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Search on : CRUZ-ROBLES, DAVID [Author]
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 Núñez-Martínez, Paulina M. et al. Familial erythrocytosis 2 and von Hippel-Lindau disease in the same pediatric patient. Bol. Med. Hosp. Infant. Mex., Aug 2021, vol.78, no.4, p.341-345. ISSN 1665-1146

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 Avila-Vanzzini, Nydia et al. The ACE I/D polymorphism is associated with nitric oxide metabolite and blood pressure levels in healthy Mexican men. Arch. Cardiol. Méx., June 2015, vol.85, no.2, p.105-110. ISSN 1405-9940

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 Márquez, Manlio F. et al. Next generation sequencing for molecular confirmation of hereditary sudden cardiac death syndromes. Arch. Cardiol. Méx., Mar 2015, vol.85, no.1, p.68-72. ISSN 1405-9940

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 Márquez, Manlio F. et al. Síndrome de Andersen-Tawil: una revisión del diagnóstico genético y clínico con énfasis en sus manifestaciones cardíacas. Arch. Cardiol. Méx., Dic 2014, vol.84, no.4, p.278-285. ISSN 1405-9940

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 Fragoso-Lona, José Manuel et al. Marcadores pro y antiinflamatorios en la enfermedad arterial coronaria y el síndrome isquémico coronario agudo. Arch. Cardiol. Méx., Mar 2009, vol.79, no.1, p.54-62. ISSN 1405-9940

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 Márquez, Manlio F et al. A novel SCN5A deletion mutation in a child with ventricular tachycardia, recurrent aborted sudden death, and Brugada electrocardiographic pattern. Arch. Cardiol. Méx., Dec 2007, vol.77, no.4, p.284-287. ISSN 1405-9940

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