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期刊名:Calcified tissue international

缩写:CALCIFIED TISSUE INT

ISSN:0171-967X

e-ISSN:1432-0827

IF/分区:3.5/Q2

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共收录本刊相关文章索引2372条
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Junwei Tian,Jianzeng Zhang,Lu Ding et al. Junwei Tian et al.
Short and long sleep duration have been linked with adverse health outcomes. However, it is unclear if sleep duration affects the risk of low bone mineral density (BMD) or osteoporosis. We systematically reviewed evidence examining the asso...
Mingliang Shi,Baocheng Niu,Cheng Ye et al. Mingliang Shi et al.
Complications from anterior decompression fusion for cervical ossification of the posterior longitudinal ligament (OPLL) are often related to the bone mineral density (BMD) of vertebral bodies and ossified masses. The aim of this study was ...
Andy K O Wong,Ali M Naraghi,Linda Probyn Andy K O Wong
To explore the hypothesis that knee osteoarthritis patients with osteoporosis represent a sub-cohort with different disease characteristics and origin of symptoms. Men and women in the Osteoarthritis Initiative (OAI) at visit 5 (36 months) ...
Jiajia Wang,Yi Yang,An Song et al. Jiajia Wang et al.
The present study aimed to assess bone strength and microstructure in patients with pseudohypoparathyroidism (PHP), nonsurgical HP (NS-HP), and healthy controls. A total of 54 PHP1 patients (14 PHP1a, 40 PHP1b), 54 age-/sex- matched NS-HP p...
Shan Su,Limin Tian Shan Su
The relationship between dietary tryptophan intake and the risk of low bone mineral density (LBMD) has not been thoroughly evaluated. This study aimed to examine the relationship between dietary tryptophan intake and LBMD. A total of 12,003...
Pascal Bizot Pascal Bizot
Osteogenesis imperfecta is a genetic disorder, mainly characterized by bone fragility. In adult with osteogenesis imperfecta, surgical treatment may be indicated as an emergency procedure in the event of a fracture, or as a scheduled proced...
Luca Celli,Mark R Garrelfs,Ralph J B Sakkers et al. Luca Celli et al.
Osteogenesis Imperfecta (OI), known as "brittle bone disease," presents a rare genetic disorder characterized by bone fragility, often accompanied by skeletal deformities and extraskeletal complications. OI is primarily associated with coll...
Silvia Vai,Alberto Falchetti,Sabrina Corbetta et al. Silvia Vai et al.
Glycogen storage disease (GSD) is the most prevalent inherited disorder of glycogen metabolism for which no causal treatment is available. In recent years, thanks to the improved clinical management, the life expectancy of these patients ex...
A H Heald,W Lu,R Williams et al. A H Heald et al.
There is important variation in the occurrence of Paget's disease in different regions and populations. There are though few data concerning the occurrence of clinically diagnosed disease in black and ethnic minority groups in the United Ki...