Ferrari M - Search Results

1

Diagnosis of Duchenne and Becker muscular dystrophies by polymerase chain reaction. A multicenter study.

Chamberlain JS, Chamberlain JR, Fenwick RG, Ward PA, Caskey CT, Dimnik LS, Bech-Hansen NT, Hoar DI, Richards S, Covone AE, Govanni R, Abbs S, Bentley DR, Bobrow M, Rysiecki G, Ray PN, Boileau C, Junien C, Boehm C, Venne VL, Fujmura FK, Spiga I, Ferrari M, Tedeschi S, Bakker E, Kneppers AL, van Ommen GJ, Jain K, Spector E, Crandall B, Kiuru A, Savontaus ML, Caskey CT, Chamberlain JS, Chamberlain JR, Rysiecki G. Chamberlain JS, et al. Among authors: ferrari m. JAMA. 1992 May 20;267(19):2609-15. doi: 10.1001/jama.1992.03480190051030. JAMA. 1992. PMID: 1573747 Clinical Trial.

2

Italian experience regarding the prevention of Duchenne and Becker muscular dystrophies.

Romeo G, Devoto M, Archidiacono N, Ferlini A, Roncuzzi L, Melis MA, Paderi E, Ferrari M, Tedeschi S, Galluzzi G, et al. Romeo G, et al. Among authors: ferrari m. Eur J Pediatr. 1988 May;147(4):412-5. doi: 10.1007/BF00496422. Eur J Pediatr. 1988. PMID: 3165066

3

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: ferrari m. Biotechniques. 1995 Aug;19(2):254-8, 260-3. Biotechniques. 1995. PMID: 8527147

4

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

5

DNA technology for prenatal diagnosis of cystic fibrosis in Italy.

Seia M, Cozzi G, Sereni L, Ferrari M, Cremonesi L, Covone AE, Fenu L, Ronchetto P, Devoto M, Romeo G. Seia M, et al. Among authors: ferrari m. Adv Exp Med Biol. 1991;290:399-401. doi: 10.1007/978-1-4684-5934-0_49. Adv Exp Med Biol. 1991. PMID: 1683101 No abstract available.

6

Multiple testing in fetal gender determination from maternal blood by polymerase chain reaction.

Lagona F, Smid M, Papasergio N, Ferrari A, Ferrari M, Cremonesi L. Lagona F, et al. Among authors: ferrari m, ferrari a. Hum Genet. 1998 Jun;102(6):687-90. doi: 10.1007/s004390050762. Hum Genet. 1998. PMID: 9703431

7

[Prenatal diagnosis of hemoglobinopathies in the 1st and 2nd pregnancy trimesters].

Ferrari M, Cantù Rajnoldi A, Cremonesi L, Donzelli C, Pietri S, Tedeschi S, Travi M, Nicolini U, Brambati B. Ferrari M, et al. Pediatr Med Chir. 1984 Nov-Dec;6(6):769-73. Pediatr Med Chir. 1984. PMID: 6545587 Italian.

8

Capillary zone electrophoresis of polymerase chain reaction-amplified DNA fragments in polymer networks: the case of GATT microsatellites in cystic fibrosis.

Gelfi C, Orsi A, Righetti PG, Brancolini V, Cremonesi L, Ferrari M. Gelfi C, et al. Among authors: ferrari m. Electrophoresis. 1994 May;15(5):640-3. doi: 10.1002/elps.1150150189. Electrophoresis. 1994. PMID: 7925242

9

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

10

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

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