Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 20 of 21

1.

Hepatic angiodynamic profile in paediatric patients with hereditary haemorrhagic telangiectasia type 1 and type 2.

Giordano P, Francavilla M, Buonamico P, Suppressa P, Lastella P, Sangerardi M, Miniello VL, Scardapane A, Lenato GM, Sabbà C.

Vasa. 2017 May;46(3):195-202. doi: 10.1024/0301-1526/a000616. Epub 2017 Mar 1.

2.

Pulmonary Arteriovenous Malformations and Cerebral Abscess Recurrence in a Child With Hereditary Hemorrhagic Telangiectasia.

Giordano P, Sangerardi M, Suppressa P, Lastella P, Attolini E, Valente F, Fiorella ML, Lenato GM, Sabbà C.

J Pediatr Hematol Oncol. 2015 Apr;37(3):e200-3. doi: 10.1097/MPH.0000000000000254.

PMID:
25222056
3.

Erratum to "hypogonadotropic hypogonadism associated with hereditary hemorrhagic telangiectasia".

Scarano V, De Santis D, Suppressa P, Lastella P, Lenato GM, Triggiani V, Sabbà C.

Case Rep Endocrinol. 2013;2013:520284. doi: 10.1155/2013/520284. Epub 2013 Jul 16. No abstract available.

4.

Hypogonadotropic hypogonadism associated with hereditary hemorrhagic telangiectasia [corrected].

Scarano V, De Santis D, Suppressa P, Lastella P, Lenato GM, Triggiani V, Sabbà C.

Case Rep Endocrinol. 2013;2013:465376. doi: 10.1155/2013/465376. Epub 2013 Apr 4. Erratum in: Case Rep Endocrinol. 2013;2013:520284. Case Rep Endocrinol. 2013;2013:520284. Scarano, Valentina (2) Valentina, Scarano (3) De Santis, Daniele (4) Daniele, De Santis (5) Suppressa, Patrizia (6) Patrizia, Suppressa (7) Patrizia, Lastella [corrected to Lastella, Patrizia]; Mariano, Lenato Gennaro [corrected to Lenato, Gennaro Mariano].

5.

Hereditary hemorrhagic telangiectasia: arteriovenous malformations in children.

Giordano P, Lenato GM, Suppressa P, Lastella P, Dicuonzo F, Chiumarulo L, Sangerardi M, Piccarreta P, Valerio R, Scardapane A, Marano G, Resta N, Quaranta N, Sabbà C.

J Pediatr. 2013 Jul;163(1):179-86.e1-3. doi: 10.1016/j.jpeds.2013.02.009. Epub 2013 Mar 25.

PMID:
23535011
6.

Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: results of an Italian multicenter study.

Resta N, Pierannunzio D, Lenato GM, Stella A, Capocaccia R, Bagnulo R, Lastella P, Susca FC, Bozzao C, Loconte DC, Sabbà C, Urso E, Sala P, Fornasarig M, Grammatico P, Piepoli A, Host C, Turchetti D, Viel A, Memo L, Giunti L, Stigliano V, Varesco L, Bertario L, Genuardi M, Lucci Cordisco E, Tibiletti MG, Di Gregorio C, Andriulli A, Ponz de Leon M; AIFEG.

Dig Liver Dis. 2013 Jul;45(7):606-11. doi: 10.1016/j.dld.2012.12.018. Epub 2013 Feb 15.

PMID:
23415580
7.

Population data for 17 Y-chromosome STRs in a sample from Apulia (Southern Italy).

Piglionica M, Baldassarra SL, Giardina E, Stella A, D'Ovidio FD, Frati P, Lenato GM, Resta N, Dell'Erba A.

Forensic Sci Int Genet. 2013 Jan;7(1):e3-4. doi: 10.1016/j.fsigen.2012.08.003. Epub 2012 Sep 7.

PMID:
22960096
8.

A long diagnostic delay in patients with Hereditary Haemorrhagic Telangiectasia: a questionnaire-based retrospective study.

Pierucci P, Lenato GM, Suppressa P, Lastella P, Triggiani V, Valerio R, Comelli M, Salvante D, Stella A, Resta N, Logroscino G, Resta F, Sabbà C.

Orphanet J Rare Dis. 2012 Jun 7;7:33.

9.

Liver involvement in hereditary hemorrhagic telangiectasia: can breath test unmask impaired hepatic first-pass effect?

