Carrera P - Search Results

1

Genomic typing for patient-specific human leukocyte antigen-alleles is an efficient tool for relapse detection of high-risk hematopoietic malignancies after stem cell transplantation from alternative donors.

Mazzi B, Clerici TD, Zanussi M, Lupo Stanghellini MT, Vago L, Sironi E, Peccatori J, Bernardi M, Carrera P, Palini A, Rossini S, Bordignon C, Bonini C, Ferrari M, Ciceri F, Fleischhauer K. Mazzi B, et al. Among authors: carrera p. Leukemia. 2008 Nov;22(11):2119-22. doi: 10.1038/leu.2008.98. Epub 2008 May 1. Leukemia. 2008. PMID: 18449202 No abstract available.

2

Capillary zone electrophoresis in polymer networks of polymerase chain reaction-amplified oligonucleotides: the case of congenital adrenal hyperplasia.

Gelfi C, Orsi A, Righetti PG, Zanussi M, Carrera P, Ferrari M. Gelfi C, et al. Among authors: carrera p. J Chromatogr B Biomed Appl. 1994 Jul 1;657(1):201-5. doi: 10.1016/0378-4347(94)80088-x. J Chromatogr B Biomed Appl. 1994. PMID: 7952069

3

Molecular diagnosis of genetic diseases.

Ferrari M, Cremonesi L, Carrera P, Bonini PA. Ferrari M, et al. Among authors: carrera p. 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.

4

Towards Automation for Molecular Diagnosis of Cancer.

Ferrari M, Carrera P. Ferrari M, et al. Among authors: carrera p. EJIFCC. 2005 May 17;16(2):66-72. eCollection 2005 May. EJIFCC. 2005. PMID: 29942240 Free PMC article. No abstract available.

5

A nonsense mutation (Gln-673-Term) in exon 17 of the human dystrophin gene detected by heteroduplex analysis.

Barbieri AM, Soriani N, Tubiello GM, Ferrari M, Carrera P. Barbieri AM, et al. Among authors: carrera p. Hum Genet. 1995 Sep;96(3):343-4. doi: 10.1007/BF00210420. Hum Genet. 1995. PMID: 7649554

6

Failure to detect Glut4-Ile383 and IR-Gln1152 variants in NIDDM (non-insulin dependent diabetes mellitus) and control subjects in an Italian population.

Esposito L, Carrera P, Pontiroli AE, Ferrari M. Esposito L, et al. Among authors: carrera p. Hum Genet. 1995 Jan;95(1):115-6. doi: 10.1007/BF00225088. Hum Genet. 1995. PMID: 7814014

7

Molecular characterization of 21-hydroxylase deficiency in 70 Italian families.

Carrera P, Ferrari M, Beccaro F, Spiga I, Zanussi M, Rigon F, Braggion F, Zacchello F, Greggio N. Carrera P, et al. Hum Hered. 1993 May-Jun;43(3):190-6. doi: 10.1159/000154176. Hum Hered. 1993. PMID: 8330883

8

Amplification of 18 dystrophin gene exons in DMD/BMD patients: simultaneous resolution by capillary electrophoresis in sieving liquid polymers.

Gelfi C, Orsi A, Leoncini F, Righetti PG, Spiga I, Carrera P, Ferrari M. Gelfi C, et al. Among authors: carrera p. Biotechniques. 1995 Aug;19(2):254-8, 260-3. Biotechniques. 1995. PMID: 8527147

9

Mutational analysis of muscle and brain specific promoter regions of dystrophin gene in DMD/BMD Italian patients by denaturing gradient gel electrophoresis (DGGE).

Tubiello G, Carrera P, Soriani N, Morandi L, Ferrari M. Tubiello G, et al. Among authors: carrera p. Mol Cell Probes. 1995 Dec;9(6):441-6. doi: 10.1006/mcpr.1995.0067. Mol Cell Probes. 1995. PMID: 8808315

10

A new polymorphism in exon 14 of the dystrophin gene detected by RT-PCR and DGGE.

Barbieri AM, Soriani N, Ferrari M, Carrera P. Barbieri AM, et al. Among authors: carrera p. Mol Cell Probes. 1997 Apr;11(2):161-2. doi: 10.1006/mcpr.1996.0092. Mol Cell Probes. 1997. PMID: 9160332 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

303 results

Search Page

Filters