Hypothyroid myopathy and its association with <i>MICU1</i> gene mutations: a clinical caseauthors

Thyroid hormones are involved in the activation of glycogenolysis and mitochondrial oxidative phosphorylation. Kocher–Debré–Semelaigne Syndrome, also known as hypothyroid myopathy, is characterized by reduced glycogenolytic activity, leading to glycogen deposition in muscles. These reserves begin to...

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Bibliografiske detaljer

Principais autores:	M. A. Perepelova, V. K. Slokva, E. A. Pigarova, A. S. Shutova, A. A. Kolodkina, A. V. Perepelov, L. K. Dzeranova
Format:	Artigo
Sprog:	Inglês
Udgivet:	Endocrinology Research Centre 2025-12-01
Serier:	Ожирение и метаболизм
Fag:	hypothyroid myopathy primary hypothyroidism myopathy with extrapyramidal symptoms
Online adgang:	https://www.omet-endojournals.ru/jour/article/view/13287
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