Buscarini E - Search Results

1

Analysis of ENG and ACVRL1 genes in 137 HHT Italian families identifies 76 different mutations (24 novel). Comparison with other European studies.

Olivieri C, Pagella F, Semino L, Lanzarini L, Valacca C, Pilotto A, Corno S, Scappaticci S, Manfredi G, Buscarini E, Danesino C. Olivieri C, et al. Among authors: buscarini e. J Hum Genet. 2007;52(10):820-829. doi: 10.1007/s10038-007-0187-5. Epub 2007 Sep 5. J Hum Genet. 2007. PMID: 17786384

2

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: buscarini l, buscarini e. 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.

3

Hepatic vascular malformations in hereditary hemorrhagic telangiectasia: Doppler sonographic screening in a large family.

Buscarini E, Buscarini L, Danesino C, Piantanida M, Civardi G, Quaretti P, Rossi S, Di Stasi M, Silva M. Buscarini E, et al. Among authors: buscarini l. J Hepatol. 1997 Jan;26(1):111-8. doi: 10.1016/s0168-8278(97)80017-7. J Hepatol. 1997. PMID: 9148001

4

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. Among authors: buscarini e. 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.

5

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: buscarini l. Ultraschall Med. 2004 Sep;25(5):348-55. doi: 10.1055/s-2004-813549. Ultraschall Med. 2004. PMID: 15368138

6

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. Ultrasound Med Biol. 2004 Sep;30(9):1089-97. doi: 10.1016/j.ultrasmedbio.2004.08.004. Ultrasound Med Biol. 2004. PMID: 15550313

7

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: buscarini e. 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.

8

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. Dig Liver Dis. 2005 Sep;37(9):635-45. doi: 10.1016/j.dld.2005.04.010. Dig Liver Dis. 2005. PMID: 15923156 Review.

9

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. Among authors: buscarini e. Genet Med. 2006 Mar;8(3):183-90. doi: 10.1097/01.gim.0000204463.77319.1c. Genet Med. 2006. PMID: 16540754 Free article.

10

Treatment of epistaxis in hereditary hemorrhagic telangiectasia patients by argon plasma coagulation with local anesthesia.

Pagella F, Semino L, Olivieri C, Corno S, Dore R, Draghi F, Lanzarini L, Vespro V, Buscarini E, Danesino C. Pagella F, et al. Among authors: buscarini e. Am J Rhinol. 2006 Jul-Aug;20(4):421-5. doi: 10.2500/ajr.2006.20.2886. Am J Rhinol. 2006. PMID: 16955772

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