Zappella M - Search Results

1

Ultrastructural study of enteric ganglia in three patients with Rett syndrome.

Malandrini A, Hayek G, Villanova M, Aucone AM, Berti G, Vernillo R, Zappella M, Guazzi GC. Malandrini A, et al. Among authors: zappella m. Brain Dev. 1998 Dec;20(8):586-8. doi: 10.1016/s0387-7604(98)00054-0. Brain Dev. 1998. PMID: 9865541 Clinical Trial.

2

Bromocriptine in the Rett syndrome.

Zappella M, Genazzani A, Facchinetti F, Hayek G. Zappella M, et al. Brain Dev. 1990;12(2):221-5. doi: 10.1016/s0387-7604(12)80329-9. Brain Dev. 1990. PMID: 2360701

3

Vitamin E serum levels in Rett syndrome.

Formichi P, Battisti C, Dotti MT, Hayek G, Zappella M, Federico A. Formichi P, et al. Among authors: zappella m. J Neurol Sci. 1998 Apr 1;156(2):227-30. doi: 10.1016/s0022-510x(98)00035-5. J Neurol Sci. 1998. PMID: 9588862

4

Reduced heart rate variability in patients affected with Rett syndrome. A possible explanation for sudden death.

Guideri F, Acampa M, Hayek G, Zappella M, Di Perri T. Guideri F, et al. Among authors: zappella m. Neuropediatrics. 1999 Jun;30(3):146-8. doi: 10.1055/s-2007-973480. Neuropediatrics. 1999. PMID: 10480210

5

Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant).

Renieri A, Mari F, Mencarelli MA, Scala E, Ariani F, Longo I, Meloni I, Cevenini G, Pini G, Hayek G, Zappella M. Renieri A, et al. Among authors: zappella m. Brain Dev. 2009 Mar;31(3):208-16. doi: 10.1016/j.braindev.2008.04.007. Epub 2008 Jun 17. Brain Dev. 2009. PMID: 18562141

6

Brain perfusion abnormalities in Rett syndrome: a qualitative and quantitative SPET study with 99Tc(m)-ECD.

Burroni L, Aucone AM, Volterrani D, Hayek Y, Bertelli P, Vella A, Zappella M, Vattimo A. Burroni L, et al. Among authors: zappella m. Nucl Med Commun. 1997 Jun;18(6):527-34. doi: 10.1097/00006231-199706000-00005. Nucl Med Commun. 1997. PMID: 9259523

7

Studies on mitochondrial pathogenesis of Rett syndrome: ultrastructural data from skin and muscle biopsies and mutational analysis at mtDNA nucleotides 10463 and 2835.

Cardaioli E, Dotti MT, Hayek G, Zappella M, Federico A. Cardaioli E, et al. Among authors: zappella m. J Submicrosc Cytol Pathol. 1999 Apr;31(2):301-4. J Submicrosc Cytol Pathol. 1999. PMID: 10457616

8

Dual X-ray absorptiometry and bone ultrasonography in patients with Rett syndrome.

Cepollaro C, Gonnelli S, Bruni D, Pacini S, Martini S, Franci MB, Gennari L, Rossi S, Hayek G, Zappella M, Gennari C. Cepollaro C, et al. Among authors: zappella m. Calcif Tissue Int. 2001 Nov;69(5):259-62. doi: 10.1007/s002230010027. Calcif Tissue Int. 2001. PMID: 11768194

9

Preserved speech variant is allelic of classic Rett syndrome.

De Bona C, Zappella M, Hayek G, Meloni I, Vitelli F, Bruttini M, Cusano R, Loffredo P, Longo I, Renieri A. De Bona C, et al. Among authors: zappella m. Eur J Hum Genet. 2000 May;8(5):325-30. doi: 10.1038/sj.ejhg.5200473. Eur J Hum Genet. 2000. PMID: 10854091 Free article.

10

MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region.

Vacca M, Filippini F, Budillon A, Rossi V, Della Ragione F, De Bonis ML, Mercadante G, Manzati E, Gualandi F, Bigoni S, Trabanelli C, Pini G, Calzolari E, Ferlini A, Meloni I, Hayek G, Zappella M, Renieri A, D'Urso M, D'Esposito M, Macdonald F, Kerr A, Dhanjal S, Hulten M. Vacca M, et al. Among authors: zappella m. Brain Dev. 2001 Dec;23 Suppl 1:S246-50. doi: 10.1016/s0387-7604(01)00343-6. Brain Dev. 2001. PMID: 11738884

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