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Scientific Reports|October 31, 2025
Real-world survival and prognostic factors in WHO 2021 classified gliomas treated with chemo-radiotherapyMateusz Bilski, Georges Noël, Krzysztof Smółka, et al.
American Journal of Obstetrics & Gynecology MFM|November 5, 2022
Longitudinal antibody response kinetics following SARS-CoV-2 messenger RNA vaccination in pregnant and nonpregnant personsMalavika Prabhu, Yawei J Yang, Carrie D Johnston, et al.
American Journal of Human Genetics|February 13, 2018
NDUFB8 Mutations Cause Mitochondrial Complex I Deficiency in Individuals with Leigh-like EncephalomyopathyDorota Piekutowska-Abramczuk, Zahra Assouline, Lavinija Mataković, et al.
Transplantation Proceedings|April 21, 2009
Effects of allopurinol on ischemia and reperfusion in rabbit liversM O Taha, M J Simões, E C Noguerol, et al.
American Journal of Human Genetics|October 11, 2011
Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulationMonika B Hartig, Arcangela Iuso, Tobias Haack, et al.
Transplantation Proceedings|April 21, 2009
l-Arginine supplementation protects against hepatic ischemia-reperfusion lesions in rabbitsM O Taha, M J Simões, M A Haddad, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 11, 2025
Characterization of plasma cell-free DNA variants as of tumor- or clonal hematopoiesis-origin in 16,812 advanced cancer patientsDaniel Magee, Valeriy Domenyuk, Jim Abraham, et al.
Brain : a Journal of Neurology|February 11, 2022
DNAJC30 defect: a frequent cause of recessive Leber hereditary optic neuropathy and Leigh syndromeSarah L Stenton, Marketa Tesarova, Natalia L Sheremet, et al.
Neurology|February 1, 2022
Association of Early MRI Characteristics With Subsequent Epilepsy and Neurodevelopmental Outcomes in Children With Tuberous Sclerosis ComplexHanna M Hulshof, Hugo J Kuijf, Katarzyna Kotulska, et al.
European Journal of Human Genetics : EJHG|September 27, 2018
Novel calcineurin A (PPP3CA) variant associated with epilepsy, constitutive enzyme activation and downregulation of protein expressionMałgorzata Rydzanicz, Małgorzata Wachowska, Erik C Cook, et al.
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