Caietta E - Search Results

1

Diagnosis and outcome of SCN4A-related severe neonatal episodic laryngospasm (SNEL): 2 new cases.

Caietta E, Milh M, Sternberg D, Lépine A, Boulay C, McGonigal A, Chabrol B. Caietta E, et al. Pediatrics. 2013 Sep;132(3):e784-7. doi: 10.1542/peds.2012-3065. Epub 2013 Aug 19. Pediatrics. 2013. PMID: 23958773

2

Cerebral (18)FluoroDeoxy-Glucose Positron Emission Tomography in paediatric anti N-methyl-D-aspartate receptor encephalitis: A case series.

Lagarde S, Lepine A, Caietta E, Pelletier F, Boucraut J, Chabrol B, Milh M, Guedj E. Lagarde S, et al. Among authors: caietta e. Brain Dev. 2016 May;38(5):461-70. doi: 10.1016/j.braindev.2015.10.013. Epub 2015 Nov 2. Brain Dev. 2016. PMID: 26542469

3

[Association of type 1 diabetes mellitus and epilepsy in children. A cohort of 10 cases].

Caietta E, Halbert C, Lépine A, Khammar A, Cano A, Gavaret M, Mancini J, Villeneuve N, Chabrol B, Simonin G, Reynaud R, Milh M. Caietta E, et al. Arch Pediatr. 2012 Jan;19(1):9-16. doi: 10.1016/j.arcped.2011.10.010. Epub 2011 Nov 22. Arch Pediatr. 2012. PMID: 22112607 French.

4

[Epilepsy and mitochondrial diseases: retrospective study on 53 epileptic children].

Caietta E, Cano A, Halbert C, Hugonenq C, Mancini J, Milh M, Lépine A, Villeneuve N, Chaussenot A, Paquis-Flucklinger V, Chabrol B. Caietta E, et al. Arch Pediatr. 2012 Aug;19(8):794-802. doi: 10.1016/j.arcped.2012.05.004. Epub 2012 Jul 11. Arch Pediatr. 2012. PMID: 22789745 French.

5

[Uncommon neonatal case of hypoglycemia: ACTH resistance syndrome].

Delmas O, Marrec C, Caietta E, Simonin G, Morel Y, Girard N, Roucher F, Sarles J, Chabrol B, Reynaud R. Delmas O, et al. Among authors: caietta e. Arch Pediatr. 2014 Dec;21(12):1353-8. doi: 10.1016/j.arcped.2014.09.010. Epub 2014 Oct 23. Arch Pediatr. 2014. PMID: 25445127 French.

6

Large in-frame intragenic deletion of OPHN1 in a male patient with a normal intelligence quotient score.

Busa T, Caietta E, Chabrol B, Girard N, Philip N, Missirian C. Busa T, et al. Among authors: caietta e. Clin Dysmorphol. 2017 Jan;26(1):47-49. doi: 10.1097/MCD.0000000000000139. Clin Dysmorphol. 2017. PMID: 27390894 No abstract available.

7

[Scurvy, an old disease still in the news: two case reports].

Pailhous S, Lamoureux S, Caietta E, Bosdure E, Chambost H, Chabrol B, Bresson V. Pailhous S, et al. Among authors: caietta e. Arch Pediatr. 2015 Jan;22(1):63-5. doi: 10.1016/j.arcped.2014.10.003. Epub 2014 Nov 20. Arch Pediatr. 2015. PMID: 25455083 French.

8

Recurrent mutations in the CDKL5 gene: genotype-phenotype relationships.

Bahi-Buisson N, Villeneuve N, Caietta E, Jacquette A, Maurey H, Matthijs G, Van Esch H, Delahaye A, Moncla A, Milh M, Zufferey F, Diebold B, Bienvenu T. Bahi-Buisson N, et al. Among authors: caietta e. Am J Med Genet A. 2012 Jul;158A(7):1612-9. doi: 10.1002/ajmg.a.35401. Epub 2012 Jun 7. Am J Med Genet A. 2012. PMID: 22678952

9

Primary Leptomeningeal Gliomatosis in Children and Adults: A Morphological and Molecular Comparative Study With Literature Review.

Tauziede-Espariat A, Maues de Paula A, Pages M, Laquerriere A, Caietta E, Delpont B, Viennet G, Medeiros de Bustos E, Moulin T, Barnerias C, Vauleon E, Grill J, Chiforeanu D, Vasiljevic A, Varlet P. Tauziede-Espariat A, et al. Among authors: caietta e. Neurosurgery. 2016 Mar;78(3):343-52. doi: 10.1227/NEU.0000000000001028. Neurosurgery. 2016. PMID: 26397750

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