Bøger af Mehmet Turgut

Written and edited by leading international authorities in the field, this book provides an in-depth review of knowledge of the incidental findings of the nervous system, with emphasis on asymptomatic brain and spinal lesions that have the potential to cause illness. It includes very informative chapters, organized into four main groups: first, incidental findings of the brain and cranium, including intracranial, intraventricular and skull base lesions, infarcts and calcification; secondly, incidental findings of the spine and spinal cord, including spinal cord tumors, syringomyelia, arteriovenous malformations and craniovertebral junction anomalies; thirdly, incidental findings of the spinal nerves and peripheral nerves, including tumors of the plexi and peripheral nerves; and fourthly, other lesions, including acquired incidental lesions of the brain and spine as well as the medicolegal and psychiatric aspects related to these lesions. The uniqueness of this compilation lies in the fact that several abnormalities exist in the nervous system that have the potential to cause life threatening illness; yet because they are asymptomatic and incidental, this leads to major management dilemmas related to whether or not to surgically the lesion. The proponents of an early surgical management subscribe to the philosophy that getting rid of an entity earlier on when it is asymptomatic, leads to an early cure and obviates any risk of it becoming aggressive and incurable later on; those opting for a ¿wait and watch¿ policy subscribe to the view that no intervention (as well as subjecting the patient to the risk of surgery) is mandated until the lesion becomes symptomatic. This may subject a person to a lifetime of anxiety related to how that lesion is going to evolve, when in all likelihood, the subject may remain asymptomatic throughout his/her life. The psychological aspects of the patient who is extremely disturbed by the presence of this incidental lesion; and, who cannot adjust to the reality that the treating doctor actually does not have a well-defined plan for it, are issues that are adequately addressed with clinical illustrations and examples. This comprehensive reference book will be an ideal source for neuroscientists at all levels, from graduate students to researchers in specific disciplines studying this region, including neurosurgeons, neurologists, neuroradiologists, neuropathologists and psychiatrists, who seek both basic and more advanced information regarding the incidental findings of the nervous system.

This book provides an in-depth review of knowledge of the corpus callosum, called white matter or terra incognita, with emphasis on anatomical, embryological, diagnostics, and surgical features. It includes very informative chapters from leaders in the field, organized into six main groups: first, the embryology, neuroanatomy, and morphometry of the corpus callosum, and animal studies related to it; secondly, neurophysiological aspects, callosal disconnection and the split brain; thirdly, neuropathology, including clinical disorders such as dementia, Tourette syndrome, and schizophrenia; fourthly, surgical procedures including partial and complete callosotomy and commissurotomy; fifthly, cognitive neuroscience; and sixthly, other features of the corpus callosum, including its medicolegal aspects and statistical shape analysis. This comprehensive reference book will be an ideal source for neuroscientists at all levels, from graduate students to researchers in specific disciplines studying this region including neuroanatomists, embryologists, neurosurgeons, neurologists, neuroradiologists and pediatricians, who seek both basic and more advanced information regarding the distinctive anatomical, physiological and pathological features of the human corpus callosum. ​

This book provides an in-depth review of the knowledge of craniospinal arachnoid cysts, with emphasis on epidemiology, genetics, neuroimaging, clinical presentations, and operative management. Sections on postoperative complications, outcome, and medicolegal aspects of this entity are also included. This richly illustrated book will help the reader in choosing the most appropriate way to manage this challenging neurosurgical disease process. This work also considers future areas of investigation and innovative therapeutic philosophies. This comprehensive reference book will be an ideal source for neuroscientists at all levels of their training in multiple different disciplines, from graduate students to specific research scientists studying this topic, including neurosurgeons, neurologists, neuroradiologists, pediatricians, and those seeking both basic and more sophisticated information regarding craniospinal arachnoid cysts.

This book provides an in-depth review of the current state of knowledge on the intracranial chronic subdural hematoma, with an emphasis on the etiology, risk factors, pathophysiology, anatomic pathology, epidemiology, clinical presentation, imaging findings, and treatment modalities, both medical and surgical. Sections on the postoperative complications, prognosis, and medicolegal aspects of this illness are also included. Lastly, the book considers future areas of investigation and innovative therapeutic philosophies.  This richly illustrated book will help the reader choose the most appropriate way to manage this challenging neurosurgical disease process. It is an ideal resource for neuroscientists at all levels, from graduate students to research scientists, including neurosurgeons, neurologists, neuroradiologists, and pediatricians, and for those seeking both basic and more advanced information regarding the craniospinal subdural hematoma, including acute, subacute and chronic ones.

This book provides an in-depth review of the sutures of the skull. The premature closure of the sutures of the skull (craniosynostosis) due to genetic or metabolic etiologies results in typical progressive skull deformity, due to both the inhibition of growth caused by the affected cranial suture and associated compensatory expansion of the skull along the open ones. Today, it is well known that early diagnosis of craniosynostosis is crucial for the best surgical outcomes and for the normal development of the brain and cosmetic appearance of the skull. As such, in addition to the anatomy, biology, genetics and embryology of the sutures of the skull, the book also covers the diagnosis and treatment of different forms of craniosynostosis such as metopism, and animal models for cranial suture research.This comprehensive work is a valuable resource for neuroscientists at all levels, from graduate students to researchers, as well as neurosurgeons, neuroanatomists, pediatricians, andneurologists seeking both basic and more advanced information on the unique structure of the sutures of the human skull.