Organic Radical Contrast Agents for Magnetic Resonance Imaging von Rajca, Andrzej, Wang, Ying, Boska, Michael, Paletta, Joseph T, Olankitwanit, Arnon, Swanson, Michael A, Mitchell, Deborah G, Eaton, Sandra S, Eaton, Gareth R, Rajca, Suchada

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Variant non-ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5 von BAKER, Peter R, FRIEDERICH, Marisa W, LEE, Wang-Tso, DESHPANDE, Charu, FRECKMANN, Mary-Louise, SHIH, Ling-Yu, WASSERSTEIN, Melissa, RASMUSSEN, Malene B, LUND, Allan M, PROCOPIS, Peter, CAMERON, Jessie M, ROBINSON, Brian H, SWANSON, Michael A, BROWN, Garry K, BROWN, Ruth M, COMPTON, Alison G, DIECKMANN, Carol L, COLLARD, Renata, COUGHLIN, Curtis R, SPECTOR, Elaine, WEMPE, Michael F, VAN HOVE, Johan L. K, SHAIKH, Tamim, BHATTACHARYA, Kaustuv, SCHARER, Gunter H, AICHER, Joseph, CREADON-SWINDELL, Geralyn, GEIGER, Elizabeth, MACLEAN, Kenneth N

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Room-Temperature Distance Measurements of Immobilized Spin-Labeled Protein by DEER/PELDOR von Meyer, Virginia, Swanson, Michael A., Clouston, Laura J., Boratyński, Przemysław J., Stein, Richard A., Mchaourab, Hassane S., Rajca, Andrzej, Eaton, Sandra S., Eaton, Gareth R.

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Identification of a novel biomarker for pyridoxine‐dependent epilepsy: Implications for newborn screening von Wempe, Michael F., Kumar, Amit, Kumar, Vijay, Choi, Yu J., Swanson, Michael A., Friederich, Marisa W., Hyland, Keith, Yue, Wyatt W., Van Hove, Johan L. K., Coughlin, Curtis R.

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Neurodevelopmental Outcome and Treatment Efficacy of Benzoate and Dextromethorphan in Siblings with Attenuated Nonketotic Hyperglycinemia von Bjoraker, Kendra J., PhD, Swanson, Michael A., PhD, Coughlin, Curtis R., MS, MBe, Christodoulou, John, MB, BS, PhD, Tan, Ee S., MB, BS, Fergeson, Mark, MD, Dyack, Sarah, MD, Ahmad, Ayesha, MD, Friederich, Marisa W., PhD, Spector, Elaine B., PhD, Creadon-Swindell, Geralyn, BS, Hodge, M. Antoinette, DPsych, Gaughan, Sommer, RD, Burns, Casey, RD, Van Hove, Johan L.K., MD, PhD

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Mutations in the mitochondrial cysteinyl-tRNA synthase gene, CARS2, lead to a severe epileptic encephalopathy and complex movement disorder von Coughlin, Curtis R, Scharer, Gunter H, Friederich, Marisa W, Yu, Hung-Chun, Geiger, Elizabeth A, Creadon-Swindell, Geralyn, Collins, Abigail E, Vanlander, Arnaud V, Coster, Rudy Van, Powell, Christopher A, Swanson, Michael A, Minczuk, Michal, Van Hove, Johan L K, Shaikh, Tamim H

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Mitochondrial energy failure in HSD10 disease is due to defective mtDNA transcript processing von Chatfield, Kathryn C, Coughlin, 2nd, Curtis R, Friederich, Marisa W, Gallagher, Renata C, Hesselberth, Jay R, Lovell, Mark A, Ofman, Rob, Swanson, Michael A, Thomas, Janet A, Wanders, Ronald J A, Wartchow, Eric P, Van Hove, Johan L K

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Deep postnatal phenotyping of a new mouse model of nonketotic hyperglycinemia von Swanson, Michael A., Jiang, Hua, Busquet, Nicolas, Carlsen, Jessica, Brindley, Connie, Benke, Tim A., Van Hove, Roxanne A., Friederich, Marisa W., MacLean, Kenneth N., Mesches, Michael H., Van Hove, Johan L. K.

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The genotypic spectrum of ALDH7A1 mutations resulting in pyridoxine dependent epilepsy: A common epileptic encephalopathy von Coughlin, Curtis R., Swanson, Michael A., Spector, Elaine, Meeks, Naomi J. L., Kronquist, Kathryn E., Aslamy, Mezhgan, Wempe, Michael F., van Karnebeek, Clara D. M., Gospe, Sidney M., Aziz, Verena G., Tsai, Becky P., Gao, Hanlin, Nagy, Peter L., Hyland, Keith, van Dooren, Silvy J. M., Salomons, Gajja S., Van Hove, Johan L. K.

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Cerebrospinal fluid amino acids glycine, serine, and threonine in nonketotic hyperglycinemia von Swanson, Michael A., Miller, Kristen, Young, Sarah P., Tong, Suhong, Ghaloul‐Gonzalez, Lina, Neira‐Fresneda, Juanita, Schlichting, Lisa, Peck, Cheryl, Gabel, Linda, Friederich, Marisa W., Van Hove, Johan L. K.

