Serum paraoxonase-3 concentration in HIV-infected patients. Evidence for a protective role against oxidation[S]
Gerard Aragonès, Anabel García-Heredia, Marta Guardiola et al. · Journal of Lipid Research · 2012
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Clinical Biochemistry
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344 papersQuestions on this topic
Characterization of bacteria in ballast water using MALDI-TOF mass spectrometry.
Kaveh Emami, Vahid Askari, Matthias Ullrich et al. · PLoS ONE · 2012
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Acidemia propiónica neonatal con deterioro neurológico, rechazo al alimento y emesis reporte de caso y revisión de la literatura
Adriana Montealegre, Erlin Robledo, José Yecid Moreno et al. · Repertorio de Medicina y Cirugía · 2012
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Phenylketonuria: nutritional advances and challenges
Giovannini Marcello, Verduci Elvira, Salvatici Elisabetta et al. · Nutrition & Metabolism · 2012
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Progress in understanding 2‐hydroxyglutaric acidurias
Martijn Kranendijk, Eduard A. Struys, Gajja S. Salomons et al. · Journal of Inherited Metabolic Disease · 2012 · Review
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Potentiation of NMDA receptor-dependent cell responses by extracellular high mobility group box 1 protein.
Marco Pedrazzi, Monica Averna, Bianca Sparatore et al. · PLoS ONE · 2012
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Suggested guidelines for the diagnosis and management of urea cycle disorders
Johannes Häberle, Nathalie Boddaert, Alberto Burlina et al. · Orphanet Journal of Rare Diseases · 2012 · Review
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Low bone strength is a manifestation of phenylketonuria in mice and is attenuated by a glycomacropeptide diet.
Patrick Solverson, Sangita G Murali, Suzanne J Litscher et al. · PLoS ONE · 2012
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X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and management
Marc Engelen, Stephan Kemp, Marianne de Visser et al. · Orphanet Journal of Rare Diseases · 2012 · Review
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Correction: Glyoxalase-I Is a Novel Prognosis Factor Associated with Gastric Cancer Progression.
Wan-Li Cheng, Ming-Ming Tsai, Chung-Ying Tsai et al. · PLoS ONE · 2012
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Neuropsychological profile and clinical effects of arginine treatment in children with creatine transport deficiency
Chilosi Annamaria, Casarano Manuela, Comparini Alessandro et al. · Orphanet Journal of Rare Diseases · 2012
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Preferential expression of mutant <it>ABCD1 </it>allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms
Salsano Ettore, Tabano Silvia, Sirchia Silvia M et al. · Orphanet Journal of Rare Diseases · 2012
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16S rRNA terminal restriction fragment length polymorphism for the characterization of the nasopharyngeal microbiota.
Silvio D Brugger, Laurence Frei, Pascal M Frey et al. · PLoS ONE · 2012
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Direct Matrix-Assisted Laser Desorption Ionization Time-of-Flight Mass Spectrometry Improves Appropriateness of Antibiotic Treatment of Bacteremia
Anne L. M. Vlek, Marc J. M. Bonten, C. H. Edwin Boel · PLoS ONE · 2012
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MR spectroscopy-based brain metabolite profiling in propionic acidaemia: metabolic changes in the basal ganglia during acute decompensation and effect of liver transplantation
McKiernan Patrick J, Chakrapani Anupam, Sun Yu et al. · Orphanet Journal of Rare Diseases · 2011
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Antioxidant and inflammatory aspects of lipoprotein-associated phospholipase A 2 (Lp-PLA 2 ): a review
Damasceno Nágila RT, Mello Ana PQ, Silva Isis T · Lipids in Health and Disease · 2011
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Chronic Immune Stimulation May Cause Moderate Impairment of Phenylalanine 4-hydroxylase
Scholl-Bürgi S, Schroecksnadel S, Jenny M et al. · Pteridines · 2011
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Neuroradiological findings of an adolescent with early treated phenylketonuria: is phenylalanine restriction enough?
Mayara Thays Beckhauser, Mirella Maccarini Peruchi, Gisele Rozone de Luca et al. · Clinics and Practice · 2011
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Neonatal astrocyte damage is sufficient to trigger progressive striatal degeneration in a rat model of glutaric acidemia-I.
Silvia Olivera-Bravo, Anabel Fernández, María Noel Sarlabós et al. · PLoS ONE · 2011
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Metilglioxal: uma toxina endógena? Is methylglyoxal an endogenous toxin?
Adriano Sartori, Etelvino José Henriques Bechara · Química Nova · 2010
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