Mandich P - Search Results

1

The D355V mutation decreases EGR2 binding to an element within the Cx32 promoter.

Musso M, Balestra P, Bellone E, Cassandrini D, Di Maria E, Doria LL, Grandis M, Mancardi GL, Schenone A, Levi G, Ajmar F, Mandich P. Musso M, et al. Among authors: mandich p. Neurobiol Dis. 2001 Aug;8(4):700-6. doi: 10.1006/nbdi.2001.0397. Neurobiol Dis. 2001. PMID: 11493034

2

Charcot-Marie-Tooth disease: evidence of a duplication at D17S122 locus.

Mandich P, Bellone E, Uccelli A, Pareyson D, Ajmar F. Mandich P, et al. Boll Soc Ital Biol Sper. 1992 Apr;68(4):225-30. Boll Soc Ital Biol Sper. 1992. PMID: 1281412

3

HMSN III phenotype due to homozygous expression of a dominant HMSN II gene.

Sghirlanzoni A, Pareyson D, Balestrini MR, Bellone E, Berta E, Ciano C, Mandich P, Marazzi R. Sghirlanzoni A, et al. Among authors: mandich p. Neurology. 1992 Nov;42(11):2201-4. doi: 10.1212/wnl.42.11.2201. Neurology. 1992. PMID: 1436537

4

Charcot-Marie-Tooth (CMT) 1a duplication at 17p11.2 in Italian families.

Bellone E, Mandich P, Mancardi GL, Schenone A, Uccelli A, Abbruzzese M, Sghirlanzoni A, Pareyson D, Ajmar F. Bellone E, et al. Among authors: mandich p. J Med Genet. 1992 Jul;29(7):492-3. J Med Genet. 1992. PMID: 1640430 Free PMC article. No abstract available.

5

Non-random association between DNA markers and Huntington disease locus in the Italian population.

Novelletto A, Mandich P, Bellone E, Malaspina P, Vivona G, Ajmar F, Frontali M. Novelletto A, et al. Among authors: mandich p. Am J Med Genet. 1991 Sep 1;40(3):374-6. doi: 10.1002/ajmg.1320400326. Am J Med Genet. 1991. PMID: 1683157

6

Polymerase chain reaction (PCR) amplification of hypervariable genomic sequences.

Mandich P, Bellone E, Massari A, Ajmar F. Mandich P, et al. Boll Soc Ital Biol Sper. 1991 Oct-Nov;67(10-11):907-13. Boll Soc Ital Biol Sper. 1991. PMID: 1687950

7

Adult polycystic kidney disease: prenatal diagnosis with DNA polymorphic markers.

Bellone E, Mandich P, Costa P, Dalerba L, Ajmar F. Bellone E, et al. Among authors: mandich p. Boll Soc Ital Biol Sper. 1991 Oct-Nov;67(10-11):915-22. Boll Soc Ital Biol Sper. 1991. PMID: 1821132

8

Genetic analysis of Huntington disease in Italy.

Ajmar F, Mandich P, Bellone E, Abbruzzese G. Ajmar F, et al. Among authors: mandich p. Am J Med Genet. 1991 May 1;39(2):211-4. doi: 10.1002/ajmg.1320390219. Am J Med Genet. 1991. PMID: 1829583

9

Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphisms.

Gasparini P, Mandich P, Novelli G, Bellone E, Sangiuolo F, De Stefano F, Potenza L, Trabetti E, Marigo M, Pignatti PF, et al. Gasparini P, et al. Among authors: mandich p. Hum Hered. 1991;41(3):174-81. doi: 10.1159/000153997. Hum Hered. 1991. PMID: 1937491

10

Autosomal dominant polycystic kidney disease: a linkage evaluation of heterogeneity in Italy. Italian Collaborative Group on Polycystic Kidney Disease.

Mandich P, Restagno G, Novelli G, Bellone E, Potenza L, Varetto O, Dallapiccola B, Carbonara A, Ajmar F. Mandich P, et al. Am J Med Genet. 1990 Apr;35(4):579-81. doi: 10.1002/ajmg.1320350426. Am J Med Genet. 1990. PMID: 2333889

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

198 results

Search Page

Filters