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Molecular Cancer Research : MCR|December 31, 2014
A vascular model of Tsc1 deficiency accelerates renal tumor formation with accompanying hemangiosarcomasJarrett D Leech, Stephen H T Lammers, Sam Goldman, et al.
Neurology. Genetics|February 8, 2021
Blended Phenotype of Silver-Russell Syndrome and SPG50 Caused by Maternal Isodisomy of Chromosome 7Marvin Ziegler, Bianca E Russell, Kathrin Eberhardt, et al.
Archives of Endocrinology and Metabolism|May 1, 2015
The association of autoimmune thyroiditis and non-functional adrenal incidentalomas with insulin resistanceMelia Karakose, Basak Karbek, Mustafa Sahin, et al.
Annali Italiani Di Chirurgia|April 10, 2018
Does digestive symptoms require esophago gastroscopy prior to bariatric procedure? Assessment of 6 years' experienceSerdar Yormaz, Kafali Yilmaz, Husnu Alptekin, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 25, 2007
A mouse model of tuberous sclerosis: neuronal loss of Tsc1 causes dysplastic and ectopic neurons, reduced myelination, seizure activity, and limited survivalLynsey Meikle, Delia M Talos, Hiroaki Onda, et al.
Journal of Clinical Medicine|February 27, 2026
Cancer Risk in Patients with Acromegaly: Insights from a Single Center in AnkaraMurat Cinel, Ozgur Demir, Rovsan Hasenov, et al.
Pediatric Neurology|December 7, 2016
Somatic GNAQ Mutation is Enriched in Brain Endothelial Cells in Sturge-Weber SyndromeLan Huang, Javier A Couto, Anna Pinto, et al.
Chemistry & Biodiversity|August 1, 2019
Metabolite Profiling by Hyphenated Liquid Chromatographic Mass Spectrometric Technique (HPLC-DAD-ESI-Q-TOF-MS/MS) and Neurobiological Potential of Haplophyllum sahinii and H. vulcanicum ExtractsEsengul Karahisar, Osman Tugay, Ilkay Erdogan Orhan, et al.
Clinical Endocrinology|April 5, 2013
Hyperprolactinaemia associated with increased thyroid volume and autoimmune thyroiditis in patients with prolactinomaMuyesser Sayki Arslan, Mustafa Sahin, Oya Topaloglu, et al.
Stem Cell Research|June 5, 2021
Generation and characterization of six human induced pluripotent stem cell lines (iPSC) from three families with AP4M1-associated hereditary spastic paraplegia (SPG50)Kathrin Eberhardt, Hellen Jumo, Angelica D'Amore, et al.
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