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European Radiology|September 1, 2021
Correlation of liver enhancement in gadoxetic acid-enhanced MRI with liver functions: a multicenter-multivendor analysis of hepatocellular carcinoma patients from SORAMIC trialOsman Öcal, Bora Peynircioglu, Christian Loewe, et al.
Cell Host & Microbe|August 8, 2025
Metatranscriptomics Uncover Diurnal Functional Shifts in Bacterial Transgenes with Profound Metabolic EffectsStephany Flores Ramos, Nicole Siguenza, Wuling Zhong, et al.
European Radiology|August 7, 2019
Consensus report from the 8th International Forum for Liver Magnetic Resonance ImagingChristoph J Zech, Ahmed Ba-Ssalamah, Thomas Berg, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|December 3, 2014
Pilot randomized trial of selective internal radiation therapy vs. chemoembolization in unresectable hepatocellular carcinomaFrank T Kolligs, Jose I Bilbao, Tobias Jakobs, et al.
Cytogenetic and Genome Research|March 19, 2020
A Case of Trisomy 13 Mosaicism Presenting with a Severe Aortic Root Dilatation and Marfanoid Habitus due to an Unpredictable Cytogenetic MechanismPauline Monin, Nicolas Reynaud, Nadine Hanna, et al.
Brain : a Journal of Neurology|March 2, 2023
Variants in ATP5F1B are associated with dominantly inherited dystoniaAlessia Nasca, Niccolò E Mencacci, Federica Invernizzi, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 30, 2021
Collagen VI Regulates Motor Circuit Plasticity and Motor Performance by Cannabinoid ModulationDaniel D Lam, Rhîannan H Williams, Ernesto Lujan, et al.
Memorias Do Instituto Oswaldo Cruz|November 30, 2011
Immunostimulatory property of a synthetic peptide belonging to the soluble ATP diphosphohydrolase isoform (SmATPDase 2) and immunolocalisation of this protein in the Schistosoma mansoni eggRita Gabriela Pedrosa Ribeiro Mendes, Michélia Antônia do Nascimento Gusmão, Ana Carolina Ribeiro Gomes Maia, et al.
Clinical Genetics|March 20, 2026
Expanding the Phenotypic Spectrum of the Recurrent De Novo FBXO31 p.Asp334Asn Variant: Evidence for a Novel Neurodevelopmental Disorder (Kruer Syndrome)Carolina I Galaz-Montoya, Sara A Lewis, Maureen K Galindo, et al.
Parkinsonism & Related Disorders|July 7, 2020
Recessive null-allele variants in MAG associated with spastic ataxia, nystagmus, neuropathy, and dystoniaMichael Zech, Theresa Brunet, Matej Škorvánek, et al.
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