Characteristics of 8 cases with congenital isolated ACTH deficiency.

Figshare2015-12-02 更新2026-04-29 收录

数据链接：

https://figshare.com/articles/dataset/_Characteristics_of_8_cases_with_congenital_isolated_ACTH_deficiency_/393890 数据链接链接失效反馈

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资源简介：

Characteristics of 8 cases with congenital isolated ACTH deficiency.

创建时间：

2015-12-02

Supplementary data for "HIGH-THROUGHPUT PROTEOMICS AND IMMUNOHISTOCHEMISTRY OF ORBITAL CONNECTIVE TISSUE IN GRAVES' ORBITOPATHY"

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This dataset contains the supplementary materials for the manuscript entitled “HIGH-THROUGHPUT PROTEOMICS AND IMMUNOHISTOCHEMISTRY OF ORBITAL CONNECTIVE TISSUE IN GRAVES' ORBITOPATHY,” submitted to Th

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Roxadustat has risks of reversible central hypothyroidism in patients undergoing hemodialysis: a single-center retrospective cohort study

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Roxadustat, a hypoxia-inducible factor-prolyl hydroxylase inhibitor, has proven efficacy in the treatment of renal anemia; however, evidence indicates that it may cause central hypothyroidism. The pre

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Supplementary Material for: Recommendations for Diagnosis and Treatment of Pseudohypoparathyroidism and Related Disorders: An Updated Practical Tool for Physicians and Patients

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Patients affected by pseudohypoparathyroidism (PHP) or related disorders are characterized by physical findings that may include brachydactyly, a short stature, a stocky build, early-onset obesity, ec

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Заболеваемость населения болезнями эндокринной системы, в т.ч. сахарным диабетом, за период 2002-2022 по данным обращаемости населения в ЛПУ на 1000 населения

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流行病学

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DataCite Commons2024-01-24 更新60

Data from " Novel CYP17A1 Variants and Functional Validation in a Large Chinese Cohort of Complete 17α-Hydroxylase Deficie ncy "

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Supplemental tables and figure from "Novel CYP17A1 Variants and Functional Validation in a Large Chinese Cohort of Complete 17α-Hydroxylase Deficiency"

Figshare2025-11-20 更新50

Characteristics of 8 cases with congenital isolated ACTH deficiency.

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