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Results of search for 'au:"Vilaseca, M"', page 5 of 7
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Authors
Aracil, A
Arias, A
Artuch, R
Artuch, Rafael
Briones, P
Cambra, F J
Campistol, J
Cardo, E
Colomé, C
Ferrer, I
García-Cazorla, A
Lambruschini, N
Mas, A
Pineda, M
Pérez-Dueñas, B
Ribes, A
Sierra, C
Vilaseca, M
Vilaseca, M A
Vilaseca, M Antonia
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Adolescent
Adult
Amino Acid Metabolism, Inborn Errors
Child
Child, Preschool
Female
Homocysteine
Humans
Infant
Infant, Newborn
Male
Mutation
Phenylketonurias
blood
chemistry
deficiency
diagnosis
genetics
metabolism
therapeutic use
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81.
[Respiratory chain and pyruvate metabolism deficiencies in pediatric patients: evaluation of biochemical tests for selective screening].
[electronic resource]
by
Artuch, R
Pineda, M
Vilaseca, M A
Briones, P
Ribes, A
Colomer, J
Vernet, A
Campistol, J
Producer:
19980616
In:
Revista de neurologia
vol. 26
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82.
[Clinical, biomedical , neurological and molecular study of 11 patients with new mutations in PAH gene].
[electronic resource]
by
Mallolas, J
Vilaseca, M A
Campistol, J
Lambruschini, N
Cambra, F J
Fusté, M E
Milà, M
Producer:
20010412
In:
Revista de neurologia
vol. 31
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83.
Oxygen consumption measurement in lymphocytes for the diagnosis of pediatric patients with oxidative phosphorylation diseases.
[electronic resource]
by
Artuch, R
Colomé, C
Playán, A
Alcaine, M J
Briones, P
Montoya, J
Vilaseca, M A
Pineda, M
Producer:
20010111
In:
Clinical biochemistry
vol. 33
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84.
Hyperlactatemia in human immunodeficiency virus-uninfected infants who are exposed to antiretrovirals.
[electronic resource]
by
Noguera, Antoni
Fortuny, Claudia
Muñoz-Almagro, Carmen
Sanchez, Emilia
Vilaseca, M Antonia
Artuch, Rafael
Pou, Jordi
Jimenez, Rafael
Producer:
20050310
In:
Pediatrics
vol. 114
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85.
[Cerebral creatine transporter deficiency: an infradiagnosed neurometabolic disease].
[electronic resource]
by
Campistol, J
Arias-Dimas, A
Poo, P
Pineda, M
Hoffman, M
Vilaseca, M A
Artuch, R
Ribes, A
Producer:
20070614
In:
Revista de neurologia
vol. 44
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86.
Long-chain polyunsaturated fatty acid concentration in patients with inborn errors of metabolism.
[electronic resource]
by
Vilaseca, M A
Gómez-López, L
Lambruschini, N
Gutiérrez, A
García, R
Meavilla, S
Moreno, J
Artuch, R
Producer:
20110901
In:
Nutricion hospitalaria
vol. 26
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87.
Polymorphisms of genes involved in homocysteine metabolism in preeclampsia and in uncomplicated pregnancies.
[electronic resource]
by
Also-Rallo, Eva
Lopez-Quesada, Eva
Urreizti, Roser
Vilaseca, M Antònia
Lailla, Josep M
Balcells, Susana
Grinberg, Daniel
Producer:
20050912
In:
European journal of obstetrics, gynecology, and reproductive biology
vol. 120
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88.
Quality of dietary control in phenylketonuric patients and its relationship with general intelligence.
[electronic resource]
by
Vilaseca, M A
Lambruschini, N
Gómez-López, Lilianne
Gutiérrez, A
Fusté, E
Gassió, R
Artuch, R
Campistol, J
Producer:
20100526
In:
Nutricion hospitalaria
vol. 25
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89.
Is deoxypyridinoline a good resorption marker to detect osteopenia in phenylketonuria?
[electronic resource]
by
Millet, Pablo
Vilaseca, M Antonia
Valls, Carme
Pérez-Dueñas, Belén
Artuch, Rafael
Gómez, Lilian
Lambruschini, Nilo
Campistol, Jaume
Producer:
20060612
In:
Clinical biochemistry
vol. 38
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90.
