Olivieri C - Search Results

1

Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: data from the French-Italian HHT network.

Lesca G, Olivieri C, Burnichon N, Pagella F, Carette MF, Gilbert-Dussardier B, Goizet C, Roume J, Rabilloud M, Saurin JC, Cottin V, Honnorat J, Coulet F, Giraud S, Calender A, Danesino C, Buscarini E, Plauchu H; French-Italian-Rendu-Osler Network. Lesca G, et al. Among authors: olivieri c. Genet Med. 2007 Jan;9(1):14-22. doi: 10.1097/gim.0b013e31802d8373. Genet Med. 2007. PMID: 17224686 Free article.

2

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

3

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.

4

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

5

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

6

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

7

Doppler ultrasonographic grading of hepatic vascular malformations in hereditary hemorrhagic telangiectasia -- results of extensive screening.

Buscarini E, Danesino C, Olivieri C, Lupinacci G, De Grazia F, Reduzzi L, Blotta P, Gazzaniga P, Pagella F, Grosso M, Pongiglione G, Buscarini L, Plauchu H, Zambelli A. Buscarini E, et al. Among authors: olivieri c. Ultraschall Med. 2004 Sep;25(5):348-55. doi: 10.1055/s-2004-813549. Ultraschall Med. 2004. PMID: 15368138

8

High prevalence of hepatic focal nodular hyperplasia in subjects with hereditary hemorrhagic telangiectasia.

Buscarini E, Danesino C, Plauchu H, de Fazio C, Olivieri C, Brambilla G, Menozzi F, Reduzzi L, Blotta P, Gazzaniga P, Pagella F, Grosso M, Pongiglione G, Cappiello J, Zambelli A. Buscarini E, et al. Among authors: olivieri c. Ultrasound Med Biol. 2004 Sep;30(9):1089-97. doi: 10.1016/j.ultrasmedbio.2004.08.004. Ultrasound Med Biol. 2004. PMID: 15550313

9

Vascular abnormalities in the fingers of patients affected with hereditary hemorrhagic telangiectasia (HHT) as assessed by color doppler sonography.

Draghi F, Precerutti M, Danesino GM, Olivieri C, Valacca C, Danesino C, Pagella F, Semino L, Lanzarini L, Buscarini E, Danesino C. Draghi F, et al. Among authors: olivieri c. Am J Med Genet A. 2005 May 15;135(1):106-9. doi: 10.1002/ajmg.a.30649. Am J Med Genet A. 2005. PMID: 15779017 No abstract available.

10

Liver involvement in hereditary haemorrhagic telangiectasia or Rendu-Osler-Weber disease.

Buscarini E, Danesino C, Olivieri C, Lupinacci G, Zambelli A. Buscarini E, et al. Among authors: olivieri c. Dig Liver Dis. 2005 Sep;37(9):635-45. doi: 10.1016/j.dld.2005.04.010. Dig Liver Dis. 2005. PMID: 15923156 Review.

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