Search
20/10/2022
Influence of clinical and neurocognitive factors in psychosocial functioning after a first episode non-affective psychosis: Differences between males and females
Serra-Navarro, M, Amoretti, S, Verdolini, N, Forte, MF, Sanchez-Torres, AM, Vieta, E, Clougher, D, Lobo, A, Gonzalez-Pinto, A, Panadero, R, Roldan, A, Carvalho, AF, de la Serna, E, Toll, A, Ramos-Quiroga, JA, Torrent, C, Cuesta, MJ, Bernardo, M. Influence of clinical and neurocognitive factors in psychosocial functioning after a first episode non-affective psychosis: Differences between males and females. Frontiers in Psychiatry. 2022; 13DOI:10.3389/fpsyt.2022.982583. PMID:36339856. IF:4.700(Q2/4D).
19/10/2022
C3 glomerulopathy associated with monoclonal gammopathy: impact of chronic histologic lesions and beneficial effects of clone-targeted therapies
Caravaca-Fontan, F, Lucientes, L, Serra, N, Cavero, T, Rodado, R, Ramos, N, Gonzalez, F, Shabaka, A, Cabello, V, Huerta, A, Pampa-Saico, S, Gutierrez, E, Quintana, LF, Lopez-Rubio, ME, Draibe, J, Titos, JA, Fernandez-Juarez, G, De Jorge, EG, Praga, M. C3 glomerulopathy associated with monoclonal gammopathy: impact of chronic histologic lesions and beneficial effects of clone-targeted therapies. NEPHROLOGY DIALYSIS TRANSPLANTATION. 2022; 37(11)DOI:10.1093/ndt/gfab302. PMID:34677610. IF:6.100(Q1/2D).
19/10/2022
The association between macrovascular complications and intensive care admission, invasive mechanical ventilation, and mortality in people with diabetes hospitalized for coronavirus disease-2019 (COVID-19)
Llaurado, G, Vlacho, B, Wargny, M, Ruan, Y, Franch-Nadal, J, Domingo, P, Gourdy, P, Saulnier, PJ, Hadjadj, S, Wild, SH, Rea, R, Cariou, B, Khunti, K, Mauricio, D. The association between macrovascular complications and intensive care admission, invasive mechanical ventilation, and mortality in people with diabetes hospitalized for coronavirus disease-2019 (COVID-19). Cardiovascular Diabetology. 2022; 21(1)DOI:10.1186/s12933-022-01657-8. PMID:36261811. IF:9.300(Q1/1D).
18/10/2022
Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke
Jaworek, T, Xu, HC, Gaynor, BJ, Cole, JW, Rannikmae, K, Stanne, TM, Tomppo, L, Abedi, V, Amouyel, P, Armstrong, ND, Attia, J, Bell, S, Benavente, OR, Boncoraglio, GB, Butterworth, A, Carcel-Marquez, J, Chen, ZM, Chong, M, Cruchaga, C, Cushman, M, Danesh, J, Debette, S, Duggan, DJ, Durda, JP, Engstrom, G, Enzinger, C, Faul, JD, Fecteau, NS, Fernandez-Cadenas, I, Gieger, C, Giese, AK, Grewal, RP, Grittner, U, Havulinna, AS, Heitsch, L, Hochberg, MC, Holliday, E, Hu, J, Ilinca, A, Irvin, MR, Jackson, RD, Jacob, MA, Rabionet, R, Jimenez-Conde, J, Johnson, JA, Kamatani, Y, Kardia, SLR, Koido, M, Kubo, M, Lange, L, Lee, JM, Lemmens, R, Levi, CR, Li, J, Li, LM, Lin, K, Lopez, H, Luke, S, Maguire, J, McArdle, PF, McDonough, CW, Meschia, JF, Metso, T, Muller-Nurasyid, M, O'Connor, TD, O'Donnell, M, Peddareddygari, LR, Pera, J, Perry, JA, Peters, A, Putaala, J, Ray, D, Rexrode, K, Ribases, M, Rosand, J, Rothwell, PM, Rundek, T, Ryan, KA, Sacco, RL, Salomaa, V, Sanchez-Mora, C, Schmidt, R, Sharma, P, Slowik, A, Smith, JA, Smith, NL, Wassertheil-Smoller, S, Soderholm, M, Stine, OC, Strbian, D, Sudlow, CLM, Tatlisumak, T, Terao, C, Thijs, V, Torres-Aguila, NP, Tregouet, DA, Tuladhar, AM, Veldink, JH, Walters, RG, Weir, DR, Woo, D, Worrall, BB, Hong, CC, Ross, OA, Zand, R, de Leeuw, FE, Lindgren, AG, Pare, G, Anderson, CD, Markus, HS, Jern, C, Malik, R, Dichgans, M, Mitchell, BD, Kittner, SJ. Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke. NEUROLOGY. 2022; 99(16)DOI:10.1212/WNL.0000000000201006. PMID:36240095. IF:9.900(Q1/1D).
