New Therapeutic Targets to Fight Type 2 Diabetes
A study led by Dr Manuel Vázquez-Carreras presents an integrative view of the most outstanding advances in understanding this process and helping to identify new pharmacological targets in the fight against type 2 diabetes mellitus.
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Automated learning app improves accessibility to medulloblastoma classification
A team from the Sant Joan de Déu Research Institute, Sant Joan de Déu Hospital, and the Polytechnic University of Catalonia, has developed an artificial intelligence-based application to make the classification of medulloblastoma subgroups more accessible, less costly, and faster
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The first living pediatric patients brain tissue laboratory in Europe
King's College London and Sant Joan de Déu have formalized an agreement to develop a new living pediatric patients brain pediatric tissue laboratory. The laboratory is set to open at the beginning of 2025 and will be led by Dr. Óscar Marín, a neuroscience expert.
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Genetic basis of ADHD and autism spectrum disorder impacts on children's school performance
A study coordinated by the Institut de Recerca Sant Joan de Déu and the Vall d'Hebron Research Institute, within the SJD MIND Schools program, has analyzed the impact of the genetic basis of these disorders on the mental health and academic outcomes of children and adolescents.
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Research into treatments to combat obesity and excessive sleepiness in children with Prader-Willi syndrome
Researchers from Sant Joan de Déu have promoted various research projects in recent years to advance the understanding of Prader-Willi syndrome and study new treatments for children affected by this rare disease.
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23% of adolescents at risk of psychosis end up developing the disorder
The study led by the Research in Child and Adolescent Mental Health team reveals that one in four adolescents at clinical risk of psychosis end up developing this mental disorder within 18 months.
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Genetic mutations are identified as causing two types of hereditary blindness
The study led by Dr. Gemma Marfany describes how mutations in the NR2E3 gene lead to the death of photoreceptor cells involved in vision and pave the way for potential treatments.
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New advances in Schaaf-Yang syndrome research
A team led by researchers from the Institut de Recerca Sant Joan de Déu · IBUB discover that mutations in the MAGEL2 gene generate non-functional truncated proteins that tend to accumulate in the cell nucleus.
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A study opens the door to designing therapies to improve the lung development of excessively small fetuses
A study, involving researchers from the Institut de Recerca Sant Joan de Déu, provides new scientific evidence that shows that problems with lung development in a fetus that grows below normal levels are related to vascular resistance.
