A. Viñuela

发表

Connections of the Superior Paraolivary Nucleus of the Rat: II. Reciprocal Connections with the Tectal Longitudinal Column

A. Berrebi, A. Viñuela, M. Aparicio, 2010, Front. Neuroanat..

The TLC: A Novel Auditory Nucleus of the Mammalian Brain

Allen F. Marshall, D. Fitzpatrick, A. Viñuela, 2007, The Journal of Neuroscience.

Projections from the inferior colliculus to the tectal longitudinal column in the rat

A. Viñuela, M. Aparicio, E. Saldaña, 2010, Neuroscience.

A mutational analysis of the SLC26A4 gene in Spanish hearing-impaired families provides new insights into the genetic causes of Pendred syndrome and DFNB4 hearing loss.

F. Moreno, C. Hernández-Chico, A. Viñuela, 2008, European Journal of Human Genetics.

Cognitive and behavioral profile in females with epilepsy with PDCH19 mutation: Two novel mutations and review of the literature

A. Viñuela, F. Mateos, R. Simón, 2012, Epilepsy & Behavior.

Unbiased stereological estimates of neuron number in subcortical auditory nuclei of the rat

R. Kulesza, A. Berrebi, A. Viñuela, 2002, Hearing Research.

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

F. Moreno, A. Viñuela, C. Morera, 2009, American journal of medical genetics. Part A.

A de novo missense mutation in the gene encoding the SOX10 transcription factor in a Spanish sporadic case of Waardenburg syndrome type IV

F. Moreno, A. Viñuela, I. del Castillo, 2008, American journal of medical genetics. Part A.

Nonsense mutations in SMPX, encoding a protein responsive to physical force, result in X-chromosomal hearing loss.

F. Wagner, P. Frommolt, G. Nürnberg, 2011, American journal of human genetics.

Relevance of complement factor H-related 1 (CFHR1) genotypes in age-related macular degeneration.

S. Rodríguez de Córdoba, A. Viñuela, I. Millán, 2012, Investigative ophthalmology & visual science.