Detalles de la búsqueda
1.
Genotype-phenotype relationship in a large cohort of osteogenesis imperfecta patients with COL1A1 mutations revealed by a new scoring system / 中华医学杂志(英文版)
Chinese Medical Journal
; (24): 145-153, 2019.
Artículo
en Inglés
| WPRIM | ID: wpr-772868
2.
Severe Hyperthyroidism-Heart Failure-Severe Liver Injury:Report of One Case and Literature Review / 中国医学科学院学报
Acta Academiae Medicinae Sinicae
; (6): 134-138, 2019.
Artículo
en Zh
| WPRIM | ID: wpr-776060
3.
A homozygous mutation in TMEM38B causes rare osteogenesis imperfecta type XIV / 基础医学与临床
Basic & Clinical Medicine
; (12): 594-599, 2018.
Artículo
en Zh
| WPRIM | ID: wpr-693948
4.
Association of GNA11 gene polymorphisms with idiopathic hypoparathyroidism and its complications / 基础医学与临床
Basic & Clinical Medicine
; (12): 145-152, 2018.
Artículo
en Zh
| WPRIM | ID: wpr-693861
5.
Clinical features of hereditary distal renal tubular acidosis and SLC4A1 gene mutation / 中国当代儿科杂志
Chinese Journal of Contemporary Pediatrics
; (12): 381-384, 2017.
Artículo
en Zh
| WPRIM | ID: wpr-351340
6.
Association Between Geranylgeranyl Pyrophosphate Synthase Gene Polymorphisms and Bone Phenotypes and Response to Alendronate Treatment in Chinese Osteoporotic Women / 中国医学科学杂志(英文版)
Chinese Medical Sciences Journal
; (4): 8-16, 2016.
Artículo
en Inglés
| WPRIM | ID: wpr-281458
7.
Value of Chloride Clearance Test in Differential Diagnosis of Gitelman Syndrome / 中国医学科学院学报
Acta Academiae Medicinae Sinicae
; (6): 275-282, 2016.
Artículo
en Inglés
| WPRIM | ID: wpr-289870
8.
Association between vitamin D insufficiency and the risk for gestational diabetes mellitus in pregnant Chinese women / 生物医学与环境科学(英文)
Biomedical and Environmental Sciences
; (12): 399-406, 2012.
Artículo
en Inglés
| WPRIM | ID: wpr-235524
9.
Surgical treatment of hyperparathyroidism due to parathyroid tumors / 中华耳鼻咽喉头颈外科杂志
Chinese Journal of Otorhinolaryngology Head and Neck Surgery
; (12): 862-864, 2012.
Artículo
en Zh
| WPRIM | ID: wpr-262460
10.
Magnetic resonance imaging findings of pituitary hyperplasia due to primary hypothyroidism / 中国医学科学院学报
Acta Academiae Medicinae Sinicae
; (6): 468-473, 2012.
Artículo
en Inglés
| WPRIM | ID: wpr-284348
11.
Exome sequencing identifies compound heterozygous PKHD1 mutations as a cause of autosomal recessive polycystic kidney disease / 中华医学杂志(英文版)
Chinese Medical Journal
; (24): 2482-2486, 2012.
Artículo
en Inglés
| WPRIM | ID: wpr-283736
12.
Expression of Ki-67, galectin-3, fragile histidine triad, and parafibromin in malignant and benign parathyroid tumors / 中华医学杂志(英文版)
Chinese Medical Journal
; (24): 2895-2901, 2012.
Artículo
en Inglés
| WPRIM | ID: wpr-244329
13.
Surgical treatment of recurrent parathyroid carcinoma with invasion of the upper aerodigestive tract / 中华耳鼻咽喉头颈外科杂志
Chinese Journal of Otorhinolaryngology Head and Neck Surgery
; (12): 901-904, 2011.
Artículo
en Zh
| WPRIM | ID: wpr-322440
14.
Generalized glucocorticoid resistance accompanied with an adrenocortical adenoma and caused by a novel point mutation of human glucocorticoid receptor gene / 中华医学杂志(英文版)
Chinese Medical Journal
; (24): 551-555, 2011.
Artículo
en Inglés
| WPRIM | ID: wpr-241558
15.
Benefit of infusions with ibandronate treatment in children with osteogenesis imperfecta / 中华医学杂志(英文版)
Chinese Medical Journal
; (24): 3049-3053, 2011.
Artículo
en Inglés
| WPRIM | ID: wpr-292756
16.
Diagnosis of thyroid nodules with ultrasound-guided fine needle aspiration: comparison of solid lesion and complex lesion / 中华超声影像学杂志
Chinese Journal of Ultrasonography
; (12): 680-683, 2011.
Artículo
en Zh
| WPRIM | ID: wpr-671604
17.
Levels and dynamic changes of serum fibroblast growth factor 23 in hypophosphatemic rickets/osteomalacia / 中华医学杂志(英文版)
Chinese Medical Journal
; (24): 1158-1162, 2010.
Artículo
en Inglés
| WPRIM | ID: wpr-352599
18.
Treatment of hypocalcemia caused by hypoparathyroidism or pseudohypoparathyroidism with domestic-made calcitriol: a prospective and self-controlled clinical trial / 中华医学杂志(英文版)
Chinese Medical Journal
; (24): 279-283, 2009.
Artículo
en Inglés
| WPRIM | ID: wpr-311876
19.
Effect of fibroblast growth factor 9 on Runx2 gene promoter activity in MC3T3-E1 and C2C12 cells / 中华医学杂志(英文版)
Chinese Medical Journal
; (24): 491-495, 2007.
Artículo
en Inglés
| WPRIM | ID: wpr-344868
20.
RET gene cys 634 trp mutation in a multiple endocrine neoplasia type 2A kindred / 中国医学科学院学报
Acta Academiae Medicinae Sinicae
; (6): 799-802, 2006.
Artículo
en Zh
| WPRIM | ID: wpr-313681