Works matching DE "GOITER"

Results: 1664
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    Clinical Characteristics and Genotype-phenotype Correlation in Turkish Patients with a Diagnosis of Resistance to Thyroid Hormone Beta.

    Published in:
    Journal of Clinical Research in Pediatric Endocrinology, 2025, v. 17, n. 2, p. 191, doi. 10.4274/jcrpe.galenos.2024.2024-8-14
    By:
    • Büyükyılmaz, Gönül;
    • Çavdarlı, Büşranur;
    • Koca, Serkan Bilge;
    • Adıgüzel, Keziban Toksoy;
    • Topaloğlu, Oya;
    • Aydın, Cevdet;
    • Hepşen, Sema;
    • Çakal, Erman;
    • Gündüz, Nur Semerci;
    • Boyraz, Mehmet;
    • Gürbüz, Fatih;
    • Demirbilek, Hüseyin
    Publication type:
    Article
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    Evaluation of clinical, biohumoral, and morphological findings of the thyroid gland as possible predictors of risk for cancer in patients with atoxic nodular and multinodular goiter.

    Published in:
    Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2024, v. 81, n. 6, p. 348, doi. 10.2298/VSP231201019M
    By:
    • Malović, Dragana;
    • Dragović, Tamara;
    • Kiković, Saša;
    • Ristić, Petar;
    • Marinković, Dejan D.;
    • Djuran, Zorana;
    • Kuzmić-Janković, Snežana;
    • Jovanović, Stevan;
    • Rakočević, Jelena;
    • Hajduković, Zoran
    Publication type:
    Article
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    Enormous Disfiguring Thyroid Swelling.

    Published in:
    Indian Journal of Surgery, 2010, v. 72, n. 5, p. 414, doi. 10.1007/s12262-010-0139-8
    By:
    • Chakravartty, Saurav;
    • Maiti, Krishnendu
    Publication type:
    Article
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    Amyloid goitre: A rare case report.

    Published in:
    Indian Journal of Surgery, 2006, v. 68, n. 2, p. 104
    By:
    • Khullar, R.;
    • Sharma, A.;
    • Goel, A.;
    • Bagchi, N.;
    • Soni, V.;
    • Baijal, M.;
    • Chowbey, P. K.
    Publication type:
    Article
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    Five novel inactivating mutations in the thyroid peroxidase gene responsible for congenital goiter and iodide organification defect (Communicated by Mark H. Paalman) Online Citation: Human Mutation, Mutation in Brief #646 (2003) Online http://www.interscience.wiley.com/humanmutation/pdf/mutation/646.pdf)

    Published in:
    Human Mutation, 2003, v. 22, n. 3, p. 259, doi. 10.1002/humu.9175
    By:
    • Carina M. Rivolta;
    • Sebastián A. Esperante;
    • Laura Gruñeiro-Papendieck;
    • Ana Chiesa;
    • Christian M. Moya;
    • Sabina Domené;
    • Viviana Varela;
    • Héctor M. Targovnik
    Publication type:
    Article
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    Five novel inactivating mutations in the thyroid peroxidase gene responsible for congenital goiter and iodide organification defectCommunicated by Mark H. PaalmanOnline Citation:Human Mutation, Mutation in Brief #646 (2003) Onlinehttp://www.interscience.wiley.com/humanmutation/pdf/mutation/646.pdf

    Published in:
    Human Mutation, 2003, v. 22, n. 3, p. 259, doi. 10.1002/humu.9175
    By:
    • Carina M. Rivolta;
    • Sebastián A. Esperante;
    • Laura Gruñeiro?Papendieck;
    • Ana Chiesa;
    • Christian M. Moya;
    • Sabina Domené;
    • Viviana Varela;
    • Héctor M. Targovnik
    Publication type:
    Article
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    Hoffmann’s Syndrome: A Case Report.

    Published in:
    Medical Principles & Practice, 2008, v. 17, n. 4, p. 346, doi. 10.1159/000129619
    By:
    • Tuncel, Deniz;
    • Cetinkaya, Ali;
    • Kaya, Berna;
    • Gokce, Mustafa
    Publication type:
    Article