Co-Authors
This is a "connection" page, showing publications co-authored by PILAR MAGOULAS and TIMOTHY LOTZE.
Connection Strength
0.152
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Autosomal dominant HK1-related neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA): An emerging mitochondrial disorder. Genet Med Open. 2025; 3:103425.
Score: 0.061
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Clinical characterization of Collagen XII-related disease caused by biallelic COL12A1 variants. Ann Clin Transl Neurol. 2025 Mar; 12(3):602-614.
Score: 0.061
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Mutations in PURA cause profound neonatal hypotonia, seizures, and encephalopathy in 5q31.3 microdeletion syndrome. Am J Hum Genet. 2014 Nov 06; 95(5):579-83.
Score: 0.030