Detalles de la búsqueda
1.
The 499th case: Roux-en-Y gastric bypass, limb weakness, and ostealgia / 中华内科杂志
Chinese Journal of Internal Medicine
; (12): 117-121, 2023.
Artículo
en Zh
| WPRIM | ID: wpr-994393
2.
Guideline for the diagnosis and management of hypophosphatemic rickets/osteomalacia / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 267-281, 2022.
Artículo
en Zh
| WPRIM | ID: wpr-933402
3.
Clinical characteristics and molecular mechanisms of hypoparathyroidism related to GATA3 gene mutation / 中华内科杂志
Chinese Journal of Internal Medicine
; (12): 66-71, 2022.
Artículo
en Zh
| WPRIM | ID: wpr-933432
4.
Identification of c.196C>T nonsense RUNX2 variant in a Chinese patient with cleidocranial dysplasia / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 526-529, 2022.
Artículo
en Zh
| WPRIM | ID: wpr-928451
5.
A case of occult malignancies with disseminated carcinomatosis of the bone marrow presenting with isolated elevation of serum alkaline phosphatase / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 1013-1016, 2021.
Artículo
en Zh
| WPRIM | ID: wpr-911419
6.
Comparative effect of eldecalcitol and alfacalcidol on bone microstructure: A preliminary report of secondary analysis of a prospective trial
Osteoporosis and Sarcopenia
; : 47-53, 2021.
Artículo
en Inglés
| WPRIM | ID: wpr-903031
7.
Clinical and genetic characteristics of patients with chronic enteropathy associated with SLCO2A1 gene / 中华内科杂志
Chinese Journal of Internal Medicine
; (12): 45-50, 2021.
Artículo
en Zh
| WPRIM | ID: wpr-885143
8.
Comparative effect of eldecalcitol and alfacalcidol on bone microstructure: A preliminary report of secondary analysis of a prospective trial
Osteoporosis and Sarcopenia
; : 47-53, 2021.
Artículo
en Inglés
| WPRIM | ID: wpr-895327
9.
Diagnostic value of 4-dimensional computed tomography in preoperative localization in patients with primary hyperparathyroidism / 中华内科杂志
Chinese Journal of Internal Medicine
; (12): 788-795, 2020.
Artículo
en Zh
| WPRIM | ID: wpr-870192
10.
GNA11 gene rs11084997 polymorphisms might be associated with risk of adult-onset non-surgical hypoparathyroidism / 中华内科杂志
Chinese Journal of Internal Medicine
; (12): 23-28, 2020.
Artículo
en Zh
| WPRIM | ID: wpr-870126
11.
GNA11 gene rs11084997 polymorphisms might be associated with risk of adult-onset non-surgical hypoparathyroidism / 中华内科杂志
Chinese Journal of Internal Medicine
; (12): 23-28, 2020.
Artículo
en Zh
| WPRIM | ID: wpr-798603
12.
Maternal mineral and bone metabolism during lactation / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 176-180, 2019.
Artículo
en Zh
| WPRIM | ID: wpr-745706
13.
Comparison of effectiveness and safety of high-dose native vitamin D versus active vitamin D in the treatment of hypoparathyroidism / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 859-863, 2019.
Artículo
en Zh
| WPRIM | ID: wpr-791728
14.
A preliminary study of the quality of life and muscle strength in patients with pseudohypoparathyroidism / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 480-485, 2019.
Artículo
en Zh
| WPRIM | ID: wpr-755669
15.
Comparison of effectiveness and safety of high-dose native vitamin D versus active vitamin D in the treatment of hypoparathyroidism / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 859-863, 2019.
Artículo
en Zh
| WPRIM | ID: wpr-796358
16.
Tumor-induced osteomalacia
Osteoporosis and Sarcopenia
; : 119-127, 2018.
Artículo
en Inglés
| WPRIM | ID: wpr-741799
17.
Clinical and immunohistopathologic study of phosphaturic mesenchymal tumor / 中华病理学杂志
Chinese Journal of Pathology
; (12): 427-431, 2018.
Artículo
en Zh
| WPRIM | ID: wpr-810018
18.
An updated hip fracture projection in Asia: The Asian Federation of Osteoporosis Societies study
Osteoporosis and Sarcopenia
; : 16-21, 2018.
Artículo
en Inglés
| WPRIM | ID: wpr-741774
19.
The Asian Federation of Osteoporosis Societies' call to action to improve the undertreatment of osteoporosis in Asia
Osteoporosis and Sarcopenia
; : 161-163, 2017.
Artículo
en Inglés
| WPRIM | ID: wpr-225119
20.
A clinical and hereditary analysis of novel complex heterozygous KCNJ1 mutation in a Bartter syndrome type Ⅱ patient / 中华内科杂志
Chinese Journal of Internal Medicine
; (12): 760-762, 2017.
Artículo
en Zh
| WPRIM | ID: wpr-662929