Miozzo M - Search Results

1

Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction.

Tabano S, Colapietro P, Cetin I, Grati FR, Zanutto S, Mandò C, Antonazzo P, Pileri P, Rossella F, Larizza L, Sirchia SM, Miozzo M. Tabano S, et al. Among authors: miozzo m. Epigenetics. 2010 May 16;5(4):313-24. doi: 10.4161/epi.5.4.11637. Epub 2010 May 28. Epigenetics. 2010. PMID: 20418667

2

19p deletion in recurring leiomyosarcoma lesions from the same patient.

Riva P, Dalprá L, Gualandri V, Volontè M, Miozzo M, Malgara R, Conti AF, Larizza L. Riva P, et al. Among authors: miozzo m. Cancer Genet Cytogenet. 2000 Jun;119(2):102-8. doi: 10.1016/s0165-4608(99)00222-8. Cancer Genet Cytogenet. 2000. PMID: 10867143

3

Patient with large 17p11.2 deletion presenting with Smith-Magenis syndrome and Joubert syndrome phenotype.

Natacci F, Corrado L, Pierri M, Rossetti M, Zuccarini C, Riva P, Miozzo M, Larizza L. Natacci F, et al. Among authors: miozzo m. Am J Med Genet. 2000 Dec 18;95(5):467-72. doi: 10.1002/1096-8628(20001218)95:5<467::aid-ajmg11>3.0.co;2-t. Am J Med Genet. 2000. PMID: 11146468

4

Post-zygotic origin of complete maternal chromosome 7 isodisomy and consequent loss of placental PEG1/MEST expression.

Miozzo M, Grati FR, Bulfamante G, Rossella F, Cribiù M, Radaelli T, Cassani B, Persico T, Cetin I, Pardi G, Simoni G. Miozzo M, et al. Placenta. 2001 Nov;22(10):813-21. doi: 10.1053/plac.2001.0728. Placenta. 2001. PMID: 11718568

5

The role of imprinted genes in fetal growth.

Miozzo M, Simoni G. Miozzo M, et al. Biol Neonate. 2002;81(4):217-28. doi: 10.1159/000056752. Biol Neonate. 2002. PMID: 12011565 Review.

6

Mapping of candidate region for chordoma development to 1p36.13 by LOH analysis.

Riva P, Crosti F, Orzan F, Dalprà L, Mortini P, Parafioriti A, Pollo B, Fuhrman Conti AM, Miozzo M, Larizza L. Riva P, et al. Among authors: miozzo m. Int J Cancer. 2003 Nov 10;107(3):493-7. doi: 10.1002/ijc.11421. Int J Cancer. 2003. PMID: 14506752 Free article.

7

Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies.

Grati FR, Sirchia SM, Gentilin B, Rossella F, Ramoscelli L, Antonazzo P, Cavallari U, Bulfamante G, Cetin I, Simoni G, Miozzo M. Grati FR, et al. Among authors: miozzo m. Eur J Hum Genet. 2004 Apr;12(4):272-8. doi: 10.1038/sj.ejhg.5201121. Eur J Hum Genet. 2004. PMID: 14673477

8

Frequency of monosomy X in women with primary biliary cirrhosis.

Invernizzi P, Miozzo M, Battezzati PM, Bianchi I, Grati FR, Simoni G, Selmi C, Watnik M, Gershwin ME, Podda M. Invernizzi P, et al. Among authors: miozzo m. Lancet. 2004 Feb 14;363(9408):533-5. doi: 10.1016/S0140-6736(04)15541-4. Lancet. 2004. PMID: 14975617

9

Fetal growth restriction: a workshop report.

Cetin I, Foidart JM, Miozzo M, Raun T, Jansson T, Tsatsaris V, Reik W, Cross J, Hauguel-de-Mouzon S, Illsley N, Kingdom J, Huppertz B. Cetin I, et al. Among authors: miozzo m. Placenta. 2004 Sep-Oct;25(8-9):753-7. doi: 10.1016/j.placenta.2004.02.004. Placenta. 2004. PMID: 15450396 Free article.

10

Prenatal search for UPD 14 and UPD 15 in 83 cases of familial and de novo heterologous Robertsonian translocations.

Ruggeri A, Dulcetti F, Miozzo M, Grati FR, Grimi B, Bellato S, Natacci F, Maggi F, Simoni G. Ruggeri A, et al. Among authors: miozzo m. Prenat Diagn. 2004 Dec 15;24(12):997-1000. doi: 10.1002/pd.961. Prenat Diagn. 2004. PMID: 15614836

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