Patrick M. Hefferan

Menkes disease: a biochemical abnormality in cultured human fibroblasts.

T J Goka, Roger E. Stevenson, Patrick M. Hefferan et al. · Proceedings of the National Academy of Sciences · 1976 · 173 citations · Full text

Iron Metabolism, Genetics, Pathology +19

ATP Depletion, a Possible Role in the Pathogenesis of Hyperuricemia in Glycogen Storage Disease Type I

Harry L. Greene, Frederick A. Wilson, Patrick M. Hefferan et al. · Journal of Clinical Investigation · 1978 · 65 citations · Full text

Familial recurrent rhabdomyolysis due to carnitine palmityl transferase deficiency

Bernard M. Patten, Jeanie McMillin Wood, Yadollah Harati et al. · The American Journal of Medicine · 1979 · 37 citations

Familial Recurrent Rhabdomyolysis, Mendelian Disorder, Genetic Disorder +4

Genetic evidence for the common identity of glucose-6-phosphatase, pyrophosphate-glucose phosphotransferase, carbamyl phosphate-glucose phosphotransferase and inorganic pyrophosphatase

Patrick M. Hefferan, R. Rodney Howell · Biochimica et Biophysica Acta (BBA) - General Subjects · 1977 · 17 citations

Common Identity, Pyrophosphate-glucose Phosphotransferase, Metabolic Pathways +12

Enzymatic and biochemical characterization of the avian glycogen body

Aaron S. Fink, Patrick M. Hefferan, R. Rodney Howell · Comparative Biochemistry and Physiology Part B Comparative Biochemistry · 1975 · 13 citations

Biochemistry, Bioanalysis, Metabolism +5