Detalles de la búsqueda
1.
Global guidance for the recognition, diagnosis, and management of tumor-induced osteomalacia.
J Intern Med;
293(3): 309-328, 2023 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-36511653
2.
Health-related quality of life of men with primary osteoporosis and its changes after bisphosphonates treatment.
BMC Musculoskelet Disord;
24(1): 309, 2023 Apr 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-37076878
3.
Specific Characteristic of Hyperplastic Callus in a Larger Cohort of Osteogenesis Imperfecta Type V.
Calcif Tissue Int;
110(4): 451-463, 2022 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-34988594
4.
Effects of Bisphosphonates on Bone of Osteoporotic Men With Different Androgen Levels: A Case-Control Study.
Endocr Pract;
28(3): 250-256, 2022 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-34968764
5.
Effects of Bisphosphonates on Osteoporosis Induced by Duchenne Muscular Dystrophy: A Prospective Study.
Endocr Pract;
26(12): 1477-1485, 2020 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-33471740
6.
Calcifediol (25-hydroxyvitamin D) improvement and calcium-phosphate metabolism of alendronate sodium/vitamin D3 combination in Chinese women with postmenopausal osteoporosis: a post hoc efficacy analysis and safety reappraisal.
BMC Musculoskelet Disord;
19(1): 210, 2018 Jul 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-29970059
7.
Novel mutations in FKBP10 in Chinese patients with osteogenesis imperfecta and their treatment with zoledronic acid.
J Hum Genet;
62(2): 205-211, 2017 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-27762305
8.
Novel Mutations in SERPINF1 Result in Rare Osteogenesis Imperfecta Type VI.
Calcif Tissue Int;
100(1): 55-66, 2017 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-27796462
9.
The diagnostic dilemma of tumor induced osteomalacia: a retrospective analysis of 144 cases.
Endocr J;
64(7): 675-683, 2017 Jul 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-28450684
10.
[Clinical features of hereditary distal renal tubular acidosis and SLC4A1 gene mutation].
Zhongguo Dang Dai Er Ke Za Zhi;
19(4): 381-384, 2017 Apr.
Artículo
en Zh
| MEDLINE | ID: mdl-28407820
11.
A novel mutant Na+ /HCO3- cotransporter NBCe1 in a case of compound-heterozygous inheritance of proximal renal tubular acidosis.
J Physiol;
594(21): 6267-6286, 2016 11 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-27338124
12.
Two novel mutations in TMEM38B result in rare autosomal recessive osteogenesis imperfecta.
J Hum Genet;
61(6): 539-45, 2016 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-26911354
13.
THE CLINICAL CHARACTERISTICS AND EFFICACY OF BISPHOSPHONATES IN AUDLT PATIENTS WITH OSTEOGENESIS IMPERGECTA.
Endocr Pract;
22(11): 1267-1276, 2016 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-27482615
14.
Association Between Geranylgeranyl Pyrophosphate Synthase Gene Polymorphisms and Bone Phenotypes and Response to Alendronate Treatment in Chinese Osteoporotic Women.
Chin Med Sci J;
31(1): 8-16, 2016 Mar 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-28031082
15.
A Common Mutation and a Novel Mutation in the HPGD Gene in Nine Patients with Primary Hypertrophic Osteoarthropathy.
Calcif Tissue Int;
97(4): 336-42, 2015 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-26135126
16.
The efficacy and safety of weekly 35-mg risedronate dosing regimen for Chinese postmenopausal women with osteoporosis or osteopenia: 1-year data.
Acta Pharmacol Sin;
36(7): 841-6, 2015 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-26051110
17.
[Infantile hypophosphatasia due to mutations in the tissue-nonspecific alkaline phosphatase gene].
Zhonghua Nei Ke Za Zhi;
52(10): 824-8, 2013 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-24378058
18.
[CDC73 gene mutation and parafibromin expression status of parathyroid carcinoma in Chinese].
Zhonghua Yi Xue Za Zhi;
93(42): 3364-8, 2013 Nov 12.
Artículo
en Zh
| MEDLINE | ID: mdl-24418033
19.
Unique mutation spectrum of progressive pseudorheumatoid dysplasia in the Chinese population: a retrospective genotype-phenotype analysis of 105 patients.
World J Pediatr;
19(7): 674-686, 2023 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-36622578
20.
Impaired bone strength and bone microstructure in a novel early-onset osteoporotic rat model with a clinically relevant PLS3 mutation.
Elife;
122023 04 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-37083757