Fritz Haverkamp
Department of Pediatrics
University of Bonn
Germany
Name/email consistency: high
- Risk analyses for the cognitive phenotype in Turner's syndrome: evidence of familial influence as a decisive factor. Haverkamp, F., Zerres, K., Rietz, C., Noeker, M., Ruenger, M. J. Child Neurol. (2004)
- Familial factors and hearing impairment modulate the neuromotor phenotype in Turner syndrome. Haverkamp, F., Keuker, T., Woelfle, J., Kaiser, G., Zerres, K., Rietz, C., Ruenger, M. Eur. J. Pediatr. (2003)
- Psychomotor development in children with early diagnosed giant interhemispheric cysts. Haverkamp, F., Heep, A., Woelfle, J. Dev. Med. Child. Neurol (2002)
- Neurodevelopmental risks in twin-to-twin transfusion syndrome: preliminary findings. Haverkamp, F., Lex, C., Hanisch, C., Fahnenstich, H., Zerres, K. Eur. J. Paediatr. Neurol. (2001)
- Evidence of a specific vulnerability for deficient sequential cognitive information processing in epilepsy. Haverkamp, F., Hanisch, C., Mayer, H., Noeker, M. J. Child Neurol. (2001)
- Growth retardation in Turner syndrome: aneuploidy, rather than specific gene loss, may explain growth failure. Haverkamp, F., Wölfle, J., Zerres, K., Butenandt, O., Amendt, P., Hauffa, B.P., Weimann, E., Bettendorf, M., Keller, E., Mühlenberg, R., Partsch, C.J., Sippell, W.G., Hoppe, C. J. Clin. Endocrinol. Metab. (1999)