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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
Ursula Heilmeier,Alexandra Siegenthaler,Ursina Meyer et al. Ursula Heilmeier et al.
Proton-pump inhibitors (PPI) are widely used among older adults and PPI intake has been associated with increased fracture risk. However, their association with bone microarchitecture and strength remains unclear as prior clinical PPI studi...
H T Holltrø,T I L Nilsen,B Schei et al. H T Holltrø et al.
Purpose: To examine the association between birth characteristics and bone mineral density (BMD) and bone mineral content (BMC) in young adults. Methods: ...
Petra Malavašič,Jasna Lojk,Marija Nika Lovšin et al. Petra Malavašič et al.
Genome-wide association studies have identified multiple loci associated with bone mineral density, a major determinant of osteoporotic fracture risk. At one such locus, genetic, bioinformatic, and zebrafish knockout data strongly prioritiz...
Yi-Lin Chiu,Tsai-Yuan Hsieh,Yu-Juei Hsu et al. Yi-Lin Chiu et al.
Chronic hepatitis C (CHC) is a risk factor for hepatic osteodystrophy, increasing osteoporosis and fracture risks. While historical pegylated interferon/ribavirin (PEG-IFN/RBV) showed variable bone effects, the newer direct-acting antiviral...
Virgínia Amorin Fróes de Moraes,Francisco Mônico Moreira,Carolina Dos Santos Santinoni et al. Virgínia Amorin Fróes de Moraes et al.
Tissue engineering creates possibilities for promoting bone regeneration, which can culminate in an ideal therapy for treating bone defects. Considering its tools, especially exosomes (Exos), inferring its efficiency is fundamental for futu...
Trine Maxel Juul,Lisbeth Koch Thomsen,Christina Møller Andreasen et al. Trine Maxel Juul et al.
Larsen syndrome is a rare genetic condition characterized by facial dysmorphism and skeletal deformities. It is caused by heterozygous pathogenic variants in the Filamin B encoding gene (FLNB). FLNB is a cytoskeletal protein that plays a ke...
Lindsay L Loundagin,Kim D Harrison,David M L Cooper Lindsay L Loundagin
It is well documented that the activation frequency of basic multicellular units (BMUs) is increased following menopause, but it is unclear if a negative BMU balance also contributes to osteoporosis-related bone loss or how remodeling dynam...
Judith Bubbear,Robin Lachmann,Elaine Murphy et al. Judith Bubbear et al.
X-linked hypophosphataemia (XLH) is a genetic phosphate-wasting disorder caused by excess fibroblast growth factor 23 (FGF23), which leads to skeletal morbidities, pain, stiffness, and impairments in physical function and health-related qua...