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1.
Eur J Paediatr Neurol ; 16(2): 203-5, 2012 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-21868270

RESUMEN

PURPOSE: evaluate the psychomotor evolution of a child with Multiple acyl-CoA dehydrogenase deficiency after treatment with L-carnitine, ubiquinone and riboflavin. METHODS: an assessment of psychomotor development was performed before the start of farmacological treatment using the Assessment Scale of Mental Development Griffiths (GMDS-R, 0-2 years). The same assessment was performed after a month and after six months of treatment to evaluate the possible benefits of treatment. RESULTS: we noticed a quick and dramatic improvement in muscular tone and motor performances after pharmacological treatment. We also observed a substantial improvement in the personal/social and hearing/language areas, suggesting the presence of intellectual/cognitive improvement. The clinical improvement correlated with the biochemical response. CONCLUSION: In our patient early therapy resulted in a optimal response in psychomotor development, motor function and muscole hypotonia. Evaluation with GMDS-R, a simple, non-invasive and multidimensional tool, represents a useful instrument to monitor the clinical response to treatment.


Asunto(s)
Acil-CoA Deshidrogenasa/deficiencia , Errores Innatos del Metabolismo de los Aminoácidos/tratamiento farmacológico , Acidosis/etiología , Acidosis/genética , Errores Innatos del Metabolismo de los Aminoácidos/enzimología , Errores Innatos del Metabolismo de los Aminoácidos/patología , Carnitina/uso terapéutico , Desarrollo Infantil , Audición/fisiología , Humanos , Hipoglucemia/etiología , Hipoglucemia/genética , Lactante , Desarrollo del Lenguaje , Masculino , Hipotonía Muscular/tratamiento farmacológico , Hipotonía Muscular/etiología , Músculo Esquelético/patología , Pruebas Neuropsicológicas , Desempeño Psicomotor/fisiología , Riboflavina/uso terapéutico , Conducta Social , Espectrometría de Masas en Tándem , Ubiquinona/uso terapéutico , Vitaminas/uso terapéutico
2.
Int J Cancer ; 63(5): 621-6, 1995 Nov 27.
Artículo en Inglés | MEDLINE | ID: mdl-7591276

RESUMEN

Over-production of gelatinase A (MMP-2) or under-production of its inhibitor (TIMP-2) may result in the matrix degradation crucial for metastasis, and early evaluation of their expression in primary tumor would offer important prognostic informations. RT-PCR amplicons of MMP-2 and TIMP-2 mRNA from tissue biopsies of 13 breast carcinomas and one fibrocystic mastopathy were quantitated. In comparison with their normal-tissue counterparts, their expression trends were not uniform: in some cases MMP-2 increased in the tumor without changes in TIMP-2, in others TIMP-2 expression also increased, although to a lesser extent than MMP-2; only in 2 cases was it slightly lower in the tumor tissue. Nevertheless, clearer insights were gained from the comparison of the ratio (R) between MMP-2tumor/normal and TIMP-2tumor/normal: as in the fibrocystic mastopathy, the R in carcinomas without lymph-node involvement (LN-) was usually lower than I in most cases. In contrast, in 5 out of 6 patients with lymph-node metastasis (LN+), the ratio ranged between 2 and 4. While the R magnitude was not related to the frequency of positive lymph nodes out of the total analyzed, nor to relapse status at follow-up (all relapse-free), the clear-cut difference between the LN- and LN+ groups was statistically significant. Results suggest that evaluation of MMP-2/TIMP-2 mRNA balance may constitute an early prognostic approach, which may also be more reliable concerning cancer aggressiveness as compared with the MMP-2 alone, and that boosting TIMP-2 expression may be a therapeutic strategy to prevent metastasis.


Asunto(s)
Neoplasias de la Mama/enzimología , Gelatinasas/análisis , Metaloendopeptidasas/análisis , Proteínas/análisis , Adulto , Anciano , Secuencia de Bases , Neoplasias de la Mama/patología , Progresión de la Enfermedad , Femenino , Expresión Génica , Humanos , Metástasis Linfática , Metaloproteinasa 2 de la Matriz , Persona de Mediana Edad , Datos de Secuencia Molecular , Estadificación de Neoplasias , Reacción en Cadena de la Polimerasa , ARN Mensajero/análisis , Inhibidor Tisular de Metaloproteinasa-2 , Transcripción Genética
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