Search research articles
Contact Us
Filters
Showing results (11-20 of 118) with videos related to
Page
of 12
Sort By:
Prenatal Diagnosis
|
June 1, 1992
A further prenatal diagnosis of mosaic tetrasomy 12p (Pallister-Killian syndrome)
M I Tejada, A Uribarren, P Briones, et al.
Revista De Neurologia
|
April 1, 2000
[Risk factors in cerebrovascular disease in childhood]
E Cardo, M Pineda, M A Vilaseca, et al.
Revista De Neurologia
|
October 21, 1999
[Ubiquinone: metabolism and functions. Ubiquinone deficiency and its implication in mitochondrial encephalopathies. Treatment with ubiquinone]
R Artuch, C Colomé, M A Vilaseca, et al.
Revista De Neurologia
|
January 1, 1996
[Primary leptomeningeal melanomatosis in a 6-year-old child]
G Monsó, A Vernet, V Cusí, et al.
European Journal of Clinical Nutrition
|
April 16, 1998
Plasma total-homocysteine in anorexia nervosa
D Moyano, M A Vilaseca, R Artuch, et al.
Journal of Inherited Metabolic Disease
|
March 21, 1998
Increased urine methylmalonic acid excretion in infants with apnoeas
R Artuch, M Calvo, A Ribes, et al.
Neuropediatrics
|
January 24, 2006
Cerebrospinal fluid concentrations of folate, biogenic amines and pterins in Rett syndrome: treatment with folinic acid
A Ormazabal, R Artuch, M A Vilaseca, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1990
Sudden death in an infant with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency
A Ribes, P Briones, M A Vilaseca, et al.
Medicina Clinica
|
October 2, 1993
[Diagnosis of ornithine carbamoyl transferase deficiency and heterozygote detection with allopurinol loading test]
M Pineda, M A Vilaseca, A Mas, et al.
Revista De Neurologia
|
December 2, 2004
[Pathogenetic mechanisms in phenylketonuria: disorders affecting the metabolism of neurotransmitters and the antioxidant system]
A Ormazábal, R Artuch, M A Vilaseca, et al.
Page
of 12
Search research articles
Search
Showing results (11-20 of 118) with videos related to
Sort By:
Page
of 12
Prenatal Diagnosis
|
June 1, 1992
A further prenatal diagnosis of mosaic tetrasomy 12p (Pallister-Killian syndrome)
M I Tejada, A Uribarren, P Briones, et al.
Revista De Neurologia
|
April 1, 2000
[Risk factors in cerebrovascular disease in childhood]
E Cardo, M Pineda, M A Vilaseca, et al.
Revista De Neurologia
|
October 21, 1999
[Ubiquinone: metabolism and functions. Ubiquinone deficiency and its implication in mitochondrial encephalopathies. Treatment with ubiquinone]
R Artuch, C Colomé, M A Vilaseca, et al.
Revista De Neurologia
|
January 1, 1996
[Primary leptomeningeal melanomatosis in a 6-year-old child]
G Monsó, A Vernet, V Cusí, et al.
European Journal of Clinical Nutrition
|
April 16, 1998
Plasma total-homocysteine in anorexia nervosa
D Moyano, M A Vilaseca, R Artuch, et al.
Journal of Inherited Metabolic Disease
|
March 21, 1998
Increased urine methylmalonic acid excretion in infants with apnoeas
R Artuch, M Calvo, A Ribes, et al.
Neuropediatrics
|
January 24, 2006
Cerebrospinal fluid concentrations of folate, biogenic amines and pterins in Rett syndrome: treatment with folinic acid
A Ormazabal, R Artuch, M A Vilaseca, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1990
Sudden death in an infant with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency
A Ribes, P Briones, M A Vilaseca, et al.
Medicina Clinica
|
October 2, 1993
[Diagnosis of ornithine carbamoyl transferase deficiency and heterozygote detection with allopurinol loading test]
M Pineda, M A Vilaseca, A Mas, et al.
Revista De Neurologia
|
December 2, 2004
[Pathogenetic mechanisms in phenylketonuria: disorders affecting the metabolism of neurotransmitters and the antioxidant system]
A Ormazábal, R Artuch, M A Vilaseca, et al.
Page
of 12