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The Iron−Sulfur Cluster of Electron Transfer Flavoprotein−Ubiquinone Oxidoreductase Is the Electron Acceptor for Electron Transfer Flavoprotein von Swanson, Michael A, Usselman, Robert J, Frerman, Frank E, Eaton, Gareth R, Eaton, Sandra S

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New insights into the phenotype of FARS2 deficiency von Vantroys, Elise, Larson, Austin, Friederich, Marisa, Knight, Kaz, Swanson, Michael A., Powell, Christopher A., Smet, Joél, Vergult, Sarah, De Paepe, Boel, Seneca, Sara, Roeyers, Herbert, Menten, Björn, Minczuk, Michal, Vanlander, Arnaud, Van Hove, Johan, Van Coster, Rudy

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Pathogenic variants in GCSH encoding the moonlighting H-protein cause combined nonketotic hyperglycinemia and lipoate deficiency von Arribas-Carreira, Laura, Dallabona, Cristina, Swanson, Michael A, Farris, Joseph, Østergaard, Elsebet, Tsiakas, Konstantinos, Hempel, Maja, Aquaviva-Bourdain, Cecile, Koutsoukos, Stefanos, Stence, Nicholas V, Magistrati, Martina, Spector, Elaine B, Kronquist, Kathryn, Christensen, Mette, Karstensen, Helena G, Feichtinger, René G, Achleitner, Melanie T, Lawrence Merritt II, J, Pérez, Belén, Ugarte, Magdalena, Grünewald, Stephanie, Riela, Anthony R, Julve, Natalia, Arnoux, Jean-Baptiste, Haldar, Kasturi, Donnini, Claudia, Santer, René, Lund, Allan M, Mayr, Johannes A, Rodriguez-Pombo, Pilar, Van Hove, Johan L K

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Biochemical and molecular predictors for prognosis in nonketotic hyperglycinemia von Swanson, Michael A., Coughlin Jr, Curtis R., Scharer, Gunter H., Szerlong, Heather J., Bjoraker, Kendra J., Spector, Elaine B., Creadon-Swindell, Geralyn, Mahieu, Vincent, Matthijs, Gert, Hennermann, Julia B., Applegarth, Derek A., Toone, Jennifer R., Tong, Suhong, Williams, Kristina, Van Hove, Johan L. K.

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The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT von Coughlin, Curtis R., Swanson, Michael A., Kronquist, Kathryn, Acquaviva, Cécile, Hutchin, Tim, Rodríguez-Pombo, Pilar, Väisänen, Marja-Leena, Spector, Elaine, Creadon-Swindell, Geralyn, Brás-Goldberg, Ana M., Rahikkala, Elisa, Moilanen, Jukka S., Mahieu, Vincent, Matthijs, Gert, Bravo-Alonso, Irene, Pérez-Cerdá, Celia, Ugarte, Magdalena, Vianey-Saban, Christine, Scharer, Gunter H., Van Hove, Johan L.K.

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Conformational Basis for Asymmetric Seeding Barrier in Filaments of Three- and Four-Repeat Tau von Siddiqua, Ayisha, Luo, Yin, Meyer, Virginia, Swanson, Michael A, Yu, Xiang, Wei, Guanghong, Zheng, Jie, Eaton, Gareth R, Ma, Buyong, Nussinov, Ruth, Eaton, Sandra S, Margittai, Martin

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Nonketotic hyperglycinemia: Functional assessment of missense variants in GLDC to understand phenotypes of the disease von Bravo‐Alonso, Irene, Navarrete, Rosa, Arribas‐Carreira, Laura, Perona, Almudena, Abia, David, Couce, María Luz, García‐Cazorla, Angels, Morais, Ana, Domingo, Rosario, Ramos, María Antonia, Swanson, Michael A., Hove, Johan L.K., Ugarte, Magdalena, Pérez, Belén, Pérez‐Cerdá, Celia, Rodríguez‐Pombo, Pilar

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Comment on Late-Onset Nonketotic Hyperglycinemia With a Heterozygous Novel Point Mutation of the GLDC Gene von Coughlin, Curtis R., Swanson, Michael A., Spector, Elaine B., Kronquist, Kathryn E., Van Hove, Johan L.K.

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Corrigendum: Swanson MA, Coughlin CR Jr, Scharer GH, et al: Biochemical and molecular predictors for prognosis in nonketotic hyperglycinemia. Ann Neurol 2015;78:606-618 von Swanson, Michael A., Coughlin Jr, Curtis R., Van Hove, Johan L. K.

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Correction: The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT von Coughlin, Curtis R, Swanson, Michael A, Kronquist, Kathryn, Acquaviva, Cécile, Hutchin, Tim, Rodríguez-Pombo, Pilar, Väisänen, Marja-Leena, Spector, Elaine, Creadon-Swindell, Geralyn, Brás-Goldberg, Ana M, Rahikkala, Elisa, Moilanen, Jukka S, Mahieu, Vincent, Matthijs, Gert, Bravo-Alonso, Irene, Pérez-Cerdá, Celia, Ugarte, Magdalena, Vianey-Saban, Christine, Scharer, Gunter H, Van Hove, Johan L K

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