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Registry of the International Society of Uterus Transplantation: First Report.
Brännström M, Tullius SG, Brucker S, Dahm-Kähler P, Flyckt R, Kisu I, Andraus W, Wei L, Carmona F, Ayoubi JM, Scollo P, Weyers S, Fronek J. Brännström M, et al. Among authors: carmona f. Transplantation. 2022 Aug 11. doi: 10.1097/TP.0000000000004286. Online ahead of print. Transplantation. 2022. PMID: 35951434
Mild controlled hypothermia for necrotizing enterocolitis treatment to preterm neonates: low technology technique description and safety analysis.
Gonçalves-Ferri WA, Ferreira CHF, Albuquerque LMS, Silva JBC, Caixeta MV, Carmona F, Calixto C, Aragon DC, Crott G, Mussi-Pinhata MM, Roosch A, Sbragia L. Gonçalves-Ferri WA, et al. Among authors: carmona f. Eur J Pediatr. 2022 Jul 15. doi: 10.1007/s00431-022-04558-w. Online ahead of print. Eur J Pediatr. 2022. PMID: 35840777
Long-term Immune Response to SARS-CoV-2 Infection Among Children and Adults After Mild Infection.
Di Chiara C, Cantarutti A, Costenaro P, Donà D, Bonfante F, Cosma C, Ferrarese M, Cozzani S, Petrara MR, Carmona F, Liberati C, Palma P, Di Salvo G, De Rossi A, Plebani M, Padoan A, Giaquinto C. Di Chiara C, et al. Among authors: carmona f. JAMA Netw Open. 2022 Jul 1;5(7):e2221616. doi: 10.1001/jamanetworkopen.2022.21616. JAMA Netw Open. 2022. PMID: 35816313 Free PMC article.
Common genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertility.
Cerván-Martín M, Bossini-Castillo L, Guzmán-Jiménez A, Rivera-Egea R, Garrido N, Lujan S, Romeu G, Santos-Ribeiro S; IVIRMA Group; Lisbon Clinical Group, Castilla JA, Gonzalvo MDC, Clavero A, Maldonado V, Vicente FJ, Burgos M, Jiménez R, González-Muñoz S, Sánchez-Curbelo J, López-Rodrigo O, Pereira-Caetano I, Marques PI, Carvalho F, Barros A, Bassas L, Seixas S, Gonçalves J, Larriba S, Lopes AM, Palomino-Morales RJ, Carmona FD. Cerván-Martín M, et al. Among authors: carmona fd. Andrology. 2022 Jun 25. doi: 10.1111/andr.13221. Online ahead of print. Andrology. 2022. PMID: 35752927
Common Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only Syndrome.
Cerván-Martín M, Bossini-Castillo L, Guzmán-Jimenez A, Rivera-Egea R, Garrido N, Luján S, Romeu G, Santos-Ribeiro S, Ivirma Group, Lisbon Clinical Group, Castilla JA, Gonzalvo MC, Clavero A, Vicente FJ, Maldonado V, González-Muñoz S, Rodríguez-Martín I, Burgos M, Jiménez R, Pinto MG, Pereira I, Nunes J, Sánchez-Curbelo J, López-Rodrigo O, Pereira-Caetano I, Marques PI, Carvalho F, Barros A, Bassas L, Seixas S, Gonçalves J, Larriba S, Lopes AM, Carmona FD, Palomino-Morales RJ. Cerván-Martín M, et al. Among authors: carmona fd. J Pers Med. 2022 Jun 4;12(6):932. doi: 10.3390/jpm12060932. J Pers Med. 2022. PMID: 35743717 Free PMC article.
Biochemical, Biophysical and Functional Characterization of an Insoluble Iron Containing Hepcidin-Ferritin Chimeric Monomer Assembled Together with Human Ferritin H/L Chains at Different Molar Ratios.
Boumaiza M, Fhoula I, Carmona F, Poli M, Asperti M, Gianoncelli A, Bertuzzi M, Arosio P, Marzouki MN. Boumaiza M, et al. Among authors: carmona f. Curr Issues Mol Biol. 2021 Dec 28;44(1):117-127. doi: 10.3390/cimb44010009. Curr Issues Mol Biol. 2021. PMID: 35723388 Free PMC article.
421 results