Peter G. Barth
Department of Paediatric Neurology
Room # G8-211
Emma Children's Hospital/Academic Medical Centre
University of Amsterdam
Netherlands
Name/email consistency: high
- 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)
- Congenital brainstem disconnection associated with a syrinx of the brainstem. Barth, P.G., de Vries, L.S., Nikkels, P.G., Troost, D. Neuropediatrics (2008)
- 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)
- 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)
- 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)
- The neuropathology of Aicardi-Goutières syndrome. Barth, P.G. Eur. J. Paediatr. Neurol. (2002)
- 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)
- 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)
- 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)
