Related content

Cutaneous Venous Malformations Related to KRIT1 Mutation: Case Report and Literature Review

By Grippaudo Francesca   Piane Maria   Amoroso Matteo   Longo Benedetto   Penco Silvana   Chessa Luciana   Giubettini Maria   Santanelli Fabio  

Journal of Molecular Neuroscience, Vol. 51, Iss. 2, 2013-10 ,pp. : 442-445

Humana Press, Inc

Access to resources Recommend Favorite

A novel PMP22 mutation Ser22Phe in a family with hereditary neuropathy with liability to pressure palsies and CMT1A phenotypes

By Kleopa Kleopas   Georgiou Domna-Maria   Nicolaou Paschalis   Koutsou Pantelitsa   Papathanasiou Eleftherios   Kyriakides Theodoros   Christodoulou Kyproula  

Neurogenetics, Vol. 5, Iss. 3, 2004-09 ,pp. : 171-175

Springer Publishing Company

Access to resources Recommend Favorite

Impaired Intracellular Trafficking Is a Common Disease Mechanism of PMP22 Point Mutations in Peripheral Neuropathies

By Naef R.   Suter U.  

Neurobiology of Disease, Vol. 6, Iss. 1, 1999-02 ,pp. : 1-14

Academic Press

Access to resources Recommend Favorite

HydroCoil embolization of a ruptured infectious aneurysm in a pediatric patient: case report and review of the literature

By Eddleman Christopher   Nikas Dimitrios   Shaibani Ali   Khan Pervez   DiPatri Arthur   Tomita Tadanori  

Child's Nervous System, Vol. 23, Iss. 6, 2007-06 ,pp. : 707-712

Springer Publishing Company

Access to resources Recommend Favorite

Anterior spinal epidural abscess due to Salmonella typhi: a report of a rare case treated conservatively and review of the literature

By Nardone Antonio   Caporlingua Federico   Lapadula Gennaro   Santoro Antonio  

Neurological Sciences, Vol. 34, Iss. 11, 2013-11 ,pp. : 2051-2052

Springer Publishing Company

Access to resources Recommend Favorite