Ferrari M - Search Results

1

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: ferrari m. 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

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: ferrari m. Hum Genet. 1995 Sep;96(3):343-4. doi: 10.1007/BF00210420. Hum Genet. 1995. PMID: 7649554

3

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. Among authors: ferrari m. Hum Genet. 1996 Dec;98(6):662-5. doi: 10.1007/s004390050280. Hum Genet. 1996. PMID: 8931696

4

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: ferrari m. Hum Genet. 1995 Jan;95(1):115-6. doi: 10.1007/BF00225088. Hum Genet. 1995. PMID: 7814014

5

Molecular diagnosis of genetic diseases.

Ferrari M, Cremonesi L, Carrera P, Bonini PA. Ferrari M, et al. 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.

6

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: ferrari m. Mol Cell Probes. 1997 Apr;11(2):161-2. doi: 10.1006/mcpr.1996.0092. Mol Cell Probes. 1997. PMID: 9160332 No abstract available.

7

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

Carrera P, Righetti PG, Gelfi C, Ferrari M. Carrera P, et al. Among authors: ferrari m. Methods Mol Biol. 2001;163:95-108. doi: 10.1385/1-59259-116-7:95. Methods Mol Biol. 2001. PMID: 11242967 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. Among authors: ferrari m. Clin Chem. 1997 Nov;43(11):2121-7. Clin Chem. 1997. PMID: 9365397

9

Substitution of Leu for Pro-193 in the insulin receptor in a patient with a genetic form of severe insulin resistance.

Carrera P, Cordera R, Ferrari M, Cremonesi L, Taramelli R, Andraghetti G, Carducci C, Dozio N, Pozza G, Taylor SI, et al. Carrera P, et al. Among authors: ferrari m. Hum Mol Genet. 1993 Sep;2(9):1437-41. doi: 10.1093/hmg/2.9.1437. Hum Mol Genet. 1993. PMID: 8242067

10

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: ferrari m. Mol Cell Probes. 1995 Dec;9(6):441-6. doi: 10.1006/mcpr.1995.0067. Mol Cell Probes. 1995. PMID: 8808315

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