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

Autosomal dominant hereditary sensory neuropathy with chronic cough and gastro-oesophageal reflux: clinical features in two families linked to chromosome 3p22–p24

By Spring Penelope J.   Kok Cindy   Nicholson Garth A.   Ing Alvin J.   Spies Judith M.   Bassett Mark L.   Cameron John   Kerlin Paul   Bowler Simon   Tuck Roger   Pollard John D.  

Brain, Vol. 128, Iss. 12, 2005-12 ,pp. : 2797-2810

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

Reciprocal inhibition and corticospinal transmission in the arm and leg in patients with autosomal dominant pure spastic paraparesis (ADPSP)

By Crone C.  

Brain, Vol. 127, Iss. 12, 2004-12 ,pp. : 2693-2702

Oxford University Press

Access to resources Recommend Favorite

A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23

By Chung M-y.  

Brain, Vol. 126, Iss. 6, 2003-06 ,pp. : 1293-1299

Oxford University Press

Access to resources Recommend Favorite