutz, P. W., Deakin, C. T., Sag, E., Simou, S., Marshall, L. R., Tansley, S. L., McHugh, N. J., Holton, J. L., Wedderburn, L. R., Jacques, T. S., Armon, Kate, Ellis‐Gage, Joe, Briggs, Vanja, Watts, Joanna, McCann, Liza, Roberts, Ian, Baildam, Eileen, Hanna, Lou, Lloyd, Olivia, Wadeson, Susan, Riley, Phil, McGovern, Ann, Ryder, Clive, Scott, Janis, Thomas, Beverley, Southwood, Taunton, Al‐Abadi, Eslam, Wyatt, Sue, Jackson, Gillian, Wood, Mark, VanRooyen, Vanessa, Burton, Deborah, Davidson, Joyce, Gardner‐Medwin, Janet, Martin, Neil, Waxman, Liz, Browne, Michael, Friswell, Mark, Foster, Helen, Swift, Alison, Stevenson, Vicky, Wade, Debbie, Sen, Ethan, Smith, Eve, Qiao, Lisa, Watson, Stuart, Duong, Claire, Venning, Helen, Satyapal, Rangaraj, Stretton, Elizabeth, Jordan, Mary, Mosley, Ellen, Frost, Anna, Crate, Lindsay, Warrier, Kishore, ord, Stefanie, Pilkington, Clarissa, Hasson, Nathan, Halkon, Elizabeth, Brown, Virginia, Juggins, Audrey, Smith, Sally, Lunt, Sian, Enayat, Elli, Kassoumeri, Laura, Beard, Laura, Arnold, Katie, Glackin, Yvonne, Simou, Stephanie, Almeida, Beverley, Nistala, Kiran, Dowle, Stefanie, Papadopoulou, Charis, Johnson‐Moore, Cer, Robinson, Emily, Murray, Kevin, Ioannou, John, Suffield, Linda, Al‐Obaidi, Muthana, Lee, Helen, Leach, Sam, McMahon, Anne‐Marie, Chisem, Heather, Kingshott, Ruth, Wilkinson, Nick, Inness, Emma, Kendall, Eunice, Mayers, David, Bailey, Kathryn, Fineman, Natalie, Pluess‐Hall, Helen, Akeroyd, Lou, Leahy, Alice, Collier, Amy, Cutts, Rebecca, Macleod, Emma, De Graaf, Hans, Hartfree, Sarah, Pratt, Danny

“…Aim Juvenile idiopathic inflammatory myopathies have been recently reclassified into clinico‐serological subgroups. Myopathological correlates of the subgroups…”
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SHH pathway inhibition is protumourigenic in adamantinomatous craniopharyngioma by Carreno, G, Boult, J K R, Apps, J, Gonzalez-Meljem, J M, Haston, S, Guiho, R, Stache, C, Danielson, L S, Koers, A, Smith, L M, Virasami, A, Panousopoulos, L, Buchfelder, M, Jacques, T S, Chesler, L, Robinson, S P, Martinez-Barbera, J P

“…Pharmacological inhibition of the sonic hedgehog (SHH) pathway can be beneficial against certain cancers but detrimental in others. Adamantinomatous…”
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