Low serum carnitine in HIV-infected children on antiretroviral treatment.
[electronic resource]
by
Vilaseca, M A
Artuch, R
Sierra, C
Pineda, J
López-Vilches, M A
Muñoz-Almagro, C
Fortuny, C
Producer:
20040308
In:
European journal of clinical nutrition
vol. 57
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91.
Treatment of severe osteoporosis with alendronate in a patient with lysinuric protein intolerance.
[electronic resource]
by
Gömez, L
García-Cazorla, A
Gutiérrez, A
Artuch, R
Varea, V
Martín, J
Pinillos, S
Vilaseca, M A
Producer:
20070117
In:
Journal of inherited metabolic disease
vol. 29
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92.
Hyperhomocysteinaemia and folate deficiency in human immunodeficiency virus-infected children.
[electronic resource]
by
Vilaseca, M A
Sierra, C
Colomé, C
Artuch, R
Valls, C
Muñoz-Almagro, C
Vilches, M A
Fortuny, C
Producer:
20020412
In:
European journal of clinical investigation
vol. 31
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93.
Requirement of high biotin doses in a case of biotinidase deficiency.
[electronic resource]
by
Riudor, E
Vilaseca, M A
Briones, P
Ribes, A
Suñé, J
Martorell, R
Macaya, A
Roig, M
Ballabriga, A
Producer:
19900305
In:
Journal of inherited metabolic disease
vol. 12
Online resources:
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94.
Secondary alteration of the transferrin isoelectric focusing pattern in a case of bacterial meningitis.
[electronic resource]
by
Quintana, E
Gala, S
García-Cazorla, A
Montero, R
Muñoz-Almagro, C
Vilaseca, M A
Briones, P
Artuch, R
Producer:
20070426
In:
Journal of inherited metabolic disease
vol. 30
Online resources:
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95.
3-phosphoglycerate dehydrogenase deficiency in a patient with West syndrome.
[electronic resource]
by
Pineda, M
Vilaseca, M A
Artuch, R
Santos, S
García González, M M
Aracil, A
Van Schaftingen, E
Jaeken, J
Producer:
20001024
In:
Developmental medicine and child neurology
vol. 42
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96.
Selective screening for hyperhomocysteinemia in pediatric patients.
[electronic resource]
by
Vilaseca, M A
Moyano, D
Artuch, R
Ferrer, I
Pineda, M
Cardo, E
Campistol, J
Pavia, C
Camacho, J A
Producer:
19980407
In:
Clinical chemistry
vol. 44
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97.
A folate-rich diet is as effective as folic acid from supplements in decreasing plasma homocysteine concentrations.
[electronic resource]
by
Pintó, Xavier
Vilaseca, M Antonia
Balcells, Susana
Artuch, Rafael
Corbella, Emili
Meco, José F
Vila, Ramon
Pujol, Ramon
Grinberg, Daniel
Publication details:
International journal of medical sciences
2005
In:
International journal of medical sciences
vol. 2
Online resources:
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98.
An atypical French form of pyruvate carboxylase deficiency.
[electronic resource]
by
Pineda, M
Campistol, J
Vilaseca, M A
Briones, P
Ribes, A
Temudo, T
Pons, M
Cusi, V
Rolland, M O
Producer:
19960117
In:
Brain & development
vol. 17
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99.
Antioxidant status in hyperphenylalaninemia.
[electronic resource]
by
Sierra, C
Vilaseca, M A
Moyano, D
Brandi, N
Campistol, J
Lambruschini, N
Cambra, F J
Deulofeu, R
Mira, A
Producer:
19981217
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 276
Online resources:
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100.
Methylmalonic aciduria with homocystinuria.
[electronic resource]
by
Ribes, A
Vilaseca, M A
Briones, P
Maya, A
Sabater, J
Pascual, P
Alvarez, L
Ros, J
Gonzalez Pascual, E
Producer:
19841119
In:
Journal of inherited metabolic disease
vol. 7 Suppl 2
Online resources:
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