Piperno A - Search Results

1

Ferroportin disease: A novel SLC40A1 mutation.

Ravasi G, Pelucchi S, Russo A, Mariani R, Piperno A. Ravasi G, et al. Among authors: piperno a. Dig Liver Dis. 2020 Jun;52(6):688-690. doi: 10.1016/j.dld.2020.03.013. Epub 2020 Apr 29. Dig Liver Dis. 2020. PMID: 32360131 No abstract available.

2

Haemochromatosis in patients with beta-thalassaemia trait.

Piperno A, Mariani R, Arosio C, Vergani A, Bosio S, Fargion S, Sampietro M, Girelli D, Fraquelli M, Conte D, Fiorelli G, Camaschella C. Piperno A, et al. Br J Haematol. 2000 Dec;111(3):908-14. Br J Haematol. 2000. PMID: 11122155 Free article.

3

Natural history of juvenile haemochromatosis.

De Gobbi M, Roetto A, Piperno A, Mariani R, Alberti F, Papanikolaou G, Politou M, Lockitch G, Girelli D, Fargion S, Cox TM, Gasparini P, Cazzola M, Camaschella C. De Gobbi M, et al. Among authors: piperno a. Br J Haematol. 2002 Jun;117(4):973-9. doi: 10.1046/j.1365-2141.2002.03509.x. Br J Haematol. 2002. PMID: 12060140 Free article. Review.

4

Increased serum ferritin is common in men with essential hypertension.

Piperno A, Trombini P, Gelosa M, Mauri V, Pecci V, Vergani A, Salvioni A, Mariani R, Mancia G. Piperno A, et al. J Hypertens. 2002 Aug;20(8):1513-8. doi: 10.1097/00004872-200208000-00013. J Hypertens. 2002. PMID: 12172312

5

Prevalence of C282Y and E168X HFE mutations in an Italian population of Northern European ancestry.

Salvioni A, Mariani R, Oberkanins C, Moritz A, Mauri V, Pelucchi S, Riva A, Arosio C, Cerutti P, Piperno A. Salvioni A, et al. Among authors: piperno a. Haematologica. 2003 Mar;88(3):250-5. Haematologica. 2003. PMID: 12651261

6

Prevalence of HFE mutations in upper Northern Italy: study of 1132 unrelated blood donors.

Mariani R, Salvioni A, Corengia C, Erba N, Lanzafame C, De Micheli V, Baldini V, Arosio C, Fossati L, Trombini P, Oberkanins C, Piperno A. Mariani R, et al. Among authors: piperno a. Dig Liver Dis. 2003 Jul;35(7):479-81. doi: 10.1016/s1590-8658(03)00220-2. Dig Liver Dis. 2003. PMID: 12870733

7

Homozygosity for transferrin receptor-2 Y250X mutation induces early iron overload.

Piperno A, Roetto A, Mariani R, Pelucchi S, Corengia C, Daraio F, Piga A, Garozzo G, Camaschella C. Piperno A, et al. Haematologica. 2004 Mar;89(3):359-60. Haematologica. 2004. PMID: 15020277

8

Gene symbol: FTL. Disease: Hyperferritinemia-cataract syndrome.

Piperno A, Pelucchi S. Piperno A, et al. Hum Genet. 2004 Mar;114(4):406. Hum Genet. 2004. PMID: 15046083 No abstract available.

9

Type 3 hemochromatosis and beta-thalassemia trait.

Riva A, Mariani R, Bovo G, Pelucchi S, Arosio C, Salvioni A, Vergani A, Piperno A. Riva A, et al. Among authors: piperno a. Eur J Haematol. 2004 May;72(5):370-4. doi: 10.1111/j.1600-0609.2004.00230.x. Eur J Haematol. 2004. PMID: 15059075

10

Iron chelation therapy in aceruloplasminaemia: study of a patient with a novel missense mutation.

Mariani R, Arosio C, Pelucchi S, Grisoli M, Piga A, Trombini P, Piperno A. Mariani R, et al. Among authors: piperno a. Gut. 2004 May;53(5):756-8. doi: 10.1136/gut.2003.030429. Gut. 2004. PMID: 15082597 Free PMC article.

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