Zobrazeno 1 - 10
of 121
pro vyhledávání: '"Hammans, Simon"'
Autor:
Currò, Riccardo, Dominik, Natalia, Facchini, Stefano, Vegezzi, Elisa, Sullivan, Roisin, Deforie, Valentina Galassi, Fernández-Eulate, Gorka, Traschütz, Andreas, Rossi, Salvatore, Garibaldi, Matteo, Kwarciany, Mariusz, Taroni, Franco, Brusco, Alfredo, Good, Jean-Marc, Cavalcanti, Francesca, Hammans, Simon, Ravenscroft, Gianina, Roxburgh, Richard H, group, RFC1 repeat expansion study, Schnekenberg, Ricardo Parolin
Publikováno v:
Brain: A Journal of Neurology; May2024, Vol. 147 Issue 5, p1887-1898, 12p
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Autor:
Cortese, Andrea, Dohrn, Maike, Curro, Riccardo, Seeman, Pavel, Stojkovic, Tanya, Hammans, Simon, Previtali, Stefano, Bolino, Alessandra, Schenone, Angelo, Kennerson, Marina, Rojas-Garcia, Ricardo, Sevilla, Teresa, Hahn, Katrin, Claeys, Kristl, Brunkhorst, Robert, Cavalcanti, Francesca, Manganelli, Fiore, Zhang, Ruxu, Houlden, Henry, Scherer, Steven, Herrmann, David, Pareyson, Davide, Reilly, Mary, Shy, Michael, Zuchner, Stephan
Publikováno v:
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::22f5313b50927fc21beb90921da54246
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=16749
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=16749
Autor:
Burke, Georgina, Hammans, Simon
Publikováno v:
In Medicine August 2012 40(8):435-439
Autor:
Wai, Htoo A, Lord, Jenny, Lyon, Matthew, Gunning, Adam, Kelly, Hugh, Cibin, Penelope, Seaby, Eleanor G, Spiers-Fitzgerald, Kerry, Lye, Jed, Ellard, Sian, Thomas, N Simon, Bunyan, David J, Douglas, Andrew G L, Baralle, Diana, Naik, Swati, Ragge, Nicola, Cox, Helen, Morton, Jenny E., O'Driscoll, Mary, Lim, Derek, Osio, Deborah, Elmslie, Frances, Huber, Camilla, Hewitt, Julie, Brandon, Heidy, McEntagart, Meriel, Mansour, Sahar, Lahiri, Nayana, Dempsey, Esther, Manalo, Merrie, Homfray, Tessa, Saggar, Anand, Li, Jin, Barwell, Julian, Chandler, Kate E., Briggs, Tracy, Douzgou, Sofia, Adlard, Julian, Kraus, Alison, Mehta, Sarju, Watford, Amy, Donaldson, Alan, Low, Karen, Jones, Gabriela, Dixit, Abhijit, King, Elizabeth, Shannon, Nora, Kaliakatsos, Marios, Joss, Shelagh, Balasubramanian, Meena, Johnson, Diana, Everest, Sarah, Salter, Claire, Harrison, Victoria, Wise, Gillian, Torokwa, Audrey, Sands, Victoria, Pyle, Esther, Thomas, Tessy, Lachlan, Katherine, Foulds, Nicola, Lotery, Andrew, Hammans, Simon R., Pond, Emily, Horton, Rachel, Kharbanda, Mira, Hunt, David, Thomas, Charlene, Side, Lucy, Willis, Catherine, Greville-Heygate, Stephanie, Mawby, Rebecca, Mercer, Catherine, Temple, Karen, Kinning, Esther, Bojovic, Ognjen, Archer, L.
