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Clinical Endocrinology|October 30, 2013
Three noninvasive methods in the evaluation of subclinical cardiovascular disease in patients with acromegaly: epicardial fat thickness, aortic stiffness and serum cell adhesion moleculesOya Topaloglu, Muyesser Sayki Arslan, Osman Turak, et al.
Thescientificworldjournal|February 6, 2015
Isolated vitamin D deficiency is not associated with nonthyroidal illness syndrome, but with thyroid autoimmunityMuyesser Sayki Arslan, Oya Topaloglu, Bekir Ucan, et al.
Endocrine Research|May 14, 2015
The relationship between cytotoxin-associated gene A positive Helicobacter pylori infection and autoimmune thyroid diseaseMuyesser Sayki Arslan, Fuat Ekiz, Murat Deveci, et al.
Pediatric Neurology|August 3, 2021
Epilepsy Is Heterogeneous in Early-Life Tuberous Sclerosis ComplexS Katie Z Ihnen, Jamie K Capal, Paul S Horn, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 31, 2015
The Stress-Induced Atf3-Gelsolin Cascade Underlies Dendritic Spine Deficits in Neuronal Models of Tuberous Sclerosis ComplexDuyu Nie, Zehua Chen, Darius Ebrahimi-Fakhari, et al.
Pediatric Neurology|October 4, 2020
Epilepsy Risk Prediction Model for Patients With Tuberous Sclerosis ComplexLaura S Farach, Melissa A Richard, Philip J Lupo, et al.
American Journal of Medical Genetics. Part A|August 23, 2021
Toward better characterization of restricted and repetitive behaviors in individuals with germline heterozygous PTEN mutationsMirko Uljarević, Thomas W Frazier, Gaëlle Rached, et al.
Cell|May 19, 2015
The Circadian Protein BMAL1 Regulates Translation in Response to S6K1-Mediated PhosphorylationJonathan O Lipton, Elizabeth D Yuan, Lara M Boyle, et al.
Case Reports in Endocrinology|November 7, 2013
Solitary fibrous tumor of neck mimicking cold thyroid nodule in 99m tc thyroid scintigraphyOya Topaloglu, Bekir Ucan, Taner Demirci, et al.
Molecular Autism|January 29, 2021
Cross-level analysis of molecular and neurobehavioral function in a prospective series of patients with germline heterozygous PTEN mutations with and without autismThomas W Frazier, Ritika Jaini, Robyn M Busch, et al.
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