Carrera P - Search Results

1

Capillary zone electrophoresis in polymer networks of polymerase chain reaction-amplified oligonucleotides: the case of congenital adrenal hyperplasia.

Gelfi C, Orsi A, Righetti PG, Zanussi M, Carrera P, Ferrari M. Gelfi C, et al. Among authors: carrera p. J Chromatogr B Biomed Appl. 1994 Jul 1;657(1):201-5. doi: 10.1016/0378-4347(94)80088-x. J Chromatogr B Biomed Appl. 1994. PMID: 7952069

2

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: carrera p. Biol Psychiatry. 1992 Apr 1;31(7):720-8. doi: 10.1016/0006-3223(92)90282-5. Biol Psychiatry. 1992. PMID: 1599988

3

CAG triplet analysis in families with androgen insensitivity syndrome by capillary electrophoresis in polymer networks.

Gelfi C, Righetti PG, Leoncini F, Brunelli V, Carrera P, Ferrari M. Gelfi C, et al. Among authors: carrera p. J Chromatogr A. 1995 Jul 7;706(1-2):463-8. doi: 10.1016/0021-9673(95)00074-w. J Chromatogr A. 1995. PMID: 7640779

4

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

5

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

6

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. Hum Mol Genet. 1993 Sep;2(9):1437-41. doi: 10.1093/hmg/2.9.1437. Hum Mol Genet. 1993. PMID: 8242067

7

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

8

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

9

HLA-DQ screening for risk assessment of insulin dependent diabetes in northern Italy.

Lampasona V, Ferrari M, Bonifacio E, Pastore MR, Carrera P, Sergi A, Genovese S, Trucco M, Dorman J, Bosi E. Lampasona V, et al. Among authors: carrera p. Acta Diabetol. 1995 Oct;32(3):137-42. doi: 10.1007/BF00838481. Acta Diabetol. 1995. PMID: 8590780

10

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.

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