Chaix Y - Search Results

1

Perturbation in dystrophin-associated glycoprotein complex in a boy with Becker muscular dystrophy.

Rivier F, Echenne B, Chaix Y, Robert A, Delisle MB, Calvas P, Mornet D. Rivier F, et al. Among authors: chaix y. Brain Dev. 2000 Jan;22(1):65-8. doi: 10.1016/s0387-7604(99)00112-6. Brain Dev. 2000. PMID: 10761838

2

Efficacy of an interventional educational programme in mitigating post-traumatic stress in parents who have witnessed a febrile seizure: a pilot before-and-after study.

Frascari F, Dreyfus I, Chaix Y, Tison-Chambellan C. Frascari F, et al. Among authors: chaix y. BMJ Paediatr Open. 2017 Dec 12;1(1):e000107. doi: 10.1136/bmjpo-2017-000107. eCollection 2017. BMJ Paediatr Open. 2017. PMID: 29637135 Free PMC article.

3

Carbimazole-induced juvenile dermatomyositis.

Alvarez F, Pagot C, Vabre-Latre CM, Uro-Coste E, Paul C, Chaix Y, Mazereeuw-Hautier J. Alvarez F, et al. Among authors: chaix y. Br J Dermatol. 2008 Jan;158(1):196-7. doi: 10.1111/j.1365-2133.2007.08289.x. Epub 2007 Nov 6. Br J Dermatol. 2008. PMID: 17986297 No abstract available.

4

Cognitive functions in children with benign childhood epilepsy with centrotemporal spikes (BECTS).

Pinton F, Ducot B, Motte J, Arbuès AS, Barondiot C, Barthez MA, Chaix Y, Cheminal R, Livet MO, Penniello MJ, Peudenier S, de Saint-Martin A, Billard C. Pinton F, et al. Among authors: chaix y. Epileptic Disord. 2006 Mar;8(1):11-23. Epileptic Disord. 2006. PMID: 16567321 Free article.

5

[Clear cell meningioma: recurrent intraspinal tumor in a child].

Cancès C, Chaix Y, Karsenty C, Boetto S, Sévely A, Delisle MB, Carrière JP. Cancès C, et al. Among authors: chaix y. Arch Pediatr. 1998 Jul;5(7):758-62. doi: 10.1016/s0929-693x(98)80062-6. Arch Pediatr. 1998. PMID: 9759276 French.

6

[Pseudotumor forms of neurosarcoidosis in children. Diagnostic difficulties and therapeutic management].

Chaix Y, Grouteau E, Sevely A, Boetto S, Delisle MB, Carrière JP. Chaix Y, et al. Rev Neurol (Paris). 1997 Dec;153(12):771-4. Rev Neurol (Paris). 1997. PMID: 9686267 Review. French.

7

Molecular characterisation of a ring chromosome 22 in a patient with severe language delay: a contribution to the refinement of the subtelomeric 22q deletion syndrome.

De Mas P, Chassaing N, Chaix Y, Vincent MC, Julia S, Bourrouillou G, Calvas P, Bieth E. De Mas P, et al. Among authors: chaix y. J Med Genet. 2002 Apr;39(4):e17. doi: 10.1136/jmg.39.4.e17. J Med Genet. 2002. PMID: 11950869 Free PMC article. No abstract available.

8

Systematic MRI in NF1 children under six years of age for the diagnosis of optic pathway gliomas. Study and outcome of a French cohort.

Blanchard G, Lafforgue MP, Lion-François L, Kemlin I, Rodriguez D, Castelnau P, Carneiro M, Meyer P, Rivier F, Barbarot S, Chaix Y; NF France network. Blanchard G, et al. Among authors: chaix y. Eur J Paediatr Neurol. 2016 Mar;20(2):275-281. doi: 10.1016/j.ejpn.2015.12.002. Epub 2015 Dec 17. Eur J Paediatr Neurol. 2016. PMID: 26774135 Free article.

9

Deficit in phonological processes: a characteristic of the neuropsychological profile of children with NF1.

Chaix Y, Lauwers-Cancès V, Faure-Marie N, Gentil C, Lelong S, Schweitzer E, Rodriguez D, Iannuzzi S, Kemlin I, Dorison N, Rivier F, Carniero M, Preclaire E, Barbarot S, Lion-François L, Castelnau P. Chaix Y, et al. Child Neuropsychol. 2018 May;24(4):558-574. doi: 10.1080/09297049.2017.1313970. Epub 2017 Apr 10. Child Neuropsychol. 2018. PMID: 28393676

10

Sporadic and Familial Variants in NF1: An Explanation of the Wide Variability in Neurocognitive Phenotype?

Biotteau M, Déjean S, Lelong S, Iannuzzi S, Faure-Marie N, Castelnau P, Rivier F, Lauwers-Cancès V, Baudou E, Chaix Y. Biotteau M, et al. Among authors: chaix y. Front Neurol. 2020 May 5;11:368. doi: 10.3389/fneur.2020.00368. eCollection 2020. Front Neurol. 2020. PMID: 32431664 Free PMC article.

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