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170 related items for PubMed ID: 22435912

  • 1. Minimally invasive follicular thyroid carcinoma developed in dyshormonogenetic multinodular goiter due to thyroid peroxidase gene mutation.
    Chertok Shacham E, Ishay A, Irit E, Pohlenz J, Tenenbaum-Rakover Y.
    Thyroid; 2012 May; 22(5):542-6. PubMed ID: 22435912
    [Abstract] [Full Text] [Related]

  • 2. Minimal Invasive Follicular Thyroid Carcinoma Developed in Dyshormonogenetic Multinodular Goiter Due to Thyroid Peroxidase Gene Mutation.
    Rakover YT, Chertok Shacham E, Ishay A, Elmalah I, Joachim P.
    Thyroid; 2012 Jan 19. PubMed ID: 22260524
    [Abstract] [Full Text] [Related]

  • 3. Congenital primary hypothyroidism with subsequent adenomatous goiter in a Turkish patient caused by a homozygous 10-bp deletion in the thyroid peroxidase (TPO) gene.
    Pfarr N, Musholt TJ, Musholt PB, Brzezinska R, Pohlenz J.
    Clin Endocrinol (Oxf); 2006 May 19; 64(5):514-8. PubMed ID: 16649969
    [Abstract] [Full Text] [Related]

  • 4. Mitotically Active Follicular Nodule in Early Childhood: A Case Report with a Novel Mutation in the Thyroglobulin Gene.
    Kızılcan Çetin S, Aycan Z, Şıklar Z, Dizbay Sak S, Ceylaner S, Özsu E, Berberoğlu M.
    J Clin Res Pediatr Endocrinol; 2024 Sep 05; 16(3):340-343. PubMed ID: 36453602
    [Abstract] [Full Text] [Related]

  • 5. New mutations in the RET protooncogene-L881V - associated with medullary thyroid carcinoma and -R770Q - in a patient with mixed medullar/follicular thyroid tumour.
    Frank-Raue K, Döhring J, Scheumann G, Rondot S, Lorenz A, Schulze E, Dralle H, Raue F, Leidig-Bruckner G.
    Exp Clin Endocrinol Diabetes; 2010 Aug 05; 118(8):550-3. PubMed ID: 20013610
    [Abstract] [Full Text] [Related]

  • 6. Case Report: Functional Analysis and Neuropsychological Evaluation of Dyshormonogenetic Fetal Goiter in Siblings Caused by Novel Compound Hyterozygous TPO Gene Mutations.
    Rodrigues TMB, Silva MMDC, Freitas MM, Duarte ZMC, Frutuoso VS, Rodrigues MT, Rubio IGS.
    Front Endocrinol (Lausanne); 2021 Aug 05; 12():671659. PubMed ID: 34220711
    [Abstract] [Full Text] [Related]

  • 7. Metastatic thyroid carcinoma arising from congenital goiter due to mutation in the thyroperoxidase gene.
    Medeiros-Neto G, Gil-Da-Costa MJ, Santos CL, Medina AM, Silva JC, Tsou RM, Sobrinho-Simões M.
    J Clin Endocrinol Metab; 1998 Nov 05; 83(11):4162-6. PubMed ID: 9814507
    [Abstract] [Full Text] [Related]

  • 8. Clinical and genetic characteristics of congenital hypothyroidism due to mutations in the thyroid peroxidase (TPO) gene in Israelis.
    Tenenbaum-Rakover Y, Mamanasiri S, Ris-Stalpers C, German A, Sack J, Allon-Shalev S, Pohlenz J, Refetoff S.
    Clin Endocrinol (Oxf); 2007 May 05; 66(5):695-702. PubMed ID: 17381485
    [Abstract] [Full Text] [Related]

  • 9. Dissociation of thyrotropin-dependent enzyme activities, reduced iodide transport, and preserved iodide organification in nonfunctioning thyroid adenoma and multinodular goiter.
    Masini-Repiso AM, Cabanillas AM, Bonaterra M, Coleoni AH.
    J Clin Endocrinol Metab; 1994 Jul 05; 79(1):39-44. PubMed ID: 8027249
    [Abstract] [Full Text] [Related]

  • 10. A germline mutation (A339V) in thyroid transcription factor-1 (TITF-1/NKX2.1) in patients with multinodular goiter and papillary thyroid carcinoma.
    Ngan ES, Lang BH, Liu T, Shum CK, So MT, Lau DK, Leon TY, Cherny SS, Tsai SY, Lo CY, Khoo US, Tam PK, Garcia-Barceló MM.
    J Natl Cancer Inst; 2009 Feb 04; 101(3):162-75. PubMed ID: 19176457
    [Abstract] [Full Text] [Related]

