Now showing items 1-6 of 6

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      Age‐related cognitive decline in myotonic dystrophy type 1: An 11‐year longitudinal follow‐up study 

      Labayru Isusquiza, Garazi; Aliri Lazcano, Jone ORCID; Zulaica, Miren; López de Munain Arregui, Adolfo José; Sistiaga Berrondo, Andone ORCID (Wiley, 2020-03)
      Background Myotonic dystrophy type 1 (DM1) is an inherited multi-systemic disease involving the central nervous system (CNS) and is consequently characterized by a range of cognitive impairments. However, whether this ...
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      Neurodegeneration Trajectory in Pediatric and Adult/Late DM1: a Follow-up MRI Study Across a Decade 

      Labayru Isusquiza, Garazi; Jiménez Marín, Antonio; Fernández, Esther; Villanua Bernues, Jorge Alberto; Zulaica, Miren; Cortés Díaz, Jesús María; Díez, Ibai; Sepulcre, Jorge; López de Munain Arregui, Adolfo José; Sistiaga Berrondo, Andone ORCID (Wiley, 2020-10)
      Objective: To characterize the progression of brain structural abnormalities in adults with pediatric and adult/late onset DM1, as well as to examine the potential predictive markers of such progression. Methods: 21 DM1 ...
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      Small for gestational age moderate to late preterm children: a neuropsychological follow-up 

      Labayru Isusquiza, Garazi; Aliri Lazcano, Jone ORCID; Santos, Andrea; Arrizabalaga Sagasta, Ane; Estévez, María; Cancela, Vanesa; Gaztañaga Echeverria, Mirari; Martí Carrera, María Itxaso; Sistiaga Berrondo, Andone ORCID (Routledge Journals, Taylor & Francis Group, 2021-05-19)
      [EN] Determine whether SGA constitutes a neurodevelopmental risk-factor of MLP, exploring if potential developmental difficulties at toddlerhood persist and are related to school-age performance. 109 SGA and 109 adequate ...
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      Social cognition in myotonic dystrophy type 1: Specific or secondary impairment? 

      Labayru Isusquiza, Garazi; Arenzana, Irati; Aliri Lazcano, Jone ORCID; Zulaica, Miren; López de Munain Arregui, Adolfo José; Sistiaga Berrondo, Andone ORCID (Public Library Science, 2018-09-24)
      Aims The cognitive profile of Myotonic Dystrophy type 1 (DM1) has been described in recent decades. Moreover, DM1 patients show lowered social engagement and difficulties in social-cognitive functions. The aim of the ...
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      Transcriptional signatures of synaptic vesicle genes define myotonic dystrophy type I neurodegeneration 

      Jiménez Marín, Antonio; Díez Palacio, Ibai; Labayru Isusquiza, Garazi; Sistiaga Berrondo, Andone ORCID; Caballero, Maria C.; Andres-Benito, Pol; Sepulcre, Jorge; Ferrer, Isidro; López de Munain Arregui, Adolfo José; Cortés Díaz, Jesús María (Wiley, 2021-12)
      Aim To delineate the neurogenetic profiles of brain degeneration patterns in myotonic dystrophy type I (DM1). Methods In two cohorts of DM1 patients, brain maps of volume loss (VL) and neuropsychological deficits (NDs) ...
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      White matter integrity changes and neurocognitive functioning in adult-late onset DM1: a follow-up DTI study 

      Labayru Isusquiza, Garazi; Camino, Borja; Jiménez Marín, Antonio; Garmendia Zaldua, Joana; Villanua Bernues, Jorge Alberto; Zulaica Ijurco, Miren; Cortés Díaz, Jesús María; López de Munain Arregui, Adolfo José; Sistiaga Berrondo, Andone ORCID (Nature Research, 2022-03)
      [EN] Myotonic Dystrophy Type 1 (DM1) is a multisystemic disease that affects gray and white matter (WM) tissues. WM changes in DM1 include increased hyperintensities and altered tract integrity distributed in a widespread ...