Conrad C. Weihl
Department of Neurology
Washington University School of Medicine
Saint Louis
MO 63110
USA
Name/email consistency: high
- Valosin containing protein associated fronto-temporal lobar degeneration: clinical presentation, pathologic features and pathogenesis. Weihl, C.C. Curr. Alzheimer. Res (2011)
- Novel GNE mutations in two phenotypically distinct HIBM2 patients. Weihl, C.C., Miller, S.E., Zaidman, C.M., Pestronk, A., Baloh, R.H., Al-Lozi, M. Neuromuscul. Disord. (2011)
- Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia. Weihl, C.C., Pestronk, A., Kimonis, V.E. Neuromuscul. Disord. (2009)
- TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementia. Weihl, C.C., Temiz, P., Miller, S.E., Watts, G., Smith, C., Forman, M., Hanson, P.I., Kimonis, V., Pestronk, A. J. Neurol. Neurosurg. Psychiatr. (2008)
- Transgenic expression of inclusion body myopathy associated mutant p97/VCP causes weakness and ubiquitinated protein inclusions in mice. Weihl, C.C., Miller, S.E., Hanson, P.I., Pestronk, A. Hum. Mol. Genet. (2007)
- Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation. Weihl, C.C., Dalal, S., Pestronk, A., Hanson, P.I. Hum. Mol. Genet. (2006)