Sensory neuronopathy as a major clinical feature of mitochondrial trifunctional protein deficiency in adults
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Neurology
Reference20 articles.
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3. Peripheral neuropathy, episodic myoglobinuria, and respiratory failure in deficiency of the mitochondrial trifunctional protein;Spiekerkoetter;Muscle Nerve,2004
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1. Sensory neuronopathies, diagnostic criteria and causes;Current Opinion in Neurology;2022-08-11
2. Reversible sensory neuropathy in mitochondrial trifunctional protein deficiency;JIMD Reports;2022-03-09
3. Diagnostic Challenges in Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: Clinical, Morphological, and Genetic Aspects;Frontiers in Neurology;2022-03-03
4. Novel mutations in the HADHB gene causing a mild phenotype of mitochondrial trifunctional protein ( MTP ) deficiency;JIMD Reports;2022-03
5. Peripheral nervous system manifestations of Shiga toxin-producing E. coli-induced haemolytic uremic syndrome in children;Italian Journal of Pediatrics;2021-09-06
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