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Journal of Neurology|May 26, 2001
Restless legs syndrome in spinocerebellar ataxia types 1, 2, and 3M Abele, K Bürk, F Laccone, et al.Human Genetics|September 16, 1998
Mutation of the start codon in the FRDA1 gene: linkage analysis of three pedigrees with the ATG to ATT transversion points to a unique common ancestorC Zühlke, F Laccone, M Cossée, et al.Human Reproduction (Oxford, England)|January 5, 2001
Pseudo dicentric chromosome (5;21): a rare example of maternal germline mosaicismU Engel, S K Bohlander, K Bink, et al.Der Orthopade|September 10, 2013
[Hip dysplasia and spinal osteochondritis (Scheuermann's disease) in a girl with type II manifesting collagenopathy]A Al Kaissi, F Laccone, C Karner, et al.Journal of Medical Genetics|May 13, 2006
Very mild cases of Rett syndrome with skewed X inactivationP Huppke, E M Maier, A Warnke, et al.Journal of Neurology|October 20, 1999
Autosomal dominant cerebellar ataxia type I: oculomotor abnormalities in families with SCA1, SCA2, and SCA3K Bürk, M Fetter, M Abele, et al.American Journal of Human Genetics|April 20, 2001
MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal originR Trappe, F Laccone, J Cobilanschi, et al.Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1997
Saccade velocity in idiopathic and autosomal dominant cerebellar ataxiaK Bürk, M Fetter, M Skalej, et al.Clinical Genetics|May 22, 2008
Dysmorphic syndrome of hereditary neuralgic amyotrophy associated with a SEPT9 gene mutation--a family studyF Laccone, M C Hannibal, J Neesen, et al.Human Heredity|March 17, 1999
Linkage disequilibrium and haplotype analysis in German Friedreich ataxia familiesC Zühlke, U Gehlken, S Purmann, et al.Pageof 4