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Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|March 10, 2020
Neurodevelopmental outcome at 2 years of corrected age in fetuses with increased nuchal translucency thickness and normal karyotype compared with matched controlsR Buffin, A Fichez, E Decullier, et al.
Archivos De La Sociedad Espanola De Oftalmologia|December 1, 2006
[Topical cyclosporine in the treatment of ocular actinic prurigo]J V Ortiz-Castillo, A Boto-de-los-Bueis, R De-Lucas-Laguna, et al.
Beneficial Microbes|March 29, 2020
Effects of <i>Lactobacillus fermentum</i> CECT5716 Lc40 on infant growth and health: a randomised clinical trial in nursing womenB Pastor-Villaescusa, J A Hurtado, M Gil-Campos, et al.
Actas Urologicas Espanolas|June 21, 2021
Role of PCA3 and SelectMDx in the optimization of active surveillance in prostate cancerD Fiorella, J L Marenco, J M Mascarós, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|February 13, 2019
Recent advances in circulating nucleic acids in oncologyA Otandault, P Anker, Z Al Amir Dache, et al.
European Journal of Pediatrics|March 24, 2026
A Mediterranean lifestyle obesity prevention intervention in preschoolers at risk: MELI-POP Study-a randomized controlled trialA Larruy-García, P De Miguel-Etayo, M Gil-Campos, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|September 16, 2017
Clinical utility of circulating DNA analysis for rapid detection of actionable mutations to select metastatic colorectal patients for anti-EGFR treatmentA R Thierry, S El Messaoudi, C Mollevi, et al.
Plos One|May 17, 2021
MADRID+90 study on factors associated with longevity: Study design and preliminary dataMiguel A Fernández-Blázquez, Teodoro Del Ser, Belén Frades-Payo, et al.
Haematologica|April 23, 2026
Novel <i>KAT6B::NUTM2B</i> fusion oncogene in congenital acute myeloid leukemia and implications for menin inhibitor therapyRebecca K Voss, Wenqing Qi, La'Ron Browne, et al.
Haematologica|December 9, 2017
Constitutional <i>SAMD9L</i> mutations cause familial myelodysplastic syndrome and transient monosomy 7Victor B Pastor, Sushree S Sahoo, Jessica Boklan, et al.
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