Carnitine insufficiency in children with inborn errors of metabolism: prevalence and treatment efficacy.

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Environmental Enteric Dysfunction is Associated with Carnitine Deficiency and Altered Fatty Acid Oxidation.Nutritional interventions in primary mitochondrial disorders: Developing an evidence base.The application of NMR-based milk metabolite analysis in milk authenticity identification.

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Carnitine insufficiency in children with inborn errors of metabolism: prevalence and treatment efficacy.

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2015 nî lūn-bûn

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Carnitine insufficiency in chi ...... alence and treatment efficacy.

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Carnitine insufficiency in chi ...... alence and treatment efficacy.

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Carnitine insufficiency in chi ...... alence and treatment efficacy.

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Irina Zolkina

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Pavel Glagovsky

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The in-depth evaluation of suspected mitochondrial disease

Carnitine Profile and Effect of Suppletion in Children with Renal Fanconi Syndrome due to Cystinosis.

Cystinosis: practical tools for diagnosis and treatment

Plasma and muscle free carnitine deficiency due to renal Fanconi syndrome.

Oral carnitine therapy in children with cystinosis and renal Fanconi syndrome.

Systemic primary carnitine deficiency: an overview of clinical manifestations, diagnosis, and management.

Mitochondrial myopathy associated with a novel mutation in mtDNA.

Primary carnitine deficiency: novel mutations and insights into the cardiac phenotype.

Carnitine deficiency in chronic critical illness.

Carnitine deficiency presenting with encephalopathy and hyperammonemia in a patient receiving chronic enteral tube feeding: a case report.

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1299-1304

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scholarly article

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10.1515/JPEM-2015-0193

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11-12

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Vladimir S. Sukhorukov

I S Mamedov

Ekaterina Nikolaeva

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2015-07-18T00:00:00Z

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26197467

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Carnitine insufficiency in children with inborn errors of metabolism: prevalence and treatment efficacy.

about

P2860

P2860

Carnitine insufficiency in children with inborn errors of metabolism: prevalence and treatment efficacy.

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