Fuki M. Hisama
Department of Neurology
Yale University School of Medicine
New Haven
Connecticut 06520-8018
USA
Name/email consistency: high
- WRN's tenth anniversary. Hisama, F.M., Bohr, V.A., Oshima, J. Sci. Aging. Knowledge. Environ (2006)
- Familial periodic paralysis and Charcot-Marie-Tooth disease in a 7-generation family. Hisama, F.M. Arch. Neurol. (2005)
- Human GABA(B) receptor 1 gene: eight novel sequence variants. Hisama, F.M., Gruen, J.R., Choi, J., Huseinovic, M., Grigorenko, E.L., Pauls, D., Mattson, R.H., Gelernter, J., Wood, F.B., Goei, V.L. Hum. Mutat. (2001)
- Clinical and molecular studies in a family with probable X-linked dominant Charcot-Marie-Tooth disease involving the central nervous system. Hisama, F.M., Lee, H.H., Vashlishan, A., Tekumalla, P., Russell, D.S., Auld, E., Goldstein, J.M. Arch. Neurol. (2001)
- GABA and the ornithine delta-aminotransferase gene in vigabatrin-associated visual field defects. Hisama, F.M., Mattson, R.H., Lee, H.H., Felice, K., Petroff, O.A. Seizure (2001)