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Hepatic Echinococcus granulosus. A case report.
Méndez-Sánchez N, Vega R, Cortés R, Corona R, Pichardo-Bahena R, Uribe M. Méndez-Sánchez N, et al. Among authors: corona r. Ann Hepatol. 2003 Apr-Jun;2(2):99-100. Ann Hepatol. 2003. PMID: 15041899 Free article.
Caroli's disease and choledochal cyst.
Hérnandez-Ortiz J, Corona R, Méndez-Sánchez N. Hérnandez-Ortiz J, et al. Among authors: corona r. Ann Hepatol. 2002 Oct-Dec;1(4):196. Ann Hepatol. 2002. PMID: 15280807 Free article. No abstract available.
Genetic variants in DDX53 contribute to autism spectrum disorder associated with the Xp22.11 locus.
Scala M, Bradley CA, Howe JL, Trost B, Salazar NB, Shum C, Mendes M, Reuter MS, Anagnostou E, MacDonald JR, Ko SY, Frankland PW, Charlebois J, Elsabbagh M, Granger L, Anadiotis G, Pullano V, Brusco A, Keller R, Parisotto S, Pedro HF, Lusk L, McDonnell PP, Helbig I, Mullegama SV; Undiagnosed Diseases Network; Douine ED, Corona RI, Russell BE, Nelson SF, Graziano C, Schwab M, Simone L, Zara F, Scherer SW. Scala M, et al. Among authors: corona ri. Am J Hum Genet. 2025 Jan 2;112(1):154-167. doi: 10.1016/j.ajhg.2024.11.003. Epub 2024 Dec 19. Am J Hum Genet. 2025. PMID: 39706195
KIF21A-associated peripheral neuropathy defined by impaired binding with TUBB3.
Borja NA, Zafeer MF, Bivona S, Peart L, Gultekin SH; Undiagnosed Diseases Network; Bademci G, Tekin M; Undiagnosed Diseases Network NIH. Borja NA, et al. J Med Genet. 2024 Dec 11:jmg-2024-109908. doi: 10.1136/jmg-2024-109908. Online ahead of print. J Med Genet. 2024. PMID: 39643435
303 results