Individual intra-digit somatotopy of all phalanges of the middle and little finger of the right and left hand was studied by functional magnetic resonance imaging in 12 healthy subjects. Phalanges were tactilely stimulated and activation in BA 3b of the human primary somatosensory cortex could be observed for each individual phalanx. Activation peaks were further analysed using the Direction/Or...

Article: Osteometric Study of Metapodial Bones and Phalanges as Indicators the Behavioural Ecology Modern Reindeer (Rangifer tarandus) Implications for Reconstruction Paleo Mobility

To ensure the high performance of a biometric system, various unimodal systems are combined to evade their constraints to form a multimodal biometric system. Here, a multimodal personal authentication systemusing palmprint, dorsal hand vein pattern and a novel biometricmodality “palm-phalanges print” is presented. Firstly, we have collected a new anterior hand database of 50 individualswith 500...

Dexamethasone (Dex) is widely used to treat chronic inflammatory diseases in the clinic. Increasingly, there is more attention being paid to the side effect of Dex. In this study, we investigated the involvement and mechanism of Dex exposure in accelerating mineralization during long bone formation. We first determined that Dex exposure could accelerate long bone mineralization in vivo, but the...

Bilateral congenital pseudoarthrosis of the clavicles is extremely rare. We report a case of this entity presenting in the neonatal period. We highlight the importance of the differential diagnosis when clavicular fracture shows no evidence of healing or occurs bilaterally.

Background: In forensic anthropological identification, we usually use body remains. Accurate sex estimation from these remains is very important and needs the knowledge of specific population standards of that area. Sometimes, human remains are damaged by environmental circumstances. So, we must examine single bones for sex estimation. One of the relatively resistant bones to environmental con...

Cleidocranial dysplasia (CCD) is an autosomal-dominant heritable skeletal disease caused by heterozygous mutations in the RUNX2 gene. We studied a Chinese family that included three affected individuals with CCD phenotypes; the clinical features of patients with CCD include delayed closure of fontanelles, frontal bossing, dysplasia of clavicles, late tooth eruption, and other skeletal anomalies...