Cognitive impairment in families with pure autosomal dominant hereditary spastic paraparesis

By Webb S   Hutchinson M  

Brain, Vol. 121, Iss. 5, 1998-05 ,pp. : 923-929

Oxford University Press

Access to resources Recommend Favorite

Locus–phenotype correlations in autosomal dominant pure hereditary spastic paraplegia

By Reid E.   Grayson C.   Rogers M. T.  

Brain, Vol. 122, Iss. 9, 1999-09 ,pp. : 1741-1755

Oxford University Press

Access to resources Recommend Favorite

Autosomal dominant hereditary spastic paraparesis with cognitive loss linked to chromosome 2p

By Webb S   Coleman D   Byrne P   Parfrey N   Burke T   Hutchinson J   Hutchinson M  

Brain, Vol. 121, Iss. 4, 1998-04 ,pp. : 601-609

Oxford University Press

Access to resources Recommend Favorite

Reduced reciprocal inhibition is seen only in spastic limbs in patients with neurolathyrism

By Crone C.   Petersen N.   Gimenéz-Roldán S.   Lungholt B.   Nyborg K.   Nielsen J.  

Experimental Brain Research, Vol. 181, Iss. 1, 2007-07 ,pp. : 193-197

Springer Publishing Company

Access to resources Recommend Favorite

Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia

By Ashley-Koch Allison   Bonner Erin R.   Gaskell P. Craig   West Sandra G.   Tim Richard   Wolpert Chantelle M.   Jones Rodney   Farrell Carolyn D.   Nance Martha   Svenson Ingrid K.   Marchuk Douglas A.   Boustany Rose-Mary N.   Vance Jeffery M.   Scott William K.   Pericak-Vance Margaret A.  

Neurogenetics, Vol. 3, Iss. 2, 2001-03 ,pp. : 91-97

Springer Publishing Company

Access to resources Recommend Favorite