G. Pitelet

Phenotype and genotype in 101 males with X-linked creatine transporter deficiency

Jiddeke M. van de Kamp, Ofir T. Betsalel, Saadet Mercimek‐Mahmutoglu et al. · Journal of Medical Genetics · 2013 · 165 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

High frequency of creatine deficiency syndromes in patients with unexplained mental retardation

Laurence Lion‐François, David Cheillan, G. Pitelet et al. · Neurology · 2006 · 102 citations

Medicine, Neurology, Pediatrics +13

LIS1-Related Isolated Lissencephaly

Yoann Saillour, Nathalie Carion, Chloé Quēlin et al. · Archives of Neurology · 2009 · 100 citations · Full text

Life Sciences, Genetics, Neurology +11

Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms

David Cheillan, Marie Joncquel-Chevalier Curt, Gilbert Briand et al. · Orphanet Journal of Rare Diseases · 2012 · 43 citations · Full text

Medicine, Neurology, Neurogenetics +6

Creatine and guanidinoacetate reference values in a French population

Marie Joncquel-Chevalier Curt, David Cheillan, Gilbert Briand et al. · Molecular Genetics and Metabolism · 2013 · 38 citations

Agriculture, Nutritional Sciences, Human Nutrition +1