Peripheral neuropathy in patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency – A follow-up EMG study of 12 patients

Author:

Tuuli Immonen,Emilia Ahola,Jussi Toppila,Risto Lapatto,Tiina Tyni,Leena Lauronen

Funder

Lea and Arvo Ylppö Foundation.

Academy of Finland.

Jane and Aatos Erkko Foundation.

Märta Donner Foundation

Publisher

Elsevier BV

Subject

Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health

Reference23 articles.

1. Disorders of mitochondrial fatty acyl-CoA β-oxidation;Wanders;J Inherit Metab Dis,1999

2. Dissecting a population genome for targeted screening of disease mutations;Pastinen;Hum Mol Genet,2001

3. Neonatal screening for defects of the mitochondrial trifunctional protein;Sanders;Mol Genet Metab,2005

4. Sudden infant death and long-chain 3-hydroxyacyl-CoA dehydrogenase;Wanders;Lancet,1989

5. Familial hypoketotic hypoglycaemia associated with peripheral neuropathy, pigmentary retinopathy and C6–C14 hydroxydicarboxylic aciduria. A new defect in fatty acid oxidation?;Poll-The;J Inherit Metab Dis,1988

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