Biomarkers of oxidative stress, inflammation, and vascular dysfunction in inherited cystathionine β‐synthase deficient homocystinuria and the impact of taurine treatment in a phase... by Van Hove, Johan L. K., Freehauf, Cynthia L., Ficicioglu, Can, Pena, Loren D. M., Moreau, Kerrie L., Henthorn, Thomas K., Christians, Uwe, Jiang, Hua, Cowan, Tina M., Young, Sarah P., Hite, Michelle, Friederich, Marisa W., Stabler, Sally P., Spector, Elaine B., Kronquist, Kathryn E., Thomas, Janet A., Emmett, Peggy, Harrington, Mary J., Pyle, Laura, Creadon‐Swindell, Geralyn, Wempe, Michael F., MacLean, Kenneth N.

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Variant non-ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5 by 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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Biochemical and molecular predictors for prognosis in nonketotic hyperglycinemia by 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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Neurodevelopmental Outcome and Treatment Efficacy of Benzoate and Dextromethorphan in Siblings with Attenuated Nonketotic Hyperglycinemia by 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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genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy due to mutations in ALDH7A1 by Scharer, Gunter, Brocker, Chad, Vasiliou, Vasilis, Creadon-Swindell, Geralyn, Gallagher, Renata C, Spector, Elaine, Van Hove, Johan L. K

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Pathogenic variants in MRPL44 causes infantile cardiomyopathy due to a mitochondrial translation defect by Friederich, Marisa W., Geddes, Gabrielle C., Wortmann, Saskia B., Punnoose, Ann, Wartchow, Eric, Knight, Kaz M., Prokisch, Holger, Creadon-Swindell, Geralyn, Mayr, Johannes A., Van Hove, Johan L.K.

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Pathogenic variants in MRPL44 cause infantile cardiomyopathy due to a mitochondrial translation defect by Friederich, Marisa W., Geddes, Gabrielle C., Wortmann, Saskia B., Punnoose, Ann, Wartchow, Eric, Knight, Kaz M., Prokisch, Holger, Creadon-Swindell, Geralyn, Mayr, Johannes A., Van Hove, Johan L.K.

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d-Glyceric aciduria does not cause nonketotic hyperglycinemia: A historic co-occurrence by Swanson, Michael A., Garcia, Stephanie M., Spector, Elaine, Kronquist, Kathryn, Creadon-Swindell, Geralyn, Walter, Melanie, Christensen, Ernst, Van Hove, Johan L.K., Sass, Jörn Oliver

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Sequencing Heavy- and Light-Chain Variable Genes of Single B-Hybridoma Cells by Total Enzymatic Amplification by Liu, Andrew H., Creadon, Geralyn, Wysocki, Lawrence J.

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An early post-mutational selection event directs expansion of autoreactive B cells in murine lupus by Portanova, Joseph P., Creadon, Geralyn, Zhang, Xianghua, Smith, Diana S., Kotzin, Brian L., Wysocki, Larry J.

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Correction: Sequencing Heavy- and Light-Chain Variable Genes of Single B- Hybridoma Cells by Total Enzymatic Amplification by Liu, Andrew H., Creadon, Geralyn, Wysocki, Lawrence J.

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