Publications by authors named "Felipe Moreno"

36Publications

Experimental model for removal of snake venom via hemoperfusion in rats.

J Vet Emerg Crit Care (San Antonio) 2020 May 29;30(3):286-294. Epub 2020 Feb 29.

Post-Graduate Program in Pharmaceutical Sciences, University of Sorocaba (UNISO), Sorocaba, São Paulo, Brazil.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/vec.12949DOI Listing
May 2020

New pharmacological insights of .

Nat Prod Res 2019 Aug 28;33(16):2389-2393. Epub 2018 Feb 28.

b Veterinary Medicine Graduate Course , University of Sorocaba (UNISO) , Sorocaba , Brazil.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1080/14786419.2018.1443086DOI Listing
August 2019

A novel splice-site mutation in the GJB2 gene causing mild postlingual hearing impairment.

PLoS One 2013 6;8(9):e73566. Epub 2013 Sep 6.

Unidad de Genética Molecular, Hospital Universitario Ramón y Cajal, Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Madrid, Spain ; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Madrid, Spain.

View Article

Download full-text PDF

Source
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0073566PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3765306PMC
June 2014

Segregation of a new mutation in SLC26A4 and p.E47X mutation in GJB2 within a consanguineous Tunisian family affected with Pendred syndrome.

Int J Pediatr Otorhinolaryngol 2012 Jun 18;76(6):832-6. Epub 2012 Mar 18.

Laboratoire de microorganismes et biomolécules, Centre de Biotechnologie de Sfax, Sfax, Tunisia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ijporl.2012.02.053DOI Listing
June 2012

Novel splice-site mutation c.1615-2A>G (IVS14-2A>G) in the SLC26A4 gene causing Pendred syndrome in a consanguineous Portuguese family.

Am J Med Genet A 2011 Apr 17;155A(4):924-7. Epub 2011 Mar 17.

Faculty of Science, Centre for Biodiversity, Functional and Integrative Genomics (BioFIG), University of Lisbon, Lisbon, Portugal.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.33740DOI Listing
April 2011

Genetic and phenotypic heterogeneity in two novel cases of Waardenburg syndrome type IV.

Am J Med Genet A 2009 Oct;149A(10):2296-302

Unidad de Genética Molecular, Hospital Universitario Ramón y Cajal, Madrid, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.33026DOI Listing
October 2009

Functional assessment of allelic variants in the SLC26A4 gene involved in Pendred syndrome and nonsyndromic EVA.

Proc Natl Acad Sci U S A 2008 Nov 18;105(47):18608-13. Epub 2008 Nov 18.

Unidad de Genética Molecular, Hospital Ramón y Cajal, Centro de Investigación Biomédica de Enfermedades Raras, ISCIII, 28034 Madrid, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1073/pnas.0805831105DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2584577PMC
November 2008

Characterization of a spontaneous, recessive, missense mutation arising in the Tecta gene.

J Assoc Res Otolaryngol 2008 Jun 2;9(2):202-14. Epub 2008 May 2.

Unidad de Genética Molecular, Hospital Ramón y Cajal, Carretera de Colmenar Km 9, 28034, Madrid, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10162-008-0116-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2504605PMC
June 2008

Persistent sinus venosus valve mimicking pulmonary stenosis and atrial tumor.

Ann Thorac Surg 2006 Mar;81(3):1123-6

Department of Pediatric Cardiology and Pediatric Cardiac Surgery, Hospital Universitario La Paz, Madrid, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.athoracsur.2005.01.047DOI Listing
March 2006

[Balloon angioplasty for native coarctation in children: immediate and medium-term results].

Rev Esp Cardiol 2005 Sep;58(9):1054-61

Servicio de Cardiología Pediátrica, Hospital Infantil La Paz, Madrid, Spain.

View Article

Download full-text PDF

Source
September 2005

[Genetic study of hearing loss in families from Argentina].

Rev Fac Cien Med Univ Nac Cordoba 2004 ;61(1):13-9

Cátedra de Bioquímica y Biología Molecular, Facultad de Ciencias Médicas, UNC, Córdoba.

View Article

Download full-text PDF

Source
March 2005

[Familial susceptibility to aminoglycoside ototoxicity due to the A1555G mutation in the mitochondrial DNA].

Med Clin (Barc) 2003 Jul;121(6):216-8

Servicio de Otorrinolaringología. Hospital Marqués de Valdecilla. Santander. Cantabria. Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/s0025-7753(03)73909-8DOI Listing
July 2003

A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29.

Hum Genet 2003 Jan 16;112(1):24-8. Epub 2002 Oct 16.

Unidad de Genética Molecular, Hospital Ramón y Cajal, Carretera de Colmenar Km 9, 28034, Madrid, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00439-002-0836-xDOI Listing
January 2003

The regulation of microcin B, C and J operons.

Biochimie 2002 May-Jun;84(5-6):521-9

Unidad de Genética Molecular, Hospital Ramón y Cajal, Ctra Colmenar Km 9 1, 28034, Madrid, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/s0300-9084(02)01452-9DOI Listing
May 2003

A deletion involving the connexin 30 gene in nonsyndromic hearing impairment.

N Engl J Med 2002 Jan;346(4):243-9

Unidad de Genética Molecular, Hospital Ramón y Cajal, Madrid, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1056/NEJMoa012052DOI Listing
January 2002