Olivieri C - Search Results

1

Interstitial deletion of chromosome 9, int del(9)(9q22.31-q31.2), including the genes causing multiple basal cell nevus syndrome and Robinow/brachydactyly 1 syndrome.

Olivieri C, Maraschio P, Caselli D, Martini C, Beluffi G, Maserati E, Danesino C. Olivieri C, et al. Eur J Pediatr. 2003 Feb;162(2):100-3. doi: 10.1007/s00431-002-1116-4. Epub 2002 Dec 10. Eur J Pediatr. 2003. PMID: 12548386

2

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. Among authors: olivieri c. Eur J Gynaecol Oncol. 1998;19(3):234-8. Eur J Gynaecol Oncol. 1998. PMID: 9641220

3

Early onset of gastric carcinoma and constitutional deletion of 18p.

Dellavecchia C, Guala A, Olivieri C, Haintink O, Cadario F, Luinetti O, Fiocca R, Minelli A, Danesino C, Bona G. Dellavecchia C, et al. Among authors: olivieri c. Cancer Genet Cytogenet. 1999 Aug;113(1):96-9. doi: 10.1016/s0165-4608(99)00003-5. Cancer Genet Cytogenet. 1999. PMID: 10459356

4

Isochromosome (7)(q10) in Shwachman syndrome without MDS/AML and role of chromosome 7 anomalies in myeloproliferative disorders.

Maserati E, Minelli A, Olivieri C, Bonvini L, Marchi A, Bozzola M, Danesino C, Scappaticci S, Pasquali F. Maserati E, et al. Among authors: olivieri c. Cancer Genet Cytogenet. 2000 Sep;121(2):167-71. doi: 10.1016/s0165-4608(00)00246-6. Cancer Genet Cytogenet. 2000. PMID: 11063802

5

Familial partial monosomy 7 and myelodysplasia: different parental origin of the monosomy 7 suggests action of a mutator gene.

Minelli A, Maserati E, Giudici G, Tosi S, Olivieri C, Bonvini L, De Filippi P, Biondi A, Lo Curto F, Pasquali F, Danesino C. Minelli A, et al. Among authors: olivieri c. Cancer Genet Cytogenet. 2001 Jan 15;124(2):147-51. doi: 10.1016/s0165-4608(00)00344-7. Cancer Genet Cytogenet. 2001. PMID: 11172908

6

Meiotic origin of trisomy in neoplasms: evidence in a case of erythroleukaemia.

Minelli A, Morerio C, Maserati E, Olivieri C, Panarello C, Bonvini L, Leszl A, Rosanda C, Lanino E, Danesino C, Pasquali F. Minelli A, et al. Among authors: olivieri c. Leukemia. 2001 Jun;15(6):971-5. doi: 10.1038/sj.leu.2402123. Leukemia. 2001. PMID: 11417485

7

Identification of 13 new mutations in the ACVRL1 gene in a group of 52 unselected Italian patients affected by hereditary haemorrhagic telangiectasia.

Olivieri C, Mira E, Delù G, Pagella F, Zambelli A, Malvezzi L, Buscarini E, Danesino C. Olivieri C, et al. J Med Genet. 2002 Jul;39(7):E39. doi: 10.1136/jmg.39.7.e39. J Med Genet. 2002. PMID: 12114496 Free PMC article. No abstract available.

8

Linkage analysis for prenatal diagnosis in a familial case of Stickler syndrome.

Lisi V, Guala A, Lopez A, Vitali M, Spadoni E, Olivieri C, Danesino C, Mottes M. Lisi V, et al. Among authors: olivieri c. Genet Couns. 2002;13(2):163-70. Genet Couns. 2002. PMID: 12150217

9

Can GH induce chromosome breaks or microsatellite instability in GH-deficient children?

Olivieri C, Danesino C, Scappaticci S, Bozzola M. Olivieri C, et al. J Endocrinol Invest. 2004 Apr;27(4):308-10. doi: 10.1007/BF03351053. J Endocrinol Invest. 2004. PMID: 15233547

10

Echocardiographic screening discloses increased values of pulmonary artery systolic pressure in 9 of 68 unselected patients affected with hereditary hemorrhagic telangiectasia.

Olivieri C, Lanzarini L, Pagella F, Semino L, Corno S, Valacca C, Plauchu H, Lesca G, Barthelet M, Buscarini E, Danesino C. Olivieri C, et al. Genet Med. 2006 Mar;8(3):183-90. doi: 10.1097/01.gim.0000204463.77319.1c. Genet Med. 2006. PMID: 16540754 Free article.

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