Wei-Jun Gu
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Explore the profile of Wei-Jun Gu including associated specialties, affiliations and a list of published articles.
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26
Citations
109
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Recent Articles
1.
Miao X, Wang X, Lyu Z, Ba J, Pei Y, Dou J, et al.
Neuro Endocrinol Lett
. 2022 Dec;
43(4):233-238.
PMID: 36528886
Objective: Parathyroid carcinoma (PC) is a rare disease with high rates of misdiagnosis and recurrence. This report summarized the clinical and pathological characteristics of 10 patients with PC at our...
2.
Shao Y, Cai W, Wang X, Chen K, Du J, Zang L, et al.
Neuro Endocrinol Lett
. 2022 Aug;
43(2):113-118.
PMID: 35933617
Objective: Patients with hypoparathyroidism always present with recurrent tetany caused by hypocalcemia. These patients are usually misdiagnosed with epilepsy and incorrectly treated with anti-epileptic drugs. This research analyzed clinical data...
3.
Qu Y, Zhang C, Wang X, Guo Q, Chen K, Zang L, et al.
Neuro Endocrinol Lett
. 2021 May;
42(1):43-47.
PMID: 34009764
Objective: Insulinoma is a rare pancreatic neuroendocrine tumor that can spontaneously produce excess endogenous insulin, resulting in recurrent and serious hypoglycemia. Patients with insulinoma always have intermittent neuroglycopenia, which has...
4.
Miao X, Wang X, Lyu Z, Ba J, Pei Y, Dou J, et al.
World J Clin Cases
. 2021 May;
9(14):3478-3486.
PMID: 34002161
Background: Paget's disease of bone (PDB) is a rare metabolic bone disease in China and is characterized by increased bone resorption and disorganized bone formation. The main clinical symptoms of...
5.
Gu Y, Gu W, Dou J, Lv Z, Li J, Zhang S, et al.
World J Clin Cases
. 2019 May;
7(8):961-971.
PMID: 31119141
Background: Adrenocorticotropic hormone (ACTH)-independent Cushing's syndrome (CS) is mostly due to unilateral tumors, with bilateral tumors rarely reported. Its common causes include primary pigmented nodular adrenocortical disease, ACTH-independent macronodular adrenal...
6.
Li J, Wang M, Zhang B, Wu X, Lin T, Liu X, et al.
World J Gastroenterol
. 2018 Dec;
24(46):5189-5202.
PMID: 30581268
Tyrosine kinase inhibitors (TKIs) have improved the overall survival of patients with gastrointestinal stromal tumors (GISTs), but their side effects can impact dose intensity and, consequently, the clinical benefit. To...
7.
Zhang Q, Zang L, Li Y, Han B, Gu W, Yan W, et al.
Medicine (Baltimore)
. 2018 Feb;
97(2):e9084.
PMID: 29480822
Pituitary stalk interruption syndrome (PSIS) is associated with simultaneous or subsequent pituitary hormone deficiencies (PHDs). Although the clinical features of multiple PHDs are well known, the status of the thyrotrophic...
8.
Zhang Q, Cui L, Gao J, Yan W, Jin N, Chen K, et al.
Endocr J
. 2017 Dec;
65(3):269-279.
PMID: 29279458
Primary macronodular adrenal hyperplasia (PMAH), also known in the past as bilateral macronodular adrenalhyperplasia or adrenocorticotropin (ACTH)-independent macronodular adrenal hyperplasia, is a rare type of Cushing's syndrome (CS) and is...
9.
Gu W, Zhang Q, Zhu J, Li J, Wei S, Mu Y
Medicine (Baltimore)
. 2017 Jun;
96(24):e6934.
PMID: 28614220
Rationale: Immunoglobulin G4 (IgG4)-related hypophysitis is a type of IgG4-related disease (IgG4-RD), which is characterized by plasma cells infiltration in the pituitary causing functional changes and (or) space-occupying effect in...
10.
Gu W, Zhang Q, Zhu W, Guo Y, Zhang L
Zhongguo Shi Yan Xue Ye Xue Za Zhi
. 2016 Oct;
24(5):1533-1538.
PMID: 27784388
Objective: To investigate the imbalance of Tc1/Tc2,Th1/Th2 and Tc/Th in patients with systemic lupus erythematosus(SLE) and its relationship with the clinical stages of SLE. Methods: The full blood culture and...