Nuttin C - Search Results

1

SPECT of the brain in childhood autism: evidence for a lack of normal hemispheric asymmetry.

Chiron C, Leboyer M, Leon F, Jambaqué I, Nuttin C, Syrota A. Chiron C, et al. Among authors: nuttin c. Dev Med Child Neurol. 1995 Oct;37(10):849-60. doi: 10.1111/j.1469-8749.1995.tb11938.x. Dev Med Child Neurol. 1995. PMID: 7493719

2

Study of regional cerebral blood flow in West syndrome.

Chiron C, Dulac O, Bulteau C, Nuttin C, Depas G, Raynaud C, Syrota A. Chiron C, et al. Among authors: nuttin c. Epilepsia. 1993 Jul-Aug;34(4):707-15. doi: 10.1111/j.1528-1157.1993.tb00450.x. Epilepsia. 1993. PMID: 8330582

3

Functional brain imaging in HIV-1-infected children born to seropositive mothers.

Depas G, Chiron C, Tardieu M, Nuttin C, Blanche S, Raynaud C, Syrota A. Depas G, et al. Among authors: nuttin c. J Nucl Med. 1995 Dec;36(12):2169-74. J Nucl Med. 1995. PMID: 8523099 Free article.

4

Brain functional imaging SPECT in agyria-pachygyria.

Chiron C, Nabbout R, Pinton F, Nuttin C, Dulac O, Syrota A. Chiron C, et al. Among authors: nuttin c. Epilepsy Res. 1996 Jun;24(2):109-17. doi: 10.1016/0920-1211(96)00002-2. Epilepsy Res. 1996. PMID: 8796359 Clinical Trial.

5

Paroxysmal EEG pattern in a child with N-methyl-D-aspartate receptor antibody encephalitis.

Gataullina S, Plouin P, Vincent A, Scalais E, Nuttin C, Dulac O. Gataullina S, et al. Among authors: nuttin c. Dev Med Child Neurol. 2011 Aug;53(8):764-7. doi: 10.1111/j.1469-8749.2011.03956.x. Epub 2011 May 19. Dev Med Child Neurol. 2011. PMID: 21592117 Free article.

6

Perisylvian dysgenesis. Clinical, EEG, MRI and glucose metabolism features in 10 patients.

Van Bogaert P, David P, Gillain CA, Wikler D, Damhaut P, Scalais E, Nuttin C, Wetzburger C, Szliwowski HB, Metens T, Goldman S. Van Bogaert P, et al. Among authors: nuttin c. Brain. 1998 Dec;121 ( Pt 12):2229-38. doi: 10.1093/brain/121.12.2229. Brain. 1998. PMID: 9874476

7

Efficacy of high dose steroid therapy in children with severe acute transverse myelitis.

Defresne P, Meyer L, Tardieu M, Scalais E, Nuttin C, De Bont B, Loftus G, Landrieu P, Kadhim H, Sébire G. Defresne P, et al. Among authors: nuttin c. J Neurol Neurosurg Psychiatry. 2001 Aug;71(2):272-4. doi: 10.1136/jnnp.71.2.272. J Neurol Neurosurg Psychiatry. 2001. PMID: 11459911 Free PMC article.

8

[Diagnostic and prognostic value of evoked potentials facing cerebral hypoxia in newborn infants].

Scalais E, François A, Nuttin C. Scalais E, et al. Among authors: nuttin c. Arch Pediatr. 1996;3 Suppl 1:251s-253s. doi: 10.1016/0929-693x(96)86058-1. Arch Pediatr. 1996. PMID: 8796033 French. No abstract available.

9

Polymerase gamma deficiency (POLG): clinical course in a child with a two stage evolution from infantile myocerebrohepatopathy spectrum to an Alpers syndrome and neuropathological findings of Leigh's encephalopathy.

Scalais E, Francois B, Schlesser P, Stevens R, Nuttin C, Martin JJ, Van Coster R, Seneca S, Roels F, Van Goethem G, Löfgren A, De Meirleir L. Scalais E, et al. Among authors: nuttin c. Eur J Paediatr Neurol. 2012 Sep;16(5):542-8. doi: 10.1016/j.ejpn.2012.01.013. Epub 2012 Feb 17. Eur J Paediatr Neurol. 2012. PMID: 22342071

10

Early myoclonic epilepsy, hypertrophic cardiomyopathy and subsequently a nephrotic syndrome in a patient with CoQ10 deficiency caused by mutations in para-hydroxybenzoate-polyprenyl transferase (COQ2).

Scalais E, Chafai R, Van Coster R, Bindl L, Nuttin C, Panagiotaraki C, Seneca S, Lissens W, Ribes A, Geers C, Smet J, De Meirleir L. Scalais E, et al. Among authors: nuttin c. Eur J Paediatr Neurol. 2013 Nov;17(6):625-30. doi: 10.1016/j.ejpn.2013.05.013. Epub 2013 Jun 28. Eur J Paediatr Neurol. 2013. PMID: 23816342

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

17 results

Search Page

Filters