Pinton F - Search Results

1

The nonmalformed hemisphere is secondarily impaired in young children with hemimegalencephaly: a pre- and postsurgery study with SPECT and EEG.

Soufflet C, Bulteau C, Delalande O, Pinton F, Jalin C, Plouin P, Bahi-Buisson N, Dulac O, Chiron C. Soufflet C, et al. Among authors: pinton f. Epilepsia. 2004 Nov;45(11):1375-82. doi: 10.1111/j.0013-9580.2004.66003.x. Epilepsia. 2004. PMID: 15509238 Free article.

2

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: pinton f. Epilepsy Res. 1996 Jun;24(2):109-17. doi: 10.1016/0920-1211(96)00002-2. Epilepsy Res. 1996. PMID: 8796359 Clinical Trial.

3

Accelerated myelination in early Sturge-Weber syndrome: MRI-SPECT correlations.

Adamsbaum C, Pinton F, Rolland Y, Chiron C, Dulac O, Kalifa G. Adamsbaum C, et al. Among authors: pinton f. Pediatr Radiol. 1996 Nov;26(11):759-62. doi: 10.1007/BF01396195. Pediatr Radiol. 1996. PMID: 8929371

4

Early single photon emission computed tomography in Sturge-Weber syndrome.

Pinton F, Chiron C, Enjolras O, Motte J, Syrota A, Dulac O. Pinton F, et al. J Neurol Neurosurg Psychiatry. 1997 Nov;63(5):616-21. doi: 10.1136/jnnp.63.5.616. J Neurol Neurosurg Psychiatry. 1997. PMID: 9408103 Free PMC article.

5

Hemispheric specialization using SPECT and stimulation tasks in children with dysphasia and dystrophia.

Chiron C, Pinton F, Masure MC, Duvelleroy-Hommet C, Leon F, Billard C. Chiron C, et al. Among authors: pinton f. Dev Med Child Neurol. 1999 Aug;41(8):512-20. doi: 10.1017/s0012162299001139. Dev Med Child Neurol. 1999. PMID: 10479040 Free article.

6

The ketogenic diet improves recently worsened focal epilepsy.

Villeneuve N, Pinton F, Bahi-Buisson N, Dulac O, Chiron C, Nabbout R. Villeneuve N, et al. Among authors: pinton f. Dev Med Child Neurol. 2009 Apr;51(4):276-81. doi: 10.1111/j.1469-8749.2008.03216.x. Epub 2008 Feb 3. Dev Med Child Neurol. 2009. PMID: 19191829 Free article.

7

Infantile spasms with basal ganglia MRI hypersignal may reveal mitochondrial disorder due to T8993G MT DNA mutation.

Desguerre I, Pinton F, Nabbout R, Moutard ML, N'Guyen S, Marsac C, Ponsot G, Dulac O. Desguerre I, et al. Among authors: pinton f. Neuropediatrics. 2003 Jun;34(5):265-9. doi: 10.1055/s-2003-43258. Neuropediatrics. 2003. PMID: 14598233

8

Specific language impairment versus Landau-Kleffner syndrome.

Billard C, Fluss J, Pinton F. Billard C, et al. Among authors: pinton f. Epilepsia. 2009 Aug;50 Suppl 7:21-4. doi: 10.1111/j.1528-1167.2009.02213.x. Epilepsia. 2009. PMID: 19682045 Free article.

9

Exclusion of the dymeclin and PAPSS2 genes in a novel form of spondyloepimetaphyseal dysplasia and mental retardation.

Geneviève D, Héron D, El Ghouzzi V, Prost-Squarcioni C, Le Merrer M, Jacquette A, Sanlaville D, Pinton F, Villeneuve N, Kalifa G, Munnich A, Cormier-Daire V. Geneviève D, et al. Among authors: pinton f. Eur J Hum Genet. 2005 May;13(5):541-6. doi: 10.1038/sj.ejhg.5201339. Eur J Hum Genet. 2005. PMID: 15726110 Free article.

10

[Progressive convulsive encephalopathy: considering a abnormality of biopterin metabolism].

Mikaeloff Y, Pinton F, Sevin C, Dhondt JL, Ponsot G. Mikaeloff Y, et al. Among authors: pinton f. Arch Pediatr. 1999 Jul;6(7):759-61. doi: 10.1016/s0929-693x(99)80360-1. Arch Pediatr. 1999. PMID: 10429818 French.

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