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Human Molecular Genetics|February 1, 1995
A molecular defect in coproporphyrinogen oxidase gene causing harderoporphyria, a variant form of hereditary coproporphyriaJ Lamoril, P Martasek, J C Deybach, et al.
Parasite (Paris, France)|June 1, 1995
Detection of Toxoplasma gondii parasitemia by polymerase chain reaction in perorally infected miceA Paugam, J Dupouy-Camet, M H Sumuyen, et al.
Blood|March 9, 1999
Inheritance in erythropoietic protoporphyria: a common wild-type ferrochelatase allelic variant with low expression accounts for clinical manifestationL Gouya, H Puy, J Lamoril, et al.
American Journal of Human Genetics|February 1, 1996
Modulation of the phenotype in dominant erythropoietic protoporphyria by a low expression of the normal ferrochelatase alleleL Gouya, J C Deybach, J Lamoril, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1992
Thyroid hormone extraction by plasma exchange: a study of extraction rateH Puy, J Lamoril, J M Marcelli, et al.
Human Molecular Genetics|March 1, 1996
Mutations in the protoporphyrinogen oxidase gene in patients with variegate porphyriaJ C Deybach, H Puy, A M Robréau, et al.
Journal of Inherited Metabolic Disease|September 14, 2002
A molecular, enzymatic and clinical study in a family with hereditary coproporphyriaU Gross, H Puy, U Meissauer, et al.
Journal of Clinical Pathology|January 1, 1996
Detection by PCR of Toxoplasma gondii in blood in the diagnosis of cerebral toxoplasmosis in patients with AIDSJ Lamoril, J M Molina, A de Gouvello, et al.
American Journal of Human Genetics|June 1, 1997
Molecular epidemiology and diagnosis of PBG deaminase gene defects in acute intermittent porphyriaH Puy, J C Deybach, J Lamoril, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 4, 1999
Evaluation of mutation screening by heteroduplex analysis in acute intermittent porphyria: comparison with denaturing gradient gel electrophoresisD Tchernitchko, J Lamoril, H Puy, et al.
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