Ngā hua rapu - Zambonin, Jessica

Injury and differentiation following inhibition of mitochondrial respiratory chain complex IV in rat oligodendrocytes mā Ziabreva, Iryna, Campbell, Graham, Rist, Julia, Zambonin, Jessica, Rorbach, Joanna, Wydro, Mateusz M, Lassmann, Hans, Franklin, Robin J M, Mahad, Don

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Loss of Myelin-Associated Glycoprotein in Kearns-Sayre Syndrome mā Lax, Nichola Z., Campbell, Graham R., Reeve, Amy K., Ohno, Nobuhiko, Zambonin, Jessica, Blakely, Emma L., Taylor, Robert W., Bonilla, Eduardo, Tanji, Kurenai, DiMauro, Salvatore, Jaros, Evelyn, Lassmann, Hans, Turnbull, Doug M., Mahad, Don J.

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Increased mitochondrial content in remyelinated axons: implications for multiple sclerosis mā Zambonin, Jessica L., Zhao, Chao, Ohno, Nobuhiko, Campbell, Graham R., Engeham, Sarah, Ziabreva, Iryna, Schwarz, Nadine, Lee, Sok Ee, Frischer, Josa M., Turnbull, Doug M., Trapp, Bruce D., Lassmann, Hans, Franklin, Robin J. M., Mahad, Don J.

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Spinocerebellar ataxia type 29 due to mutations in ITPR1: a case series and review of this emerging congenital ataxia mā Zambonin, Jessica L., Bellomo, Allison, Ben-Pazi, Hilla, Everman, David B., Frazer, Lee M., Geraghty, Michael T., Harper, Amy D., Jones, Julie R., Kamien, Benjamin, Kernohan, Kristin, Koenig, Mary Kay, Lines, Matthew, Palmer, Elizabeth Emma, Richardson, Randal, Segel, Reeval, Tarnopolsky, Mark, Vanstone, Jason R., Gibbons, Melissa, Collins, Abigail, Fogel, Brent L., Dudding-Byth, Tracy, Boycott, Kym M.

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Early infantile epileptic encephalopathy due to biallelic pathogenic variants in PIGQ: Report of seven new subjects and review of the literature mā Johnstone, Devon L., Nguyen, Thi Tuyet Mai, Zambonin, Jessica, Kernohan, Kristin D., St‐Denis, Anik, Baratang, Nissan V., Hartley, Taila, Geraghty, Michael T., Richer, Julie, Majewski, Jacek, Bareke, Eric, Guerin, Andrea, Pendziwiat, Manuela, Pena, Loren D. M., Braakman, Hilde M. H., Gripp, Karen W., Edmondson, Andrew C., He, Miao, Spillmann, Rebecca C., Eklund, Erik A., Bayat, Allan, McMillan, Hugh J., Boycott, Kym M., Campeau, Philippe M.

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Bi-allelic variants in the mitochondrial RNase P subunit PRORP cause mitochondrial tRNA processing defects and pleiotropic multisystem presentations mā Hochberg, Irit, Demain, Leigh A.M., Richer, Julie, Thompson, Kyle, Urquhart, Jill E., Rea, Alessandro, Pagarkar, Waheeda, Rodríguez-Palmero, Agustí, Schlüter, Agatha, Verdura, Edgard, Pujol, Aurora, Quijada-Fraile, Pilar, Amberger, Albert, Deutschmann, Andrea J., Demetz, Sandra, Gillespie, Meredith, Belyantseva, Inna A., McMillan, Hugh J., Barzik, Melanie, Beaman, Glenda M., Motha, Reeya, Ng, Kah Ying, O’Sullivan, James, Williams, Simon G., Bhaskar, Sanjeev S., Lawrence, Isabella R., Jenkinson, Emma M., Zambonin, Jessica L., Blumenfeld, Zeev, Yalonetsky, Sergey, Oerum, Stephanie, Rossmanith, Walter, Yue, Wyatt W., Zschocke, Johannes, Munro, Kevin J., Battersby, Brendan J., Friedman, Thomas B., Taylor, Robert W., O’Keefe, Raymond T., Newman, William G.

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