Torrado M - Search Results

1

Characterization of alterations in carbohydrate metabolism in children with Prader-Willi syndrome.

Krochik AG, Ozuna B, Torrado M, Chertkoff L, Mazza C. Krochik AG, et al. Among authors: torrado m. J Pediatr Endocrinol Metab. 2006 Jul;19(7):911-8. doi: 10.1515/jpem.2006.19.7.911. J Pediatr Endocrinol Metab. 2006. PMID: 16995571

2

Clinical-etiologic correlation in children with Prader-Willi syndrome (PWS): an interdisciplinary study.

Torrado M, Araoz V, Baialardo E, Abraldes K, Mazza C, Krochik G, Ozuna B, Leske V, Caino S, Fano V, Chertkoff L. Torrado M, et al. Am J Med Genet A. 2007 Mar 1;143A(5):460-8. doi: 10.1002/ajmg.a.31520. Am J Med Genet A. 2007. PMID: 17163531

3

Thyroid axis dysfunction in patients with Prader-Willi syndrome during the first 2 years of life.

Vaiani E, Herzovich V, Chaler E, Chertkoff L, Rivarola MA, Torrado M, Belgorosky A. Vaiani E, et al. Among authors: torrado m. Clin Endocrinol (Oxf). 2010 Oct;73(4):546-50. doi: 10.1111/j.1365-2265.2010.03840.x. Clin Endocrinol (Oxf). 2010. PMID: 20560980

4

[Angelman syndrome: the electroclinical characteristics in 35 patients].

Cersósimo R, Caraballo R, Espeche A, Cassar L, Torrado MV, Chertkoff L, Baialardo E, Arroyo HA, Fejerman N. Cersósimo R, et al. Among authors: torrado mv. Rev Neurol. 2003 Jul 1-15;37(1):14-8. Rev Neurol. 2003. PMID: 12861501 Free article. Spanish.

5

Combined cytogenetic and molecular analyses for the diagnosis of Prader-Willi/Angelman syndromes.

Borelina D, Engel N, Esperante S, Ferreiro V, Ferrer M, Torrado M, Goldschmidt E, Francipane L, Szijan I. Borelina D, et al. Among authors: torrado m. J Biochem Mol Biol. 2004 Sep 30;37(5):522-6. doi: 10.5483/bmbrep.2004.37.5.522. J Biochem Mol Biol. 2004. PMID: 15479613

6

Loss of function of the cytoplasmic isoform of the protein laforin (EPM2A) causes Lafora progressive myoclonus epilepsy.

Ianzano L, Young EJ, Zhao XC, Chan EM, Rodriguez MT, Torrado MV, Scherer SW, Minassian BA. Ianzano L, et al. Among authors: torrado mv. Hum Mutat. 2004 Feb;23(2):170-176. doi: 10.1002/humu.10306. Hum Mutat. 2004. PMID: 14722920

7

Terminal osseous dysplasia with pigmentary defects (TODPD) due to a recurrent filamin A (FLNA) mutation.

Brunetti-Pierri N, Torrado M, Fernandez Mdel C, Tello AM, Arberas CL, Cardinale A, Piccolo P, Bacino CA. Brunetti-Pierri N, et al. Among authors: torrado m. Mol Genet Genomic Med. 2014 Nov;2(6):467-71. doi: 10.1002/mgg3.90. Epub 2014 Aug 8. Mol Genet Genomic Med. 2014. PMID: 25614868 Free PMC article.

8

Chemoenzymatic synthesis and binding affinity of novel (R)- and (S)-3-aminomethyl-1-tetralones, potential atypical antipsychotics.

Caro Y, Torrado M, Masaguer CF, Raviña E, Padín F, Brea J, Loza MI. Caro Y, et al. Among authors: torrado m. Bioorg Med Chem Lett. 2004 Feb 9;14(3):585-9. doi: 10.1016/j.bmcl.2003.11.064. Bioorg Med Chem Lett. 2004. PMID: 14741248

9

Synthesis and biological evaluation of a series of aminoalkyl-tetralones and tetralols as dual dopamine/serotonin ligands.

Carro L, Torrado M, Raviña E, Masaguer CF, Lage S, Brea J, Loza MI. Carro L, et al. Among authors: torrado m. Eur J Med Chem. 2014 Jan;71:237-49. doi: 10.1016/j.ejmech.2013.10.066. Epub 2013 Nov 20. Eur J Med Chem. 2014. PMID: 24316025

10

Brain-derived neurotrophic factor modulation in response to oxidative stress and corticosterone: role of scopolamine and mirtazapine.

Correia AS, Torrado M, Costa-Coelho T, Carvalho ED, Inteiro-Oliveira S, Diógenes MJ, Pêgo AP, Santos SD, Sebastião AM, Vale N. Correia AS, et al. Among authors: torrado m. Life Sci. 2024 Dec 1;358:123133. doi: 10.1016/j.lfs.2024.123133. Epub 2024 Oct 15. Life Sci. 2024. PMID: 39413901 Free article.

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