Boddaert N - Search Results

1

Prenatally diagnosed periventricular nodular heterotopia: Further delineation of the imaging phenotype and outcome.

Deloison B, Sonigo P, Millischer-Bellaiche AE, Quibel T, Cavallin M, Benoist G, Quelin C, Jouk PS, Lev D, Alison M, Baumann C, Beldjord C, Razavi F, Bessières B, Boddaert N, Ville Y, Salomon LJ, Bahi-Buisson N. Deloison B, et al. Among authors: boddaert n. Eur J Med Genet. 2018 Dec;61(12):773-782. doi: 10.1016/j.ejmg.2018.10.015. Epub 2018 Nov 1. Eur J Med Genet. 2018. PMID: 30391507

2

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

3

Intellectual prognosis of the Dandy-Walker malformation in children: the importance of vermian lobulation.

Boddaert N, Klein O, Ferguson N, Sonigo P, Parisot D, Hertz-Pannier L, Baraton J, Emond S, Simon I, Chigot V, Schmit P, Pierre-Kahn A, Brunelle F. Boddaert N, et al. Neuroradiology. 2003 May;45(5):320-4. doi: 10.1007/s00234-003-0980-6. Epub 2003 Apr 8. Neuroradiology. 2003. PMID: 12682795

4

Atypical case of hemiconvulsions-hemiplegia-epilepsy syndrome revealing contralateral focal cortical dysplasia.

Bahi-Buisson N, Kossorotoff M, Barnerias C, Boddaert N, Bourgeois M, Dulac O, Plouin P, Chiron C, Hertz-Pannier L. Bahi-Buisson N, et al. Among authors: boddaert n. Dev Med Child Neurol. 2005 Dec;47(12):830-4. doi: 10.1017/S0012162205001751. Dev Med Child Neurol. 2005. PMID: 16288674 Free article.

5

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.

6

Contribution of fetal MR imaging in the prenatal diagnosis of Zellweger syndrome.

Mochel F, Grébille AG, Benachi A, Martinovic J, Razavi F, Rabier D, Simon I, Boddaert N, Brunelle F, Sonigo P. Mochel F, et al. Among authors: boddaert n. AJNR Am J Neuroradiol. 2006 Feb;27(2):333-6. AJNR Am J Neuroradiol. 2006. PMID: 16484405 Free PMC article.

7

Molar tooth sign and superior vermian dysplasia: a radiological, clinical, and genetic study.

Romano S, Boddaert N, Desguerre I, Hubert L, Salomon R, Seidenwurm D, Bahi-Buisson N, Nabbout R, Sonigo P, Lyonnet S, Brunelle F, Munnich A, de Lonlay P. Romano S, et al. Among authors: boddaert n. Neuropediatrics. 2006 Feb;37(1):42-5. doi: 10.1055/s-2006-923838. Neuropediatrics. 2006. PMID: 16541367

8

1H MRS spectroscopy evidence of cerebellar high lactate in mitochondrial respiratory chain deficiency.

Boddaert N, Romano S, Funalot B, Rio M, Sarzi E, Lebre AS, Bahi-Buisson N, Valayannopoulos V, Desguerre I, Seidenwurm D, Brunelle F, Brami-Zylberberg F, Rötig A, Munnich A, de Lonlay P. Boddaert N, et al. Mol Genet Metab. 2008 Jan;93(1):85-8. doi: 10.1016/j.ymgme.2007.09.003. Epub 2007 Oct 22. Mol Genet Metab. 2008. PMID: 17950645

9

Risk assessment of acute vascular events in congenital disorder of glycosylation type Ia.

Arnoux JB, Boddaert N, Valayannopoulos V, Romano S, Bahi-Buisson N, Desguerre I, de Keyzer Y, Munnich A, Brunelle F, Seta N, Dautzenberg MD, de Lonlay P. Arnoux JB, et al. Among authors: boddaert n. Mol Genet Metab. 2008 Apr;93(4):444-9. doi: 10.1016/j.ymgme.2007.11.006. Epub 2008 Feb 21. Mol Genet Metab. 2008. PMID: 18093857

10

Transient magnetic resonance diffusion abnormalities in West syndrome: the radiological expression of non-convulsive status epilepticus?

Desguerre I, Marti I, Valayannopoulos V, Bahi-Buisson N, Dulac O, Plouin P, Delonlay P, Hertz-Pannier L, Boddaert N. Desguerre I, et al. Among authors: boddaert n. Dev Med Child Neurol. 2008 Feb;50(2):112-6. doi: 10.1111/j.1469-8749.2007.02017.x. Dev Med Child Neurol. 2008. PMID: 18201300 Free article.

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