Perri M - Search Results

1

Male-specific phosphorylated SR proteins in adult flies of the Mediterranean fruitfly Ceratitis capitata.

Saccone G, Louis C, Zhang H, Petrella V, Di Natale M, Perri M, Salvemini M. Saccone G, et al. Among authors: perri m. BMC Genet. 2014;15 Suppl 2(Suppl 2):S6. doi: 10.1186/1471-2156-15-S2-S6. Epub 2014 Dec 1. BMC Genet. 2014. PMID: 25472723 Free PMC article.

2

Absence of association between Alzheimer disease and the regulatory region polymorphism of the PS2 gene in an Italian population.

Di Natale M, Perri M, Kawarai T, Maletta R, Tomaino C, Sato C, Nacmias B, Shibata N, Sorbi S, St George-Hyslop PH, Bruni AC, Rogaeva E. Di Natale M, et al. Among authors: perri m. Neurosci Lett. 2003 Jun 12;343(3):210-2. doi: 10.1016/s0304-3940(03)00335-5. Neurosci Lett. 2003. PMID: 12770698

3

Nicastrin gene in familial and sporadic Alzheimer's disease.

Confaloni A, Terreni L, Piscopo P, Crestini A, Campeggi LM, Frigerio CS, Blotta I, Perri M, Di Natale M, Maletta R, Marcon G, Franceschi M, Bruni AC, Forloni G, Cantafora A. Confaloni A, et al. Among authors: perri m. Neurosci Lett. 2003 Dec 15;353(1):61-5. doi: 10.1016/j.neulet.2003.09.007. Neurosci Lett. 2003. PMID: 14642438

4

A family with Alzheimer disease and strokes associated with A713T mutation of the APP gene.

Rossi G, Giaccone G, Maletta R, Morbin M, Capobianco R, Mangieri M, Giovagnoli AR, Bizzi A, Tomaino C, Perri M, Di Natale M, Tagliavini F, Bugiani O, Bruni AC. Rossi G, et al. Among authors: perri m. Neurology. 2004 Sep 14;63(5):910-2. doi: 10.1212/01.wnl.0000137048.80666.86. Neurology. 2004. PMID: 15365148

5

A large Calabrian kindred segregating frontotemporal dementia.

Curcio SA, Kawarai T, Paterson AD, Maletta RG, Puccio G, Perri M, Di Natale M, Palermo S, Foncin JF, Hyslop PH, Bruni AC. Curcio SA, et al. Among authors: perri m. J Neurol. 2002 Jul;249(7):911-22. doi: 10.1007/s00415-002-0759-4. J Neurol. 2002. PMID: 12140677

6

The effects of APOE and tau gene variability on risk of frontotemporal dementia.

Bernardi L, Maletta RG, Tomaino C, Smirne N, Di Natale M, Perri M, Longo T, Colao R, Curcio SA, Puccio G, Mirabelli M, Kawarai T, Rogaeva E, St George Hyslop PH, Passarino G, De Benedictis G, Bruni AC. Bernardi L, et al. Among authors: perri m. Neurobiol Aging. 2006 May;27(5):702-9. doi: 10.1016/j.neurobiolaging.2005.03.008. Neurobiol Aging. 2006. PMID: 15904995

7

Interpreting elevated fetal hemoglobin in pathology and health at the basic laboratory level: new and known γ- gene mutations associated with hereditary persistence of fetal hemoglobin.

Amato A, Cappabianca MP, Perri M, Zaghis I, Grisanti P, Ponzini D, Di Biagio P. Amato A, et al. Among authors: perri m. Int J Lab Hematol. 2014 Feb;36(1):13-9. doi: 10.1111/ijlh.12094. Epub 2013 Apr 29. Int J Lab Hematol. 2014. PMID: 23621512 Review.

8

Hb Filottrano [codon 120 (-A)]: a novel frameshift mutation in exon 3 of the β-globin gene causing dominantly inherited β-thalassemia intermedia.

Amato A, Cappabianca MP, Perri M, Zaghis I, Mastropietro F, Ponzini D, Di Biagio P, Piscitelli R. Amato A, et al. Among authors: perri m. Hemoglobin. 2012;36(5):480-4. doi: 10.3109/03630269.2012.718309. Hemoglobin. 2012. PMID: 22992010

9

Current Genetic Epidemiology of β-Thalassemias and Structural Hemoglobin Variants in the Lazio Region (Central Italy) Following Recent Migration Movements.

Amato A, Cappabianca MP, Colosimo A, Perri M, Grisanti P, Zaghis I, Ponzini D, Lerone M. Amato A, et al. Among authors: perri m. Adv Hematol. 2010;2010:317542. doi: 10.1155/2010/317542. Epub 2010 Oct 5. Adv Hematol. 2010. PMID: 20975770 Free PMC article.

10

Carrier screening for inherited haemoglobin disorders among secondary school students and young adults in Latium, Italy.

Amato A, Cappabianca MP, Lerone M, Colosimo A, Grisanti P, Ponzini D, Di Biagio P, Perri M, Gianni D, Rinaldi S, Piscitelli R. Amato A, et al. Among authors: perri m. J Community Genet. 2014 Jul;5(3):265-8. doi: 10.1007/s12687-013-0171-z. Epub 2013 Oct 27. J Community Genet. 2014. PMID: 24163007 Free PMC article.

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