Autosomal dominant congenital fibre type disproportion: a clinicopathological and imaging study of a large family

By Sobrido M. J.  

Brain, Vol. 128, Iss. 7, 2005-07 ,pp. : 1716-1727

Oxford University Press

Access to resources Recommend Favorite

The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlates

By Giunti P   Sabbadini G   Sweeney MG   Davis MB   Veneziano L   Mantuano E   Federico A   Plasmati R   Frontali M   Wood NW  

Brain, Vol. 121, Iss. 3, 1998-03 ,pp. : 459-467

Oxford University Press

Access to resources Recommend Favorite

Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study

By Gouider-Khouja N.   Larnaout A.   Amouri R.   Sfar S.   Belal S.   Ben Hamida C.   Ben Hamida M.   Hattori N.   Mizuno Y.   Hentati F.  

Parkinsonism and Related Disorders, Vol. 9, Iss. 5, 2003-06 ,pp. : 247-251

Elsevier

Access to resources Recommend Favorite

Migraine in women. Epidemiological, clinical, genetic, and experimental aspects

By Mattsson Peter  

Nordic Journal of Psychiatry, Vol. 54, Iss. 4, 2000-11 ,pp. : 297-298

Informa Healthcare

Access to resources Recommend Favorite

Late onset autosomal dominant Charcot–Marie–Tooth 2 neuropathy in a Costa Rican family

By Berghoff Corinna   Berghoff Martin   Leal Alejandro   Morera Bernal   Contreras Carlos   Barrantes Ramiro   Rautenstrauss Bernd   Del Valle Gerardo   Heuss Dieter  

Neurological Research, Vol. 31, Iss. 3, 2009-04 ,pp. : 283-288

Maney Publishing

Access to resources Recommend Favorite