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Human Genetics
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December 22, 1999
Mutational spectrum of phenylalanine hydroxylase deficiency in the population resident in Catalonia: genotype-phenotype correlation
J Mallolas, M A Vilaseca, J Campistol, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences
|
July 18, 2009
Comparison between high performance liquid chromatography and capillary zone electrophoresis for the diagnosis of congenital disorders of glycosylation
Ester Quintana, Raquel Montero, Mercedes Casado, et al.
Molecular Genetics and Metabolism
|
August 9, 2011
Neurological complications and behavioral problems in patients with phenylketonuria in a follow-up unit
María J González, Alfonso P Gutiérrez, Rosa Gassió, et al.
Rehabilitacion
|
September 7, 2021
[Efficacy of collagen infiltrations in the pelvic pain caused by episiotomy and caesarean scars. Pilot randomized clinical trial]
G Romero-Cullerés, A Amela-Arévalo, C Jané-Feixas, et al.
Developmental Medicine and Child Neurology
|
March 13, 1999
Fatal haemorrhagic infarct in an infant with homocystinuria
E Cardo, J Campistol, J Caritg, et al.
Anales Espanoles De Pediatria
|
September 27, 2000
[Proposed protocol for the study of cerebrovascular disease in childhood]
E Cardo Jalón, M Pineda Marfà, R Artuch Iriberri, et al.
Anales Espanoles De Pediatria
|
May 1, 1991
[Ornithine transcarbamylase deficiency. Biochemical studies in the diagnosis of 4 cases and the identification of carriers]
P Briones Godino, M A Vilaseca Busca, L Alvarez Dominguez, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
Platelet serotonin concentrations in PKU patients under dietary control and tetrahydrobiopterin treatment
A Ormazabal, M A Vilaseca, B Pérez-Dueñas, et al.
The International Journal of Eating Disorders
|
January 30, 1999
Antioxidant status in anorexia nervosa
D Moyano, C Sierra, N Brandi, et al.
Journal of Inherited Metabolic Disease
|
August 7, 2001
Plasma phenylalanine is associated with decreased serum ubiquinone-10 concentrations in phenylketonuria
R Artuch, C Colomé, M A Vilaseca, et al.
Page
of 14
Search research articles
Search
Showing results (41-50 of 133) with videos related to
Sort By:
Page
of 14
Human Genetics
|
December 22, 1999
Mutational spectrum of phenylalanine hydroxylase deficiency in the population resident in Catalonia: genotype-phenotype correlation
J Mallolas, M A Vilaseca, J Campistol, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences
|
July 18, 2009
Comparison between high performance liquid chromatography and capillary zone electrophoresis for the diagnosis of congenital disorders of glycosylation
Ester Quintana, Raquel Montero, Mercedes Casado, et al.
Molecular Genetics and Metabolism
|
August 9, 2011
Neurological complications and behavioral problems in patients with phenylketonuria in a follow-up unit
María J González, Alfonso P Gutiérrez, Rosa Gassió, et al.
Rehabilitacion
|
September 7, 2021
[Efficacy of collagen infiltrations in the pelvic pain caused by episiotomy and caesarean scars. Pilot randomized clinical trial]
G Romero-Cullerés, A Amela-Arévalo, C Jané-Feixas, et al.
Developmental Medicine and Child Neurology
|
March 13, 1999
Fatal haemorrhagic infarct in an infant with homocystinuria
E Cardo, J Campistol, J Caritg, et al.
Anales Espanoles De Pediatria
|
September 27, 2000
[Proposed protocol for the study of cerebrovascular disease in childhood]
E Cardo Jalón, M Pineda Marfà, R Artuch Iriberri, et al.
Anales Espanoles De Pediatria
|
May 1, 1991
[Ornithine transcarbamylase deficiency. Biochemical studies in the diagnosis of 4 cases and the identification of carriers]
P Briones Godino, M A Vilaseca Busca, L Alvarez Dominguez, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
Platelet serotonin concentrations in PKU patients under dietary control and tetrahydrobiopterin treatment
A Ormazabal, M A Vilaseca, B Pérez-Dueñas, et al.
The International Journal of Eating Disorders
|
January 30, 1999
Antioxidant status in anorexia nervosa
D Moyano, C Sierra, N Brandi, et al.
Journal of Inherited Metabolic Disease
|
August 7, 2001
Plasma phenylalanine is associated with decreased serum ubiquinone-10 concentrations in phenylketonuria
R Artuch, C Colomé, M A Vilaseca, et al.
Page
of 14