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Brain Pathology (Zurich, Switzerland)|December 18, 2024
Molecular profile of adult primary leptomeningeal gliomatosis aligns with glioblastoma, IDH-wildtypeYi Zhu, Darin D Carabenciov, Derek R Johnson, et al.
European Journal of Medical Genetics|November 4, 2022
Intrafamilial phenotypic variability in autosomal recessive DOCK6-related Adams-Oliver syndromeLuz Consuelo Zepeda-Romero, Martin Zenker, Denny Schanze, et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|November 5, 2025
Maternal RSV vaccination for infant protection: A systematic review and meta-analysis of phase 3 trials with an integrated economic evaluationJohnatan Torres-Torres, Lourdes Rojas-Zepeda, José Rafael Villafan-Bernal, et al.
Nature|October 27, 2017
In situ X-ray diffraction measurement of shock-wave-driven twinning and lattice dynamicsC E Wehrenberg, D McGonegle, C Bolme, et al.
Cureus|May 6, 2026
Atypical Presentation of a Malignant Tumor of the Appendix: A Case ReportMaria H Garcia Ramírez, Jose M Zepeda Torres, Luis O Suárez Carreón, et al.
Haematologica|May 14, 2026
CSF3R-mutated chronic neutrophilic leukemia: a two-center study of 44 consecutive patientsAbiola B Bolarinwa, Natasha Szuber, Janick Caron-Lecuyer, et al.
Ambio|November 2, 2021
Between uncertainty and hope: Young leaders as agents of change in sustainable small-scale fisheriesAlejandro Espinoza-Tenorio, Romana Gabriela Ehuan-Noh, Gabriela Alejandra Cuevas-Gómez, et al.
Stem Cell Research & Therapy|July 4, 2026
Identification and enrichment of human retinal organoid-derived red/green cone-competent precursors with enhanced axon dynamicsPraveen J Susaimanickam, Elizabeth Capowski, Mai N Xiong, et al.
European Journal of Human Genetics : EJHG|July 7, 2016
Estrogen-related receptor gamma implicated in a phenotype including hearing loss and mild developmental delaySamantha Lp Schilit, Benjamin B Currall, Ruen Yao, et al.
Molecular Syndromology|April 17, 2023
First Report of Mexican Patients with PACS1-Related Neurodevelopmental Disorder and Review of the PACS1-, PACS2-, and WDR37-Related Ophthalmological ManifestationsJorge Román Corona-Rivera, Juan Carlos Zenteno, Leopoldo Gildardo López-Pérez, et al.
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