FERNANDO SCAGLIA to Muscular Diseases
This is a "connection" page, showing publications FERNANDO SCAGLIA has written about Muscular Diseases.
Connection Strength
0.623
-
Outcomes of kidney transplantation in three patients with single large-scale mitochondrial DNA deletion syndromes. Mol Genet Metab. 2026 Mar; 147(3):109731.
Score: 0.217
-
Disorders of carnitine biosynthesis and transport. Mol Genet Metab. 2015 Nov; 116(3):107-12.
Score: 0.106
-
MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options. Mol Genet Metab. 2015 Sep-Oct; 116(1-2):4-12.
Score: 0.104
-
Improvement of regressive autism symptoms in a child with TMLHE deficiency following carnitine supplementation. Am J Med Genet A. 2015 Sep; 167A(9):2162-7.
Score: 0.104
-
Molecular and clinical characterization of the myopathic form of mitochondrial DNA depletion syndrome caused by mutations in the thymidine kinase (TK2) gene. Mol Genet Metab. 2013 Sep-Oct; 110(1-2):153-61.
Score: 0.092