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pro vyhledávání: '"M L, Couce Pico"'
Autor:
E, Narbona López, J, Uberos Fernández, M I, Armadá Maresca, M L, Couce Pico, G, Rodríguez Martínez, M, Saenz de Pipaon
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 81(6)
Clinical practice guidelines are an important tool for improving healthcare. In recent years there has been accumulating evidence on the impact of nutritional supplementation with probiotics in the very low birth weight infants. With no uniformity in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cecdc51736311851940e8c319f3b23c0
https://pubmed.ncbi.nlm.nih.gov/25106928
https://pubmed.ncbi.nlm.nih.gov/25106928
Autor:
L Vázquez, García, I Oulego, Erroz, M Maneiro, Freire, A Pérez, Muñuzuri, A Baña, Souto, M L Couce, Pico, J M Fraga, Bermúdez
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 76(3)
Extrauterine growth restriction affects most premature newborns. Early and higher parenteral protein intake seems to improve postnatal growth and associated comorbidities. We evaluate the impact of a new parenteral nutrition protocol based on early a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::216ec278bd6ba12bbc3c1aba2d348d95
https://pubmed.ncbi.nlm.nih.gov/22056312
https://pubmed.ncbi.nlm.nih.gov/22056312
Autor:
O, López-Suárez, M L, Couce Pico, A, Pérez-Muñuzuri, D E, Castiñeiras Ramos, J R, Fernández-Lorenzo
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 72(3)
Excess methionine can cause central nervous system disorders such as diffuse cerebral edema and disorders of myelin.A retrospective and prospective (ambispective) observational study in preterm newborns admitted to our hospital over a period of 15 mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f78b9a46cf681e0fba99dad6a2e40560
https://pubmed.ncbi.nlm.nih.gov/20117063
https://pubmed.ncbi.nlm.nih.gov/20117063
Autor:
M L, Couce Pico, D E, Castiñeiras Ramos, M, López Sousa, M J, Fernández Seara, J, Eirís Puñal, J A, Cocho de Juan
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 69(3)
Glutaric Acidaemia type I (GA-I) is an autosomal recessive progressive neurodegenerative inborn error of metabolism caused by deficient activity of the enzyme glutaryl-CoA dehydrogenase (GCDH). In most cases, the diagnosis is established biochemicall
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8c64051f9aab3caddc69230d841e753e
https://pubmed.ncbi.nlm.nih.gov/18775269
https://pubmed.ncbi.nlm.nih.gov/18775269
Autor:
M L, Couce Pico, D E, Castiñeiras Ramos, M D, Bóveda Fontán, A J, Iglesias Rodríguez, J A, Cocho de Juan, J M, Fraga Bermúdez
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 67(4)
Maple syrup urine disease (MSUD) is a rare autosomal recessive disorder caused by an inherited deficiency of branched chain alpha-ketoacid dehydrogenase activity. Accumulation of the amino acids leucine, isoleucine, valine and alloisoleucine and thei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7924d8342fc9d7f7975768732ec9c838
https://pubmed.ncbi.nlm.nih.gov/17949643
https://pubmed.ncbi.nlm.nih.gov/17949643
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Publikováno v:
Anales espanoles de pediatria. 30(2)
In order to investigate effects produced by external cranial irradiation on neuroendocrine systems. GH secretion (elicited by oral clonidine and by GRF-29 as iv bolus) and TSH and PRL responses to an iv bolus of TRH were evaluated in children previou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7ac43b775a38a3f5a419ed1bffa8bf6c
https://pubmed.ncbi.nlm.nih.gov/2719421
https://pubmed.ncbi.nlm.nih.gov/2719421