Peter Huppke
Department of Pediatrics and Pediatric Neurology
Faculty of Medicine
Georg August University
Göttingen
Germany
Name/email consistency: high
- Molecular and biochemical characterization of a unique mutation in CCS, the human copper chaperone to superoxide dismutase. Huppke, P., Brendel, C., Korenke, G.C., Marquardt, I., Donsante, A., Yi, L., Hicks, J.D., Steinbach, P.J., Wilson, C., Elpeleg, O., Møller, L.B., Christodoulou, J., Kaler, S.G., Gärtner, J. Hum. Mutat. (2012)
- Neuromyelitis optica and NMO-IgG in European pediatric patients. Huppke, P., Blüthner, M., Bauer, O., Stark, W., Reinhardt, K., Huppke, B., Gärtner, J. Neurology (2010)
- A practical guide to pediatric multiple sclerosis. Huppke, P., Gärtner, J. Neuropediatrics (2010)
- Immunoglobulin therapy in idiopathic hypothalamic dysfunction. Huppke, P., Heise, A., Rostasy, K., Huppke, B., Gärtner, J. Pediatr. Neurol. (2009)
- Treatment of epilepsy in Rett syndrome. Huppke, P., Köhler, K., Brockmann, K., Stettner, G.M., Gärtner, J. Eur. J. Paediatr. Neurol. (2007)
- Very mild cases of Rett syndrome with skewed X inactivation. Huppke, P., Maier, E.M., Warnke, A., Brendel, C., Laccone, F., Gärtner, J. J. Med. Genet. (2006)
- Perisylvian polymicrogyria in Landau-Kleffner syndrome. Huppke, P., Kallenberg, K., Gärtner, J. Neurology (2005)
- Mutation analysis of the HDAC 1, 2, 8 and CDKL5 genes in Rett syndrome patients without mutations in MECP2. Huppke, P., Ohlenbusch, A., Brendel, C., Laccone, F., Gärtner, J. Am. J. Med. Genet. A (2005)
- Molecular diagnosis of Rett syndrome. Huppke, P., Gärtner, J. J. Child Neurol. (2005)
- Indication for genetic testing: a checklist for Rett syndrome. Huppke, P., Köhler, K., Laccone, F., Hanefeld, F. J. Pediatr. (2003)
- The spectrum of phenotypes in females with Rett Syndrome. Huppke, P., Held, M., Laccone, F., Hanefeld, F. Brain Dev. (2003)
- Influence of mutation type and location on phenotype in 123 patients with Rett syndrome. Huppke, P., Held, M., Hanefeld, F., Engel, W., Laccone, F. Neuropediatrics (2002)
- Altered methylation pattern of the G6 PD promoter in Rett syndrome. Huppke, P., Bohlander, S., Krämer, N., Laccone, F., Hanefeld, F. Neuropediatrics (2002)
- Eosinophilic fasciitis leading to painless contractures. Huppke, P., Wilken, B., Brockmann, K., Sattler, B., Hanefeld, F. Eur. J. Pediatr. (2002)
- Two brothers with Hennekam syndrome and cerebral abnormalities. Huppke, P., Christen, H.J., Sattler, B., Hanefeld, F. Clin. Dysmorphol. (2000)