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Human Genetics|June 1, 1996
A family segregating a Friedreich ataxia phenotype that is not linked to the FRDA locusP Smeyers, E Monrós, J Vílchez, et al.
The Journal of International Advanced Otology|May 31, 2017
Audiological Findings in Charcot-Marie-Tooth Disease Type 4CRafael Sivera, Laura Cavalle, Juan J Vílchez, et al.
Revista Clinica Espanola|October 1, 1989
[The presence of oligoclonal bands in the cerebrospinal fluid in various neurologic diseases]F Coret, J J Vílchez, M J Enguídanos, et al.
Investigacion Clinica|September 1, 1996
[Leydig cell function in hyper- or hypoprolactinemic states in healthy men]G Marín-López, J Vílchez-Martínez, L Hernández-Yañez, et al.
Brain : a Journal of Neurology|June 25, 2003
Clinical, electrophysiological and morphological findings of Charcot-Marie-Tooth neuropathy with vocal cord palsy and mutations in the GDAP1 geneTeresa Sevilla, Ana Cuesta, María José Chumillas, et al.
Journal of Endocrinological Investigation|September 3, 2010
Alterations in arterial pressure in patients with Type 1 diabetes are associated with long-term poor metabolic control and a more atherogenic lipid profileF J Vílchez-López, F Carral-Sanlaureano, C Coserria-Sánchez, et al.
Neurologia (Barcelona, Spain)|December 19, 2002
[Nonsystemic vasculitic neuropathy]M Garcés Sánchez, V E Villanueva-Haba, T Sevilla Mantecón, et al.
Human Molecular Genetics|September 12, 2009
Missense mutations in the SH3TC2 protein causing Charcot-Marie-Tooth disease type 4C affect its localization in the plasma membrane and endocytic pathwayVincenzo Lupo, Máximo I Galindo, Dolores Martínez-Rubio, et al.
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