Hyperhomocysteinemia and Neurologic Disorders: a Review

por Ansari, Ramin, Mahta, Ali, Mallack, Eric, Luo, Jin Jun
Publicado 2014

Erratum: Hyperhomocysteinemia and Neurologic Disorders: a Review

por Ansari, Ramin, Mahta, Ali, Mallack, Eric, Luo, Jin Jun
Publicado 2015

Structure and Function of the ABCD1 Variant Database: 20 Years, 940 Pathogenic Variants, and 3400 Cases of Adrenoleukodystrophy

por Mallack, Eric J., Gao, Kerry, Engelen, Marc, Kemp, Stephan
Publicado 2022

Practical Approaches and Knowledge Gaps in the Care for Children With Leukodystrophies

por Keller, Stephanie R., Mallack, Eric J., Rubin, Jennifer P., Accardo, Jennifer A., Brault, Jennifer A., Corre, Camille S., Elizondo, Camila, Garafola, Jennifer, Jackson-Garcia, April C., Rhee, Jullie, Seeger, Elisa, Shullanberger, Kaprice C., Tourjee, Amanda, Trovato, Melissa K., Waldman, Amy T., Wallace, Jenna L., Wallace, Michael R., Werner, Klaus, White, Angela, Ess, Kevin C., Becker, Catherine, Eichler, Florian S.
Publicado 2020

Biomarker-based risk prediction for the onset of neuroinflammation in X-linked adrenoleukodystrophy

por Weinhofer, Isabelle, Rommer, Paulus, Gleiss, Andreas, Ponleitner, Markus, Zierfuss, Bettina, Waidhofer-Söllner, Petra, Fourcade, Stéphane, Grabmeier-Pfistershammer, Katharina, Reinert, Marie-Christine, Göpfert, Jens, Heine, Anne, Yska, Hemmo A.F., Casasnovas, Carlos, Cantarín, Verónica, Bergner, Caroline G., Mallack, Eric, Forss-Petter, Sonja, Aubourg, Patrick, Bley, Annette, Engelen, Marc, Eichler, Florian, Lund, Troy C., Pujol, Aurora, Köhler, Wolfgang, Kühl, Jörn-Sven, Berger, Johannes
Publicado 2023

International Recommendations for the Diagnosis and Management of Patients With Adrenoleukodystrophy: A Consensus-Based Approach

por Engelen, Marc, van Ballegoij, Wouter J.C., Mallack, Eric James, Van Haren, Keith P., Köhler, Wolfgang, Salsano, Ettore, van Trotsenburg, A.S.P., Mochel, Fanny, Sevin, Caroline, Regelmann, Molly O., Tritos, Nicholas A., Halper, Alyssa, Lachmann, Robin H., Davison, James, Raymond, Gerald V., Lund, Troy C., Orchard, Paul J., Kuehl, Joern-Sven, Lindemans, Caroline A., Caruso, Paul, Turk, Bela Rui, Moser, Ann B., Vaz, Frédéric M., Ferdinandusse, Sacha, Kemp, Stephan, Fatemi, Ali, Eichler, Florian S., Huffnagel, Irene C.
Publicado 2022

TLR7 gain-of-function genetic variation causes human lupus

por Brown, Grant J., Cañete, Pablo F., Wang, Hao, Medhavy, Arti, Bones, Josiah, Roco, Jonathan A., He, Yuke, Qin, Yuting, Cappello, Jean, Ellyard, Julia I., Bassett, Katharine, Shen, Qian, Burgio, Gaetan, Zhang, Yaoyuan, Turnbull, Cynthia, Meng, Xiangpeng, Wu, Phil, Cho, Eun, Miosge, Lisa A., Andrews, T. Daniel, Field, Matt A., Tvorogov, Denis, Lopez, Angel F., Babon, Jeffrey J., López, Cristina Aparicio, Gónzalez-Murillo, África, Garulo, Daniel Clemente, Pascual, Virginia, Levy, Tess, Mallack, Eric J., Calame, Daniel G., Lotze, Timothy, Lupski, James R., Ding, Huihua, Ullah, Tomalika R., Walters, Giles D., Koina, Mark E., Cook, Matthew C., Shen, Nan, de Lucas Collantes, Carmen, Corry, Ben, Gantier, Michael P., Athanasopoulos, Vicki, Vinuesa, Carola G.
Publicado 2022