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Work (Reading, Mass.)|December 4, 2022
Evaluation and comparison of selected methodologies to investigate occupational accidentsF Salguero-Caparrós, J C Rubio-RomeroAccident; Analysis and Prevention|February 4, 2014
Modeling injury rates as a function of industrialized versus on-site construction techniquesJ C Rubio-Romero, M Suárez-Cebador, Jesús AbadEarly Human Development|April 2, 1999
Biological roles of L-carnitine in perinatal metabolismJ Arenas, J C Rubio, M A Martín, et al.Neuromuscular Disorders : NMD|March 14, 2000
A missense mutation T487N in the myophosphorylase gene in a Spanish patient with McArdle's diseaseJ C Rubio, M A Martín, Y Campos, et al.Journal of Mass Spectrometry : JMS|April 1, 1996
Evaluation of flow injection sample to standard addition method for the inductively coupled plasma mass spectrometric determination of aluminium in biological tissuesA G Coedo, M T Dorado, J Ruiz, et al.Revista Espanola De Cirugia Ortopedica Y Traumatologia|April 24, 2013
[Medial versus lateral plating in distal tibial fractures: a prospective study of 40 fractures]C A Encinas-Ullán, R Fernandez-Fernandez, J C Rubio-Suárez, et al.Muscle & Nerve|December 11, 1999
A missense mutation W797R in the myophosphorylase gene in a Spanish patient with McArdle's diseaseJ C Rubio, M A Martín, Y Campos, et al.Human Mutation|February 19, 2000
Two homozygous mutations (R193W and 794/795 delAA) in the myophosphorylase gene in a patient with McArdle's diseaseM A Martín, J C Rubio, Y Campos, et al.Neuromuscular Disorders : NMD|November 5, 1997
Association of genetically proven deficiencies of myophosphorylase and AMP deaminase: a second case of 'double trouble'J C Rubio, M A Martín, J Bautista, et al.Neuromuscular Disorders : NMD|July 19, 2000
A homozygous missense mutation (A659D) in the myophosphorylase gene in a Spanish patient with McArdle's diseaseM A Martín, J C Rubio, Y Campos, et al.Pageof 5