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Journal of Medical Genetics|July 26, 2011
Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene in patients with a non-classic phenotypeAhmed Alfares, Laura Dempsey Nunez, Khalid Al-Thihli, et al.Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|June 7, 2019
A STRATIFIED CROSS-SECTIONAL CLUSTER MODEL SURVEY OF IODINE NUTRITION IN ARMENIA AFTER A DECADE OF UNIVERSAL SALT IODIZATIONNicholas Hutchings, Elena Aghajanova, Sisak Baghdasaryan, et al.Journal of Systems and Integrative Neuroscience|January 31, 2022
Induction of homeostatic biological parameters in reward deficiency as a function of an iron-free multi-nutrient complex: Promoting hemoglobinization, aerobic metabolism, viral immuno-competence, and neuroinflammatory regulationKenneth Blum, Bernard W Downs, Manashi Bagchi, et al.Proceedings of the National Academy of Sciences of the United States of America|May 23, 2007
Oncogenic inhibition by a deleted in liver cancer gene requires cooperation between tensin binding and Rho-specific GTPase-activating protein activitiesXiaolan Qian, Guorong Li, Holly K Asmussen, et al.Journal of Applied Genetics|February 11, 2010
Rhizomelic chondrodysplasia punctata type 1: report of mutations in 3 children from IndiaS R Phadke, N Gupta, K M Girisha, et al.Clinical Endocrinology|June 9, 2007
Clinical features of thyroid autoimmunity are associated with thyroiditis on histology and are not predictive of malignancy in 570 patients with indeterminate nodules on cytology who had a thyroidectomyT Rago, G Di Coscio, C Ugolini, et al.Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|November 29, 2012
Iodine nutrition during pregnancy in Toronto, CanadaPamela M Katz, Angela M Leung, Lewis E Braverman, et al.CPQ Neurology and Psychology|February 22, 2023
How to Combat the Global Opioid CrisisCatherine Dennen A, Kenneth Blum, Eric Braverman R, et al.Neurogenetics|June 22, 2014
A homozygous mutation in the NDUFS1 gene presents with a mild cavitating leukoencephalopathyAlireza Kashani, Isabelle Thiffault, Marie-Emmanuelle Dilenge, et al.Blood Advances|May 29, 2024
AMPK drives both glycolytic and oxidative metabolism in murine and human T cells during graft-versus-host diseaseArchana Ramgopal, Erica L Braverman, Lee-Kai Sun, et al.Pageof 166