New insights into genotype―phenotype correlations for the doublecortin-related lissencephaly spectrumBAHI-BUISSON, Nadia; SOUVILLE, Isabelle; LOUIS LEGER, Pierre et al.Brain. 2013, Vol 136, pp 223-244, issn 0006-8950, 22 p., 1Article

The wide spectrum of tubulinopathies: what are the key features for the diagnosis?BAHI-BUISSON, Nadia; POIRIER, Karine; LASCELLES, Karine et al.Brain. 2014, Vol 137, pp 1676-1700, issn 0006-8950, 25 p., 6Article

The location of DCX mutations predicts malformation severity in X-linked lissencephalyLEGER, Pierre-Louis; SOUVILLE, Isabelle; RENARD, Jean Louis et al.Neurogenetics (Oxford. Print). 2008, Vol 9, Num 4, pp 277-285, issn 1364-6745, 9 p.Article

Mosaic DCX deletion causes subcortical band heterotopia in malesQUELIN, Chloé; SAILLOUR, Yoann; BELDJORD, Cherif et al.Neurogenetics (Oxford. Print). 2012, Vol 13, Num 4, pp 367-373, issn 1364-6745, 7 p.Article

CDKL5 and ARX mutations are not responsible for early onset severe myoclonic epilepsy in infancyNABBOUT, Rima; DEPIENNE, Christel; LEGUERN, Eric et al.Epilepsy research. 2009, Vol 87, Num 1, pp 25-30, issn 0920-1211, 6 p.Article

Combination of infantile spasms, non-epileptic seizures and complex movement disorder : A new case of ARX-related epilepsyPOIRIER, Karine; EISERMANN, Monika; LASCELLES, Karine et al.Epilepsy research. 2008, Vol 80, Num 2-3, pp 224-228, issn 0920-1211, 5 p.Article

Case reports: A novel missense mutation A1081P in the cystic fibrosis transmembrane conductance regulator (CFTR) gene identified in a laotian patient with congenital bilateral absence of the vas deferensNGUKARN, Angele; JACQUEMONT, Marie Line; SOUVILLE, Isabelle et al.Journal of tropical pediatrics (1980). 2004, Vol 50, Num 4, pp 239-240, issn 0142-6338, 2 p.Article

MECP2 is highly mutated in X-linked mental retardationCOUVERT, Philippe; BIENVENU, Thierry; STEFFANN, Julie et al.Human molecular genetics (Print). 2001, Vol 10, Num 9, pp 941-946, issn 0964-6906Article