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There are 28957 results for: content related to: Delayed onset congenital hypothyroidism in a patient with DUOX2 mutations and maternal iodine excess

  1. Pseudodominant inheritance in a family with nonautoimmune hypothyroidism due to biallelic DUOX2 mutations

    Clinical Endocrinology

    Volume 83, Issue 3, September 2015, Pages: 394–398, Kiyomi Abe, Satoshi Narumi, Ayuko S. Suwanai, Takashi Hamajima and Tomonobu Hasegawa

    Article first published online : 7 NOV 2014, DOI: 10.1111/cen.12622

  2. You have free access to this content
    Compound heterozygosity for a novel hemizygous missense mutation and a partial deletion affecting the catalytic core of the H2O2-generating enzyme DUOX2 associated with transient congenital hypothyroidism

    Human Mutation

    Volume 31, Issue 4, April 2010, Pages: E1304–E1319, Candice Hoste, Sabrina Rigutto, Guy Van Vliet, Françoise Miot and Xavier De Deken

    Article first published online : 25 FEB 2010, DOI: 10.1002/humu.21227

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    Persistent mild hypothyroidism associated with novel sequence variants of the DUOX2 gene in two siblings

    Human Mutation

    Volume 26, Issue 4, October 2005, Page: 395, Maria Cristina Vigone, Laura Fugazzola, Ilaria Zamproni, Arianna Passoni, Stefania Di Candia, Giuseppe Chiumello, Luca Persani and Giovanna Weber

    Article first published online : 30 AUG 2005, DOI: 10.1002/humu.9372

  4. Genotypes and phenotypes of congenital goitre and hypothyroidism caused by mutations in dual oxidase 2 genes

    Clinical Endocrinology

    Volume 81, Issue 3, September 2014, Pages: 452–457, Fang Wang, Kunna Lu, Zhifeng Yang, Shasha Zhang, Wei Lu, Liqin Zhang, Shiguo Liu and Shengli Yan

    Article first published online : 19 MAY 2014, DOI: 10.1111/cen.12469

  5. Expression of dual oxidases and secreted cytokines in chronic rhinosinusitis

    International Forum of Allergy & Rhinology

    Volume 3, Issue 5, May 2013, Pages: 376–383, Do-Yeon Cho, Jayakar V. Nayak, Dawn T. Bravo, Wei Le, Alan Nguyen, Justin A. Edward, Peter H. Hwang, Beate Illek and Horst Fischer

    Article first published online : 21 DEC 2012, DOI: 10.1002/alr.21133

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    Structure, regulation and evolution of Nox-family NADPH oxidases that produce reactive oxygen species

    FEBS Journal

    Volume 275, Issue 13, July 2008, Pages: 3249–3277, Hideki Sumimoto

    Article first published online : 28 JUN 2008, DOI: 10.1111/j.1742-4658.2008.06488.x

    Corrected by:


    Vol. 275, Issue 15, 3984, Article first published online: 11 JUL 2008

  7. Thyroid Dysfunction: Molecular Genetics

    Standard Article


    Marian Ludgate and Dagmar Fuhrer

    Published Online : 27 JAN 2006, DOI: 10.1038/npg.els.0006176

  8. The Thyroid

    Brook's Clinical Pediatric Endocrinology, Sixth Edition

    Charles G. D. Brook, Peter E. Clayton, Rosalind S. Brown, Pages: 250–282, 2010

    Published Online : 20 JUN 2010, DOI: 10.1002/9781444316728.ch12

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    Roles of Nox1 and other Nox isoforms in cancer development

    Cancer Science

    Volume 100, Issue 8, August 2009, Pages: 1382–1388, Tohru Kamata

    Article first published online : 4 MAY 2009, DOI: 10.1111/j.1349-7006.2009.01207.x

  10. Congenital hypothyroidism caused by new mutations in the thyroid oxidase 2 (THOX2) gene

    Clinical Endocrinology

    Volume 65, Issue 6, December 2006, Pages: 810–815, Nicole Pfarr, Eckhard Korsch, Stefan Kaspers, Antje Herbst, Armin Stach, Claudia Zimmer and Joachim Pohlenz

    Article first published online : 8 SEP 2006, DOI: 10.1111/j.1365-2265.2006.02672.x

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    Roflumilast N-oxide, a PDE4 inhibitor, improves cilia motility and ciliated human bronchial epithelial cells compromised by cigarette smoke in vitro

    British Journal of Pharmacology

    Volume 166, Issue 8, August 2012, Pages: 2243–2262, J Milara, M Armengot, P Bañuls, H Tenor, Rolf Beume, E Artigues and J Cortijo

