Browsing by Author Houlden, Henry

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Issue DateTitleAuthor(s)
14-Aug-2023Frequency and phenotypic spectrum of spinocerebellar ataxia <scp>27B</scp> and other genetic ataxias in a Spanish cohort of late‐onset cerebellar ataxiaIruzubieta, Pablo; Pellerin, David; Bergareche, Alberto; Albajar, Inés; Mondragón, Elisabet; Vinagre, Ana; Fernández‐torrón, Roberto; Moreno, Fermín; Equiza, Jon; Campo‐caballero, David; Poza, Juan José; Ruibal, Marta; Formica, Alessandro; Dicaire, Marie‐josée; Danzi, Matt C.; Zuchner, Stephan; Croitoru, Ioana; Ruiz, Montserrat; Schlüter, Agatha; Casasnovas, Carlos; Pujol, Aurora; Brais, Bernard; Houlden, Henry; López de munain, Adolfo; Ruiz‐martínez, Javier
1-Jul-2019PDXK mutations cause polyneuropathy responsive to pyridoxal 5'-phosphate supplementationChelban, Viorica; Wilson, Matthew P.; Chardon, Jodi Warman; Vandrovcova, Jana; Zanetti, M. Natalia; Zamba-Papanicolaou, Eleni; Efthymiou, Stephanie; Pope, Simon; Conte, Maria R.; Abis, Giancarlo; Liu, Yo-Tsen; Tribollet, Eloise; Haridy, Nourelhoda A.; Botía, Juan A.; Ryten, Mina; Nicolaou, Paschalis; Minaidou, Anna; Christodoulou, Kyproula; Kernohan, Kristin D.; Eaton, Alison; Osmond, Matthew; Ito, Yoko; Bourque, Pierre; Jepson, James E.C.; Bello, Oscar; Bremner, Fion; Cordivari, Carla; Reilly, Mary M.; Foiani, Martha; Heslegrave, Amanda; Zetterberg, Henrik; Heales, Simon J.R.; Wood, Nicholas W.; Rothman, James E.; Boycott, Kym M.; Mills, Philippa B.; Clayton, Peter T.; Houlden, Henry; Care4Rare Canada Consortium; the SYNaPS Study Group.