  • 11. Toxic multinodular goitre in a patient with generalized resistance to thyroid hormone who harbours the R429Q mutation in the thyroid hormone receptor beta gene.
    Taniyama M, Ishikawa N, Momotani N, Ito K, Ban Y.
    Clin Endocrinol (Oxf); 2001 Jan 04; 54(1):121-4. PubMed ID: 11167935
    [Abstract] [Full Text] [Related]

  • 12. A Novel Mutation in Thyroid Peroxidase Gene Causing Congenital Goitrous Hypothyroidism in a German-Thai Patient.
    Sriphrapradang C, Thewjitcharoen Y, Chanprasertyothin S, Nakasatien S, Himathongkam T, Trachoo O.
    J Clin Res Pediatr Endocrinol; 2016 Jun 05; 8(2):241-5. PubMed ID: 26761947
    [Abstract] [Full Text] [Related]

  • 13. Defective organification of iodide causing congenital goitrous hypothyroidism.
    Ishikawa N, Eguchi K, Ohmori T, Momotani N, Nagayama Y, Hosoya T, Oguchi H, Mimura T, Kimura S, Nagataki S, Ito K.
    J Clin Endocrinol Metab; 1996 Jan 05; 81(1):376-83. PubMed ID: 8550781
    [Abstract] [Full Text] [Related]

  • 14. Aggressive metastatic follicular thyroid carcinoma with anaplastic transformation arising from a long-standing goiter in a patient with Pendred's syndrome.
    Camargo R, Limbert E, Gillam M, Henriques MM, Fernandes C, Catarino AL, Soares J, Alves VA, Kopp P, Medeiros-Neto G.
    Thyroid; 2001 Oct 05; 11(10):981-8. PubMed ID: 11716048
    [Abstract] [Full Text] [Related]

  • 15. Long-Term Outcome of Patients with TPO Mutations.
    Tobias L, Elias-Assad G, Khayat M, Admoni O, Almashanu S, Tenenbaum-Rakover Y.
    J Clin Med; 2021 Aug 30; 10(17):. PubMed ID: 34501348
    [Abstract] [Full Text] [Related]

  • 16. Evaluation and management of multinodular goiter.
    Hurley DL, Gharib H.
    Otolaryngol Clin North Am; 1996 Aug 30; 29(4):527-40. PubMed ID: 8844728
    [Abstract] [Full Text] [Related]

  • 17. Biallelic p.R2223H mutation in the thyroglobulin gene causes thyroglobulin retention and severe hypothyroidism with subsequent development of thyroid carcinoma.
    Raef H, Al-Rijjal R, Al-Shehri S, Zou M, Al-Mana H, Baitei EY, Parhar RS, Al-Mohanna FA, Shi Y.
    J Clin Endocrinol Metab; 2010 Mar 30; 95(3):1000-6. PubMed ID: 20089614
    [Abstract] [Full Text] [Related]

  • 18. TPO gene mutations associated with thyroid carcinoma: Case report and literature review.
    Zhu H, Peng YG, Ma SG, Liu H.
    Cancer Biomark; 2015 Mar 30; 15(6):909-13. PubMed ID: 26406404
    [Abstract] [Full Text] [Related]

  • 19. Thyroidectomy in a patient with multinodular dyshormonogenetic goitre--a case of Pendred syndrome confirmed by mutations in the PDS/SLC26A4 gene.
    Banghova K, Cinek O, Al Taji E, Zapletalova J, Vidura R, Lebl J.
    J Pediatr Endocrinol Metab; 2008 Dec 30; 21(12):1179-84. PubMed ID: 19189692
    [Abstract] [Full Text] [Related]

  • 20. Quantification of Thyroid Cancer and Multinodular Goiter Risk in the DICER1 Syndrome: A Family-Based Cohort Study.
    Khan NE, Bauer AJ, Schultz KAP, Doros L, Decastro RM, Ling A, Lodish MB, Harney LA, Kase RG, Carr AG, Rossi CT, Field A, Harris AK, Williams GM, Dehner LP, Messinger YH, Hill DA, Stewart DR.
    J Clin Endocrinol Metab; 2017 May 01; 102(5):1614-1622. PubMed ID: 28323992
    [Abstract] [Full Text] [Related]

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