Annals of Pediatric Endocrinology & Metabolism

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Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the TSHR gene

Won Kyoung Cho, Moon-Bae Ahn, Woori Jang, Hyojin Chae, Myungshin Kim, Byung-Kyu Suh

Ann Pediatr Endocrinol Metab. 2018;23(4):235-239. Published online December 31, 2018
DOI: https://doi.org/10.6065/apem.2018.23.4.235

Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the TSHR gene

Won Kyoung Cho, Moon-Bae Ahn, Woori Jang, Hyojin Chae, Myungshin Kim, Byung-Kyu Suh

Annals of Pediatric Endocrinology & Metabolism. 2018;23(4):235-239

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Subclinical hyperthyroidism due to a thyrotropin receptor (TSHR) gene mutation (S505R)

Joachim Pohlenz, Nicole Pfarr, Silvia Krüger, Volker Hesse

Acta Paediatrica. 2006;95(12):1685-1687

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MON-264 Familial Neonatal Nonautoimmune Hyperthyroidism Due To A Thyrotropin Receptor Gene Mutation (A619G).

Doris Taha, Amita Adhikari, Rajeev Thirunagari, Rajan Senguttuvan, Leigh Anne Flore

Journal of the Endocrine Society. 2019;3(Supplement_1):

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Sporadic Nonautoimmune Congenital Hyperthyroidism due to a Strong Activating Mutation of the Thyrotropin Receptor Gene

M. Tonacchera, P. Agretti, V. Rosellini, G. Ceccarini, A. Perri, M. Zampolli, R. Longhi, D. Larizza, A. Pinchera, P. Vitti, L. Chiovato

Thyroid. 2000;10(10):859-863

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Congenital Nonautoimmune Hyperthyroidism in a Nonidentical Twin Caused by a Sporadic Germline Mutation in the Thyrotropin Receptor Gene

PETER KOPP, J. LARRY JAMESON, THOMAS F. ROE

Thyroid. 1997;7(5):765-770

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MON-265 Congenital Hypothyroidism and Bilateral Ptosis Due to a Novel TSHR Gene Mutation

Andreea Marinescu, Francesco De Luca, Elizabeth Suarez

Journal of the Endocrine Society. 2019;3(Supplement_1):

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Long-Term Carbimazole Treatment of Neonatal Nonautoimmune Hyperthyroidism due to a New Activating TSH Receptor Gene Mutation (Ala428Val)

Kirsten Börgel, Joachim Pohlenz, Hans G. Koch, Jurgen H. Bramswig

Hormone Research in Paediatrics. 2005;64(4):203-208

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Sporadic congenital nonautoimmune hyperthyroidism caused by P639S mutation in thyrotropin receptor gene

Patrizia Agretti, Giuseppina De Marco, Martina Biagioni, Antonio Iannilli, Marco Marigliano, Aldo Pinchera, Paolo Vitti, Valentino Cherubini, Massimo Tonacchera

European Journal of Pediatrics. 2012;171(7):1133-1137

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Premature birth and low birth weight associated with nonautoimmune hyperthyroidism due to an activating thyrotropin receptor gene mutation

Bijay Vaidya, Viv Campbell, John H. Tripp, Gill Spyer, Andrew T. Hattersley, Sian Ellard

Clinical Endocrinology. 2004;60(6):711-718

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A Japanese family with nonautoimmune hyperthyroidism caused by a novel heterozygous thyrotropin receptor gene mutation

Akie Nakamura, Shuntaro Morikawa, Hayato Aoyagi, Katsura Ishizu, Toshihiro Tajima

Pediatric Research. 2014;75(6):749-753

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