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Page 1
Spinal Muscular Atrophy Update in Best Practices: Recommendations for Diagnosis Considerations.
Schroth M, Deans J, Arya K, Castro D, De Vivo DC, Gibbons MA, Ionita C, Kuntz NL, Lakhotia A, Neil Knierbein E, Scoto M, Sejersen T, Servais L, Tian C, Waldrop MA, Vázquez-Costa JF. Schroth M, et al. Among authors: ionita c. Neurol Clin Pract. 2024 Aug;14(4):e200310. doi: 10.1212/CPJ.0000000000200310. Epub 2024 May 24. Neurol Clin Pract. 2024. PMID: 38915908 Free PMC article.
Multicenter comparison using two AI stroke CT perfusion software packages for determining thrombectomy eligibility.
Alwood BT, Meyer DM, Ionita C, Snyder KV, Santos R, Perrotta L, Crooks R, Van Orden K, Torres D, Poynor B, Pham N, Kelly S, Meyer BC, Bolar DS. Alwood BT, et al. Among authors: ionita c. J Stroke Cerebrovasc Dis. 2024 Jul;33(7):107750. doi: 10.1016/j.jstrokecerebrovasdis.2024.107750. Epub 2024 May 2. J Stroke Cerebrovasc Dis. 2024. PMID: 38703875 Free PMC article.
Clinical situations for which 3D printing is considered an appropriate representation or extension of data contained in a medical imaging examination: pediatric congenital heart disease conditions.
Ryan JR, Ghosh R, Sturgeon G, Ali A, Arribas E, Braden E, Chadalavada S, Chepelev L, Decker S, Huang YH, Ionita C, Lee J, Liacouras P, Parthasarathy J, Ravi P, Sandelier M, Sommer K, Wake N, Rybicki F, Ballard D. Ryan JR, et al. Among authors: ionita c. 3D Print Med. 2024 Jan 29;10(1):3. doi: 10.1186/s41205-023-00199-3. 3D Print Med. 2024. PMID: 38282094 Free PMC article. Review.
Clinical situations for which 3D Printing is considered an appropriate representation or extension of data contained in a medical imaging examination: vascular conditions.
Lee J, Chadalavada SC, Ghodadra A, Ali A, Arribas EM, Chepelev L, Ionita CN, Ravi P, Ryan JR, Santiago L, Wake N, Sheikh AM, Rybicki FJ, Ballard DH. Lee J, et al. Among authors: ionita cn. 3D Print Med. 2023 Nov 30;9(1):34. doi: 10.1186/s41205-023-00196-6. 3D Print Med. 2023. PMID: 38032479 Free PMC article. Review.
Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections.
Jeffries L, Mis EK, McWalter K, Donkervoort S, Brodsky NN, Carpier JM, Ji W, Ionita C, Roy B, Morrow JS, Darbinyan A, Iyer K, Aul RB, Banka S, Chao KR, Cobbold L, Cohen S, Custodio HM, Drummond-Borg M, Elmslie F, Finanger E, Hainline BE, Helbig I, Hewson S, Hu Y, Jackson A, Josifova D, Konstantino M, Leach ME, Mak B, McCormick D, McGee E, Nelson S, Nguyen J, Nugent K, Ortega L, Goodkin HP, Roeder E, Roy S, Sapp K, Saade D, Sisodiya SM, Stals K, Towner S, Wilson W; Deciphering Developmental Disorders; Genomics England Research Consortium; Undiagnosed Disease Network; Khokha MK, Bönnemann CG, Lucas CL, Lakhani SA. Jeffries L, et al. Among authors: ionita c. Genet Med. 2024 Feb;26(2):101023. doi: 10.1016/j.gim.2023.101023. Epub 2023 Nov 7. Genet Med. 2024. PMID: 37947183
241 results