The epidemiology of lumbar degenerative spondylolisthesis (DS) remains controversial. We
performed a systematic review with the aim of gaining a better understanding of the …

Abstract Purpose of Review Spondylolysis remains one of the most common causes of lower
back pain in the pediatric and adolescent populations and is particularly prevalent in young …

Sulfation is a widespread modification of biomolecules that has been incompletely explored
to date. Through cross-phenotype meta-analysis of bone mineral density in up to 426,824 …

Autism spectrum disorder (ASD) represents a set of complex neurodevelopmental disorders
with large degrees of heritability and heterogeneity. We sequenced 136 microcephaly or …

Study Design. A retrospective review of prospectively collected data. Objective. The aim of
this study was to investigate recent outcomes of conservative treatment for bony healing in …

Tooth agenesis is one of the most common developmental anomalies in humans.
Oligodontia, a severe form of tooth agenesis, is genetically and phenotypically a …

Purpose To investigate the association of spinal anomalies with lumbar spondylolysis and
spina bifida occulta (SBO). Methods A total of 1190 patients with thoracic, abdominal, and …

Skeletal dysplasia with multiple dislocations are severe disorders characterized by
dislocations of large joints and short stature. The majority of them have been linked to …

ABSTRACT SLC26 family members are multifunctional transporters of small anions,
including Cl−, HCO3−, sulfate, oxalate, and formate. Most SLC26 isoforms act as secondary …

Background Mutations in the SLC26A2 gene cause a spectrum of currently incurable human
chondrodysplasias. However, genotype-phenotype relationships of SLC26A2-deficient …