Browsing Artículos by Author "Gadalla, Shahinaz M."

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      Leukocyte telomere length in patients with myotonic dystrophy type I: a pilot study 

      Wang, Youjin; Best, Ana; Fernández Torrón, Roberto; Alsaggaf, Rotana; García Puga, Mikel; Dagnall, Casey L.; Hicks, Belynda; Thompson, Mone’t; Matheu Fernández, Ander; Zulaica Ijurco, Miren; Greene, Mark H.; López de Munain Arregui, Adolfo José; Gadalla, Shahinaz M. (Wiley, 2019-12)
      Myotonic dystrophy type I (DM1) is an autosomal dominant disease of which clinical manifestations resemble premature aging. We evaluated the contribution of telomere length in pathogenesis in 361 DM1 patients (12 with ...
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      Senescence plays a role in myotonic dystrophy type 1 br 

      García Puga, Mikel; Sáenz Antoñanzas, Ander; Gereñu Lopetegi, Gorka; Arrieta Legorburu, Alex; Fernández Torrón, Roberto; Zulaica Ijurco, Miren; Sáenz Peña, Amets; Elizazu Pérez, Joseba; Nogales Gadea, Gisela; Gadalla, Shahinaz M.; Araúzo Bravo, Marcos J.; López de Munain Arregui, Adolfo José; Matheu Fernández, Ander (American Society for Clinical Investigation, 2022-10)
      Myotonic dystrophy type 1 (DM1; MIM #160900) is an autosomal dominant disorder, clinically characterized by progressive muscular weakness and multisystem degeneration. The broad phenotypes observed in patients with DM1 ...