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Общее количество найденных документов : 8
Показаны документы с 1 по 8
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1.
| Identification and quantification of intermediates of unsaturated fatty acid metabolism in plasma of patients with fatty acid oxidation disorders // Clin. Chem., 1995. Vol. 41, N 10.-С.1467-1474
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2.
| Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship // Hum. Mutat., 2001. Vol. 18, N 3.-С.169-189
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3.
| Schatz Ulrich A. The clinical manifestation of MCAD deficiency: Challenges towards adulthood in the screened population // J. Inherit. Metab. Disease, 2010. Vol. 33, N 5.-С.513-520
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4.
| Benentt M.J. Pathophysiology of fatty acid oxidation disorders // J. Inherit. Metab. Disease, 2010. Vol. 33, N 5.-С.533-537
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5.
| Wilcken Fatty acid oxidation disorders: Outcome and long-term prognosis // J. Inherit. Metab. Disease, 2010. Vol. 33, N 5.-С.501-506
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6.
| Spiekerkoetter Mitochondrial fatty acid oxidation disorders: Pathophysiological studies in mouse models // J. Inherit. Metab. Disease, 2010. Vol. 33, N 5.-С.539-546
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7.
| Current issues regarding treatment of mitochondrial fatty acid oxidation disorders // J. Inherit. Metab. Disease, 2010. Vol. 33, N 5.-С.555-561
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8.
| Variability in the clinical management of fatty acid oxidation disorders: Results of a survey of Canadian metabolic physicians // J. Inherit. Metab. Disease, 2012. Vol. 35, N 1.-С.115-123
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