Cremonesi L - Search Results

1

Molecular diagnosis of genetic diseases.

Ferrari M, Cremonesi L, Carrera P, Bonini PA. Ferrari M, et al. Among authors: cremonesi l. Clin Biochem. 1996 Jun;29(3):201-8. doi: 10.1016/0009-9120(95)02022-e. Clin Biochem. 1996. PMID: 8740505 Review. No abstract available.

2

Molecular diagnostics by microelectronic microchips.

Ferrari M, Stenirri S, Bonini P, Cremonesi L. Ferrari M, et al. Among authors: cremonesi l. Clin Chem Lab Med. 2003 Apr;41(4):462-7. doi: 10.1515/CCLM.2003.069. Clin Chem Lab Med. 2003. PMID: 12747587 Review.

3

Molecular diagnostics by microelectronic microchips.

Ferrari M, Cremonesi L, Bonini P, Stenirri S, Foglieni B. Ferrari M, et al. Among authors: cremonesi l. Expert Rev Mol Diagn. 2005 Mar;5(2):183-92. doi: 10.1586/14737159.5.2.183. Expert Rev Mol Diagn. 2005. PMID: 15833048 Review.

4

Single-nucleotide polymorphism and mutation identification by the nanogen microelectronic chip technology.

Ferrari M, Cremonesi L, Bonini P, Foglieni B, Stenirri S. Ferrari M, et al. Among authors: cremonesi l. Methods Mol Med. 2005;114:93-106. doi: 10.1385/1-59259-923-0:93. Methods Mol Med. 2005. PMID: 16156099

5

Different approaches for noninvasive prenatal diagnosis of genetic diseases based on PNA-mediated enriched PCR.

Galbiati S, Restagno G, Foglieni B, Bonalumi S, Travi M, Piga A, Sbaiz L, Chiari M, Damin F, Smid M, Valsecchi L, Pasi F, Ferrari A, Ferrari M, Cremonesi L. Galbiati S, et al. Among authors: cremonesi l. Ann N Y Acad Sci. 2006 Sep;1075:137-43. doi: 10.1196/annals.1368.018. Ann N Y Acad Sci. 2006. PMID: 17108203

6

2. Post-Natal Molecular Diagnosis of Inherited Diseases.

Ferrari M, Cremonesi L, Stenirri S. Ferrari M, et al. Among authors: cremonesi l. EJIFCC. 2008 Apr 3;19(1):7-12. eCollection 2008 Apr. EJIFCC. 2008. PMID: 27683285 Free PMC article. No abstract available.

7

Multiplex PCR for rapid detection of three mutations in the cystic fibrosis gene.

Cremonesi L, Belloni E, Magnani C, Seia M, Ferrari M. Cremonesi L, et al. PCR Methods Appl. 1992 May;1(4):297-8. doi: 10.1101/gr.1.4.297. PCR Methods Appl. 1992. PMID: 1477665 Free article. No abstract available.

8

Rapid detection of 1717-1G----A mutation in CFTR gene by PCR-mediated site-directed mutagenesis.

Cremonesi L, Seia M, Magnani C, Ferrari M. Cremonesi L, et al. Clin Chem. 1991 Nov;37(11):1967. Clin Chem. 1991. PMID: 1718633 No abstract available.

9

Simultaneous detection of delta F508, G542X, N1303K and 1717-1G-->A mutations in cystic fibrosis by capillary electrophoresis in polymer networks.

Gelfi C, Righetti PG, Magnani C, Cremonesi L, Ferrari M. Gelfi C, et al. Among authors: cremonesi l. Clin Chim Acta. 1994 Sep;229(1-2):181-9. doi: 10.1016/0009-8981(94)90240-2. Clin Chim Acta. 1994. PMID: 7527312 No abstract available.

10

Informativity of intragenic microsatellites for carrier detection and prenatal diagnosis of cystic fibrosis in the Italian population.

Magnani C, Cremonesi L, Belloni E, Ferrari M, Seia M, Russo MP, Devoto M, Ronchetto P, Romeo G. Magnani C, et al. Among authors: cremonesi l. Clin Genet. 1994 Mar;45(3):135-9. doi: 10.1111/j.1399-0004.1994.tb04010.x. Clin Genet. 1994. PMID: 7913006

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