Candelli M, Pompili M, Suppressa P, Lenato GM, Bosco G, Rapaccini GL, Gasbarrini A, Scardapane A, Sabbà C.

Intern Emerg Med. 2012 Aug;7(4):323-9. doi: 10.1007/s11739-011-0531-9. Epub 2011 Feb 9.

PMID:
21305365
10.

Effects of VEGF on phenotypic severity in children with hereditary hemorrhagic telangiectasia.

Giordano P, Lenato GM, Pierucci P, Suppressa P, Altomare M, Del Vecchio G, Di Bitonto G, De Mattia D, Guanti G, Sabbà C.

J Pediatr Hematol Oncol. 2009 Aug;31(8):577-82. doi: 10.1097/MPH.0b013e3181a1c104.

PMID:
19636272
11.

Liver involvement in a large cohort of patients with hereditary hemorrhagic telangiectasia: echo-color-Doppler vs multislice computed tomography study.

Buonamico P, Suppressa P, Lenato GM, Pasculli G, D'Ovidio F, Memeo M, Scardapane A, Sabbà C.

J Hepatol. 2008 May;48(5):811-20. doi: 10.1016/j.jhep.2007.12.022. Epub 2008 Feb 14.

PMID:
18321607
12.

Hereditary haemorrhagic telangiectasia: a rare disease as a model for the study of human atherosclerosis.

Lenato GM, Suppressa P, Giordano P, Guanti G, Guastamacchia E, Triggiani V, Amati L, Resta F, Covelli V, Jirillo E, Sabbà C.

Curr Pharm Des. 2007;13(36):3656-64.

PMID:
18220803
13.

Hereditary hemorrhagic telangiectasia: clinical features in ENG and ALK1 mutation carriers.

Sabbà C, Pasculli G, Lenato GM, Suppressa P, Lastella P, Memeo M, Dicuonzo F, Guant G.

J Thromb Haemost. 2007 Jun;5(6):1149-57.

14.

Screening for children from families with Rendu-Osler-Weber disease: from geneticist to clinician.

Giordano P, Nigro A, Lenato GM, Guanti G, Suppressa P, Lastella P, DE Mattia D, Sabbà C.

J Thromb Haemost. 2006 Jun;4(6):1237-45.

15.

Hereditary Haemorrhagic Telangiectasia (HHT): genetic and molecular aspects.

Lenato GM, Guanti G.

Curr Pharm Des. 2006;12(10):1173-93. Review.

PMID:
16611099
16.

Life expectancy in patients with hereditary haemorrhagic telangiectasia.

Sabbà C, Pasculli G, Suppressa P, D'Ovidio F, Lenato GM, Resta F, Assennato G, Guanti G.

QJM. 2006 May;99(5):327-34. Epub 2006 Apr 4.

PMID:
16595564
17.

Mutation study of Spanish patients with hereditary hemorrhagic telangiectasia and expression analysis of Endoglin and ALK1.

Fernandez-L A, Sanz-Rodriguez F, Zarrabeitia R, Perez-Molino A, Morales C, Restrepo CM, Ramirez JR, Coto E, Lenato GM, Bernabeu C, Botella LM.

Hum Mutat. 2006 Mar;27(3):295.

PMID:
16470589
18.

DHPLC-based mutation analysis of ENG and ALK-1 genes in HHT Italian population.

Lenato GM, Lastella P, Di Giacomo MC, Resta N, Suppressa P, Pasculli G, Sabbà C, Guanti G.

Hum Mutat. 2006 Feb;27(2):213-4.

PMID:
16429404
19.

Capillaroscopy of the dorsal skin of the hands in hereditary hemorrhagic telangiectasia.

Pasculli G, Quaranta D, Lenato GM, Suppressa P, Lastella P, Guanti G, Sabbà C.

QJM. 2005 Oct;98(10):757-63. Epub 2005 Aug 26.

PMID:
16126740
20.

A large interstitial deletion encompassing the amelogenin gene on the short arm of the Y chromosome.

Lattanzi W, Di Giacomo MC, Lenato GM, Chimienti G, Voglino G, Resta N, Pepe G, Guanti G.

Hum Genet. 2005 Apr;116(5):395-401. Epub 2005 Feb 22.

PMID:
15726419

Supplemental Content

Loading ...
Support Center