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

Life Sciences, Biochemistry, Pathology +14

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 · 347 citations · Full text

Life Sciences, Biochemistry, Pediatrics +8

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 · 294 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

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 · 269 citations

Life Sciences, Biochemistry, Cell Biology +10

Phenylketonuria in adulthood: A collaborative study

Richard Koch, Barbara K. Burton, George Hoganson et al. · Journal of Inherited Metabolic Disease · 2002 · 215 citations

Medicine, Endocrinology, Pediatrics +3