Carrera P - Search Results

1

Dominant LMNA mutations can cause combined muscular dystrophy and peripheral neuropathy.

Benedetti S, Bertini E, Iannaccone S, Angelini C, Trisciani M, Toniolo D, Sferrazza B, Carrera P, Comi G, Ferrari M, Quattrini A, Previtali SC. Benedetti S, et al. Among authors: carrera p. J Neurol Neurosurg Psychiatry. 2005 Jul;76(7):1019-21. doi: 10.1136/jnnp.2004.046110. J Neurol Neurosurg Psychiatry. 2005. PMID: 15965218 Free PMC article.

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

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

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

5

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

6

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

7

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

8

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

9

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.

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

303 results

Search Page

Filters