Hypoparathyroidism
What's New
Last Posted: Jan 07, 2022
- [Clinical characteristics and molecular mechanisms of hypoparathyroidism related to GATA3 gene mutation].
Yang J et al. Zhonghua nei ke za zhi 2022 61(1) 66-71 - Real-life use of BRAF-V600E mutation analysis in thyroid nodule fine needle aspiration: consequences on clinical decision-making.
Brigante Giulia et al. Endocrine 2021 - Genetic screening in a large Chinese cohort of childhood onset hypoparathyroidism by next-generation sequencing combined with TBX1-MLPA.
Wang Yabing et al. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2019 Aug - Smith-Lemli-Opitz syndrome: clinical and biochemical correlates.
Donoghue Sarah E et al. Journal of pediatric endocrinology & metabolism : JPEM 2018 Mar 31(4) 451-459 - CLINGEN Actionability Report for Multiple Endocrine Neoplasia IIA, Familial Medullary Thyroid Cancer - RET
ClinGen Actionability Working Group - Is new American Thyroid Association risk classification for hereditary medullary thyroid carcinoma applicable to Chinese patients? A single-center study.
Zhang Xiwei et al. Chinese journal of cancer research = Chung-kuo yen cheng yen chiu 2017 Jun 29(3) 223-230 - Mitochondrial disease and endocrine dysfunction.
Chow Jasmine et al. Nature reviews. Endocrinology 2017 Feb 13(2) 92-104 - Hypoparathyroidism
From NCATS Genetic and Rare Diseases Information Center - Hypoparathyroidism familial isolated
From NCATS Genetic and Rare Diseases Information Center - Hypoparathyroidism X-linked
From NCATS Genetic and Rare Diseases Information Center
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- Page last reviewed:Feb 1, 2024
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