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Clinical Chemistry
|
November 4, 1998
Serum ubiquinone-10 in a pediatric population
R Artuch, J Moreno, M Quintana, et al.
Revista De Neurologia
|
August 31, 2006
[Diagnosis and treatment of brain creatine deficiency syndromes]
A Arias-Dimas, M A Vilaseca, R Artuch, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1995
Biochemical follow-up in late-treated nephropathic cystinosis
M A Vilaseca, J A Camacho, P Briones, et al.
Neuropediatrics
|
May 6, 2004
Cerebrospinal fluid concentrations of idebenone in Friedreich ataxia patients
R Artuch, A Aracil, A Mas, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
August 26, 1999
Evaluation of hyperhomocysteinaemia in children with stroke
E Cardo, M A Vilaseca, J Campistol, et al.
Diabetes Care
|
June 17, 2000
Total homocysteine in patients with type 1 diabetes
C Pavía, I Ferrer, C Valls, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
the allopurinol test in patients with Rett syndrome
M Pineda, M A Vilaseca, A Vernet, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Fatal hepatic failure with lactic acidaemia, Fanconi syndrome and defective activity of succinate:cytochrome c reductase
M A Vilaseca, P Briones, A Ribes, et al.
Developmental Medicine and Child Neurology
|
January 9, 1999
Glutaric aciduria type I with high residual glutaryl-CoA dehydrogenase activity
M Pineda, A Ribes, C Busquets, et al.
Clinical Chemistry and Laboratory Medicine
|
January 5, 2001
Personal experience with the application of carbohydrate-deficient transferrin (CDT) assays to the detection of congenital disorders of glycosylation
C Colomé, I Ferrer, R Artuch, et al.
Page
of 12
Search research articles
Search
Showing results (21-30 of 118) with videos related to
Sort By:
Page
of 12
Clinical Chemistry
|
November 4, 1998
Serum ubiquinone-10 in a pediatric population
R Artuch, J Moreno, M Quintana, et al.
Revista De Neurologia
|
August 31, 2006
[Diagnosis and treatment of brain creatine deficiency syndromes]
A Arias-Dimas, M A Vilaseca, R Artuch, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1995
Biochemical follow-up in late-treated nephropathic cystinosis
M A Vilaseca, J A Camacho, P Briones, et al.
Neuropediatrics
|
May 6, 2004
Cerebrospinal fluid concentrations of idebenone in Friedreich ataxia patients
R Artuch, A Aracil, A Mas, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
August 26, 1999
Evaluation of hyperhomocysteinaemia in children with stroke
E Cardo, M A Vilaseca, J Campistol, et al.
Diabetes Care
|
June 17, 2000
Total homocysteine in patients with type 1 diabetes
C Pavía, I Ferrer, C Valls, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
the allopurinol test in patients with Rett syndrome
M Pineda, M A Vilaseca, A Vernet, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Fatal hepatic failure with lactic acidaemia, Fanconi syndrome and defective activity of succinate:cytochrome c reductase
M A Vilaseca, P Briones, A Ribes, et al.
Developmental Medicine and Child Neurology
|
January 9, 1999
Glutaric aciduria type I with high residual glutaryl-CoA dehydrogenase activity
M Pineda, A Ribes, C Busquets, et al.
Clinical Chemistry and Laboratory Medicine
|
January 5, 2001
Personal experience with the application of carbohydrate-deficient transferrin (CDT) assays to the detection of congenital disorders of glycosylation
C Colomé, I Ferrer, R Artuch, et al.
Page
of 12