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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.
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.
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.
Bioconjugate Chemistry
|
November 1, 1993
Protein conjugates of defined structure: synthesis and use of a new carrier molecule
L A Vilaseca, K Rose, R Werlen, et al.
Clinical Biochemistry
|
December 2, 2009
Long-chain polyunsaturated fatty acid status in phenylketonuric patients treated with tetrahydrobiopterin
Maria A Vilaseca, Nilo Lambruschini, Lilianne Gómez-López, et al.
European Journal of Clinical Nutrition
|
September 25, 2003
Low serum carnitine in HIV-infected children on antiretroviral treatment
M A Vilaseca, R Artuch, C Sierra, et al.
Clinical Biochemistry
|
November 14, 2000
Oxygen consumption measurement in lymphocytes for the diagnosis of pediatric patients with oxidative phosphorylation diseases
R Artuch, C Colomé, A Playán, et al.
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of 14
Search research articles
Search
Showing results (61-70 of 133) with videos related to
Sort By:
Page
of 14
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.
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.
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.
Bioconjugate Chemistry
|
November 1, 1993
Protein conjugates of defined structure: synthesis and use of a new carrier molecule
L A Vilaseca, K Rose, R Werlen, et al.
Clinical Biochemistry
|
December 2, 2009
Long-chain polyunsaturated fatty acid status in phenylketonuric patients treated with tetrahydrobiopterin
Maria A Vilaseca, Nilo Lambruschini, Lilianne Gómez-López, et al.
European Journal of Clinical Nutrition
|
September 25, 2003
Low serum carnitine in HIV-infected children on antiretroviral treatment
M A Vilaseca, R Artuch, C Sierra, et al.
Clinical Biochemistry
|
November 14, 2000
Oxygen consumption measurement in lymphocytes for the diagnosis of pediatric patients with oxidative phosphorylation diseases
R Artuch, C Colomé, A Playán, et al.
Page
of 14