Arosio P - Search Results

1

Denaturing HPLC analysis of DNA deletions and insertions.

Cremonesi L, Stenirri S, Fermo I, Paroni R, Ferrari M, Cazzola M, Arosio P. Cremonesi L, et al. Among authors: arosio p. Hum Mutat. 2003 Jul;22(1):98-102. doi: 10.1002/humu.10234. Hum Mutat. 2003. PMID: 12815600

2

Scanning mutations of the 5'UTR regulatory sequence of L-ferritin by denaturing high-performance liquid chromatography: identification of new mutations.

Cremonesi L, Paroni R, Foglieni B, Galbiati S, Fermo I, Soriani N, Belloli S, Ruggeri G, Biasiotto G, Cazzola M, Ferrari F, Ferrari M, Arosio P. Cremonesi L, et al. Among authors: arosio p. Br J Haematol. 2003 Apr;121(1):173-9. doi: 10.1046/j.1365-2141.2003.04253.x. Br J Haematol. 2003. PMID: 12670350 Free article.

3

Identification of two novel mutations in the 5'-untranslated region of H-ferritin using denaturing high performance liquid chromatography scanning.

Cremonesi L, Foglieni B, Fermo I, Cozzi A, Paroni R, Ruggeri G, Belloli S, Levi S, Fargion S, Ferrari M, Arosio P. Cremonesi L, et al. Among authors: arosio p. Haematologica. 2003 Oct;88(10):1110-6. Haematologica. 2003. PMID: 14555306

4

Microelectronic DNA chip for hereditary hyperferritinemia cataract syndrome, a model for large-scale analysis of disorders of iron metabolism.

Ferrari F, Foglieni B, Arosio P, Camaschella C, Daraio F, Levi S, García Erce JA, Beaumont C, Cazzola M, Ferrari M, Cremonesi L. Ferrari F, et al. Among authors: arosio p. Hum Mutat. 2006 Feb;27(2):201-8. doi: 10.1002/humu.20294. Hum Mutat. 2006. PMID: 16395671

5

Analysis of ferritin genes in Parkinson disease.

Foglieni B, Ferrari F, Goldwurm S, Santambrogio P, Castiglioni E, Sessa M, Volontè MA, Lalli S, Galli C, Wang XS, Connor J, Sironi F, Canesi M, Biasiotto G, Pezzoli G, Levi S, Ferrari M, Arosio P, Cremonesi L. Foglieni B, et al. Among authors: arosio p. Clin Chem Lab Med. 2007;45(11):1450-6. doi: 10.1515/CCLM.2007.307. Clin Chem Lab Med. 2007. PMID: 17970701

6

Double-gradient denaturing gradient gel electrophoresis assay for identification of L-ferritin iron-responsive element mutations responsible for hereditary hyperferritinemia-cataract syndrome: identification of the new mutation C14G.

Cremonesi L, Fumagalli A, Soriani N, Ferrari M, Levi S, Belloli S, Ruggeri G, Arosio P. Cremonesi L, et al. Among authors: arosio p. Clin Chem. 2001 Mar;47(3):491-7. Clin Chem. 2001. PMID: 11238302

7

Case report: a subject with a mutation in the ATG start codon of L-ferritin has no haematological or neurological symptoms.

Cremonesi L, Cozzi A, Girelli D, Ferrari F, Fermo I, Foglieni B, Levi S, Bozzini C, Camparini M, Ferrari M, Arosio P. Cremonesi L, et al. Among authors: arosio p. J Med Genet. 2004 Jun;41(6):e81. doi: 10.1136/jmg.2003.011718. J Med Genet. 2004. PMID: 15173247 Free PMC article. No abstract available.

8

Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3).

Cazzola M, Cremonesi L, Papaioannou M, Soriani N, Kioumi A, Charalambidou A, Paroni R, Romtsou K, Levi S, Ferrari M, Arosio P, Christakis J. Cazzola M, et al. Among authors: arosio p. Br J Haematol. 2002 Nov;119(2):539-46. doi: 10.1046/j.1365-2141.2002.03946.x. Br J Haematol. 2002. PMID: 12406098 Free article.

9

Sequence variations in mitochondrial ferritin: distribution in healthy controls and different types of patients.

Castiglioni E, Finazzi D, Goldwurm S, Levi S, Pezzoli G, Garavaglia B, Nardocci N, Malcovati L, Porta MG, Gallì A, Forni GL, Girelli D, Maccarinelli F, Poli M, Ferrari M, Cremonesi L, Arosio P. Castiglioni E, et al. Among authors: arosio p. Genet Test Mol Biomarkers. 2010 Dec;14(6):793-6. doi: 10.1089/gtmb.2010.0076. Epub 2010 Oct 12. Genet Test Mol Biomarkers. 2010. PMID: 20939738

10

Analysis of nucleotide variations in genes of iron management in patients of Parkinson's disease and other movement disorders.

Castiglioni E, Finazzi D, Goldwurm S, Pezzoli G, Forni G, Girelli D, Maccarinelli F, Poli M, Ferrari M, Cremonesi L, Arosio P. Castiglioni E, et al. Among authors: arosio p. Parkinsons Dis. 2010 Oct 17;2011:827693. doi: 10.4061/2011/827693. Parkinsons Dis. 2010. PMID: 20981230 Free PMC article.

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