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Revista De Neurologia
|
August 10, 2000
[Aspects of neuropathy in mitochondrial diseases]
J Colomer, C Iturriaga, M Bestué, et al.
Journal of Inherited Metabolic Disease
|
August 1, 1997
A new case of multiple mitochondrial enzyme deficiencies with decreased amount of heat shock protein 60
P Briones, M A Vilaseca, A Ribes, et al.
Revista De Neurologia
|
April 9, 1998
[Respiratory chain and pyruvate metabolism deficiencies in pediatric patients: evaluation of biochemical tests for selective screening]
R Artuch, M Pineda, M A Vilaseca, et al.
Archives of Disease in Childhood
|
March 1, 1996
Normal pubertal development in a female with carbohydrate deficient glycoprotein syndrome
M Pineda, C Pavia, M A Vilaseca, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 30, 2001
Anti-epileptic drug treatment in children: hyperhomocysteinaemia, B-vitamins and the 677C-->T mutation of the methylenetetrahydrofolate reductase gene
M A Vilaseca, E Monrós, R Artuch, et al.
Revista De Neurologia
|
March 14, 2001
[Clinical, biomedical , neurological and molecular study of 11 patients with new mutations in PAH gene]
J Mallolas, M A Vilaseca, J Campistol, et al.
Anales Espanoles De Pediatria
|
March 23, 2001
[Evolution of a case of tyrosinemia type I treated with NTBC]
J Ros Viladoms, M A Vilaseca Buscà, N Lambruschini Ferri, et al.
Journal of Inherited Metabolic Disease
|
July 27, 2006
Treatment of severe osteoporosis with alendronate in a patient with lysinuric protein intolerance
L Gömez, A García-Cazorla, A Gutiérrez, et al.
Nutricion Hospitalaria
|
March 6, 2010
Quality of dietary control in phenylketonuric patients and its relationship with general intelligence
M A Vilaseca, N Lambruschini, Lilianne Gómez-López, et al.
Nutricion Hospitalaria
|
April 27, 2011
Long-chain polyunsaturated fatty acid concentration in patients with inborn errors of metabolism
M A Vilaseca, L Gómez-López, N Lambruschini, et al.
Page
of 12
Search research articles
Search
Showing results (61-70 of 118) with videos related to
Sort By:
Page
of 12
Revista De Neurologia
|
August 10, 2000
[Aspects of neuropathy in mitochondrial diseases]
J Colomer, C Iturriaga, M Bestué, et al.
Journal of Inherited Metabolic Disease
|
August 1, 1997
A new case of multiple mitochondrial enzyme deficiencies with decreased amount of heat shock protein 60
P Briones, M A Vilaseca, A Ribes, et al.
Revista De Neurologia
|
April 9, 1998
[Respiratory chain and pyruvate metabolism deficiencies in pediatric patients: evaluation of biochemical tests for selective screening]
R Artuch, M Pineda, M A Vilaseca, et al.
Archives of Disease in Childhood
|
March 1, 1996
Normal pubertal development in a female with carbohydrate deficient glycoprotein syndrome
M Pineda, C Pavia, M A Vilaseca, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 30, 2001
Anti-epileptic drug treatment in children: hyperhomocysteinaemia, B-vitamins and the 677C-->T mutation of the methylenetetrahydrofolate reductase gene
M A Vilaseca, E Monrós, R Artuch, et al.
Revista De Neurologia
|
March 14, 2001
[Clinical, biomedical , neurological and molecular study of 11 patients with new mutations in PAH gene]
J Mallolas, M A Vilaseca, J Campistol, et al.
Anales Espanoles De Pediatria
|
March 23, 2001
[Evolution of a case of tyrosinemia type I treated with NTBC]
J Ros Viladoms, M A Vilaseca Buscà, N Lambruschini Ferri, et al.
Journal of Inherited Metabolic Disease
|
July 27, 2006
Treatment of severe osteoporosis with alendronate in a patient with lysinuric protein intolerance
L Gömez, A García-Cazorla, A Gutiérrez, et al.
Nutricion Hospitalaria
|
March 6, 2010
Quality of dietary control in phenylketonuric patients and its relationship with general intelligence
M A Vilaseca, N Lambruschini, Lilianne Gómez-López, et al.
Nutricion Hospitalaria
|
April 27, 2011
Long-chain polyunsaturated fatty acid concentration in patients with inborn errors of metabolism
M A Vilaseca, L Gómez-López, N Lambruschini, et al.
Page
of 12