L Phung

Acute intermittent porphyria: prevalence of mutations in the porphobilinogen deaminase gene in blood donors in France

Y Nordmann, Hervé Puy, V. Da Silva et al. · Journal of Internal Medicine · 1997 · 128 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Harderoporphyria: a variant hereditary coproporphyria.

Y Nordmann, Bernard Grandchamp, Hubert de Verneuil et al. · Journal of Clinical Investigation · 1983 · 102 citations · Full text

Life Sciences, Biochemistry, Genetics +16

Recurrence risk estimation of acute intermittent porphyria based on analysis of porphobilinogen deaminase activity: A Bayesian approach

Catherine Bonaïti‐Pellié, L Phung, Y Nordmann · American Journal of Medical Genetics · 1984 · 27 citations

Life Sciences, Biochemistry, Genetics +13

Coexistent hereditary coproporphyria and congenital erythropoietic porphyria (Günther disease)

Y Nordmann, Daniel Amram, Jean‐Charles Deybach et al. · Journal of Inherited Metabolic Disease · 1990 · 25 citations

Life Sciences, Genetics, Human Genetics +9

[Drug risk of hepatic porphyria. Development of an animal experiment model].

Jean‐Charles Deybach, V. Da Silva, L Phung et al. · PubMed · 1987 · 14 citations

Medicine, Pharmacology, Experimental Pharmacology +6