001476521 000__ 06389cam\\22006377a\4500 001476521 001__ 1476521 001476521 003__ OCoLC 001476521 005__ 20231003174425.0 001476521 006__ m\\\\\o\\d\\\\\\\\ 001476521 007__ cr\un\nnnunnun 001476521 008__ 230902s2023\\\\sz\\\\\\o\\\\\000\0\eng\d 001476521 019__ $$a1395946472 001476521 020__ $$a9783031349812$$q(electronic bk.) 001476521 020__ $$a3031349814$$q(electronic bk.) 001476521 020__ $$z3031349806 001476521 020__ $$z9783031349805 001476521 0247_ $$a10.1007/978-3-031-34981-2$$2doi 001476521 035__ $$aSP(OCoLC)1396064811 001476521 040__ $$aEBLCP$$beng$$cEBLCP$$dYDX$$dEBLCP$$dGW5XE 001476521 049__ $$aISEA 001476521 050_4 $$aRD768 001476521 08204 $$a616.7/3$$223/eng/20230912 001476521 24500 $$aSpinal Dysraphic Malformations :$$bScience and Surgery -- Volume 47 /$$cDachling Pang, Kyu-Chang Wang, editors. 001476521 260__ $$aCham :$$bSpringer,$$c2023. 001476521 300__ $$a1 online resource (293 p.). 001476521 4901_ $$aAdvances and Technical Standards in Neurosurgery ;$$vv.47 001476521 500__ $$aNeurourological Findings 001476521 5050_ $$aIntro -- Preface -- Contents -- Gastrulation and Split Cord Malformation -- Definition -- Nomenclature -- Epidemiology -- Pathology -- Aetiology -- Embryology: Germinal Phase -- Embryology: Gastrulation -- Dysraphism and Embryology -- Split Cord Malformation and Embryology -- Split Cord Malformation and Experimental Evidence -- Signs and Symptoms -- Associated Conditions -- Neuroimaging -- Management -- Surgery for Type 1 SCM -- Surgery for Type 2 SCM -- Complications -- Prognosis -- Conclusion -- References -- Fetal Surgery for Myelomeningocele: Neurosurgical Perspectives 001476521 5058_ $$aIntroduction and Experimental Background -- Clinical Studies -- Neurosurgery Perspectives -- Hydrocephalus -- Chiari II Malformation -- Motor Function -- Anatomical Level -- MMC Sac vs No Sac -- Gestational Age at the Time of Fetal Repair -- Bladder Function -- Cognitive Function -- Complications at the Myelomeningocele Repair Site -- Problems of Wound Healing -- Inclusion Cysts -- Re-tethering of Spinal Cord -- Selection Criteria for Fetal Surgery -- Operative Technique: Standard Open Fetal Repair of MMC -- Abdominal Opening -- Hysterotomy -- Fetal Monitoring -- Standard Open Repair 001476521 5058_ $$aSkin Patch Repair -- Alternative Techniques -- Fetoscopic Repair (FSBAR) -- Mini-Hysterotomy -- Future Perspectives -- References -- A New Surgical Paradigm for Postnatal Repair of Open Neural Tube Defects Using Intraoperative Neurophysiology Monitoring -- Primary Neurulation Defect -- Disadvantages of Traditional Repair of Open Neural Tube Defects -- Advantages of the New Paradigm for Repair of Open Neural Tube Defects -- Patient Series -- Intraoperative Neurophysiological Monitoring (IONM) -- Surgical Technique -- Intraoperative Surgical and IONM Findings 001476521 5058_ $$aFirst Illustrative Case: Terminal Lumbar Non-functional Placode (Case #2 in Table 1) -- Second Illustrative Case: Preservation of Segmental Lumbar Placode with L5 Functional Level (Case #8 in Table 1) -- Histopathology of the Resected Placode -- Neurological, Urological and Imaging Follow-Up -- Discussion -- Conclusion -- References -- Focal Spinal Nondisjunctional Disorders: Including a Discussion on the Embryogenesis of Cranial Focal Nondisjunctional Lesions -- Introduction -- Embryogenetic Mechanisms of Focal Nondisjunctional Disorders -- Normal Primary Neurulation 001476521 5058_ $$aOn the Caudal End of the Primary Neural Tube -- Relevant Features in the Rostral End of Primary Neural Tube -- Faults in Embryogenesis in Focal Nondisjunctional Disorders -- Molecular Mechanisms of Focal Nondisjunctional Malformations -- Embryogenetic Mechanisms of the Subtypes of Focal Spinal Nondisjunctional Disorders -- Embryogenetic Mechanisms of Cranial Focal Nondisjunctional Disorders -- Pathological Anatomy and Clinical Manifestations of FSND -- Pure CSDST -- Pathological Anatomy -- Clinical Manifestations -- Pure LDM -- Pathological Anatomy -- Clinical Manifestations -- Cutaneous Markers 001476521 506__ $$aAccess limited to authorized users. 001476521 520__ $$aThis book includes detailed discussions of the latest science in the embryogenesis of spinal dysraphic malformations, and a well-illustrated guide to their surgical repair. In addition to covering the actual malformations, and because, with the probable exception of prenatal closure of the open neural tube defect, all surgical repairs of other dysraphic malformations require sophisticated intraoperative neurophysiological monitoring (IONM), an in-depth chapter is devoted to the physics, physiology, techniques, parameters and patterns of electrophysiological responses in representative dysraphic lesions. As the evaluation of bladder function is crucial for the assessment of the pre-operative clinical status and long-term outcome of the patient with spinal dysraphism, an entire chapter is devoted to the neurophysiology of micturition, the symptoms of neuropathic bladder, and to the explanation of the complexities of proper urodynamics. The book will be an invaluable tool for paediatric neurosurgical consultants interested in spinal dysraphism and for fellows and other trainees in this discipline. 001476521 588__ $$aOnline resource; title from PDF title page (SpringerLink, viewed September 12, 2023). 001476521 650_0 $$aSpine$$xAbnormalities. 001476521 650_0 $$aSpine$$xAbnormalities$$xSurgery. 001476521 655_0 $$aElectronic books. 001476521 7001_ $$aPang, Dachling. 001476521 7001_ $$aWang, Kyu-Chang. 001476521 77608 $$iPrint version:$$aPang, Dachling$$tSpinal Dysraphic Malformations$$dCham : Springer International Publishing AG,c2023$$z9783031349805 001476521 830_0 $$aAdvances and technical standards in neurosurgery ;$$vv. 47. 001476521 852__ $$bebk 001476521 85640 $$3Springer Nature$$uhttps://univsouthin.idm.oclc.org/login?url=https://link.springer.com/10.1007/978-3-031-34981-2$$zOnline Access$$91397441.1 001476521 909CO $$ooai:library.usi.edu:1476521$$pGLOBAL_SET 001476521 980__ $$aBIB 001476521 980__ $$aEBOOK 001476521 982__ $$aEbook 001476521 983__ $$aOnline 001476521 994__ $$a92$$bISE