Minelli A - Search Results

1

Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies.

Maserati E, Minelli A, Pressato B, Valli R, Crescenzi B, Stefanelli M, Menna G, Sainati L, Poli F, Panarello C, Zecca M, Curto FL, Mecucci C, Danesino C, Pasquali F. Maserati E, et al. Among authors: minelli a. Genes Chromosomes Cancer. 2006 Apr;45(4):375-82. doi: 10.1002/gcc.20301. Genes Chromosomes Cancer. 2006. PMID: 16382447

2

A homozygous missense arginine to histidine substitution at position 482 of the beta-galactosidase in an Italian infantile GM1-gangliosidosis patient.

Mosna G, Fattore S, Tubiello G, Brocca S, Trubia M, Gianazza E, Gatti R, Danesino C, Minelli A, Piantanida M. Mosna G, et al. Among authors: minelli a. Hum Genet. 1992 Nov;90(3):247-50. doi: 10.1007/BF00220071. Hum Genet. 1992. PMID: 1487238

3

Gene dosage effect in acquired monosomy 7: distinct behaviour of beta-glucuronidase and phosphoserine phosphatase.

Minelli A, Piantanida M, Maserati E, Campagnoli E, Pasquali F, Danesino C. Minelli A, et al. Genes Chromosomes Cancer. 1990 Jan;1(3):216-20. doi: 10.1002/gcc.2870010305. Genes Chromosomes Cancer. 1990. PMID: 1964582

4

Gene dosage effect in cells with monosomy of chromosome 22 derived from human meningiomas.

Casalone R, Minelli A, Butti G, Gaetani P, Silvani V, Solero CL, Danesino C. Casalone R, et al. Among authors: minelli a. Acta Neurochir Suppl (Wien). 1988;43:114-7. doi: 10.1007/978-3-7091-8978-8_24. Acta Neurochir Suppl (Wien). 1988. PMID: 2975141

5

The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications.

Floridia G, Piantanida M, Minelli A, Dellavecchia C, Bonaglia C, Rossi E, Gimelli G, Croci G, Franchi F, Gilgenkrantz S, Grammatico P, Dalprá L, Wood S, Danesino C, Zuffardi O. Floridia G, et al. Among authors: minelli a. Am J Hum Genet. 1996 Apr;58(4):785-96. Am J Hum Genet. 1996. PMID: 8644743 Free PMC article.

6

Hereditary haemorrhagic telangiectasia with extensive liver involvement is not caused by either HHT1 or HHT2.

Piantanida M, Buscarini E, Dellavecchia C, Minelli A, Rossi A, Buscarini L, Danesino C. Piantanida M, et al. Among authors: minelli a. J Med Genet. 1996 Jun;33(6):441-3. doi: 10.1136/jmg.33.6.441. J Med Genet. 1996. PMID: 8782041 Free PMC article.

7

Constitutional trisomy 8 as first mutation in multistep carcinogenesis: clinical, cytogenetic, and molecular data on three cases.

Seghezzi L, Maserati E, Minelli A, Dellavecchia C, Addis P, Locatelli F, Angioni A, Balloni P, Miano C, Cavalli P, Danesino C, Pasquali F. Seghezzi L, et al. Among authors: minelli a. Genes Chromosomes Cancer. 1996 Oct;17(2):94-101. doi: 10.1002/(SICI)1098-2264(199610)17:2<94::AID-GCC4>3.0.CO;2-W. Genes Chromosomes Cancer. 1996. PMID: 8913726

8

Ring chromosome 13 with loss of the region D13S317-D13S285: phenotypic overlap with XK syndrome.

Guala A, Dellavecchia C, Mannarino S, Rognone F, Giglio S, Minelli A, Danesino C. Guala A, et al. Among authors: minelli a. Am J Med Genet. 1997 Oct 31;72(3):319-23. Am J Med Genet. 1997. PMID: 9332662 Review.

9

Ph-positive CML in blastic phase with monosomy 7 in a Down syndrome patient. Monitoring by interphase cytogenetics and demonstration of maternal allelic loss.

Seghezzi L, Dellavecchia C, Maserati E, Minelli A, Carrà A, Locatelli F, Argusti A, Lo Curto F, Danesino C, Pasquali F. Seghezzi L, et al. Among authors: minelli a. Cancer Genet Cytogenet. 1997 Nov;99(1):77-80. doi: 10.1016/s0165-4608(96)00431-1. Cancer Genet Cytogenet. 1997. PMID: 9352800

10

Concurrent cytogenetic and molecular investigations in uterine and ovarian neoplasms.

Minelli A, Capra E, Dellavecchia C, Danesino C, Olivieri C, Tateo S, Tenti P, Scappaticci S. Minelli A, et al. Eur J Gynaecol Oncol. 1998;19(3):234-8. Eur J Gynaecol Oncol. 1998. PMID: 9641220

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