ENFERMEDADES NEUROMUSCULARES

Corrigendum to "Temporo-spatial analysis of amyotrophic lateral sclerosis in Spain: Altitude and land use as new determinants of the disease" [Sci. Total Environ., 957 (2024), 177796]..

Santurtún A, Medín P, Riancho JA, Santiago-Setién M, Ortiz F, López de Munain A, Almendra R, Riancho J.

Science of The Total Environment, 1015 (2026)

DOI: 10.1016/j.scitotenv.2026.181474

Targeted plasma proteomics uncover proteins associated with KIF5A-linked SPG10 and ALS spectrum disorders..

Dulski J, Boddapati AK, Risi B, Iruzubieta P, Orlacchio A, Fernández-Torrón R, Castillo-Triviño T, López de Munain A, Vucic S, Padovani A, Kaat LD, Barakat TS, Petrucelli L, Prudencio M, Landers JE, Weishaupt JH, Prokop A, Filosto M, Wszolek ZK, Pant DC.

Human Genetics and Genomics Advances, 7 (2026)

DOI: 10.1016/j.xhgg.2025.100498

Neural damage and inflammation in myotonic dystrophy type 1: Longitudinal analysis of serum NFL, GFAP, and IL-6..

Garmendia J, Labayru G, Alberro A, Martins-Almeida L, Otaegui D, Iruzubieta P, Lopez de Munain A, Sistiaga A.

BRAIN RESEARCH BULLETIN, 234 (2026)

DOI: 10.1016/j.brainresbull.2025.111688

Mitochondria and Lipid Defects in Hereditary Progranulin-Related Frontotemporal Dementia.

Ondaro, J, Zúñiga-Elizari, JL, Zufiría, M, Garciandia-Arcelus, M, Molleda, AS, Zulaica, M, Lafarga, M, Riancho, J, de Munaín, AL, Moreno, F, Gil-Bea, FJ, Gerenu, G.

Cells, 15 (2026)

DOI: 10.3390/cells15030276

Mitochondrial DNA replication is regulated by endoplasmic reticulum-mitochondrial contact sites, the mitochondrial calcium uniporter, and manganese.

Lopez de Arbina, A, Zamudio-Ochoa, A, Muñoz-Oreja, M, Perez-Rodriguez, D, Mosqueira-Martín, L, Lasalandra, R, Villar-Fernandez, M, Fernandez-Pelayo, U, Rodriguez-Gomez, L, Lee, S, Gil-Bea, F, Osinalde, N, Vallejo-Illaramendi, A, Temiakov, D, Spinazzola, A, Holt, IJ.

NUCLEIC ACIDS RESEARCH, 54 (2026)

DOI: 10.1093/nar/gkag233

Enhanced muscle uptake of chemically optimized miR-23b antisense oligonucleotides as lead compounds for myotonic dystrophy type 1.

González-Martínez, I, Cerro-Herreros, E, Carrascosa-Sàez, M, García-Rey, A, Piqueras-Losilla, D, Colom-Rodrigo, A, Moreno, N, Chakraborty, M, Huguet-Lachon, A, González-Barriga, A, Naldaiz-Gastesi, N, Dehesa, M, Díaz-Maqueda, A, Barquero, N, Varela, MA, Munain, ALD, Eritja, R, Gourdon, G, López-Castel, A, Pérez-Alonso, M, Llamusi, B, Artero, R.

AMERICAN JOURNAL OF HUMAN GENETICS, 113 (2026)

DOI: 10.1016/j.ajhg.2026.01.016

Formulation and 3D Printing of Collagen/Chitosan Inks: Tailoring the Scaffold Properties.

Carranza, T, Andonegui, M, Hernáez, R, Aiastui, A, Zhang, Y, de la Caba, K, Guerrero, P.

Gels, 12 (2026)

DOI: 10.3390/gels12030261

The role of endothelial dysfunction in the age-related poor prognosis of stroke patients undergoing endovascular treatment.

de la Riva, Patricia, Rodriguez-Antiguedad, Jon, Marta-Enguita, Juan, Gomez, Virginia, Arenaza, Gorka, Gorostidi, Ana, Diez, Noemi, De Arce, Ana, Garmendia, Enaut, Zumeta, Eider, Larrea, Jose Angel, Bergareche, Alberto, Arregui, Adolfo Lopez de Munain.

JOURNAL OF STROKE & CEREBROVASCULAR DISEASES, 34 (2025)

DOI: 10.1016/j.jstrokecerebrovasdis.2025.108412

Common Characteristics Between Frailty and Myotonic Dystrophy Type 1: A Narrative Review..

Garmendia J, Labayru G, Souto Barreto P, Vergara I, de Munain AL, Sistiaga A.

AGING AND DISEASE (2025)

DOI: 10.14336/AD.2024.0950

Translating Muscle RNAseq Into the Clinic for the Diagnosis of Muscle Diseases.

Segarra-Casas, Alba, Dominguez-Gonzalez, Cristina, Natera-de Benito, Daniel, Kapetanovic, Solange, Hernandez-Lain, Aurelio, Estevez-Arias, Berta, Llanso, Laura, Ortez, Carlos, Jou, Cristina, Marti-Carrera, Itxaso, Lopez-Marquez, Aristides, Rodriguez, Maria Jose, Gonzalez-Mera, Laura, Nedkova, Velina, Fernandez-Torron, Roberto, Rodriguez-Santiago, Benjamin, Jimenez-Mallebrera, Cecilia, Juntas-Morales, Raul, Lopez-de Munain, Adolfo, Surralles, Jordi, Nascimento, Andres, Gallardo, Eduard, Olive, Montse, Gallano, Pia, Gonzalez-Quereda, Lidia.

Annals of Clinical and Translational Neurology, 12 (2025)

DOI: 10.1002/acn3.70078