P. Byrne

Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome

Sylvain Hanein, Elodie Martin, Amir Boukhris et al. · The American Journal of Human Genetics · 2008 · 211 citations · Full text

Including Kjellin Syndrome, Genetics, Spg15 Gene +4

REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31

Christian Beetz, Rebecca Schüle, Tine Deconinck et al. · Brain · 2008 · 180 citations · Full text

SPG15, a new locus for autosomal recessive complicated HSP on chromosome 14q

C. A. Hughes, P. Byrne, Stewart Webb et al. · Neurology · 2001 · 76 citations

Cytogenetics, Genetics, Pathology +17

Dementia in SPG4 hereditary spastic paraplegia

Sinéad M. Murphy, Gráinne S. Gorman, Christian Beetz et al. · Neurology · 2009 · 58 citations · Full text

The hereditary spastic paraplegia protein spartin localises to mitochondria

Jianping Lu, Faiza Rashid, P. Byrne · Journal of Neurochemistry · 2006 · 57 citations · Full text