Aicardi–Goutières syndrome presenting atypically as a sub-acute leukoencephalopathy by Orcesi, S, Pessagno, A, Biancheri, R, La Piana, R, Mascaretti, M, Rossi, A, Rice, G.I, Crow, Y.J, Fazzi, E, Veneselli, E

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Neprilysin, obesity and the metabolic syndrome by Standeven, K.F, Hess, K, Carter, A.M, Rice, G.I, Cordell, P.A, Balmforth, A.J, Lu, B, Scott, D.J, Turner, A.J, Hooper, N.M, Grant, P.J

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Comprehensive molecular screening strategy of OCLN in band‐like calcification with simplified gyration and polymicrogyria by Jenkinson, E.M., Livingston, J.H., O'Driscoll, M.C., Desguerre, I., Nabbout, R., Boddaert, N., Soares, G., Gonçalves da Rocha, M., D'Arrigo, S., Rice, G.I., Crow, Y.J.

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Cerebroretinal microangiopathy with calcifications and cysts (CRMCC) by Briggs, T.A., Abdel-Salam, G.M.H., Balicki, M., Baxter, P., Bertini, E., Bishop, N., Browne, B.H., Chitayat, D., Chong, W.K., Eid, M.M., Halliday, W., Hughes, I., Klusmann-Koy, A., Kurian, M., Nischal, K.K., Rice, G.I., Stephenson, J.B.P., Surtees, R., Talbot, J.F., Tehrani, N.N., Tolmie, J.L., Toomes, C., van der Knaap, M.S., Crow, Y.J.

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Band-like intracranial calcification with simplified gyration and polymicrogyria: A distinct "pseudo-TORCH" phenotype by Briggs, T.A., Wolf, N.I., D'Arrigo, S., Ebinger, F., Harting, I., Dobyns, W.B., Livingston, J.H., Rice, G.I., Crooks, D., Rowland-Hill, C.A., Squier, W., Stoodley, N., Pilz, D.T., Crow, Y.J.

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Two further cases of spondyloenchondrodysplasia (SPENCD) with immune dysregulation by Navarro, V., Scott, C., Briggs, T.A., Barete, S., Frances, C., Lebon, P., Maisonobe, T., Rice, G.I., Wouters, C.H., Crow, Y.J.

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2FC3.3 Identification and characterization of a novel inborn error of metabolism caused by a defect in Dihydrofolate reductase by Banka, S., Blom, H.J., Walter, J., Aziz, M., Urquhart, J.E., Clouthier, C.M., Rice, G.I., de Brouwer, A.P.M., Hilton, E., Vassallo, G., Will, A., Smith, D.E.C., Smulders, Y.M., Wevers, R.A., Steinfeld, R., Heales, S., Crow, Y.J., Pelletier, J.N., Jones, S., Newman, W.G.

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DOENÇA ARTICULAR NA INTERFERONPATIA TIPO 1 RELACIONADA AO MDA‐5 ‐ UMA FORMA MENDELIANA DA ARTROPATIA DE JACCOUD by Souza, F.F.L., Carvalho, L.M., Ehmke, N., Ngoumou, G., Kitabayashi, N., Melki, I., Deigendesch, N., Nogueira-Barbosa, M.H., Ferriani, V., Louzada-Junior, P., Marques Junior, W., Lourenço, C.M., Horn, D., Kallinich, T., Stenzel, W., Rice, G.I., Crow, Y.J.

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Neprilysin, obesity and the metabolic syndrome by Standeven, K.F, Hess, K, Carter, A.M, Rice, G.I, Cordell, P.A, Balmforth, A.J, Lu, B, Scott, D.J, Turner, A.J, Hooper, N.M, Grant, P.J

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Neprilysin, obesity and the metabolic syndrome by Standeven, K.F, Hess, K, Carter, A.M, Rice, G.I, Cordell, P.A, Balmforth, A.J, Lu, B, Scott, D.J, Turner, A.J, Hooper, N.M, Grant, P.J

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Two further cases of spondyloenchondrodysplasia (SPENCD) with immune dysregulation by Navarro, V., Scott, C., Briggs, T.A., Barete, S., Frances, C., Lebon, P., Maisonobe, T., Rice, G.I., Wouters, C.H., Crow, Y.J.

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Cocaine cross-sensitization to dopamine uptake inhibitors: Unique effects of GBR12909 by Elmer, G.I., Brockington, A., Gorelick, D.A., Carrol, F.I., Rice, K.C., Matecka, D., Goldberg, S.R., Rothman, R.B.

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