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There are 2503188 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

    Version of Record online : 7 NOV 2014, DOI: 10.1111/cen.12622

  2. Missed congenital hypothyroidism in an identical twin

    Journal of Paediatrics and Child Health

    Volume 48, Issue 10, October 2012, Pages: 936–938, Anita Azam, Wayne Cutfield, Fran Mouat, Paul L Hofman, Craig Jefferies, Dianne Webster and Alistair Jan Gunn

    Version of Record online : 12 SEP 2012, DOI: 10.1111/j.1440-1754.2012.02554.x

  3. Measurement of thyroglobulin in newborn screening specimens from normal and hypothyroid infants

    Clinical Endocrinology

    Volume 42, Issue 5, May 1995, Pages: 523–527, M. L. Mitchell and R. J. Hermos

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1365-2265.1995.tb02672.x

  4. Integration of new genetic diseases into statewide newborn screening: New England experience

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 125C, Issue 1, 15 February 2004, Pages: 35–41, Anne Marie Comeau, Cecilia Larson and Roger B. Eaton

    Version of Record online : 14 JAN 2004, DOI: 10.1002/ajmg.c.30001

  5. The Thyroid and its Disorders

    Clinical Pediatric Endocrinology, Fifth Edition

    Rosalind S. Brown, Stephen Huang, Pages: 218–253, 2007

    Published Online : 4 OCT 2007, DOI: 10.1002/9780470987117.ch12

  6. The screening programme for congenital hypothyroidism in Greece: evidence of iodine deficiency in some areas of the country

    Acta Paediatrica

    Volume 83, Issue s394, March 1994, Pages: 47–51, C Mengreli, L Yiannakou and S Pantelakis

    Version of Record online : 21 JAN 2008, DOI: 10.1111/j.1651-2227.1994.tb13214.x

  7. Population study of congenital hypothyroidism and associated birth defects, Atlanta, 1979-1992

    American Journal of Medical Genetics

    Volume 71, Issue 1, 11 July 1997, Pages: 29–32, Helen E. Roberts, Cynthia A. Moore, Paul M. Fernhoff, Ann L. Brown and Muin J. Khoury

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19970711)71:1<29::AID-AJMG5>3.0.CO;2-L

  8. Quality of life of young adults with congenital hypothyroidism

    Pediatrics International

    Volume 51, Issue 1, February 2009, Pages: 126–131, Hirokazu Sato, 1,2 Nobue Nakamura, 3 Shohei Harada, 4 Naoko Kakee and 4 Nozomu Sasaki 2

    Version of Record online : 18 SEP 2008, DOI: 10.1111/j.1442-200X.2008.02686.x

  9. The Development and Organization of Newborn Screening Programs in Turkey

    Journal of Clinical Laboratory Analysis

    Volume 28, Issue 1, January 2014, Pages: 63–69, Başak Tezel, Dilek Dilli, Hilal Bolat, Hatice Şahman, Sema Özbaş, Deniz Acıcan, Mustafa Ertek, Mehmet Rıfat Köse and Uğur Dilmen, Scientific Committee of Turkish National Newborn Screening Programme

    Version of Record online : 27 DEC 2013, DOI: 10.1002/jcla.21645

  10. The clinical aspects of newborn screening: Importance of newborn screening follow-up

    Mental Retardation and Developmental Disabilities Research Reviews

    Volume 12, Issue 4, 2006, Pages: 246–254, Philip M. James and Harvey L. Levy

    Version of Record online : 20 DEC 2006, DOI: 10.1002/mrdd.20120

  11. 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

    Version of Record online : 23 JUL 2009, DOI: 10.1111/j.1442-200X.2008.02790.x

  12. 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

  13. Evaluation of the revised New Zealand national newborn screening protocol for congenital hypothyroidism

    Clinical Endocrinology

    Volume 86, Issue 3, March 2017, Pages: 431–437, Natasha L. Heather, Paul L. Hofman, Mark de Hora, Joan Carll, José G.B. Derraik and Dianne Webster

    Version of Record online : 21 OCT 2016, DOI: 10.1111/cen.13250

  14. 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

    Version of Record online : 20 MAR 2014, DOI: 10.1111/1754-9485.12166

  15. Congenital hypothyroidism with delayed rise in serum TSH missed on newborn screening

    Pediatrics International

    Volume 37, Issue 5, October 1995, Pages: 634–637, TADASHI ASAMI, NAOKO OTABE, MARIKO WAKABAYASHI, TOURU KIKUCHI and MAKOTO UCHIYAMA

    Version of Record online : 19 JAN 2011, DOI: 10.1111/j.1442-200X.1995.tb03392.x

  16. Universal newborn screening and adverse medical outcomes: A historical note

    Mental Retardation and Developmental Disabilities Research Reviews

    Volume 12, Issue 4, 2006, Pages: 262–269, Jeffrey P. Brosco, Michael I. Seider and Angela C. Dunn

    Version of Record online : 20 DEC 2006, DOI: 10.1002/mrdd.20123

  17. A 7-year experience with low blood TSH cutoff levels for neonatal screening reveals an unsuspected frequency of congenital hypothyroidism (CH)

    Clinical Endocrinology

    Volume 71, Issue 5, November 2009, Pages: 739–745, Carlo Corbetta, Giovanna Weber, Francesca Cortinovis, Davide Calebiro, Arianna Passoni, Maria C. Vigone, Paolo Beck-Peccoz, Giuseppe Chiumello and Luca Persani

    Version of Record online : 28 MAY 2009, DOI: 10.1111/j.1365-2265.2009.03568.x

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    Long-term follow-up of newborn screening often falls short

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 9, September 2012, Pages: viii–ix,

    Version of Record online : 24 AUG 2012, DOI: 10.1002/ajmg.a.35646

  19. Present newborn screening for phenylketonuria

    Mental Retardation and Developmental Disabilities Research Reviews

    Volume 5, Issue 2, 1999, Pages: 144–149, Frances E. Dougherty and Harvey L. Levy

    Version of Record online : 20 MAY 1999, DOI: 10.1002/(SICI)1098-2779(1999)5:2<144::AID-MRDD9>3.0.CO;2-B

  20. Permanent and transient congenital hypothyroidism in preterm infants

    Acta Paediatrica

    Volume 101, Issue 4, April 2012, Pages: e179–e182, Ramesh Srinivasan, Sundeep Harigopal, Steve Turner and Tim Cheetham

    Version of Record online : 9 DEC 2011, DOI: 10.1111/j.1651-2227.2011.02536.x