R. Eisensmith

发表

In vivo gene therapy for hyperlipidemia: phenotypic correction in Watanabe rabbits by hepatic delivery of the rabbit LDL receptor gene.

I. Nasonkin, A. Hughes, M. Mims, 1995, The Journal of clinical investigation.

Gene therapy for phenylketonuria

S. Woo, R. Eisensmith, 1994, European journal of pediatrics.

Gene therapy for hemophilia B: host immunosuppression prolongs the therapeutic effect of adenovirus-mediated factor IX expression.

M. Kay, C. Landen, D. Bellinger, 1995, Human gene therapy.

Macrophage depletion increases the safety, efficacy and persistence of adenovirus-mediated gene transfer in vivo

M. Finegold, R. Eisensmith, A. Kuzmin, 1997, Gene Therapy.

Prenatal diagnosis by minisatellite analysis in italian families with phenylketonuria

P. Bosco, I. Dianzani, V. Romano, 1994, Prenatal diagnosis.

Haplotypes and mutations of the PAH locus in Egyptian families with PKU

N. Meguid, M. El-Awady, S. Temtamy, 1999, European Journal of Human Genetics.

Population genetics of phenylketonuria

S. Woo, R. Eisensmith, 1994, Acta paediatrica (Oslo, Norway : 1992). Supplement.

Gene therapy for phenylketonuria: phenotypic correction in a genetically deficient mouse model by adenovirus-mediated hepatic gene transfer.

S. Woo, W. Dove, M. Finegold, 1994, Gene therapy.

RFLP discordance in a PKU family due to a deletion in the PAH gene.

P. Bosco, F. Calì, G. Novelli, 1996, The Turkish journal of pediatrics.