George Hoganson

Cytochrome <i>c</i> oxidase deficiency in leigh syndrome

Salvatore DiMauro, Serenella Servidei, Massimo Zeviani et al. · Annals of Neurology · 1987 · 363 citations

Recombinant human acid α-glucosidase enzyme therapy for infantile glycogen storage disease type II: Results of a phase I/II clinical trial

Andrea Amalfitano, A. Resai Bengur, Richard P. Morse et al. · Genetics in Medicine · 2001 · 346 citations · Full text

Translational Medicine, Biochemistry, Inherited Metabolic Disease +5

Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation

Patrick Tarpey, F. Lucy Raymond, Lam Son Nguyen et al. · Nature Genetics · 2007 · 284 citations · Full text

Developmental Biology, Genetic Disorder, Genetics +7

Role of Tyrosinase as the Determinant of Pigmentation in Cultured Human Melanocytes

Ken Iozumi, George Hoganson, Raffaele Pennella et al. · Journal of Investigative Dermatology · 1993 · 267 citations

Natural Pigments, Carotenoid, Biochemistry +6

Phenylketonuria in adulthood: A collaborative study

Richard Koch, Barbara K. Burton, George Hoganson et al. · Journal of Inherited Metabolic Disease · 2002 · 213 citations