Oscullo G., de la Rosa D., Clemente, MG, Giron R., Golpe R., Máiz L., Martinez-Garcia M.A.. The role of precision medicine in bronchiectasis: emerging data and clinical implications. Expert Review of Respiratory Medicine. 2023; 17(4)DOI:10.1080/17476348.2023.2205125. PMID:37077039. IF:2.900(Q2/4D).

Esteve-Valverde E., Alijotas-Reig J., Belizna C., Marques-Soares J., Anunciacion-Llunell A., Feijóo-Massó C., Sáez-Comet L., Mekinian A., Ferrer-Oliveras R., Lefkou E., Morales-Pérez S., Hoxha A., Tincani A., Nalli C., Pardos-Gea J., Marozio L., Maina A., Espinosa G., Cervera R., De Carolis S., Latino O., Udry S., Llurba E., Garrido-Gimenez C., Trespidi L., Gerosa M., Chighizola C.B., Rovere-Querini P., Canti V., Mayer-Pickel K., Tabacco S., Arnau A., Miró-Mur F.. Low complement levels are related to poor obstetric outcomes in women with obstetric antiphospholipid syndrome. The EUROAPS Registry Study Group. PLACENTA. 2023; 136DOI:10.1016/j.placenta.2023.04.001. PMID:37028222. IF:3.000(Q1/3D).

Vazquez-Costa, JF, Borrego-Hernandez, D, Paradas, C, Gomez-Caravaca, MT, Rojas-Garcia, R, Varona, L, Povedano, M, Garcia-Sobrino, T, Pascual, IJ, Gutierrez, A, Riancho, J, Turon-Sans, J, Assialioui, A, Perez-Tur, J, Sevilla, T, Perez, JE, Garcia-Redondo, A. Characterizing SOD1 mutations in Spain: The impact of genotype, age and sex in the natural history of the disease. EUROPEAN JOURNAL OF NEUROLOGY. 2023; 30(4)DOI:10.1111/ene.15661. PMID:36484631. IF:4.500(Q1/2D).

Segarra-Casas, A, Collet, R, Gonzalez-Quereda, L, Vesperinas, A, Caballero-Avila, M, Carbayo, A, Diaz-Manera, J, Rodriguez, MJ, Gallardo, E, Gallano, P, Olive, M. A new homozygous missense variant in LMOD3 gene causing mild nemaline myopathy with prominent facial weakness. NEUROMUSCULAR DISORDERS. 2023; 33(4)DOI:10.1016/j.nmd.2023.02.006. PMID:36893608. IF:2.700(Q2/4D).