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Isabelle Creveaux

French Institute of Health and Medical Research

33

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Paracetamol and Pain Modulation by TRPV1, UGT2B15, SULT1A1 Genotypes: A Randomized Clinical Trial in Healthy Volunteers

2019 Pain Medicine
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TREX1 est-il impliqué dans les manifestations neuropsychiatriques du lupus systémique ? Étude du génotype sur une cohorte française

2012 Revue de Médecine Interne
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Élévation de la transcription d’IL-1β dans les abcès aseptiques

2010 Revue de Médecine Interne
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lvation de la transcription dIL-1 dans les abcs aseptiques

2010 Revue de Médecine Interne
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Identification of new FOXP3 mutations and prenatal diagnosis of IPEX syndrome

2010 Prenatal Diagnosis
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Intra-familial phenotypic heterogeneity in adult onset vanishing white matter disease

2008 Clinical Neurology and Neurosurgery
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Leucoencephalopathy with vanishing white matter may cause progressive myoclonus epilepsy.

2008 Epilepsia
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Leucoencephalopathy with vanishing white matter as a cause of progressive myoclonus epilepsy

2007 Neurology
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Vanishing white matter disease presenting as progressive myoclonus epilepsy

2005 Epilepsia
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Mouse SCO-spondin, a gene of the thrombospondin type 1 repeat (TSR) superfamily expressed in the brain.

2003 Gene
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Citations (12)