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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2018 | 1 |
2019 | 1 |
2021 | 1 |
2023 | 2 |
2024 | 0 |
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5 results
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Page 1
Internal jugular access using pocket ultrasound in a simulated model: comparison between biplane and monoplane visualization techniques.
Ultrasound J. 2023 Oct 10;15(1):42. doi: 10.1186/s13089-023-00335-4.
Ultrasound J. 2023.
PMID: 37815637
Free PMC article.
Correction: Uveitis and Multiple Sclerosis: Potential Common Causal Mutations.
de-la-Torre A, Silva-Aldana CT, Muñoz-Ortiz J, Piñeros-Hernández LB, Otero-Marquez O, Domínguez A, Faciolince LA, Arcos-Holzinger M, Mastronardi C, Contreras-Bravo NC, Restrepo CM, Arcos-Burgos M.
de-la-Torre A, et al. Among authors: pineros hernandez lb.
Mol Neurobiol. 2023 May;60(5):2969. doi: 10.1007/s12035-023-03265-3.
Mol Neurobiol. 2023.
PMID: 36781740
Free PMC article.
No abstract available.
Item in Clipboard
A Pharmacogenetic Study of CYP2C19 in Acute Coronary Syndrome Patients of Colombian Origin Reveals New Polymorphisms Potentially Related to Clopidogrel Therapy.
Angulo-Aguado M, Panche K, Tamayo-Agudelo CA, Ruiz-Torres DA, Sambracos-Parrado S, Niño-Orrego MJ, Páez N, Piñeros-Hernandez LB, Castillo-León LF, Pardo-Oviedo JM, Abaunza KP, Laissue P, Contreras N, Calderón-Ospina CA, Fonseca-Mendoza DJ.
Angulo-Aguado M, et al. Among authors: pineros hernandez lb.
J Pers Med. 2021 May 12;11(5):400. doi: 10.3390/jpm11050400.
J Pers Med. 2021.
PMID: 34065778
Free PMC article.
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Uveitis and Multiple Sclerosis: Potential Common Causal Mutations.
de-la-Torre A, Silva-Aldana CT, Muñoz-Ortiz J, Piñeros-Hernández LB, Otero O, Domínguez A, Faciolince LA, Arcos-Holzinger M, Mastronardi C, Contreras-Bravo NC, Restrepo CM, Arcos-Burgos M.
de-la-Torre A, et al. Among authors: pineros hernandez lb.
Mol Neurobiol. 2019 Dec;56(12):8008-8017. doi: 10.1007/s12035-019-1630-2. Epub 2019 Jun 3.
Mol Neurobiol. 2019.
PMID: 31161422
Free PMC article.
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A combined linkage, microarray and exome analysis suggests MAP3K11 as a candidate gene for left ventricular hypertrophy.
Silva CT, Zorkoltseva IV, Niemeijer MN, van den Berg ME, Amin N, Demirkan A, van Leeuwen E, Iglesias AI, Piñeros-Hernández LB, Restrepo CM, Kors JA, Kirichenko AV, Willemsen R, Oostra BA, Stricker BH, Uitterlinden AG, Axenovich TI, van Duijn CM, Isaacs A.
Silva CT, et al. Among authors: pineros hernandez lb.
BMC Med Genomics. 2018 Mar 5;11(1):22. doi: 10.1186/s12920-018-0339-9.
BMC Med Genomics. 2018.
PMID: 29506515
Free PMC article.
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