Publikováno v:
Genetics in Medicine
Wai, H A, Lord, J, Lyon, M, Gunning, A, Kelly, H, Cibin, P, Seaby, E G, Spiers-Fitzgerald, K, Lye, J, Ellard, S, Thomas, N S, Bunyan, D J, Douglas, A G L, Baralle, D, Splicing and disease working group, Naik, S, Ragge, N, Cox, H, Morton, J E, O'Driscoll, M, Lim, D, Osio, D, Elmslie, F, Huber, C, Hewitt, J, Brandon, H, McEntagart, M, Mansour, S, Lahiri, N, Dempsey, E, Manalo, M, Homfray, T, Saggar, A, Li, J, Barwell, J, Chandler, K E, Briggs, T, Douzgou, S, Adlard, J, Kraus, A, Mehta, S, Watford, A, Donaldson, A, Low, K, Jones, G, Dixit, A, King, E, Shannon, N, Kaliakatsos, M, Manalo, M, Joss, S, Balasubramanian, M, Johnson, D, Everest, S, Salter, C, Harrison, V, Wise, G, Torokwa, A, Sands, V, Pyle, E, Thomas, T, Lachlan, K, Foulds, N, Lotery, A, Douglas, A G L, Hammans, S R, Pond, E, Horton, R, Kharbanda, M, Hunt, D, Thomas, C, Side, L, Willis, C, Greville-Heygate, S, Mawby, R, Mercer, C, Temple, K, Kinning, E, Bojovic, O & Archer, L 2020, ' Blood RNA analysis can increase clinical diagnostic rate and resolve variants of uncertain significance ', Genetics in medicine : official journal of the American College of Medical Genetics, vol. 22, no. 6, pp. 1005-1014 . https://doi.org/10.1038/s41436-020-0766-9
Wai, H A, Lord, J, Lyon, M, Gunning, A, Kelly, H, Cibin, P, Seaby, E G, Spiers-Fitzgerald, K, Lye, J, Ellard, S, Thomas, N S, Bunyan, D J, Douglas, A G L, Baralle, D, Splicing and disease working group, Naik, S, Ragge, N, Cox, H, Morton, J E, O'Driscoll, M, Lim, D, Osio, D, Elmslie, F, Huber, C, Hewitt, J, Brandon, H, McEntagart, M, Mansour, S, Lahiri, N, Dempsey, E, Manalo, M, Homfray, T, Saggar, A, Li, J, Barwell, J, Chandler, K E, Briggs, T, Douzgou, S, Adlard, J, Kraus, A, Mehta, S, Watford, A, Donaldson, A, Low, K, Jones, G, Dixit, A, King, E, Shannon, N, Kaliakatsos, M, Manalo, M, Joss, S, Balasubramanian, M, Johnson, D, Everest, S, Salter, C, Harrison, V, Wise, G, Torokwa, A, Sands, V, Pyle, E, Thomas, T, Lachlan, K, Foulds, N, Lotery, A, Douglas, A G L, Hammans, S R, Pond, E, Horton, R, Kharbanda, M, Hunt, D, Thomas, C, Side, L, Willis, C, Greville-Heygate, S, Mawby, R, Mercer, C, Temple, K, Kinning, E, Bojovic, O & Archer, L 2020, ' Blood RNA analysis can increase clinical diagnostic rate and resolve variants of uncertain significance ', Genetics in medicine : official journal of the American College of Medical Genetics, vol. 22, no. 6, pp. 1005-1014 . https://doi.org/10.1038/s41436-020-0766-9
Diagnosis of genetic disorders is hampered by large numbers of variants of uncertain significance (VUSs) identified through next-generation sequencing. Many such variants may disrupt normal RNA splicing. We examined effects on splicing of a large coh
Akademický článek
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Autor:
Burke, Georgina, Hammans, Simon
Publikováno v:
In Medicine 2008 36(10):540-544
Autor:
Hammans, Simon, McMonagle, Paul
Publikováno v:
In Medicine 2004 32(9):23-27
Autor:
Hammans, Simon R.
Publikováno v:
Practical Neurology; Feb2021, Vol. 21 Issue 1, p43-47, 5p