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Refinement of cortical dysgeneses spectrum associated with TUBA1A mutations.
Bahi-Buisson N, Poirier K, Boddaert N, Saillour Y, Castelnau L, Philip N, Buyse G, Villard L, Joriot S, Marret S, Bourgeois M, Van Esch H, Lagae L, Amiel J, Hertz-Pannier L, Roubertie A, Rivier F, Pinard JM, Beldjord C, Chelly J. Bahi-Buisson N, et al. Among authors: boddaert n. J Med Genet. 2008 Oct;45(10):647-53. doi: 10.1136/jmg.2008.058073. Epub 2008 Aug 26. J Med Genet. 2008. PMID: 18728072
Intracranial venous anomalies associated with atretic cephalocoeles.
Brunelle F, Baraton J, Renier D, Teillac D, Simon I, Sonigo P, Hertz-Pannier L, Emond S, Boddaert N, Chigot V, Lellouch-Tubiana A. Brunelle F, et al. Among authors: boddaert n. Pediatr Radiol. 2000 Nov;30(11):743-7. doi: 10.1007/s002470000328. Pediatr Radiol. 2000. PMID: 11100489
Respiratory chain deficiency in a female with Aicardi-Goutières syndrome.
Barnérias C, Giurgea I, Hertz-Pannier L, Bahi-Buisson N, Boddaert N, Rustin P, Rotig A, Desguerre I, Munnich A, de Lonlay P. Barnérias C, et al. Among authors: boddaert n. Dev Med Child Neurol. 2006 Mar;48(3):227-30. doi: 10.1017/S001216220600048X. Dev Med Child Neurol. 2006. PMID: 16483401 Free article.
478 results