Found: 19
Select item for more details and to access through your institution.
Influence of Obesity and Changes in Weight or BMI on Incident Fractures in Postmenopausal Women: From Peking Vertebral Fracture Study.
- Published in:
- Calcified Tissue International, 2023, v. 113, n. 5, p. 483, doi. 10.1007/s00223-023-01129-5
- By:
- Publication type:
- Article
Evaluation of Volumetric Bone Mineral Density, Bone Microarchitecture, and Bone Strength in Patients with Achondroplasia Caused by FGFR3 c.1138G > A Mutation.
- Published in:
- Calcified Tissue International, 2023, v. 112, n. 1, p. 13, doi. 10.1007/s00223-022-01027-2
- By:
- Publication type:
- Article
Functioning gonadotroph adenomas in premenopausal women: clinical and molecular characterization and review of the literature.
- Published in:
- Pituitary, 2022, v. 25, n. 3, p. 454, doi. 10.1007/s11102-021-01205-9
- By:
- Publication type:
- Article
Clinical, Biochemical, Radiological, Genetic and Therapeutic Analysis of Patients with COMP Gene Variants.
- Published in:
- Calcified Tissue International, 2022, v. 110, n. 3, p. 313, doi. 10.1007/s00223-021-00920-6
- By:
- Publication type:
- Article
Corrigendum: Clinical Characteristics of Short-Stature Patients With Collagen Gene Mutation and the Therapeutic Response to rhGH.
- Published in:
- 2022
- By:
- Publication type:
- Correction Notice
Clinical Characteristics of Short-Stature Patients With Collagen Gene Mutation and the Therapeutic Response to rhGH.
- Published in:
- Frontiers in Endocrinology, 2022, v. 13, p. 1, doi. 10.3389/fendo.2022.820001
- By:
- Publication type:
- Article
A Chinese Case of Cornelia de Lange Syndrome Caused by a Pathogenic Variant in SMC3 and a Literature Review.
- Published in:
- Frontiers in Endocrinology, 2021, v. 12, p. 1, doi. 10.3389/fendo.2021.604500
- By:
- Publication type:
- Article
Clinical Characteristics of Short-Stature Patients With an NPR2 Mutation and the Therapeutic Response to rhGH.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2021, v. 106, n. 2, p. 431, doi. 10.1210/clinem/dgaa842
- By:
- Publication type:
- Article
Dwarfism in Troyer syndrome: a family with SPG20 compound heterozygous mutations and a literature review.
- Published in:
- Annals of the New York Academy of Sciences, 2020, v. 1462, n. 1, p. 118, doi. 10.1111/nyas.14229
- By:
- Publication type:
- Article
Incident vertebral fracture and longitudinal BMD change in Chinese postmenopausal women with early CKD: Peking Vertebral Fracture Study.
- Published in:
- Archives of Osteoporosis, 2023, v. 18, n. 1, p. 1, doi. 10.1007/s11657-023-01324-9
- By:
- Publication type:
- Article
Relationships between sclerostin and morphometric vertebral fractures, bone mineral density, and bone microarchitecture in postmenopausal women.
- Published in:
- Archives of Osteoporosis, 2023, v. 18, n. 1, p. 1, doi. 10.1007/s11657-023-01235-9
- By:
- Publication type:
- Article
A Chinese case of CHST3-related skeletal dysplasia and a systematic review.
- Published in:
- Endocrine (1355008X), 2023, v. 80, n. 3, p. 658, doi. 10.1007/s12020-023-03303-z
- By:
- Publication type:
- Article
Serum Irisin level is associated with fall risk, muscle strength, and cortical porosity in postmenopausal women.
- Published in:
- Frontiers in Endocrinology, 2023, v. 14, p. 1, doi. 10.3389/fendo.2023.1096950
- By:
- Publication type:
- Article
Clinical characteristics and the influence of rs1800470 in patients with Camurati-Engelmann disease.
- Published in:
- Frontiers in Endocrinology, 2022, v. 13, p. 01, doi. 10.3389/fendo.2022.1041061
- By:
- Publication type:
- Article
Na-Cl Co-transporter (NCC) gene inactivation is associated with improved bone microstructure.
- Published in:
- Osteoporosis International, 2022, v. 33, n. 10, p. 2193, doi. 10.1007/s00198-022-06471-2
- By:
- Publication type:
- Article
A Chinese Case of X-Linked Acrogigantism and Systematic Review.
- Published in:
- Neuroendocrinology, 2021, v. 111, n. 12, p. 1164, doi. 10.1159/000512240
- By:
- Publication type:
- Article
The phenotype and rhGH treatment response of ring Chromosome 15 Syndrome: Case report and literature review.
- Published in:
- Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 12, p. 1, doi. 10.1002/mgg3.1842
- By:
- Publication type:
- Article
Case Report: A Clinical and Genetic Analysis of Childhood Growth Hormone Deficiency With Familial Hypercholesterolemia.
- Published in:
- Frontiers in Endocrinology, 2021, v. 12, p. 1, doi. 10.3389/fendo.2021.691490
- By:
- Publication type:
- Article
Identification and In Vitro Functional Verification of Two Novel Mutations of GHR Gene in the Chinese Children with Laron Syndrome.
- Published in:
- Frontiers in Endocrinology, 2021, v. 11, p. N.PAG, doi. 10.3389/fendo.2021.605736
- By:
- Publication type:
- Article