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Acta Paediatrica (Oslo, Norway : 1992)
|
September 12, 2002
New approach to osteopenia in phenylketonuric patients
B Pérez-Dueñas, F J Cambra, M A Vilaseca, et al.
Neurology
|
April 12, 2006
Global and regional volume changes in the brains of patients with phenylketonuria
B Pérez-Dueñas, J Pujol, C Soriano-Mas, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 25, 1997
Tocopherol in inborn errors of intermediary metabolism
D Moyano, M A Vilaseca, M Pineda, et al.
Revista De Neurologia
|
August 10, 2000
[Aspects of neuropathy in mitochondrial diseases]
J Colomer, C Iturriaga, M Bestué, et al.
Bioconjugate Chemistry
|
May 1, 1991
Preparation of well-defined protein conjugates using enzyme-assisted reverse proteolysis
K Rose, L A Vilaseca, R Werlen, et al.
Neurochemical Research
|
May 12, 2010
Selenium concentration in cerebrospinal fluid samples from a paediatric population
Mireia Tondo, Juan Moreno, Mercedes Casado, et al.
Journal of Inherited Metabolic Disease
|
August 1, 1997
A new case of multiple mitochondrial enzyme deficiencies with decreased amount of heat shock protein 60
P Briones, M A Vilaseca, A Ribes, et al.
Clinical Biochemistry
|
February 20, 2004
A longitudinal study of antioxidant status in phenylketonuric patients
Rafael Artuch, Catrina Colomé, Cristina Sierra, et al.
Revista De Neurologia
|
April 9, 1998
[Respiratory chain and pyruvate metabolism deficiencies in pediatric patients: evaluation of biochemical tests for selective screening]
R Artuch, M Pineda, M A Vilaseca, et al.
Archives of Disease in Childhood
|
March 1, 1996
Normal pubertal development in a female with carbohydrate deficient glycoprotein syndrome
M Pineda, C Pavia, M A Vilaseca, et al.
Page
of 14
Search research articles
Search
Showing results (51-60 of 133) with videos related to
Sort By:
Page
of 14
Acta Paediatrica (Oslo, Norway : 1992)
|
September 12, 2002
New approach to osteopenia in phenylketonuric patients
B Pérez-Dueñas, F J Cambra, M A Vilaseca, et al.
Neurology
|
April 12, 2006
Global and regional volume changes in the brains of patients with phenylketonuria
B Pérez-Dueñas, J Pujol, C Soriano-Mas, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 25, 1997
Tocopherol in inborn errors of intermediary metabolism
D Moyano, M A Vilaseca, M Pineda, et al.
Revista De Neurologia
|
August 10, 2000
[Aspects of neuropathy in mitochondrial diseases]
J Colomer, C Iturriaga, M Bestué, et al.
Bioconjugate Chemistry
|
May 1, 1991
Preparation of well-defined protein conjugates using enzyme-assisted reverse proteolysis
K Rose, L A Vilaseca, R Werlen, et al.
Neurochemical Research
|
May 12, 2010
Selenium concentration in cerebrospinal fluid samples from a paediatric population
Mireia Tondo, Juan Moreno, Mercedes Casado, et al.
Journal of Inherited Metabolic Disease
|
August 1, 1997
A new case of multiple mitochondrial enzyme deficiencies with decreased amount of heat shock protein 60
P Briones, M A Vilaseca, A Ribes, et al.
Clinical Biochemistry
|
February 20, 2004
A longitudinal study of antioxidant status in phenylketonuric patients
Rafael Artuch, Catrina Colomé, Cristina Sierra, et al.
Revista De Neurologia
|
April 9, 1998
[Respiratory chain and pyruvate metabolism deficiencies in pediatric patients: evaluation of biochemical tests for selective screening]
R Artuch, M Pineda, M A Vilaseca, et al.
Archives of Disease in Childhood
|
March 1, 1996
Normal pubertal development in a female with carbohydrate deficient glycoprotein syndrome
M Pineda, C Pavia, M A Vilaseca, et al.
Page
of 14