Francalanci P - Search Results

1

Fibrinogen storage disease caused by Aguadilla mutation presenting with hypobeta-lipoproteinemia and considerable liver disease.

Sogo T, Nagasaka H, Komatsu H, Inui A, Miida T, Callea F, Francalanci P, Hirano K, Kitamura H, Yorifuji T, Fujisawa T. Sogo T, et al. Among authors: francalanci p. J Pediatr Gastroenterol Nutr. 2009 Jul;49(1):133-6. doi: 10.1097/MPG.0b013e31817ed7ea. J Pediatr Gastroenterol Nutr. 2009. PMID: 19458552 No abstract available.

2

CD44-v6 expression in smooth muscle cells in the postnatal remodeling process of ductus arteriosus.

Francalanci P, Camassei FD, Orzalesi M, Danhaive O, Callea F. Francalanci P, et al. Am J Cardiol. 2006 Apr 1;97(7):1056-9. doi: 10.1016/j.amjcard.2005.10.046. Epub 2006 Feb 17. Am J Cardiol. 2006. PMID: 16563915

3

Severe liver disease in early childhood due to fibrinogen storage and de novo gamma375Arg-->Trp gene mutation.

Francalanci P, Santorelli FM, Talini I, Boldrini R, Devito R, Camassei FD, Maggiore G, Callea F. Francalanci P, et al. J Pediatr. 2006 Mar;148(3):396-8. doi: 10.1016/j.jpeds.2005.10.007. J Pediatr. 2006. PMID: 16615976

4

A new ABCB11 mutation in two Italian children with familial intrahepatic cholestasis.

Nobili V, Di Giandomenico S, Francalanci P, Callea F, Marcellini M, Santorelli FM. Nobili V, et al. Among authors: francalanci p. J Gastroenterol. 2006 Jun;41(6):598-603. doi: 10.1007/s00535-006-1816-z. J Gastroenterol. 2006. PMID: 16868810

5

Z and Mmalton-1-antitrypsin deficiency-associated hepatocellular carcinoma: a genetic study.

Francalanci P, Santorelli FM, Saccani S, Bonetti MF, Medicina D, Coni P, Faa G, Callea F. Francalanci P, et al. Liver Int. 2009 Nov;29(10):1593-6. doi: 10.1111/j.1478-3231.2009.02091.x. Epub 2009 Sep 10. Liver Int. 2009. PMID: 19744266

6

Tyrosinemia type 1: metastatic hepatoblastoma with a favorable outcome.

Nobili V, Jenkner A, Francalanci P, Castellano A, Holme E, Callea F, Dionisi-Vici C. Nobili V, et al. Among authors: francalanci p. Pediatrics. 2010 Jul;126(1):e235-8. doi: 10.1542/peds.2009-1639. Epub 2010 Jun 14. Pediatrics. 2010. PMID: 20547648

7

Two novel mutations in African and Asian children with progressive familial intrahepatic cholestasis type 3.

Giovannoni I, Santorelli FM, Candusso M, Di Rocco M, Bellacchio E, Callea F, Francalanci P. Giovannoni I, et al. Among authors: francalanci p. Dig Liver Dis. 2011 Jul;43(7):567-70. doi: 10.1016/j.dld.2011.03.004. Epub 2011 Apr 21. Dig Liver Dis. 2011. PMID: 21514256

8

Bile salt export pump deficiency: A de novo mutation in a child compound heterozygous for ABCB11. Laboratory investigation to study pathogenic role and transmission of two novel ABCB11 mutations.

Francalanci P, Giovannoni I, Candusso M, Bellacchio E, Callea F. Francalanci P, et al. Hepatol Res. 2013 Mar;43(3):315-9. doi: 10.1111/j.1872-034X.2012.01061.x. Hepatol Res. 2013. PMID: 23437912

9

Alpha-1-antitrypsin deficiency: from genoma to liver disease. PiZ mouse as model for the development of liver pathology in human.

Giovannoni I, Callea F, Stefanelli M, Mariani R, Santorelli FM, Francalanci P. Giovannoni I, et al. Among authors: francalanci p. Liver Int. 2015 Jan;35(1):198-206. doi: 10.1111/liv.12504. Epub 2014 Mar 11. Liver Int. 2015. PMID: 24529185

10

Malignant pheochromocytoma in a 16-year-old patient with neurofibromatosis type 1.

Giovannoni I, Callea F, Boldrini R, Inserra A, Cozza R, Francalanci P. Giovannoni I, et al. Among authors: francalanci p. Pediatr Dev Pathol. 2014 Mar-Apr;17(2):126-9. doi: 10.2350/13-10-1397-CR.1. Epub 2014 Feb 20. Pediatr Dev Pathol. 2014. PMID: 24555864

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