Abnormal antioxidant system in inborn errors of intermediary metabolism
Vilaseca-Buscà, M A, Artuch-Iriberri, R, Colomé-Mallolas, C, Brandi-Tarrau, N, Campistol, J, Pineda- Marfá, M, Sierra-March, C
Published in Revista de neurologiá (01.06.2002)
Published in Revista de neurologiá (01.06.2002)
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Management of phenylketonuria in Europe: Survey results from 19 countries
Blau, Nenad, Bélanger-Quintana, Amaya, Demirkol, Mübeccel, Feillet, François, Giovannini, Marcello, MacDonald, Anita, Trefz, Friedrich K., Spronsen, Francjan van
Published in Molecular genetics and metabolism (01.02.2010)
Published in Molecular genetics and metabolism (01.02.2010)
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Alteraciones del sistema antioxidante en errores congénitos del metabolismo intermediario
Vilaseca Buscà, Maria Antònia, Artuch Iriberri, Rafael, Colomé Mallolas, Catrina, Brandi Tarrau, Núria, Campistol Plana, Jaume, Pineda Marfà, Mercè, Sierra March, Cristina
Published in Revista de neurologiá (01.06.2002)
Published in Revista de neurologiá (01.06.2002)
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Proposed protocol for the study of cerebrovascular disease in childhood
Cardo Jalón, E, Pineda Marfà, M, Artuch Iriberri, R, Vilaseca Buscà, M A, Campistol Plana, J
Published in Anales españoles de pediatría (01.05.2000)
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Published in Anales españoles de pediatría (01.05.2000)
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Evolution of a case of tyrosinemia type I treated with NTBC
Ros Viladoms, J, Vilaseca Buscà, M A, Lambruschini Ferri, N, Mas Comas, A, González Pascual, E, Holme, E
Published in Anales españoles de pediatría (01.03.2001)
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Published in Anales españoles de pediatría (01.03.2001)
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Embryonic pathology caused by maternal phenylketonuria. A cause of underdiagnosed mental retardation. A report of 8 cases
Campistol Plana, J, Arellano Pedrola, M, Poo Argüelles, P, Escofet Sotera, C, Pérez Olarte, P, Vilaseca Buscà, M A
Published in Anales españoles de pediatría (01.08.1999)
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Published in Anales españoles de pediatría (01.08.1999)
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Hyperhomocystinemia and 677C T methylenetetrahydrofolate reductase polymorphism as a cardiovascular risk factor in childhood
Mainou Cid, C, García Giralt, N, Vilaseca Buscà, M A, Ferrer Codina, I, Meco López, José F, Mainou Pintó, A, Pintó Sala, X, Grinberg Vaisman, D, Balcells Comas, S
Published in Anales españoles de pediatría (01.05.2002)
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Published in Anales españoles de pediatría (01.05.2002)
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Reye-like syndrome as initial manifestation of mitochondrial disease
Quintillá Martínez, J M, Campistol Plana, J, Boleda Vall-Llobera, M D, Vilaseca Buscà, M A, Artuch Iriberri, R, Palomeque Rico, A, Briones Godino, P, Ribes Rubio, A
Published in Anales españoles de pediatría (01.05.2000)
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Published in Anales españoles de pediatría (01.05.2000)
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Ornithine transcarbamylase deficiency. Biochemical studies in the diagnosis of 4 cases and the identification of carriers
Briones Godino, P, Vilaseca Busca, M A, Alvarez Dominguez, L, Rodes Monegal, M, Campistol Plana, J
Published in Anales españoles de pediatría (01.05.1991)
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Published in Anales españoles de pediatría (01.05.1991)
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The neonatal form of propionic acidemia
Figueras Aloy, J, Ribes Rubio, A, Vilaseca Busca, M A, Lluch Mir, M, Brines Godino, P, Jiménez González, R, Cruz Hernández, M
Published in Anales españoles de pediatría (01.12.1988)
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Published in Anales españoles de pediatría (01.12.1988)
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Argininosuccinic aciduria. Comparative studies and detection of carriers in 3 affected families
Briones Godino, P, Rodes Monegal, M, Vilaseca Busca, M A, Maya Victoria, A, Lizárraga Vidaurreta, I, Barbero Aguirre, P, Pascual Castroviejo, I
Published in Anales españoles de pediatría (01.01.1988)
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Published in Anales españoles de pediatría (01.01.1988)
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