Associated Papers
Mitochondrial carnitine palmitoyltransferase-II dysfunction: A possible novel mechanism for nonalcoholic fatty liver disease in hepatocarcinogenesis.
Yao M et al.
World Journal of Gastroenterology, 2023
Muscle Carnitine Palmitoyltransferase II (CPT II) Deficiency: A Conceptual Approach.
Joshi PR et al.
Molecules (basel, Switzerland), 2020
Allelic and phenotypic heterogeneity in 49 Italian patients with the muscle form of CPT-II deficiency.
Fanin M et al.
Clinical Genetics, 2012
Genotype-phenotype correlations in a large series of patients with muscle type CPT II deficiency.
Anichini A et al.
Neurological Research, 2011
Pseudometabolic presentation of dystrophinopathy due to a missense mutation.
Veerapandiyan A et al.
Muscle & Nerve, 2010
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