Demori E - Search Results

1

Genomic organization and chromosome mapping of the human homeobox gene HHEX.

Morgutti M, Demori E, Pecile V, Amoroso A, Rustighi A, Manfioletti G. Morgutti M, et al. Among authors: demori e. Cytogenet Cell Genet. 2001;94(1-2):30-2. doi: 10.1159/000048778. Cytogenet Cell Genet. 2001. PMID: 11701950

2

Supernumerary ring chromosome 8: clinical and molecular cytogenetic characterization in a case report.

Demori E, Devescovi R, Benussi DG, Dolce S, Carrozzi M, Villa N, Miertus J, Amoroso A, Pecile V. Demori E, et al. Am J Med Genet A. 2004 Oct 15;130A(3):288-94. doi: 10.1002/ajmg.a.20677. Am J Med Genet A. 2004. PMID: 15378554 Review.

3

Fragile X syndrome, mental retardation and macroorchidism.

Vatta S, Cigui I, Demori E, Morgutti M, Pecile V, Benussi DG, Serra C, Amoroso A. Vatta S, et al. Among authors: demori e. Clin Genet. 1998 Oct;54(4):366-7. doi: 10.1034/j.1399-0004.1998.5440420.x. Clin Genet. 1998. PMID: 9831354 No abstract available.

4

In situ RT-PCR allows the detection of ornithine decarboxylase mRNA in paraffin embedded archival human hyperplastic breast tissues.

Clerico L, Mancuso T, Da Prato L, Marziliano N, Garagna S, Pecile V, Demori E, Morgutti M, Città A, Parodi S, Amoroso A, Crovella S. Clerico L, et al. Among authors: demori e. Eur J Histochem. 1999;43(3):179-83. Eur J Histochem. 1999. PMID: 10563250

5

Detection of ornithine decarboxylase mRNA in human breast cancer MCF-7 cells by in situ RT-PCR.

Clerico L, Mancuso T, Crovella S, Amoroso A, Morgutti M, Demori E, Parodi S. Clerico L, et al. Among authors: demori e. Int J Oncol. 2000 Feb;16(2):241-4. doi: 10.3892/ijo.16.2.241. Int J Oncol. 2000. PMID: 10639565

6

Anthracyclines in Nijmegen breakage syndrome.

Barth E, Demori E, Pecile V, Zanazzo GA, Malorgio C, Tamaro P. Barth E, et al. Among authors: demori e. Med Pediatr Oncol. 2003 Feb;40(2):122-4. doi: 10.1002/mpo.10079. Med Pediatr Oncol. 2003. PMID: 12461799 No abstract available.

7

Diagnosis of triploidy in metaphases from uncultured amniocytes.

Pecile V, Demori E, Gambel Benussi D, Dolce S, Amoroso A. Pecile V, et al. Among authors: demori e. Prenat Diagn. 2002 Jan;22(1):78-9. doi: 10.1002/pd.229. Prenat Diagn. 2002. PMID: 11810658 No abstract available.

8

Chromosome instability and nibrin protein variants in NBS heterozygotes.

Tanzanella C, Antoccia A, Spadoni E, di Masi A, Pecile V, Demori E, Varon R, Marseglia GL, Tiepolo L, Maraschio P. Tanzanella C, et al. Among authors: demori e. Eur J Hum Genet. 2003 Apr;11(4):297-303. doi: 10.1038/sj.ejhg.5200962. Eur J Hum Genet. 2003. PMID: 12708449

9

Fluorescent RT in situ PCR detection of MRP1 mRNA in human HCV infected liver.

Pascolo L, Bogoni S, Spanò A, Demori E, Amoroso A, Crovella S. Pascolo L, et al. Among authors: demori e. Eur J Histochem. 2001;45(1):105-8. doi: 10.4081/1620. Eur J Histochem. 2001. PMID: 11411859 No abstract available.

10

CACNA1C haploinsufficiency accounts for the common features of interstitial 12p13.33 deletion carriers.

Mio C, Passon N, Baldan F, Bregant E, Monaco E, Mancini L, Demori E, Damante G. Mio C, et al. Among authors: demori e. Eur J Med Genet. 2020 Apr;63(4):103843. doi: 10.1016/j.ejmg.2020.103843. Epub 2020 Jan 14. Eur J Med Genet. 2020. PMID: 31953239

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