Pubblicazioni scientifiche indicizzate in PubMed:  dalla 41 alla 60

41.

Preserved speech variants of the Rett syndrome: molecular and clinical analysis.

Zappella M, Meloni I, Longo I, Hayek G, Renieri A.

Am J Med Genet. 2001 Nov 15;104(1):14-22.PMID: 11746022 [PubMed - indexed for MEDLINE]Related citations

42.

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.

Brain Dev. 2001 Dec;23 Suppl 1:S246-50.PMID: 11738884 [PubMed - indexed for MEDLINE]Related citations

43.

Possible case of Pitt-Hopkins syndrome in sibs.

Orrico A, Galli L, Zappella M, Lam CW, Bonifacio S, Torricelli F, Hayek G.

Am J Med Genet. 2001 Oct 1;103(2):157-9.PMID: 11568923 [PubMed - indexed for MEDLINE]Related citations

44.

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.

J Child Neurol. 2001 May;16(5):370-3.PMID: 11392524 [PubMed - indexed for MEDLINE]Related citations

45.

Additional case of Marden-Walker syndrome: support for the autosomal-recessive inheritance adn refinement of phenotype in a surviving patient.

Orrico A, Galli L, Zappella M, Orsi A, Hayek G.

J Child Neurol. 2001 Feb;16(2):150-3.PMID: 11292226 [PubMed - indexed for MEDLINE]Related citations

46.

Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females.

Vacca M, Filippini F, Budillon A, Rossi V, 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, Hultén M.

J Mol Med. 2001;78(11):648-55.PMID: 11269512 [PubMed - indexed for MEDLINE]Related citations

47.

Influence of donor age on bovine pancreatic islet isolation.

Figliuzzi M, Zappella S, Morigi M, Rossi P, Marchetti P, Remuzzi A.

Transplantation. 2000 Oct 15;70(7):1032-7.PMID: 11045639 [PubMed - indexed for MEDLINE]Related citations

48.

MECP2 mutation in male patients with non-specific X-linked mental retardation.

Orrico A, Lam C, Galli L, Dotti MT, Hayek G, Tong SF, Poon PM, Zappella M, Federico A, Sorrentino V.

FEBS Lett. 2000 Sep 22;481(3):285-8.PMID: 11007980 [PubMed - indexed for MEDLINE]Related citations

49.

17beta-estradiol corrects hemostasis in uremic rats by limiting vascular expression of nitric oxide synthases.

Noris M, Todeschini M, Zappella S, Bonazzola S, Zoja C, Corna D, Gaspari F, Marchetti G, Aiello S, Remuzzi G.

Am J Physiol Renal Physiol. 2000 Oct;279(4):F626-35. Erratum in: Am J Physiol Renal Physiol 2001 Feb;280(2):preceding F181. Am J Physiol Renal Physiol 2001 Jun;280(6):section F following table of contents. Marchetti, F [corrected to Marchetti, G].PMID: 10997912 [PubMed - indexed for MEDLINE]Free ArticleRelated citations

50.

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.

Eur J Hum Genet. 2000 May;8(5):325-30.PMID: 10854091 [PubMed - indexed for MEDLINE]Free ArticleRelated citations

51.

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.

Neuropediatrics. 1999 Jun;30(3):146-8.PMID: 10480210 [PubMed - indexed for MEDLINE]Related citations

52.

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.

J Submicrosc Cytol Pathol. 1999 Apr;31(2):301-4.PMID: 10457616 [PubMed - indexed for MEDLINE]Related citations

53.

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study.

Philippe A, Martinez M, Guilloud-Bataille M, Gillberg C, Råstam M, Sponheim E, Coleman M, Zappella M, Aschauer H, Van Maldergem L, Penet C, Feingold J, Brice A, Leboyer M.

Hum Mol Genet. 1999 May;8(5):805-12. Erratum in: Hum Mol Genet 1999 Jul;8(7):1353. van Malldergerme L [corrected to Van Maldergem L].PMID: 10196369 [PubMed - indexed for MEDLINE]Free ArticleRelated citations

54.

The preserved speech variant: a subgroup of the Rett complex: a clinical report of 30 cases.

Zappella M, Gillberg C, Ehlers S.

J Autism Dev Disord. 1998 Dec;28(6):519-26.PMID: 9932238 [PubMed - indexed for MEDLINE]Related citations

55.

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.

Brain Dev. 1998 Dec;20(8):586-8.PMID: 9865541 [PubMed - indexed for MEDLINE]Related citations

56.

Holding has grown old.

Zappella M.

Eur Child Adolesc Psychiatry. 1998 Jun;7(2):119-21. No abstract available.PMID: 9712379 [PubMed - indexed for MEDLINE]Related citations

57.

Upregulation of renal and systemic cyclooxygenase-2 in patients with active lupus nephritis.

Tomasoni S, Noris M, Zappella S, Gotti E, Casiraghi F, Bonazzola S, Benigni A, Remuzzi G.

J Am Soc Nephrol. 1998 Jul;9(7):1202-12.PMID: 9644630 [PubMed - indexed for MEDLINE]Free ArticleRelated citations

58.

Vitamin E serum levels in Rett syndrome.

Formichi P, Battisti C, Dotti MT, Hayek G, Zappella M, Federico A.

J Neurol Sci. 1998 Apr 1;156(2):227-30.PMID: 9588862 [PubMed - indexed for MEDLINE]Related citations

59.

Renal and systemic nitric oxide synthesis in rats with renal mass reduction.

Aiello S, Noris M, Todeschini M, Zappella S, Foglieni C, Benigni A, Corna D, Zoja C, Cavallotti D, Remuzzi G.

Kidney Int. 1997 Jul;52(1):171-81.PMID: 9211360 [PubMed - indexed for MEDLINE]Related citations

60.

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.

Nucl Med Commun. 1997 Jun;18(6):527-34.PMID: 9259523 [PubMed - indexed for MEDLINE]Related citations