Zappella M - Search Results

1

Epilepsy, electroencephalographic abnormalities, and regression in children with autism.

Canitano R, Luchetti A, Zappella M. Canitano R, et al. Among authors: zappella m. J Child Neurol. 2005 Jan;20(1):27-31. doi: 10.1177/08830738050200010401. J Child Neurol. 2005. PMID: 15791919

2

Autistic epileptiform regression.

Canitano R, Zappella M. Canitano R, et al. Among authors: zappella m. Funct Neurol. 2006 Apr-Jun;21(2):97-101. Funct Neurol. 2006. PMID: 16796825

3

Study of MECP2 gene in Rett syndrome variants and autistic girls.

Zappella M, Meloni I, Longo I, Canitano R, Hayek G, Rosaia L, Mari F, Renieri A. Zappella M, et al. Am J Med Genet B Neuropsychiatr Genet. 2003 May 15;119B(1):102-7. doi: 10.1002/ajmg.b.10070. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12707946

4

Chromosome 2 deletion encompassing the MAP2 gene in a patient with autism and Rett-like features.

Pescucci C, Meloni I, Bruttini M, Ariani F, Longo I, Mari F, Canitano R, Hayek G, Zappella M, Renieri A. Pescucci C, et al. Among authors: zappella m. Clin Genet. 2003 Dec;64(6):497-501. doi: 10.1046/j.1399-0004.2003.00176.x. Clin Genet. 2003. PMID: 14986829

5

Three Rett patients with both MECP2 mutation and 15q11-13 rearrangements.

Longo I, Russo L, Meloni I, Ricci I, Ariani F, Pescucci C, Giordano CT, Canitano R, Hayek G, Zappella M, Neri G, Renieri A, Gurrieri F. Longo I, et al. Among authors: zappella m. Eur J Hum Genet. 2004 Aug;12(8):682-5. doi: 10.1038/sj.ejhg.5201198. Eur J Hum Genet. 2004. PMID: 15069458

6

Attention-deficit/hyperactivity disorder (ADHD) and variable clinical expression of Aarskog-Scott syndrome due to a novel FGD1 gene mutation (R408Q).

Orrico A, Galli L, Buoni S, Hayek G, Luchetti A, Lorenzini S, Zappella M, Pomponi MG, Sorrentino V. Orrico A, et al. Among authors: zappella m. Am J Med Genet A. 2005 May 15;135(1):99-102. doi: 10.1002/ajmg.a.30700. Am J Med Genet A. 2005. PMID: 15809997

7

Autism and hypomelanosis of Ito in twins.

Zappella M. Zappella M. Dev Med Child Neurol. 1993 Sep;35(9):826-32. doi: 10.1111/j.1469-8749.1993.tb11734.x. Dev Med Child Neurol. 1993. PMID: 8354433

8

The preserved speech variant of the Rett complex: a report of 8 cases.

Zappella M. Zappella M. Eur Child Adolesc Psychiatry. 1997;6 Suppl 1:23-5. Eur Child Adolesc Psychiatry. 1997. PMID: 9452915 Review.

9

Progressive cardiac dysautonomia observed in patients affected by classic Rett syndrome and not in the preserved speech variant.

Guideri F, Acampa M, DiPerri T, Zappella M, Hayek Y. Guideri F, et al. Among authors: zappella m. J Child Neurol. 2001 May;16(5):370-3. doi: 10.1177/088307380101600512. J Child Neurol. 2001. PMID: 11392524

10

Autistic regression with and without EEG abnormalities followed by favourable outcome.

Zappella M. Zappella M. Brain Dev. 2010 Oct;32(9):739-45. doi: 10.1016/j.braindev.2010.05.004. Epub 2010 Aug 12. Brain Dev. 2010. PMID: 20708360

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