Organelle pathology in metabolic neuromuscular disease: an overview.

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Phylogeny of 54 representative strains of species in the family Pasteurellaceae as determined by comparison of 16S rRNA sequences.Comparison of three methods for mitochondria isolation from the human liver cell line (HepG2).

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Organelle pathology in metabolic neuromuscular disease: an overview.

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Organelle pathology in metabolic neuromuscular disease: an overview.

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Organelle pathology in metabolic neuromuscular disease: an overview.

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Organelle pathology in metabolic neuromuscular disease: an overview.

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Organelle pathology in metabolic neuromuscular disease: an overview.

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Becker LE

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A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study

The inborn errors of mitochondrial fatty acid oxidation

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

Neuronal lipidosis and neuroaxonal dystrophy in cerebro-hepato-renal (Zellweger) syndrome.

Molecular genetic studies in the neuropsychiatric disorders.

Structure and function of mitochondria: their organization and disorders.

Mitochondrial myopathies involving the respiratory chain: a biochemical analysis.

Biochemical defects in mitochondrial cytopathies: a new classification.

Current perspectives in the study of human mitochondriopathies.

New approaches in peroxisomal disorders.

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1990-01-01T00:00:00Z

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Organelle pathology in metabolic neuromuscular disease: an overview.

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P2860

P2860

Organelle pathology in metabolic neuromuscular disease: an overview.

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P1433

P1476

P2093

P2860

P304

P31

P433

P478

P577

P698

P932

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P1476

P2093

P2860

P304

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P433

P478

P577

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