Edwardo Ramos to Mutation
This is a "connection" page, showing publications Edwardo Ramos has written about Mutation.
Connection Strength
1.079
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Ramos E, Pardo S, Mas Rodr?guez MF, V?lez J. Limb-Girdle Muscular Dystrophy Type 2A Resulting From c.C479G and c.G1818A Mutations in the Calpain-3 Gene. J Clin Neuromuscul Dis. 2015 Dec; 17(2):59-62.
Score: 0.378
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Noriega E, Ramos E. New mutation in periaxin gene causing Charcot Marie Tooth disease in a Puerto Rican young male. J Clin Neuromuscul Dis. 2013 Dec; 15(2):63-8.
Score: 0.329
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Otero-Loperena E, Ortiz-Santiago A, Ramos E. Familial Hyperckemia and Calf Hypertrophy Secondary to a Caveolin-3 Mutation. Am J Phys Med Rehabil. 2021 07 01; 100(7):e101-e103.
Score: 0.139
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Ortiz-Santiago A, Ramos E. Childhood onset homozygous recessive GDAP1 (p.Pro231Leu) mutation in a 9-year-old puerto rican pediatric female with axonal Charcot-Marie-Tooth disease: A case report. J Pediatr Rehabil Med. 2021; 14(3):533-537.
Score: 0.135
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Ramos E, Conde JG, Berrios RA, Pardo S, G?mez O, Mas Rodr?guez MF. Prevalence and Genetic Profile of Duchene and Becker Muscular Dystrophy in Puerto Rico. J Neuromuscul Dis. 2016 05 27; 3(2):261-266.
Score: 0.098