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Revista De Neurologia|September 11, 2002
[Molecular genetics of disorders of the mitochondrial respiratory chain]Y Campos, M A Martín, J ArenasNeurologia (Barcelona, Spain)|December 1, 1995
[Molecular genetics of mitochondrial cytopathologies]J Arenas, Y Campos, M A MartínEarly Human Development|April 2, 1999
Biological roles of L-carnitine in perinatal metabolismJ Arenas, J C Rubio, M A Martín, et al.Neurology|October 1, 1996
Single large-scale mitochondrial DNA deletion in a patient with mitochondrial myopathy associated with multiple symmetric lipomatosisY Campos, M A Martín, C Navarro, 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.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 51