Hayek J - Search Results

1

EEG features and epilepsy in MECP2-mutated patients with the Zappella variant of Rett syndrome.

Buoni S, Zannolli R, De Felice C, De Nicola A, Guerri V, Guerra B, Casali S, Pucci B, Corbini L, Mari F, Renieri A, Zappella M, Hayek J. Buoni S, et al. Among authors: hayek j. Clin Neurophysiol. 2010 May;121(5):652-7. doi: 10.1016/j.clinph.2010.01.003. Epub 2010 Feb 12. Clin Neurophysiol. 2010. PMID: 20153689

2

Myoclonic encephalopathy in the CDKL5 gene mutation.

Buoni S, Zannolli R, Colamaria V, Macucci F, di Bartolo RM, Corbini L, Orsi A, Zappella M, Hayek J. Buoni S, et al. Among authors: hayek j. Clin Neurophysiol. 2006 Jan;117(1):223-7. doi: 10.1016/j.clinph.2005.09.008. Epub 2005 Dec 2. Clin Neurophysiol. 2006. PMID: 16326141

3

Drug-resistant epilepsy and epileptic phenotype-EEG association in MECP2 mutated Rett syndrome.

Buoni S, Zannolli R, Felice CD, Saponari S, Strambi M, Dotti MT, Castrucci E, Corbini L, Orsi A, Hayek J. Buoni S, et al. Among authors: hayek j. Clin Neurophysiol. 2008 Nov;119(11):2455-8. doi: 10.1016/j.clinph.2008.08.015. Epub 2008 Oct 7. Clin Neurophysiol. 2008. PMID: 18842453

4

Rett syndrome and plasma leptin levels.

Blardi P, de Lalla A, D'Ambrogio T, Zappella M, Cevenini G, Ceccatelli L, Auteri A, Hayek J. Blardi P, et al. Among authors: hayek j. J Pediatr. 2007 Jan;150(1):37-9. doi: 10.1016/j.jpeds.2006.10.061. J Pediatr. 2007. PMID: 17188610

5

Focal cortical dysplasia type 1b as a cause of severe epilepsy with multiple independent spike foci.

Buoni S, Zannolli R, Miracco C, Macucci F, Hayek J, Burroni L, di Pietro G, Sardo L, Mussa F, Giordano F, Genitori L. Buoni S, et al. Among authors: hayek j. Brain Dev. 2008 Jan;30(1):53-8. doi: 10.1016/j.braindev.2007.05.010. Epub 2007 Jun 20. Brain Dev. 2008. PMID: 17583458

6

Silent increase of urinary ethylmalonic acid is an indicator of nonspecific brain dysfunction.

Zannolli R, Buoni S, Tassini M, De Nicola A, Betti G, De Felice C, Orsi A, Varetti MC, Ferrara F, Messina M, Giannini C, Mohn A, Chiarelli F, Liberati M, Strambi M, Funghini S, Vivi A, Wevers RA, Hayek J. Zannolli R, et al. Among authors: hayek j. NMR Biomed. 2010 May;23(4):353-8. doi: 10.1002/nbm.1468. Epub 2010 Feb 25. NMR Biomed. 2010. PMID: 20187168

7

SCN1A (2528delG) novel truncating mutation with benign outcome of severe myoclonic epilepsy of infancy.

Buoni S, Orrico A, Galli L, Zannolli R, Burroni L, Hayek J, Fois A, Sorrentino V. Buoni S, et al. Among authors: hayek j. Neurology. 2006 Feb 28;66(4):606-7. doi: 10.1212/01.WNL.0000198504.41315.B1. Neurology. 2006. PMID: 16505326 No abstract available.

8

Neurocutaneous syndrome with mental delay, autism, blockage in intracellular vescicular trafficking and melanosome defects.

Buoni S, Zannolli R, de Santi M, Macucci F, Hayek J, Orsi A, Scarinci R, Buscalferri A, Cuccia A, Zappella M, Miracco C. Buoni S, et al. Among authors: hayek j. Eur J Neurol. 2006 Aug;13(8):842-51. doi: 10.1111/j.1468-1331.2006.01305.x. Eur J Neurol. 2006. PMID: 16879294

9

Kabuki syndrome with trichrome vitiligo, ectodermal defect and hypogammaglobulinemia A and G.

Zannolli R, Buoni S, Macucci F, Scarinci R, Viviano M, Orsi A, de Aloe G, Fimiani M, Volterrani L, de Santi MM, Miracco C, Zappella M, Hayek J. Zannolli R, et al. Among authors: hayek j. Brain Dev. 2007 Jul;29(6):373-6. doi: 10.1016/j.braindev.2006.11.004. Epub 2006 Dec 14. Brain Dev. 2007. PMID: 17174051

10

Polydactyly with ectodermal defect, osteopenia, and mental delay.

Zannolli R, Buoni S, Viviano M, Macucci F, D'Ambrosio A, Livi W, Mazzei MA, Mazzei F, Sacco P, Volterrani L, Vonella G, Orsi A, Zappella M, Hayek J. Zannolli R, et al. Among authors: hayek j. J Child Neurol. 2008 Jun;23(6):683-9. doi: 10.1177/0883073807309778. Epub 2008 Jan 8. J Child Neurol. 2008. PMID: 18182642

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