Background Osteogenesis imperfecta (OI) is an hereditary bone disease in which increased
bone fragility leads to frequent fractures and other complications, usually in an autosomal …

The mechanisms controlling axon guidance are of fundamental importance in understanding
brain development. Growing corticospinal and somatosensory axons cross the midline in …

Study Design. A retrospective case review was performed. Objective. To assess the value,
rapidity, and safety of combined multiple-pulse transcranial electric stimulation motor-evoked …

To the Editor: We read with interest the recent paper by Alanay et al., who describe the first
human patients with FKBP10 (MIM 607063) mutations and conclude that this adds to the …

Bruck syndrome (BS) is an autosomal recessive syndromic form of osteogenesis imperfecta
(OI) that is characterized by the additional presence of pterygium formation. We have …

The objective of this study was to improve upon leg somatosensory-evoked potential (SEP)
monitoring that halves paraplegia risk but can be slow, miss or falsely imply motor injury and …

Hereditary sensory autonomic neuropathy type IV (HSAN‐IV) is a rare autosomal recessive
disorder that usually begins in infancy and is characterized by anhidrosis, insensitivity to …

Horizontal gaze palsy and progressive scoliosis (HGPPS) is an autosomal recessive neurologic
disorder caused by homozygous or compound heterozygous mutations in the ROBO3 …

Motor, sensory, and integrative activities of the brain are coordinated by a series of midline-bridging
neuronal commissures whose development is tightly regulated. Here we report a …

Introduction: Posterior spinal instrumented fusion remains the mainstay treatment for adolescent
idiopathic scoliosis (AIS) with acceptable post-operative patient satisfaction. However, …