Philippe de Mazancourt

X‐chromosome inactivation in female patients with Fabry disease

Lucía Echevarría, Karelle Bénistan, Anne Toussaint et al. · Clinical Genetics · 2015 · 417 citations

Life Sciences, Genetics, Molecular Genetics +15

Mutation in WNT10A Is Associated with an Autosomal Recessive Ectodermal Dysplasia: The Odonto-onycho-dermal Dysplasia

Lynn Adaimy, Éliane Chouery, Hala Mégarbané et al. · The American Journal of Human Genetics · 2007 · 249 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

A High-Performance Liquid Chromatography Method with Photodiode-Array UV Detection for Therapeutic Drug Monitoring of the Nontricyclic Antidepressant Drugs

Charlotte Duverneuil, Geoffroy Lorin de la Grandmaison, Philippe de Mazancourt et al. · Therapeutic Drug Monitoring · 2003 · 149 citations

Pharmacy, Pharmaceutical Analysis, Pharmacology +17

Mild forms of hypophosphatasia mostly result from dominant negative effect of severe alleles or from compound heterozygosity for severe and moderate alleles

Delphine Fauvert, Isabelle Brun‐Heath, Anne-Sophie Lia-Baldini et al. · BMC Medical Genetics · 2009 · 148 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Simultaneous determination of thirteen β-blockers and one metabolite by gradient high-performance liquid chromatography with photodiode-array UV detection

Magali Delamoye, Charlotte Duverneuil, François Paraire et al. · Forensic Science International · 2004 · 130 citations

Pharmacy, Pharmaceutical Analysis, Pharmacology +17