Journals / Journal of Clinical Research in Pediatric Endocrinology / 2020 / Cilt: 12 - Sayı: 2

Novel MTTP Gene Mutation in a Case of Abetalipoproteinemia with Central Hypothyroidism

Pages
223–224
DOI
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ACAR, S. (2020). Novel MTTP Gene Mutation in a Case of Abetalipoproteinemia with Central Hypothyroidism. Journal of Clinical Research in Pediatric Endocrinology, Cilt: 12 - Sayı: 2, 223–224. https://ajindex.com/articles/166585

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References (4)

  1. Soylu Üstkoyuncu P, Gökay S, Eren E, Doğan D, Yıldız G, Yılmaz A, Türkan Mutlu F. Novel MTTP Gene Mutation in a Case of Abetalipoproteinemia with Central Hypothyroidism. J Clin Res Pediatr Endocrinol 2020
  2. Persani L, Brabant G, Dattani M, Bonomi M, Feldt-Rasmussen U, Fliers E, Gruters A, Maiter D, Schoenmakers N, van Trotsenburg ASP. 2018 European Thyroid Association (ETA) Guidelines on the Diagnosis and Management of Central Hypothyroidism. Eur Thyroid J 2018;7:225- 237. Epub 2018 Jul 19 3. Alexopoulou O, Beguin C, De Nayer P, Maiter D. Clinical and hormonal characteristics of central hypothyroidism at diagnosis and during follow-up in adult patients. Eur J Endocrinol 2004;150:1-8
  3. Lee S, Farwell AP. Euthyroid sick syndrome. Compr Physiol 2016;6:1071- 1080
  4. Jonklaas J, Sathasivam A, Wang H, Gu J, Burman KD, Soldin SJ. Total and free thyroxine and triiodothyronine: measurement discrepancies, particularly in inpatients. Clin Biochem 2014;47:1272-1278. Epub 2014 Jun 14