Johan L. K. Van Hove
Department of Pediatrics
The University of Colorado at Denver Health Sciences Center and The Children's Hospital
Denver
CO 80045
USA
Name/email consistency: high
- Infantile cardiomyopathy caused by the T14709C mutation in the mitochondrial tRNA glutamic acid gene. Van Hove, J.L., Freehauf, C., Miyamoto, S., Vladutiu, G.D., Pancrudo, J., Bonilla, E., Lovell, M.A., Mierau, G.W., Thomas, J.A., Shanske, S. Eur. J. Pediatr. (2008)
- Management of a patient with holocarboxylase synthetase deficiency. Van Hove, J.L., Josefsberg, S., Freehauf, C., Thomas, J.A., Thuy, L.P., Barshop, B.A., Woontner, M., Mock, D.M., Chiang, P.W., Spector, E., Meneses-Morales, I., Cervantes-Roldán, R., León-Del-Río, A. Mol. Genet. Metab. (2008)
- Expanded motor and psychiatric phenotype in autosomal dominant Segawa syndrome due to GTP cyclohydrolase deficiency. Van Hove, J.L., Steyaert, J., Matthijs, G., Legius, E., Theys, P., Wevers, R., Romstad, A., Møller, L.B., Hedrich, K., Goriounov, D., Blau, N., Klein, C., Casaer, P. J. Neurol. Neurosurg. Psychiatr. (2006)
- Clericuzio type poikiloderma with neutropenia is distinct from Rothmund-Thomson syndrome. Van Hove, J.L., Jaeken, J., Proesmans, M., Boeck, K.D., Minner, K., Matthijs, G., Verbeken, E., Demunter, A., Boogaerts, M. Am. J. Med. Genet. A (2005)
- Benzoate treatment and the glycine index in nonketotic hyperglycinaemia. Van Hove, J.L., Vande Kerckhove, K., Hennermann, J.B., Mahieu, V., Declercq, P., Mertens, S., De Becker, M., Kishnani, P.S., Jaeken, J. J. Inherit. Metab. Dis. (2005)
