Antioxidant properties of natural compounds used in popular medicine for gastric ulcers von Repetto, M G, Llesuy, S F

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The oxidative stress induced in vivo by Shiga toxin‐2 contributes to the pathogenicity of haemolytic uraemic syndrome von Gomez, S. A., Abrey‐Recalde, M. J., Panek, C. A., Ferrarotti, N. F., Repetto, M. G., Mejías, M. P., Fernández, G. C., Vanzulli, S., Isturiz, M. A., Palermo, M. S.

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Brain oxidative stress in rat with chronic iron or copper overload von Sebio, R. Musacco, Ferrarotti, N., Lairion, F., Magriñá, C. Saporito, Fuda, J., Torti, H., Boveris, A., Repetto, M.G.

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Clinical features of chromosome 22q11.2 microdeletion syndrome in 208 Chilean patients von Repetto, GM, Guzmán, ML, Puga, A, Calderón, JF, Astete, CP, Aracena, M, Arriaza, M, Aravena, T, Sanz, P

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PUF60-related developmental disorder: A case series and phenotypic analysis of 10 additional patients with monoallelic PUF60 variants von Grimes, H, Ansari, M, Ashraf, T, Cueto-González, Anna Mª, Calder, A, Day, M, Fernandez Alvarez, P, Foster, A, Lahiri, N, Repetto, G M, Scurr, I, Varghese, V, Low, Karen J

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The COVID‐19 pandemic's impact on worry and medical disruptions reported by individuals with chromosome 22q11.2 copy number variants and their caregivers von White, L. K., Crowley, T. B., Finucane, B., Garcia‐Minaur, S., Repetto, G. M., Bree, M., Fischer, M., Jacquemont, S., Barzilay, R., Maillard, A. M., Donald, K. A., Gur, R. E., Bassett, A. S., Swillen, A., McDonald‐McGinn, D. M.

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Redox dyshomeostasis in the experimental chronic hepatic overloads with iron or copper von Musacco Sebio, R., Ferrarotti, N., Saporito Magriñá, C., Fuda, J., Torti, H., Lairión, F., Boveris, A., Repetto, M.G.

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Peripheral markers of oxidative stress in probable Alzheimer patients von REPETTO, M. G, REIDES, C. G, EVELSON, P, KOHAN, S, DE LUSTIG, E. S, LLESUY, S. F

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Insulin, glucose and glycated hemoglobin in Alzheimer’s and vascular dementia with and without superimposed Type II diabetes mellitus condition von Domínguez, R. O., Marschoff, E. R., Guareschi, E. M., Repetto, M. G., Famulari, A. L., Pagano, M. A., Serra, J. A.

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DESDE ANOMALÍAS CONGÉNITAS A ENFERMEDAD NEURODEGENERATIVA: 22 AÑOS DE MICRODELECIÓN 22q11.2 von Lisboa, MG Repetto

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Molecular diagnosis in patients with retinoblastoma: Report of a series of cases von Ossandón, D, Zanolli, M, López, J P, Benavides, F, Pérez, V, Repetto, G M

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Genomic imprinting and human chromosome 15 von Repetto, G M

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Interstitial duplications of chromosome region 15q11q13: Clinical and molecular characterization von Repetto, Gabriela M., White, Lisa M., Bader, Patricia J., Johnson, Debra, Knoll, Joan H.M.

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Complex familial rearrangement of chromosome 9p24.3 detected by FISH von Repetto, Gabriela M., Wagstaff, Joseph, Korf, Bruce R., Knoll, Joan H.M.

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Identification of a common mutation in mucopolysaccharidosis IVA: correlation among genotype, phenotype, and keratan sulfate von Tomatsu, Shunji, Dieter, Tatiana, Schwartz, Ida V., Sarmient, Piedad, Giugliani, Roberto, Barrera, Luis A., Guelbert, Norberto, Kremer, Raquel, Repetto, Gabriela M., Gutierrez, Monica A., Nishioka, Tatsuo, Serrato, Olga Peña, Montaño, Adriana Maria, Yamaguchi, Seiji, Noguchi, Akihiko

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Cardiovascular autonomic function in anthracycline-treated breast cancer patients von VINIEGRA, M, MARCHETTI, M, REPETTO, M. G, CHWOJNIK, A, BOSCARO, M, MAZZEI, J. A, CHACON, R. D, POLITI, P. M, LOSSO, M, NAVIGANTE, A, LITOVSKA, S, SENDEROWICZ, A, BORGHI, L, LEBRON, J, PUJATO, D, MARRERO, H

