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Page 1
Thymic Carcinoma Associated with Cerebellar Degeneration.
Cuartero IG, Galdeano MR, Pinar MP, Del Pozo JSG. Cuartero IG, et al. Among authors: del pozo jsg. Eur J Case Rep Intern Med. 2018 Mar 21;5(3):000780. doi: 10.12890/2018_000780. eCollection 2018. Eur J Case Rep Intern Med. 2018. PMID: 30756016 Free PMC article.
A bibliometric evaluation of the top 100 cited natalizumab articles.
García-Fernández FJ, García-Fernández AE, Nava E, Del Pozo JSG, Ikuta I, Jordan J, Galindo MF. García-Fernández FJ, et al. Among authors: del pozo jsg. J Neuroimmunol. 2020 Dec 15;349:577379. doi: 10.1016/j.jneuroim.2020.577379. Epub 2020 Sep 8. J Neuroimmunol. 2020. PMID: 33007648
Deep Vein Thrombosis in Upper Limb in a Weightlifter.
Pinar MP, Toledo RP, Viana LB, Del Pozo JSG. Pinar MP, et al. Among authors: del pozo jsg. Open Access Maced J Med Sci. 2017 Mar 6;5(2):228-230. doi: 10.3889/oamjms.2017.027. eCollection 2017 Apr 15. Open Access Maced J Med Sci. 2017. PMID: 28507633 Free PMC article.
CNS involvement in OFD1 syndrome: a clinical, molecular, and neuroimaging study.
Del Giudice E, Macca M, Imperati F, D'Amico A, Parent P, Pasquier L, Layet V, Lyonnet S, Stamboul-Darmency V, Thauvin-Robinet C, Franco B; Oral-Facial-Digital Type I (OFD1) Collaborative Group. Del Giudice E, et al. Orphanet J Rare Dis. 2014 May 10;9:74. doi: 10.1186/1750-1172-9-74. Orphanet J Rare Dis. 2014. PMID: 24884629 Free PMC article.
EDA, EDAR, EDARADD and WNT10A allelic variants in patients with ectodermal derivative impairment in the Spanish population.
Martínez-Romero MC, Ballesta-Martínez MJ, López-González V, Sánchez-Soler MJ, Serrano-Antón AT, Barreda-Sánchez M, Rodriguez-Peña L, Martínez-Menchon MT, Frías-Iniesta J, Sánchez-Pedreño P, Carbonell-Meseguer P, Glover-López G, Guillén-Navarro E; GIEDE (Spanish multidisciplinary research group for ectodermal dysplasia). Martínez-Romero MC, et al. Orphanet J Rare Dis. 2019 Dec 3;14(1):281. doi: 10.1186/s13023-019-1251-x. Orphanet J Rare Dis. 2019. PMID: 31796081 Free PMC article.
Further delineation of neuropsychiatric findings in Tatton-Brown-Rahman syndrome due to disease-causing variants in DNMT3A: seven new patients.
Tenorio J, Alarcón P, Arias P, Dapía I, García-Miñaur S, Palomares Bralo M, Campistol J, Climent S, Valenzuela I, Ramos S, Monseny AM, Grondona FL, Botet J, Serrano M, Solís M, Santos-Simarro F, Álvarez S, Teixidó-Tura G, Fernández Jaén A, Gordo G, Bardón Rivera MB, Nevado J, Hernández A, Cigudosa JC, Ruiz-Pérez VL, Tizzano EF; SOGRI Consortium; Lapunzina P. Tenorio J, et al. Eur J Hum Genet. 2020 Apr;28(4):469-479. doi: 10.1038/s41431-019-0485-3. Epub 2019 Nov 4. Eur J Hum Genet. 2020. PMID: 31685998 Free PMC article.
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