Clinical, electrophysiological and morphological findings of Charcot–Marie–Tooth neuropathy with vocal cord palsy and mutations in the GDAP1 gene

By Sevilla T.  

Brain, Vol. 126, Iss. 9, 2003-09 ,pp. : 2023-2033

Oxford University Press

Access to resources Recommend Favorite

Severe infantile neuropathy with diaphragmatic weakness and its relationship to SMARD1

By Pitt Matthew  

Brain, Vol. 126, Iss. 12, 2003-12 ,pp. : 2682-2692

Oxford University Press

Access to resources Recommend Favorite

Mutations in the ganglioside-induced differentiation-associated protein-1 ( GDAP1 ) gene in intermediate type autosomal recessive Charcot–Marie–Tooth neuropathy

By Zerres K.  

Brain, Vol. 126, Iss. 3, 2003-03 ,pp. : 642-649

Oxford University Press

Access to resources Recommend Favorite

Optico-cochleo-dentate degeneration associated with severe peripheral neuropathy and caused by peroxisomal D-bifunctional protein deficiency

By Schröder J.   Hackel V.   Wanders R.   Göhlich-Ratmann G.   Voit T.  

Acta Neuropathologica, Vol. 108, Iss. 2, 2004-08 ,pp. : 154-167

Springer Publishing Company

Access to resources Recommend Favorite

Isolated abducens nerve paresis associated with high titer of anti-asialo-GM1 following Campylobacter jejuni enteritis

By Katchanov Juri   Lünemann Jan   Masuhr Florian   Meisel Andreas   Möller Helgard   Zschenderlein Rolf  

Journal of Neurology, Vol. 251, Iss. 11, 2004-11 ,pp. : 1404-1405

Springer Publishing Company

Access to resources Recommend Favorite