Carrera P - Search Results

1

Concurrence of NMOSD and ALS in a patient with hexanucleotide repeat expansions of C9orf72.

Falzone YM, Radaelli M, Agosta F, Domi T, Guerrieri S, Spinelli EG, Pozzi L, Carrera P, Ferrari M, Comi G, Filippi M, Quattrini A, Riva N. Falzone YM, et al. Among authors: carrera p. Amyotroph Lateral Scler Frontotemporal Degener. 2019 Aug;20(5-6):449-452. doi: 10.1080/21678421.2019.1604761. Epub 2019 Apr 22. Amyotroph Lateral Scler Frontotemporal Degener. 2019. PMID: 31007077

2

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

3

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

4

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.

5

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

6

Seven novel additional small mutations and a new alternative splicing in the human dystrophin gene detected by heteroduplex analysis and restricted RT-PCR heteroduplex analysis of illegitimate transcripts.

Barbieri AM, Soriani N, Ferlini A, Michelato A, Ferrari M, Carrera P. Barbieri AM, et al. Among authors: carrera p. Eur J Hum Genet. 1996;4(3):183-7. doi: 10.1159/000472193. Eur J Hum Genet. 1996. PMID: 8840119

7

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.

8

Rapid detection of 21-hydroxylase deficiency mutations by allele-specific in vitro amplification and capillary zone electrophoresis.

Carrera P, Barbieri AM, Ferrari M, Righetti PG, Perego M, Gelfi C. Carrera P, et al. Clin Chem. 1997 Nov;43(11):2121-7. Clin Chem. 1997. PMID: 9365397

9

Amplification refractory mutation system analysis of point mutations by capillary electrophoresis.

Carrera P, Righetti PG, Gelfi C, Ferrari M. Carrera P, et al. Methods Mol Biol. 2001;163:95-108. doi: 10.1385/1-59259-116-7:95. Methods Mol Biol. 2001. PMID: 11242967 No abstract available.

10

Familial hemiplegic migraine: a ion channel disorder.

Carrera P, Stenirri S, Ferrari M, Battistini S. Carrera P, et al. Brain Res Bull. 2001 Oct-Nov 1;56(3-4):239-41. doi: 10.1016/s0361-9230(01)00570-6. Brain Res Bull. 2001. PMID: 11719257 Review.

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