id	author	title	date	pages	extension	mime	words	sentences	flesch	summary	cache	txt
work_vkpgxwrsbzdfjapfq6eakpv4sm	E Reid	Pure hereditary spastic paraplegia	1997.0	5	.pdf	application/pdf	5065	830	63	Keywords: pure hereditary spastic paraplegia; differential diagnosis; molecular genetics The diagnosis of pHSP in a family where several members have typical clinical features is the differential diagnosis include dopa responsive dystonia, which should actively be excluded in families where age of onset is early the neural cell adhesion molecule LI (LiCAM) at Xq28 are responsible for a complicated form of spastic paraplegia, in which Thus, the X linked hereditary spastic paraplegias indicate that mutations in the same Hereditary "pure" spastic paraplegia: a clinical spastic paraplegia: a study of nine families. familial spastic paraplegia type I: clinical and genetic analysis of a large North American family. locus for autosomal dominant familial spastic paraplegia to locus for autosomal dominant familial spastic paraplegia to Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one familial spastic paraplegia: tight linkage to chromosome Molecular genetics of familial spastic paraplegia: a multitude of responsible "pure" autosomal recessive familial spastic paraplegia to	./cache/work_vkpgxwrsbzdfjapfq6eakpv4sm.pdf	./txt/work_vkpgxwrsbzdfjapfq6eakpv4sm.txt