Relative carnitine deficiency in autism (Q36023375)

11 August 2017

Relative carnitine deficiency in autism (English)

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11 August 2017

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2

Jenifer Juranek

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11 August 2017

Pauline A Filipek

1

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11 August 2017

Minh T Nguyen

series ordinal

3

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11 August 2017

Christa Cummings

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4

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11 August 2017

J Jay Gargus

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5

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11 August 2017

language of work or name

English

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publication date

1 December 2004

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Journal of Autism and Developmental Disorders

11 August 2017

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11 August 2017

34

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11 August 2017

615-623

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11 August 2017

6

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https://scigraph.springernature.com/pub.10.1007/s10803-004-5283-1

11 August 2017

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cites work

Primary and secondary carnitine deficiency syndromes.

1 reference

12 December 2020

l-Carnitine Supplementation in Childhood Epilepsy: Current Perspectives

1 reference

12 December 2020

Stimulation of mitochondrial gene expression and proliferation of mitochondria following impairment of cellular energy transfer by inhibition of the phosphocreatine circuit in rat hearts

1 reference

12 December 2020

Mitochondrial dysfunction in autistic patients with 15q inverted duplication

1 reference

12 December 2020

Effect of sports activity on carnitine metabolism. Measurement of free carnitine, gamma-butyrobetaine and acylcarnitines by tandem mass spectrometry

1 reference

12 December 2020

Defective urinary carnitine transport in heterozygotes for primary carnitine deficiency

1 reference

12 December 2020

Practice parameter: screening and diagnosis of autism: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Child Neurology Society

1 reference

12 December 2020

L-Carnitine Insufficiency in Disorders of Organic acid Metabolism: Response to L-Carnitine by Patients with Methylmalonic Aciduria and 3-Hydroxy-3-methylglutaric Aciduria

1 reference

12 December 2020

Interstitial duplications of chromosome region 15q11q13: clinical and molecular characterization.

1 reference

12 December 2020

Carnitine in neonatal nutrition

1 reference

12 December 2020

Value of a clinical morphology examination in autism.

1 reference

12 December 2020

Regression in pervasive developmental disorders: seizures and epileptiform electroencephalogram correlates.

1 reference

12 December 2020

Carnitine Deficiency of Human Skeletal Muscle with Associated Lipid Storage Myopathy: A New Syndrome

1 reference

12 December 2020

The Screening and Diagnosis of Autistic Spectrum Disorders

1 reference

12 December 2020

Sudden and unexpected neonatal death: a protocol for the postmortem diagnosis of fatty acid oxidation disorders

1 reference

12 December 2020

Carnitine deficiency syndromes

1 reference

12 December 2020

Carnitine--metabolism and functions

1 reference

12 December 2020

Food selectivity and problem behavior in children with developmental disabilities. Analysis and intervention.

1 reference

12 December 2020

Craniofacial anomalies and malformations in respiratory chain deficiency

1 reference

12 December 2020

Valproate-induced coma with ketosis and carnitine insufficiency

1 reference

12 December 2020

Subnormal carnitine levels and their correction in artificially fed patients from a neurological intensive care unit: a pilot study

1 reference

12 December 2020

Ethylmalonic/adipic aciduria: effects of oral medium-chain triglycerides, carnitine, and glycine on urinary excretion of organic acids, acylcarnitines, and acylglycines

1 reference

12 December 2020

Secondary carnitine deficiency and impaired docosahexaenoic (22:6n-3) acid synthesis: a common denominator in the pathophysiology of diseases of oxidative phosphorylation and beta-oxidation

1 reference

12 December 2020

Genetic disorders of carnitine metabolism and their nutritional management

1 reference

12 December 2020

Physical activity as a metabolic stressor

1 reference

12 December 2020

Causes of death in autism

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12 December 2020

Serum carnitine concentrations in coeliac disease

1 reference

12 December 2020

Cloning of the human carnitine-acylcarnitine carrier cDNA and identification of the molecular defect in a patient

1 reference

12 December 2020

Acquired carnitine abnormalities in critically ill children

1 reference

12 December 2020

Respiratory complex II defect in siblings associated with a symptomatic secondary block in fatty acid oxidation

1 reference

12 December 2020

An assessment of food acceptance in children with autism or pervasive developmental disorder-not otherwise specified.

1 reference

12 December 2020

Carnitine deficiency and hyperammonemia associated with valproic acid therapy

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12 December 2020

Plasma fatty acid levels in autistic children

1 reference

12 December 2020

Docosahexaenoic acid, a ligand for the retinoid X receptor in mouse brain

1 reference

12 December 2020

Gastrointestinal abnormalities in children with autistic disorder

1 reference

12 December 2020

Phenotype and genotype variation in primary carnitine deficiency

1 reference

12 December 2020

Inhibition of carnitine biosynthesis by valproic acid in rats--the biochemical mechanism of inhibition

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12 December 2020

[Plasma L-carnitine levels in children with celiac disease]

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12 December 2020

10.1007/S10803-004-5283-1

Identifiers

DOI

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11 August 2017

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