Carrera P - Search Results

1

Early visual function impairment in CADASIL.

Parisi V, Pierelli F, Fattapposta F, Bianco F, Parisi L, Restuccia R, Malandrini A, Ferrari M, Carrera P. Parisi V, et al. Among authors: carrera p. Neurology. 2003 Jun 24;60(12):2008-10. doi: 10.1212/01.wnl.0000070411.13217.7e. Neurology. 2003. PMID: 12821756

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

Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy.

Malandrini A, Carrera P, Palmeri S, Cavallaro T, Fabrizi GM, Villanova M, Fattapposta M, Vismara L, Brancolini V, Tanganelli P, Calì A, Morocutti C, Zeviani M, Ferrari M, Guazzi GC. Malandrini A, et al. Among authors: carrera p. Acta Neuropathol. 1996 Aug;92(2):115-22. doi: 10.1007/s004010050498. Acta Neuropathol. 1996. PMID: 8841656

6

Point mutations in Italian patients with classic, non-classic, and cryptic forms of steroid 21-hydroxylase deficiency.

Carrera P, Bordone L, Azzani T, Brunelli V, Garancini MP, Chiumello G, Ferrari M. Carrera P, et al. Hum Genet. 1996 Dec;98(6):662-5. doi: 10.1007/s004390050280. Hum Genet. 1996. PMID: 8931696

7

Unusual clinical features and early brain MRI lesions in a family with cerebral autosomal dominant arteriopathy.

Malandrini A, Carrera P, Ciacci G, Gonnelli S, Villanova M, Palmeri S, Vismara L, Brancolini V, Signorini E, Ferrari M, Guazzi GC. Malandrini A, et al. Among authors: carrera p. Neurology. 1997 May;48(5):1200-3. doi: 10.1212/wnl.48.5.1200. Neurology. 1997. PMID: 9153443

8

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.

9

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

10

Comparison of clinical-radiological and molecular findings in hypochondroplasia.

Prinster C, Carrera P, Del Maschio M, Weber G, Maghnie M, Vigone MC, Mora S, Tonini G, Rigon F, Beluffi G, Severi F, Chiumello G, Ferrari M. Prinster C, et al. Among authors: carrera p. Am J Med Genet. 1998 Jan 6;75(1):109-12. doi: 10.1002/(sici)1096-8628(19980106)75:1<109::aid-ajmg22>3.0.co;2-p. Am J Med Genet. 1998. PMID: 9450868

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