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Page 1
Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene.
Gras D, Jonard L, Roze E, Chantot-Bastaraud S, Koht J, Motte J, Rodriguez D, Louha M, Caubel I, Kemlin I, Lion-François L, Goizet C, Guillot L, Moutard ML, Epaud R, Héron B, Charles P, Tallot M, Camuzat A, Durr A, Polak M, Devos D, Sanlaville D, Vuillaume I, Billette de Villemeur T, Vidailhet M, Doummar D. Gras D, et al. Among authors: caubel i. J Neurol Neurosurg Psychiatry. 2012 Oct;83(10):956-62. doi: 10.1136/jnnp-2012-302505. Epub 2012 Jul 24. J Neurol Neurosurg Psychiatry. 2012. PMID: 22832740
[Gaucher's disease ].
Belmatoug N, Caubel I, Stirnemann J, Billette de Villemeur T. Belmatoug N, et al. Among authors: caubel i. J Soc Biol. 2002;196(2):141-9. J Soc Biol. 2002. PMID: 12360743 Review. French.
West Syndrome Is an Exceptional Presentation of Pyridoxine- and Pyridoxal Phosphate-Dependent Epilepsy: Data From a French Cohort and Review of the Literature.
Gibaud M, Barth M, Lefranc J, Mention K, Villeneuve N, Schiff M, Maurey H, Barthez MA, Caubel I, Chouchane M, Doummar D, Kossorotoff M, Lamblin MD, Roubertie A, Nabbout R, Van Bogaert P. Gibaud M, et al. Among authors: caubel i. Front Pediatr. 2021 Mar 5;9:621200. doi: 10.3389/fped.2021.621200. eCollection 2021. Front Pediatr. 2021. PMID: 33748042 Free PMC article.
Early development of occipital horns in a classical Menkes patient.
Gérard-Blanluet M, Birk-Møller L, Caubel I, Gélot A, Billette de Villemeur T, Horn N. Gérard-Blanluet M, et al. Among authors: caubel i. Am J Med Genet A. 2004 Oct 1;130A(2):211-3. doi: 10.1002/ajmg.a.30155. Am J Med Genet A. 2004. PMID: 15372525 Review. No abstract available.
[Neurotoxicity of cytostatic treatments in pediatrics].
Caubel I, Landman-Parker J, Pellegrino B, de Villemeur TB. Caubel I, et al. Arch Pediatr. 2001 May;8 Suppl 2:322s-324s. doi: 10.1016/s0929-693x(01)80060-9. Arch Pediatr. 2001. PMID: 11394102 French. No abstract available.
Epilepsy diagnostic and treatment needs identified with a collaborative database involving tertiary centers in France.
Chipaux M, Szurhaj W, Vercueil L, Milh M, Villeneuve N, Cances C, Auvin S, Chassagnon S, Napuri S, Allaire C, Derambure P, Marchal C, Caubel I, Ricard-Mousnier B, N'Guyen The Tich S, Pinard JM, Bahi-Buisson N, de Baracé C, Kahane P, Gautier A, Hamelin S, Coste-Zeitoun D, Rosenberg SD, Clerson P, Nabbout R, Kuchenbuch M, Picot MC, Kaminska A; GRENAT Group. Chipaux M, et al. Among authors: caubel i. Epilepsia. 2016 May;57(5):757-69. doi: 10.1111/epi.13368. Epub 2016 Apr 1. Epilepsia. 2016. PMID: 27037674 Free article.
Combination of infantile spasms, non-epileptic seizures and complex movement disorder: a new case of ARX-related epilepsy.
Poirier K, Eisermann M, Caubel I, Kaminska A, Peudonnier S, Boddaert N, Saillour Y, Dulac O, Souville I, Beldjord C, Lascelles K, Plouin P, Chelly J, Bahi-Buisson N. Poirier K, et al. Among authors: caubel i. Epilepsy Res. 2008 Aug;80(2-3):224-8. doi: 10.1016/j.eplepsyres.2008.03.019. Epub 2008 May 12. Epilepsy Res. 2008. PMID: 18468866
11 results