Olivieri C - Search Results

1

Pleomorphic Parotid Adenoma in a Child Affected with Cri du Chat Syndrome: Clinical, Cytogenetic, and Molecular Analysis.

Danesino C, Biglioli F, Moneghini L, Valli R, Olivieri C, Testa B, Baldo C, Malacarne M, Guala A. Danesino C, et al. Among authors: olivieri c. Int J Mol Sci. 2024 Oct 3;25(19):10664. doi: 10.3390/ijms251910664. Int J Mol Sci. 2024. PMID: 39408992 Free PMC article.

2

Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability.

Valli R, Minelli A, Galbiati M, D'Amico G, Frattini A, Montalbano G, Khan AW, Porta G, Millefanti G, Olivieri C, Cipolli M, Cesaro S, Pasquali F, Danesino C, Cazzaniga G, Maserati E. Valli R, et al. Among authors: olivieri c. Br J Haematol. 2019 Mar;184(6):974-981. doi: 10.1111/bjh.15729. Epub 2018 Dec 26. Br J Haematol. 2019. PMID: 30585299 Free article.

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

Hereditary Hemorrhagic Telangiectasia in Pediatric Age: Focus on Genetics and Diagnosis.

Danesino C, Cantarini C, Olivieri C. Danesino C, et al. Among authors: olivieri c. Pediatr Rep. 2023 Feb 10;15(1):129-142. doi: 10.3390/pediatric15010011. Pediatr Rep. 2023. PMID: 36810341 Free PMC article. Review.

5

Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene.

Valli R, Vinti L, Frattini A, Fabbri M, Montalbano G, Olivieri C, Minelli A, Locatelli F, Pasquali F, Maserati E. Valli R, et al. Among authors: olivieri c. Mol Cytogenet. 2018 Jan 11;11:2. doi: 10.1186/s13039-017-0352-2. eCollection 2018. Mol Cytogenet. 2018. PMID: 29344089 Free PMC article.

6

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

7

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

8

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

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

Hereditary Hemorrhagic Telangiectasia: Breakpoint Characterization of a Novel Large Deletion in ACVRL1 Suggests the Causing Mechanism.

Boeri L, Radi O, Canzonieri C, Buscarini E, Scatigno A, Minelli A, Ornati F, Pagella F, Danesino C, Olivieri C. Boeri L, et al. Among authors: olivieri c. Mol Syndromol. 2013 Mar;4(3):119-24. doi: 10.1159/000347029. Epub 2013 Feb 28. Mol Syndromol. 2013. PMID: 23653583 Free PMC article.

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