18/10/2022
Case report: De novo pathogenic variant in WFS1 causes Wolfram-like syndrome debuting with congenital bilateral deafness
Alias, L, de Heredia, ML, Luna, S, Cliville, N, Gonzalez-Quereda, L, Gallano, P, de Juan, J, Pujol, A, Diez, S, Boronat, S, Orus, C, Lasa, A, Venegas, MD. Case report: De novo pathogenic variant in WFS1 causes Wolfram-like syndrome debuting with congenital bilateral deafness. Frontiers in Genetics. 2022; 13DOI:10.3389/fgene.2022.998898. PMID:36330437. IF:3.700(Q2/4D).
18/10/2022
Prognostic Impact of Nutritional Status After Transcatheter Edge-to-Edge Mitral Valve Repair: The MIVNUT Registry
Caneiro-Queija, B, Raposeiras-Roubin, S, Adamo, M, Freixa, X, Arzamendi, D, Benito-Gonzalez, T, Montefusco, A, Pascual, I, Nombela-Franco, L, Rodes-Cabau, J, Shuvy, M, Portoles-Hernandez, A, Godino, C, Haberman, D, Lupi, L, Regueiro, A, Li, CH, Fernandez-Vazquez, F, Frea, S, Avanzas, P, Tirado-Conte, G, Paradis, JM, Peretz, A, Monivas, V, Baz, JA, Galasso, M, Branca, L, Sanchis, L, Asmarats, L, Garrote-Coloma, C, Angelini, F, Leon, V, de Agustin, JA, Alperi, A, Beeri, R, Maccagni, G, Sabate, M, Fernandez-Peregrina, E, Gualis, J, Bocchino, PP, Curello, S, Iniguez-Romo, A, Estevez-Loureiro, R. Prognostic Impact of Nutritional Status After Transcatheter Edge-to-Edge Mitral Valve Repair: The MIVNUT Registry. Journal of the American Heart Association. 2022; 11(20)DOI:10.1161/JAHA.121.023121. PMID:36216434. IF:5.400(Q2/3D).
18/10/2022
Validating left atrial fractionation and low-voltage substrate during atrial fibrillation and sinus rhythm-A high-density mapping study in persistent atrial fibrillation
Huang, TY, Chen, J, Muller-Edenborn, B, Mayer, L, Eichenlaub, M, Weidmann, ZM, Allgeier, J, Bohnen, M, Lehrmann, H, Trenk, D, Schoechlin, S, Westermann, D, Arentz, T, Jadidi, A. Validating left atrial fractionation and low-voltage substrate during atrial fibrillation and sinus rhythm-A high-density mapping study in persistent atrial fibrillation. Frontiers in Cardiovascular Medicine. 2022; 9DOI:10.3389/fcvm.2022.1000027. PMID:36330001. IF:3.600(Q2/5D).
18/10/2022
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors
Thibord, F, Klarin, D, Brody, JA, Chen, MH, Levin, MG, Chasman, DI, Goode, EL, Hveem, K, Teder-Laving, M, Martinez-Perez, A, Aissi, D, Daian-Bacq, D, Ito, K, Natarajan, P, Lutsey, PL, Nadkarni, GN, de Vries, PS, Cuellar-Partida, G, Wolford, BN, Pattee, JW, Kooperberg, C, Braekkan, SK, Li-Gao, RF, Saut, N, Sept, C, Germain, M, Judy, RL, Wiggins, KL, Ko, D, O'Donnell, CJ, Taylor, KD, Giulianini, F, De Andrade, M, Nost, TH, Boland, A, Empana, JP, Koyama, S, Gilliland, T, Do, R, Huffman, JE, Wang, X, Zhou, W, Soria, JM, Souto, JC, Pankratz, N, Haessler, J, Hindberg, K, Rosendaal, FR, Turman, C, Olaso, R, Kember, RL, Bartz, TM, Lynch, JA, Heckbert, SR, Armasu, SM, Brumpton, B, Smadja, DM, Jouven, X, Komuro, I, Clapham, KR, Loos, RJF, Willer, CJ, Sabater-Lleal, M, Pankow, JS, Reiner, AP, Morelli, VM, Ridker, PM, Vlieg, AV, Deleuze, JF, Kraft, P, Rader, DJ, Lee, KM, Psaty, BM, Skogholt, AH, Emmerich, J, Suchon, P, Rich, SS, Vy, HT, Tang, WH, Jackson, RD, Hansen, JB, Morange, PE, Kabrhel, C, Tregouet, DA, Damrauer, SM, Johnson, AD, Smith, NL. Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors. CIRCULATION. 2022; 146(16)DOI:10.1161/CIRCULATIONAHA.122.059675. PMID:36154123. IF:37.800(Q1/1D).