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Correction: Technical evolution of pediatric neurosurgery: craniosynostosis from 1972 to 2023 and beyond
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Article
Open AccessProtocol for the multicentre prospective paediatric craniectomy and cranioplasty registry (pedCCR) under the auspices of the European Society for Paediatric Neurosurgery (ESPN)
In the paediatric age group, the overall degree of evidence regarding decompressive craniectomy (DC) and cranioplasty is low, whereas in adults, randomised controlled trials and prospective multicentre registr...
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Open AccessDiagnosis and treatment of Chiari malformation type 1 in children: the International Consensus Document
Chiari malformation type 1 (CM1) is a rare condition where agreed classification and treatment are still missing. The goal of this study is to achieve a consensus on the diagnosis and treatment of CM1 in child...
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Article
Open AccessClinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia
X-linked hypophosphataemia (XLH) is the most common cause of inherited phosphate wasting and is associated with severe complications such as rickets, lower limb deformities, pain, poor mineralization of the te...
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Article
Correction to: Management of split cordmalformation in children: the Lyon experience
The original version of this article unfortunately contained an error. The authors have been published with inverted given and family names. Given in this article are the corrected author names.
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Open AccessMultimodal optical analysis discriminates freshly extracted human sample of gliomas, metastases and meningiomas from their appropriate controls
Delineating tumor margins as accurately as possible is of primordial importance in surgical oncology: extent of resection is associated with survival but respect of healthy surrounding tissue is necessary for ...
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Article
The mysteries of Blaise Pascal’s sutures
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Open AccessDouble Xp11.22 deletion including SHROOM4 and CLCN5 associated with severe psychomotor retardation and Dent disease
Here we report the clinical and molecular characterization of two Xp11.22 deletions including SHROOM4 and CLCN5 genes. These deletions appeared in the same X chromosome of the same patient.
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About hierarchical log linear analysis of admission blood parameters and clinical outcome following traumatic brain injury
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Article
Spinal epidural hematoma in hemophilic children: controversies in management
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Successful conservative treatment of traumatic subacute subdural haematomas in neonates with haemophilia A
The aim of this report is to enlighten the role of an early diagnosis and treatment of haemophilia A during the management of an intracranial haemorrhage as well as to discuss the efficiency of a subdural tran...