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There are 16927 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

    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. Thyroid function abnormalities among first-degree relatives of Iranian congenital hypothyroidism neonates

    Pediatrics International

    Volume 52, Issue 3, June 2010, Pages: 467–471, Mahin Hashemipour, Nasibeh Hasani, Masood Amini, Kamal Heidari, Ali Sajadi, Masoomeh Dastanpour, Ali Ajami, Silva Hovsepian, Ashraf Aminorroaya, Bahar Dehghan and Roya Kelishadi

    Article first published online : 3 DEC 2009, DOI: 10.1111/j.1442-200X.2009.03016.x

  3. 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

  5. Diagnostic spectrum of congenital hypothyroidism in Turkish children

    Pediatrics International

    Volume 51, Issue 4, August 2009, Pages: 464–468, Müge Tamam, Isık Adalet, Barış Bakır, Cüneyt Türkmen, Feyza Darendeliler, Firdevs Baş, Yasemin Sanlı and Serkan Kuyumcu

    Article first published online : 23 JUL 2009, DOI: 10.1111/j.1442-200X.2008.02790.x

  6. 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

  7. You have free access to this content
    PprA: a novel protein from Deinococcus radiodurans that stimulates DNA ligation

    Molecular Microbiology

    Volume 54, Issue 1, October 2004, Pages: 278–285, Issay Narumi, Katsuya Satoh, Suzhen Cui, Tomoo Funayama, Shigeru Kitayama and Hiroshi Watanabe

    Article first published online : 3 AUG 2004, DOI: 10.1111/j.1365-2958.2004.04272.x

  8. Incidence of iodine deficiency in Turkish patients with congenital hypothyroidism

    Pediatrics International

    Volume 50, Issue 3, June 2008, Pages: 276–280, Olcay Evliyaoğlu, 1 Alev Kutlu, 2 Cengiz Kara and 2 Sevil G. Atavci 3

    Article first published online : 29 MAY 2008, DOI: 10.1111/j.1442-200X.2008.02569.x

  9. The role of scintigraphy and ultrasound in the imaging of neonatal hypothyroidism: 5-year retrospective review of single-centre experience

    Journal of Medical Imaging and Radiation Oncology

    Volume 58, Issue 4, August 2014, Pages: 422–430, Ami De Silva, Ian Jong, Glenda McLean, Philip Bergman, Christina Rodda, Justin Brown and Dee Nandurkar

    Article first published online : 20 MAR 2014, DOI: 10.1111/1754-9485.12166

  10. Dyshormonogenetic goiter-like changes in a child with congenital hypothyroidism and a euthyroid adult

    Diagnostic Cytopathology

    Volume 41, Issue 8, August 2013, Pages: 720–724, Kyle D. Perry, Jason Hope and Jack Yang

    Article first published online : 23 FEB 2012, DOI: 10.1002/dc.21861

  11. Congenital hypothyroidism and dysmaturity syndrome in foals: First reported cases in Europe

    Equine Veterinary Education

    Volume 26, Issue 4, April 2014, Pages: 181–189, K. Koikkalainen, A. Knuuttila, N. Karikoski, P. Syrjä and M. Hewetson

    Article first published online : 13 FEB 2014, DOI: 10.1111/eve.12124

  12. 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

  13. 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

  14. Contributions of bone maturation measurements to the differential diagnosis of neonatal transient hypothyroidism versus dyshormonogenetic congenital hypothyroidism

    Acta Paediatrica

    Volume 93, Issue 10, October 2004, Pages: 1301–1306, DM Niu, B Hwang, CM Tiu, LP Tsai, JL Yen, NC Lee and CY Lin

    Article first published online : 2 JAN 2007, DOI: 10.1111/j.1651-2227.2004.tb02927.x

  15. 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

  16. EFFECTS OF NOREPINEPHRINE ON THE MORPHOLOGY AND SOME ENZYME ACTIVITIES OF PRIMARY MONOLAYER CULTURES FROM RAT BRAIN

    Journal of Neurochemistry

    Volume 31, Issue 6, December 1978, Pages: 1479–1490, S. Narumi, H. K. Kimelberg and R. S. Bourke

    Article first published online : 5 OCT 2006, DOI: 10.1111/j.1471-4159.1978.tb06575.x

  17. Stimulation of Carbonic Anhydrase Activity and Phosphorylation in Primary Astroglial Cultures by Norepinephrine

    Journal of Neurochemistry

    Volume 34, Issue 4, April 1980, Pages: 873–879, G. A. Church, H. K. Kimelberg and V. S. Sapirstein

    Article first published online : 5 OCT 2006, DOI: 10.1111/j.1471-4159.1980.tb09660.x

  18. Morphological abnormalities in children with thyroidal congenital hypothyroidism

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 5, May 2009, Pages: 943–951, Marlies J.E. Kempers, Heval M. Ozgen, Thomas Vulsma, Johannes H. Merks, Koos H. Zwinderman, Jan J.M. de Vijlder and Raoul C.M. Hennekam

    Article first published online : 14 APR 2009, DOI: 10.1002/ajmg.a.32777

  19. Neonatal screening for congenital hypothyroidism in West Black Sea area, Turkey

    International Journal of Clinical Practice

    Volume 59, Issue 3, March 2005, Pages: 336–341, E. Simsek, M. Karabay and K. Kocabay

    Article first published online : 6 OCT 2004, DOI: 10.1111/j.1742-1241.2004.00222.x

  20. CONGENITAL PRIMARY HYPOTHYROIDISM AND HLA

    Acta Paediatrica

    Volume 71, Issue 6, November 1982, Pages: 919–922, B. BROCK JACOBSEN, N. J. BRANDT and A. SVEJGAARD

    Article first published online : 21 JAN 2008, DOI: 10.1111/j.1651-2227.1982.tb09549.x