Ferrari M - Search Results

1

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. Among authors: ferrari m. Hum Hered. 1993 May-Jun;43(3):190-6. doi: 10.1159/000154176. Hum Hered. 1993. PMID: 8330883

2

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

3

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

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

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: ferrari m. Eur J Hum Genet. 1996;4(3):183-7. doi: 10.1159/000472193. Eur J Hum Genet. 1996. PMID: 8840119

6

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

7

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.

8

Genetic heterogeneity in Italian families with familial hemiplegic migraine.

Carrera P, Piatti M, Stenirri S, Grimaldi LM, Marchioni E, Curcio M, Righetti PG, Ferrari M, Gelfi C. Carrera P, et al. Among authors: ferrari m. Neurology. 1999 Jul 13;53(1):26-33. doi: 10.1212/wnl.53.1.26. Neurology. 1999. PMID: 10408532

9

A genetic linkage study of schizophrenia to chromosome 5 markers in a northern Italian population.

Macciardi F, Kennedy JL, Ruocco L, Giuffra L, Carrera P, Marino C, Rinaldi V, Smeraldi E, Ferrari M. Macciardi F, et al. Among authors: ferrari m. Biol Psychiatry. 1992 Apr 1;31(7):720-8. doi: 10.1016/0006-3223(92)90282-5. Biol Psychiatry. 1992. PMID: 1599988

10

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.

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