Sökresultat - Li, Abi
- Visas 1 - 12 av 12 resultat
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PINK1 deficiency in β-cells increases basal insulin secretion and improves glucose tolerance in mice av Deas, Emma, Piipari, Kaisa, Machhada, Asif, Li, Abi, Gutierrez-del-Arroyo, Ana, Withers, Dominic J., Wood, Nicholas W., Abramov, Andrey Y.
Publicerad 2014Text -
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Neuropathological features of genetically confirmed DYT1 dystonia: investigating disease-specific inclusions av Paudel, Reema, Kiely, Aoife, Li, Abi, Lashley, Tammaryn, Bandopadhyay, Rina, Hardy, John, Jinnah, Hyder A, Bhatia, Kailash, Houlden, Henry, Holton, Janice L
Publicerad 2014Text -
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Widespread Lewy body and tau accumulation in childhood and adult onset dystonia-parkinsonism cases with PLA2G6 mutations av Paisán-Ruiz, Coro, Li, Abi, Schneider, Susanne A., Holton, Janice L., Johnson, Robert, Kidd, Desmond, Chataway, Jeremy, Bhatia, Kailash P., Lees, Andrew J., Hardy, John, Revesz, Tamas, Houlden, Henry
Publicerad 2012Text -
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Dysregulation of glucose metabolism is an early event in sporadic Parkinson's disease() av Dunn, Laura, Allen, George FG., Mamais, Adamantios, Ling, Helen, Li, Abi, Duberley, Kate E., Hargreaves, Iain P., Pope, Simon, Holton, Janice L., Lees, Andrew, Heales, Simon J., Bandopadhyay, Rina
Publicerad 2014Text -
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Mutational analysis of parkin and PINK1 in multiple system atrophy av Brooks, Janet A., Houlden, Henry, Melchers, Anna, Islam, Ansha J., Ding, Jinhui, Li, Abi, Paudel, Reema, Revesz, Tamas, Holton, Janice L., Wood, Nick, Lees, Andrew, Singleton, Andrew B., Scholz, Sonja W.
Publicerad 2010Text -
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Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease av Neumann, Juliane, Bras, Jose, Deas, Emma, O'Sullivan, Sean S., Parkkinen, Laura, Lachmann, Robin H., Li, Abi, Holton, Janice, Guerreiro, Rita, Paudel, Reema, Segarane, Badmavady, Singleton, Andrew, Lees, Andrew, Hardy, John, Houlden, Henry, Revesz, Tamas, Wood, Nicholas W.
Publicerad 2009Text -
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Clinical, pathological and functional characterization of riboflavin-responsive neuropathy av Manole, Andreea, Jaunmuktane, Zane, Hargreaves, Iain, Ludtmann, Marthe H R, Salpietro, Vincenzo, Bello, Oscar D, Pope, Simon, Pandraud, Amelie, Horga, Alejandro, Scalco, Renata S, Li, Abi, Ashokkumar, Balasubramaniem, Lourenço, Charles M, Heales, Simon, Horvath, Rita, Chinnery, Patrick F, Toro, Camilo, Singleton, Andrew B, Jacques, Thomas S, Abramov, Andrey Y, Muntoni, Francesco, Hanna, Michael G, Reilly, Mary M, Revesz, Tamas, Kullmann, Dimitri M, Jepson, James E C, Houlden, Henry
Publicerad 2017Text -
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Neuropathy target esterase impairments cause Oliver–McFarlane and Laurence–Moon syndromes av Hufnagel, Robert B, Arno, Gavin, Hein, Nichole D, Hersheson, Joshua, Prasad, Megana, Anderson, Yvonne, Krueger, Laura A, Gregory, Louise C, Stoetzel, Corinne, Jaworek, Thomas J, Hull, Sarah, Li, Abi, Plagnol, Vincent, Willen, Christi M, Morgan, Thomas M, Prows, Cynthia A, Hegde, Rashmi S, Riazuddin, Saima, Grabowski, Gregory A, Richardson, Rudy J, Dieterich, Klaus, Huang, Taosheng, Revesz, Tamas, Martinez-Barbera, J P, Sisk, Robert A, Jefferies, Craig, Houlden, Henry, Dattani, Mehul T, Fink, John K, Dollfus, Helene, Moore, Anthony T, Ahmed, Zubair M
Publicerad 2014Text -
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SNCA Variants Are Associated with Increased Risk for Multiple System Atrophy av Scholz, Sonja W., Houlden, Henry, Schulte, Claudia, Sharma, Manu, Li, Abi, Berg, Daniela, Melchers, Anna, Paudel, Reema, Gibbs, J. Raphael, Simon-Sanchez, Javier, Paisan-Ruiz, Coro, Bras, Jose, Ding, Jinhui, Chen, Honglei, Traynor, Bryan J., Arepalli, Sampath, Zonozi, Ryan R., Revesz, Tamas, Holton, Janice, Wood, Nick, Lees, Andrew, Oertel, Wolfgang, Wüllner, Ullrich, Goldwurm, Stefano, Pellecchia, Maria Teresa, Illig, Thomas, Riess, Olaf, Fernandez, Hubert H., Rodriguez, Ramon L., Okun, Michael S., Poewe, Werner, Wenning, Gregor K., Hardy, John A., Singleton, Andrew B., Gasser, Thomas
Publicerad 2009Text