Perandones C - Search Results

1

Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2.

Zeiger JS, Hetmanski JB, Beaty TH, VanderKolk CA, Wyszynski DF, Bailey-Wilson JE, de Luna RO, Perandones C, Tolarova MM, Mosby T, Bennun R, Segovia M, Calda P, Pugh EW, Doheny K, McIntosh I. Zeiger JS, et al. Among authors: perandones c. Eur J Hum Genet. 2003 Nov;11(11):835-9. doi: 10.1038/sj.ejhg.5201052. Eur J Hum Genet. 2003. PMID: 14571267

2

Family environment of individuals with oral clefts in Argentina.

Wyszynski DF, Perandones C, Yannibelli P, Bennun RD. Wyszynski DF, et al. Among authors: perandones c. Cleft Palate Craniofac J. 2005 Mar;42(2):185-91. doi: 10.1597/03-118.1. Cleft Palate Craniofac J. 2005. PMID: 15748110

3

Attitudes toward prenatal diagnosis, termination of pregnancy, and reproduction by parents of children with nonsyndromic oral clefts in Argentina.

Wyszynski DF, Perandones C, Bennun RD. Wyszynski DF, et al. Among authors: perandones c. Prenat Diagn. 2003 Sep;23(9):722-7. doi: 10.1002/pd.674. Prenat Diagn. 2003. PMID: 12975781

4

Nonsurgical correction of nasal deformity in unilateral complete cleft lip: a 6-year follow-up.

Bennun RD, Perandones C, Sepliarsky VA, Chantiri SN, Aguirre MI, Dogliotti PL. Bennun RD, et al. Among authors: perandones c. Plast Reconstr Surg. 1999 Sep;104(3):616-30. doi: 10.1097/00006534-199909030-00002. Plast Reconstr Surg. 1999. PMID: 10456510

5

Microcephaly, characteristic facies, joint abnormalities, and deficient leucocyte chemotaxis: a further case of the syndrome of Say et al.

Perandones C, Cerretini RI, Vargas Vera RM, Aranda EI, Alba LG, Pivetta OH. Perandones C, et al. J Med Genet. 1996 Mar;33(3):227-9. doi: 10.1136/jmg.33.3.227. J Med Genet. 1996. PMID: 8728697 Free PMC article. Review.

6

Differential expression of CPD1 during postnatal development in the mouse cerebellum.

Radrizzani M, Vilá-Ortiz G, Cafferata EG, Di Tella MC, González-Guerrico A, Perandones C, Pivetta OH, Carminatti H, Idoyaga Vargas VP, Santa-Coloma TA. Radrizzani M, et al. Among authors: perandones c. Brain Res. 2001 Jul 13;907(1-2):162-74. doi: 10.1016/s0006-8993(01)02351-4. Brain Res. 2001. PMID: 11430900

7

Correlation between synaptogenesis and the PTEN phosphatase expression in dendrites during postnatal brain development.

Perandones C, Costanzo RV, Kowaljow V, Pivetta OH, Carminatti H, Radrizzani M. Perandones C, et al. Brain Res Mol Brain Res. 2004 Sep 10;128(1):8-19. doi: 10.1016/j.molbrainres.2004.05.021. Brain Res Mol Brain Res. 2004. PMID: 15337313

8

Anp32e/Cpd1 regulates protein phosphatase 2A activity at synapses during synaptogenesis.

Costanzo RV, Vilá-Ortíz GJ, Perandones C, Carminatti H, Matilla A, Radrizzani M. Costanzo RV, et al. Among authors: perandones c. Eur J Neurosci. 2006 Jan;23(2):309-24. doi: 10.1111/j.1460-9568.2005.04555.x. Eur J Neurosci. 2006. PMID: 16420440

9

Different conformations of phosphatase and tensin homolog, deleted on chromosome 10 (PTEN) protein within the nucleus and cytoplasm of neurons.

Moncalero VL, Costanzo RV, Perandones C, Radrizzani M. Moncalero VL, et al. Among authors: perandones c. PLoS One. 2011 Apr 29;6(4):e18857. doi: 10.1371/journal.pone.0018857. PLoS One. 2011. PMID: 21559530 Free PMC article.

10

Dystonia in a Patient with Autosomal-Dominant Progressive External Ophthalmoplegia Type 1 Caused by Mutation in the POLG Gene.

Rossi M, Medina Escobar A, Radrizzani M, Tenembaum S, Perandones C, Merello M. Rossi M, et al. Among authors: perandones c. Mov Disord Clin Pract. 2016 Jul 8;4(2):266-269. doi: 10.1002/mdc3.12397. eCollection 2017 Mar-Apr. Mov Disord Clin Pract. 2016. PMID: 30838265 Free PMC article. No abstract available.

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