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Turkish Neurosurgery|March 5, 2019
Evaluation of the Effect of Daptomycin, a Glycopeptide Agent, on Intact Intervertebral Disc TissueNecati Kaplan, Ibrahim Yilmaz, Numan Karaarslan, et al.
Thyroid : Official Journal of the American Thyroid Association|December 31, 2010
Shared sporadic and somatic thyrotropin receptor mutations display more active in vitro activities than familial thyrotropin receptor mutationsJulia Lueblinghoff, Markus Eszlinger, Holger Jaeschke, et al.
Thyroid : Official Journal of the American Thyroid Association|May 7, 2005
Two novel mutations in the sixth transmembrane segment of the thyrotropin receptor gene causing hyperfunctioning thyroid nodulesHulya Gozu, Melike Avsar, Rifat Bircan, et al.
Thyroid : Official Journal of the American Thyroid Association|January 27, 2005
Does a Leu 512 Arg thyrotropin receptor mutation cause an autonomously functioning papillary carcinoma?Hulya Gozu, Melike Avsar, Rifat Bircan, et al.
Endocrine Journal|March 18, 2006
A case of McCune-Albright syndrome associated with Gs alpha mutation in the bone tissueHaluk Sargin, Hulya Gozu, Rifat Bircan, et al.
European Journal of Endocrinology|September 23, 2006
Similar prevalence of somatic TSH receptor and Gsalpha mutations in toxic thyroid nodules in geographical regions with different iodine supply in TurkeyHulya Iliksu Gozu, Rifat Bircan, Knut Krohn, et al.
Thyroid : Official Journal of the American Thyroid Association|April 15, 2020
Sensitive Sequencing Analysis Suggests Thyrotropin Receptor and Guanine Nucleotide-Binding Protein G Subunit Alpha as Sole Driver Mutations in Hot Thyroid NodulesAlexandra Stephenson, Markus Eszlinger, Paul Stewardson, et al.
Endokrynologia Polska|May 29, 2019
BRAF V600E mutation in papillary thyroid cancer is correlated with adverse clinicopathological features but not with iodine exposureSerhat Özçelik, Rifat Bircan, Şükran Sarıkaya, et al.
Thyroid : Official Journal of the American Thyroid Association|May 10, 2008
A new silent germline mutation of the TSH receptor: coexpression in a hyperthyroid family member with a second activating somatic mutationHulya Iliksu Gozu, Sandra Mueller, Rifat Bircan, et al.
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