The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Peter G. Barth

Department of Paediatric Neurology

Room # G8-211

Emma Children's Hospital/Academic Medical Centre

University of Amsterdam



Name/email consistency: high



  • Department of Paediatric Neurology, Room # G8-211, Emma Children's Hospital/Academic Medical Centre, University of Amsterdam, Netherlands. 1998 - 2008
  • Emma Children's Hospital, Department of Pediatrics, Amsterdam, Netherlands. 1999


  1. Rhabdomyolysis in pontocerebellar hypoplasia type 2 (PCH-2). Barth, P.G., Ryan, M.M., Webster, R.I., Aronica, E., Kan, A., Ramkema, M., Jardine, P., Poll-The, B.T. Neuromuscul. Disord. (2008) [Pubmed]
  2. Congenital brainstem disconnection associated with a syrinx of the brainstem. Barth, P.G., de Vries, L.S., Nikkels, P.G., Troost, D. Neuropediatrics (2008) [Pubmed]
  3. Pontocerebellar hypoplasia type 2: a neuropathological update. Barth, P.G., Aronica, E., de Vries, L., Nikkels, P.G., Scheper, W., Hoozemans, J.J., Poll-The, B.T., Troost, D. Acta Neuropathol. (2007) [Pubmed]
  4. Neuroimaging of peroxisome biogenesis disorders (Zellweger spectrum) with prolonged survival. Barth, P.G., Majoie, C.B., Gootjes, J., Wanders, R.J., Waterham, H.R., van der Knaap, M.S., de Klerk, J.B., Smeitink, J., Poll-The, B.T. Neurology (2004) [Pubmed]
  5. X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): an update. Barth, P.G., Valianpour, F., Bowen, V.M., Lam, J., Duran, M., Vaz, F.M., Wanders, R.J. Am. J. Med. Genet. A (2004) [Pubmed]
  6. The neuropathology of Aicardi-Goutières syndrome. Barth, P.G. Eur. J. Paediatr. Neurol. (2002) [Pubmed]
  7. Late onset white matter disease in peroxisome biogenesis disorder. Barth, P.G., Gootjes, J., Bode, H., Vreken, P., Majoie, C.B., Wanders, R.J. Neurology (2001) [Pubmed]
  8. X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060). Barth, P.G., Wanders, R.J., Vreken, P., Janssen, E.A., Lam, J., Baas, F. J. Inherit. Metab. Dis. (1999) [Pubmed]
  9. Infantile fibre type disproportion, myofibrillar lysis and cardiomyopathy: a disorder in three unrelated Dutch families. Barth, P.G., Wanders, R.J., Ruitenbeek, W., Roe, C., Scholte, H.R., van der Harten, H., van Moorsel, J., Duran, M., Dingemans, K.P. Neuromuscul. Disord. (1998) [Pubmed]
WikiGenes - Universities