Therapies in Aicardi–Goutières syndrome von Crow, Y. J., Vanderver, A., Orcesi, S., Kuijpers, T. W., Rice, G. I.

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Heterozygous Mutations in TREX1 Cause Familial Chilblain Lupus and Dominant Aicardi-Goutières Syndrome von Rice, Gillian, Newman, William G., Dean, John, Patrick, Teresa, Parmar, Rekha, Flintoff, Kim, Robins, Peter, Harvey, Scott, Hollis, Thomas, O’Hara, Ann, Herrick, Ariane L., Bowden, Andrew P., Perrino, Fred W., Lindahl, Tomas, Barnes, Deborah E., Crow, Yanick J.

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The prototypical interferonopathy: Aicardi‐Goutières syndrome from bedside to bench von Hofer, Markus J., Modesti, Nicholson, Coufal, Nicole G., Wang, Qingde, Sase, Sunetra, Miner, Jonathan J., Vanderver, Adeline, Bennett, Mariko L.

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Comment on: Diagnosis of Aicardi‐Goutières Syndrome in Adults von Pereira, Eduardo R., Franklin, Gustavo L., Raskin, Salmo, Teive, Hélio A. G.

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A novel pathogenic variant p.Asp797Val in IFIH1 in a Japanese boy with overlapping Singleton‐Merten syndrome and Aicardi‐Goutières syndrome von Hasegawa, Kosei, Tanaka, Hiroyuki, Futagawa, Natsuko, Miyahara, Hiroyuki, Higuchi, Yousuke, Tsukahara, Hirokazu

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Aicardi-Goutières syndrome: An update and results of interferon-α studies von GoutièRes, Françoise, Aicardi, Jean, Barth, Peter G., Lebon, Pierre

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Biochemical functions and structure of Caenorhabditis elegans ZK177.8 protein: Aicardi–Goutières syndrome SAMHD1 dNTPase ortholog von Maehigashi, Tatsuya, Lim, Christopher, Wade, Lydia R., Bowen, Nicole E., Knecht, Kirsten M., Alvarez, Natalie N., Kelly, William G., Schinazi, Raymond F., Kim, Dong-Hyun, Xiong, Yong, Kim, Baek

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Variable expression in SAMHD1-associated familial Aicardi-Goutières syndrome von Urban, Michael, Uren, Caitlin, Möller, Marlo, Esser, Monika M., Crow, Yanick J., Glanzmann, Brigitte, Durrheim, Glenda, Glashoff, Richard, Hoal, Eileen G., Rice, Gillian I., Kinnear, Craig J., van Coller, Ansia, Abraham, Deepthi R.

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MRI Features Predictive of Aicardi-Goutieres Syndrome von Millichap, J Gordon

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Congenital glaucoma and brain stem atrophy as features of Aicardi–Goutières syndrome von Crow, Yanick J., Massey, R.F., Innes, J.R., Pairaudeau, P.W., Rowland Hill, C.A., Woods, C.G., Ali, M., Livingston, J.H., Lebon, P., Nischall, K., McEntagart, M., Hindocha, N., Winter, R.M.

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Reconciling neuroimaging and clinical findings in Aicardi-Goutières syndrome: an autoimmune-mediated encephalopathy von Ramantani, G, Niggemann, P, Bast, T, Lee-Kirsch, M A

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Retention of Cobalt, Cesium, and Strontium in the Hydrates of C3S, C3A, and Gypsum von LAMEILLE, J.M., GOUTIERE, G., PETIT, JEAN-CLAUDE, REGOURD, MICHELINE

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Aicardi-Goutières syndrome : a genetic microangiopathy? von BARTH, P. G, WALTER, A, VAN GELDEREN, I

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Cree encephalitis is allelic with Aicardi-Goutiéres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolism von Crow, Y J, Black, D N, Ali, M, Bond, J, Jackson, A P, Lefson, M, Michaud, J, Roberts, E, Stephenson, J B P, Woods, C G, Lebon, P

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Aicardi-Goutières syndrome presenting with haematemesis in infancy von Hall, D, Rice, GI, Akbar, N, Meager, A, Crow, YJ, Lim, MJ

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Aicardi-Goutières Syndrome Displays Genetic Heterogeneity with One Locus ( AGS1) on Chromosome 3p21 von Crow, Y.J., Jackson, A.P., Roberts, E., van Beusekom, E., Barth, P., Corry, P., Ferrie, C.D., Hamel, B.C.J., Jayatunga, R., Karbani, G., Kálmánchey, R., Kelemen, A., King, M., Kumar, R., Livingstone, J., Massey, R., McWilliam, R., Meager, A., Rittey, C., Stephenson, J.B.P., Tolmie, J.L., Verrips, A., Voit, T., van Bokhoven, H., Brunner, H.G., Woods, C.G.

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Janus Kinase Inhibition in the Aicardi–Goutières Syndrome von Vanderver, Adeline, Adang, Laura, Gavazzi, Francesco, McDonald, Katherine, Helman, Guy, Frank, David B, Jaffe, Nicole, Yum, Sabrina W, Collins, Abigail, Keller, Stephanie R, Lebon, Pierre, Meritet, Jean-François, Rhee, Jullie, Takanohashi, Asako, Armangue, Thais, Ulrick, Nicole, Sherbini, Omar, Koh, Jamie, Peer, Kyle, Besnier, Constance, Scher, Carly, Boyle, Katherine, Dubbs, Holly, Kramer-Golinkoff, Julia, Pizzino, Amy, Woidill, Sarah, Shults, Justine

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Aicardi–Goutières syndrome and the type I interferonopathies von Crow, Yanick J., Manel, Nicolas

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Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus von Bonthron, David T, Lindahl, Tomas, Ali, Manir, Ponsot, Gerard, Robins, Peter, Voit, Thomas, van Bokhoven, Hans, Barnes, Deborah E, Livingston, John H, Massey, Roger F, Crow, Yanick J, Parmar, Rekha, Lebon, Pierre, Jackson, Andrew P, Hayward, Bruce E, Hamel, Ben C, Leitch, Andrea, Klepper, Joerg, Cowan, Frances M, Frints, Suzanne G, Black, Deborah N, Lynch, Sally Ann, Meritet, Jean François, Brunner, Han G, Corry, Peter C, Michaud, Jacques L

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Aicardi–Goutières syndrome presenting atypically as a sub-acute leukoencephalopathy von 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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