    Article first published online : 24 JUL 2012, DOI: 10.1111/j.1476-5381.2012.01929.x

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    Genetic evidence that thyroid hormone is indispensable for prepubertal insulin-like growth factor–I expression and bone acquisition in mice

    Journal of Bone and Mineral Research

    Volume 27, Issue 5, May 2012, Pages: 1067–1079, Weirong Xing, Kristen E Govoni, Leah Rae Donahue, Chandrasekhar Kesavan, Jon Wergedal, Carlin Long, JH Duncan Bassett, Apostolos Gogakos, Anna Wojcicka, Graham R Williams and Subburaman Mohan

    Article first published online : 18 APR 2012, DOI: 10.1002/jbmr.1551

  13. Dual oxidase 2 is essential for house dust mite-induced pro-inflammatory cytokine production in human keratinocytes

    Experimental Dermatology

    Volume 24, Issue 12, December 2015, Pages: 936–941, Eunbi Ko, Hyun Choi, Kkot-Nara Park, Ju-Yearl Park, Tae Ryong Lee, Dong Wook Shin and Yun Soo Bae

    Article first published online : 21 AUG 2015, DOI: 10.1111/exd.12808

  14. Two compound heterozygous mutations (c.215delA/c.2422T[RIGHTWARDS ARROW]C and c.387delC/c.1159G[RIGHTWARDS ARROW]A) in the thyroid peroxidase gene responsible for congenital goitre and iodide organification defect

    Clinical Endocrinology

    Volume 67, Issue 2, August 2007, Pages: 238–246, Carina M. Rivolta, Mariana Louis-Tisserand, Viviana Varela, Laura Gruñeiro-Papendieck, Ana Chiesa, Rogelio González-Sarmiento and Héctor M. Targovnik

    Article first published online : 15 APR 2007, DOI: 10.1111/j.1365-2265.2007.02869.x

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    Prostaglandin pathways in duodenal chemosensing

    Journal of Gastroenterology and Hepatology

    Volume 29, Issue S4, December 2014, Pages: 93–98, Yasutada Akiba and Jonathan D Kaunitz

    Article first published online : 18 DEC 2014, DOI: 10.1111/jgh.12731

  16. Congenital goitrous hypothyroidism: mutation analysis in the thyroid peroxidase gene

    Clinical Endocrinology

    Volume 76, Issue 4, April 2012, Pages: 568–576, Fiorella S. Belforte, Mirta B. Miras, María C. Olcese, Gabriela Sobrero, Graciela Testa, Liliana Muñoz, Laura Gruñeiro-Papendieck, Ana Chiesa, Rogelio González-Sarmiento, Héctor M. Targovnik and Carina M. Rivolta

    Article first published online : 7 MAR 2012, DOI: 10.1111/j.1365-2265.2011.04249.x

  17. Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community

    Clinical Endocrinology

    Volume 79, Issue 2, August 2013, Pages: 275–281, Hakan Cangul, Zehra Aycan, Alvaro Olivera-Nappa, Halil Saglam, Nadia A. Schoenmakers, Kristien Boelaert, Semra Cetinkaya, Omer Tarim, Ece Bober, Feyza Darendeliler, Veysel Bas, Korcan Demir, Banu K. Aydin, Michaela Kendall, Trevor Cole, Wolfgang Högler, V. Krishna K. Chatterjee, Timothy G. Barrett and Eamonn R. Maher

    Article first published online : 6 MAY 2013, DOI: 10.1111/cen.12127

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    Published Only

    Journal of Digestive Diseases

    Volume 16, Issue S1, September 2015, Pages: 29–146,

    Article first published online : 31 AUG 2015, DOI: 10.1111/1751-2980.12277

  19. Thyrotrophin-blocking antibodies in congenital hypothyroidism

    Journal of Paediatrics and Child Health

    Volume 28, Issue 1, February 1992, Pages: 50–53, A. W. C. KUNG and L. C. K. LOW

    Article first published online : 10 MAR 2008, DOI: 10.1111/j.1440-1754.1992.tb02617.x

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    Limited concentration of RecA delays DNA double-strand break repair in Deinococcus radiodurans R1

    Molecular Microbiology

    Volume 59, Issue 1, January 2006, Pages: 338–349, Edmond Jolivet, François Lecointe, Geneviève Coste, Katsuya Satoh, Issay Narumi, Adriana Bailone and Suzanne Sommer

    Article first published online : 15 NOV 2005, DOI: 10.1111/j.1365-2958.2005.04946.x