Cremonesi L - Search Results

1

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. 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.

2

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: cremonesi l. 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.

3

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. Hum Mutat. 2003 Jul;22(1):98-102. doi: 10.1002/humu.10234. Hum Mutat. 2003. PMID: 12815600

4

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. Haematologica. 2003 Oct;88(10):1110-6. Haematologica. 2003. PMID: 14555306

5

Denaturing HPLC profiling of the ABCA4 gene for reliable detection of allelic variations.

Stenirri S, Fermo I, Battistella S, Galbiati S, Soriani N, Paroni R, Manitto MP, Martina E, Brancato R, Allikmets R, Ferrari M, Cremonesi L. Stenirri S, et al. Among authors: cremonesi l. Clin Chem. 2004 Aug;50(8):1336-43. doi: 10.1373/clinchem.2004.033241. Epub 2004 Jun 10. Clin Chem. 2004. PMID: 15192030

6

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: cremonesi l. Hum Mutat. 2006 Feb;27(2):201-8. doi: 10.1002/humu.20294. Hum Mutat. 2006. PMID: 16395671

7

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: cremonesi l. Clin Chem Lab Med. 2007;45(11):1450-6. doi: 10.1515/CCLM.2007.307. Clin Chem Lab Med. 2007. PMID: 17970701

8

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. Clin Chem. 2001 Mar;47(3):491-7. Clin Chem. 2001. PMID: 11238302

9

Genetic and clinical heterogeneity of ferroportin disease.

Cremonesi L, Forni GL, Soriani N, Lamagna M, Fermo I, Daraio F, Galli A, Pietra D, Malcovati L, Ferrari M, Camaschella C, Cazzola M. Cremonesi L, et al. Br J Haematol. 2005 Dec;131(5):663-70. doi: 10.1111/j.1365-2141.2005.05815.x. Br J Haematol. 2005. PMID: 16351644 Free article.

10

High resolution melting for the identification of mutations in the iron responsive element of the ferritin light chain gene.

Castiglioni E, Soriani N, Girelli D, Camaschella C, Spiga I, Della Porta MG, Ferrari M, Cremonesi L. Castiglioni E, et al. Among authors: cremonesi l. Clin Chem Lab Med. 2010 Oct;48(10):1415-8. doi: 10.1515/CCLM.2010.281. Epub 2010 Jun 27. Clin Chem Lab Med. 2010. PMID: 20578964

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