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Revista De Neurologia
|
March 27, 2007
[Cerebral creatine transporter deficiency: an infradiagnosed neurometabolic disease]
J Campistol, A Arias-Dimas, P Poo, et al.
Clinical Biochemistry
|
April 9, 2002
Ubiquinone-10 content in lymphocytes of phenylketonuric patients
Catrina Colomé, Rafael Artuch, Maria A Vilaseca, et al.
Anales Espanoles De Pediatria
|
September 25, 1999
[Embryonic pathology caused by maternal phenylketonuria. A cause of underdiagnosed mental retardation. A report of 8 cases]
J Campistol Plana, M Arellano Pedrola, P Poo Argüelles, et al.
Journal of Inherited Metabolic Disease
|
March 21, 2007
Secondary alteration of the transferrin isoelectric focusing pattern in a case of bacterial meningitis
E Quintana, S Gala, A García-Cazorla, et al.
European Journal of Clinical Investigation
|
December 12, 2001
Hyperhomocysteinaemia and folate deficiency in human immunodeficiency virus-infected children
M A Vilaseca, C Sierra, C Colomé, et al.
Brain & Development
|
July 1, 1995
An atypical French form of pyruvate carboxylase deficiency
M Pineda, J Campistol, M A Vilaseca, et al.
Anales Espanoles De Pediatria
|
July 1, 1993
[Homocystinuria: effectiveness of the treatment with pyridoxine, folic acid, and betaine]
C Montero Brens, J Dalmau Serra, M L Cabello Tomás, et al.
Journal of Inherited Metabolic Disease
|
December 25, 2004
Two successful pregnancies in pyridoxine-nonresponsive homocystinuria
M A Vilaseca, M L Cuartero, M Martinez de Salinas, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
October 6, 1998
Antioxidant status in hyperphenylalaninemia
C Sierra, M A Vilaseca, D Moyano, et al.
Anales Espanoles De Pediatria
|
February 1, 1990
[Sudden death of a patient with 3-hydroxy-3-methylglutaryl coenzyme A lyase deficiency]
M A Vilaseca Busca, A Ribes Rubio, P Briones Godino, et al.
Page
of 14
Search research articles
Search
Showing results (71-80 of 133) with videos related to
Sort By:
Page
of 14
Revista De Neurologia
|
March 27, 2007
[Cerebral creatine transporter deficiency: an infradiagnosed neurometabolic disease]
J Campistol, A Arias-Dimas, P Poo, et al.
Clinical Biochemistry
|
April 9, 2002
Ubiquinone-10 content in lymphocytes of phenylketonuric patients
Catrina Colomé, Rafael Artuch, Maria A Vilaseca, et al.
Anales Espanoles De Pediatria
|
September 25, 1999
[Embryonic pathology caused by maternal phenylketonuria. A cause of underdiagnosed mental retardation. A report of 8 cases]
J Campistol Plana, M Arellano Pedrola, P Poo Argüelles, et al.
Journal of Inherited Metabolic Disease
|
March 21, 2007
Secondary alteration of the transferrin isoelectric focusing pattern in a case of bacterial meningitis
E Quintana, S Gala, A García-Cazorla, et al.
European Journal of Clinical Investigation
|
December 12, 2001
Hyperhomocysteinaemia and folate deficiency in human immunodeficiency virus-infected children
M A Vilaseca, C Sierra, C Colomé, et al.
Brain & Development
|
July 1, 1995
An atypical French form of pyruvate carboxylase deficiency
M Pineda, J Campistol, M A Vilaseca, et al.
Anales Espanoles De Pediatria
|
July 1, 1993
[Homocystinuria: effectiveness of the treatment with pyridoxine, folic acid, and betaine]
C Montero Brens, J Dalmau Serra, M L Cabello Tomás, et al.
Journal of Inherited Metabolic Disease
|
December 25, 2004
Two successful pregnancies in pyridoxine-nonresponsive homocystinuria
M A Vilaseca, M L Cuartero, M Martinez de Salinas, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
October 6, 1998
Antioxidant status in hyperphenylalaninemia
C Sierra, M A Vilaseca, D Moyano, et al.
Anales Espanoles De Pediatria
|
February 1, 1990
[Sudden death of a patient with 3-hydroxy-3-methylglutaryl coenzyme A lyase deficiency]
M A Vilaseca Busca, A Ribes Rubio, P Briones Godino, et al.
Page
of 14