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Probable identity-by-descent for a mutation in the Dyggve-Melchior-Clausen/Smith-McCort dysplasia (Dymeclin) gene among patients from Guam, Chile, Argentina, and Spain von Pogue, Robert, Ehtesham, Nadia, Repetto, Gabriela M., Carrero-Valenzuela, Roque, de Casella, Cristina Bazán, de Pons, Silvia Pintos, Martínez-Frías, Maria Luisa, Heuertz, Solange, Cormier-Daire, Valerie, Cohn, Daniel H.

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High cognitive outcome in an adolescent with mut− methylmalonic acidemia von Varvogli, Liza, Repetto, Gabriela M., Waisbren, Susan E., Levy, Harvey L.

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Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs von Sønderby, IE, Ching, CRK, Thomopoulos, SI, van der Meer, D, Sun, D, Villalon-Reina, JE, Agartz, I, Amunts, K, Arango, C, Armstrong, NJ, Ayesa-Arriola, R, Bakker, G, Bassett, AS, Boomsma, DI, Bülow, R, Butcher, NJ, Calhoun, VD, Caspers, S, Chow, EWC, Cichon, S, Ciufolini, S, Craig, MC, Crespo-Facorro, B, Cunningham, AC, Dale, AM, Dazzan, P, de Zubicaray, GI, Doherty, JL, Donohoe, G, Draganski, B, Durdle, CA, Ehrlich, S, Emanuel, BS, Espeseth, T, Fisher, SE, Ge, T, Glahn, DC, Grabe, HJ, Gur, RE, Gutman, BA, Håberg, AK, Hansen, LA, Hashimoto, R, Hibar, DP, Holmes, AJ, Hottenga, J-J, Hulshoff Pol, HE, Jalbrzikowski, M, Knowles, EEM, Kushan, L, Linden, DEJ, Liu, J, Lundervold, AJ, Martin-Brevet, S, Martínez, K, Mather, KA, Mathias, SR, McDonald-McGinn, DM, McRae, AF, Medland, SE, Moberget, T, Modenato, C, Monereo Sánchez, J, Moreau, CA, Mühleisen, TW, Paus, T, Pausova, Z, Prieto, C, Ragothaman, A, Reis Marques, T, Repetto, GM, Reymond, A, Roalf, DR, Rodriguez-Herreros, B, Rucker, JJ, Sachdev, PS, Schmitt, JE, Schofield, PR, Silva, AI, Stefansson, H, Stein, DJ, Tamnes, CK, Tordesillas-Gutiérrez, D, Ulfarsson, MO, Vajdi, A, van 't Ent, D, van den Bree, MBM, Vassos, E, Vázquez-Bourgon, J, Vila-Rodriguez, F, Walters, GB, Wen, W, Westlye, LT, Zackai, EH, Stefánsson, K, Thompson, PM, Bearden, CE, Andreassen, OA, ENIGMA-CNV Working Group, ENIGMA 22q11.2 Deletion Syndrome Working Group

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Clinical, neuroimaging, and molecular spectrum of TECPR2‐associated hereditary sensory and autonomic neuropathy with intellectual disability von Neuser, S, Brechmann, B, Heimer, G, Brösse, I, Schubert, S, O'Grady, L, Zech, M, Srivastava, S, Sweetser, DA, Dincer, Y, Mall, V, Winkelmann, J, Behrends, C, Darras, BT, Graham, RJ, Jayakar, P, Byrne, B, Bar-Aluma, BE, Haberman, Y, Szeinberg, A, Aldhalaan, HM, Hashem, M, Al Tenaiji, A, Ismayl, O, Al Nuaimi, AE, Maher, K, Ibrahim, S, Khan, F, Houlden, H, Ramakumaran, VS, Pagnamenta, AT, Posey, JE, Lupski, JR, Tan, W-H, ElGhazali, G, Herman, I, Muñoz, T, Repetto, GM, Seitz, A, Krumbiegel, M, Poli, MC, Kini, U, Efthymiou, S, Meiler, J, Maroofian, R, Alkuraya, FS, Abou Jamra, R, Popp, B, Ben-Zeev, B, Ebrahimi-Fakhari, D

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