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Complications of CSF Shunting in Hydrocephalus
  • Language: en
  • Pages: 320

Complications of CSF Shunting in Hydrocephalus

  • Type: Book
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  • Published: 2014-12-02
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  • Publisher: Springer

Written and edited by leading international authorities in the field, this book provides an in-depth review of knowledge of complications of CSF shunting, with emphasis on prevention, identification, and management. It covers the full range of shunt-related complications and the various associated adverse consequences that remain common despite significant improvements in imaging techniques and therapeutic methods. The chapters are organized into two parts: complications of extrathecal CSF shunt devices and complications of endoscopy. In addition to providing clinicians and investigators with the most pertinent current evidence, the book looks forward to future areas of hydrocephalus research and to innovative therapeutic philosophies. This comprehensive reference book will be an ideal source for neurosurgeons seeking both basic and more sophisticated information and procedures relating to the complications associated with CSF shunting.

Neurosurgery
  • Language: en
  • Pages: 651

Neurosurgery

In a specialized field such as neurosurgery, highly specific knowledge is required. Training programs in the EU vary, making it difficult to standardize medical training. This manual forms the basis for a European consensus in neurosurgery. It is written for residents, students and physicians with a special interest in neurosurgery. Diagnostic and therapeutic procedures are detailed according to localization (cranial, spinal, peripheral nerves) with special consideration given to congenital defects and pediatric neurosurgical disorders, functional and stereotactic neurosurgery, as well as critical neurosurgical care. Each chapter contains the basics of anatomy and physiology. The book is well-organized and clearly structured according to each entity and its neurosurgical treatment options. A better understanding of specific neurosurgical problems will help practicing neurosurgeons provide better medical care for their patients, and will also provide the neurosurgery resident with a reliable European standard for step-by-step management of neurosurgical problems, which will prove useful when preparing for the board examination.

Annual Review of Hydrocephalus
  • Language: en
  • Pages: 176

Annual Review of Hydrocephalus

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Big and Small
  • Language: en
  • Pages: 373

Big and Small

A groundbreaking work that explores human size as a distinctive cultural marker in Western thought Author, scholar, and editor Lynne Vallone has an international reputation in the field of child studies. In this analytical tour-de-force, she explores bodily size difference--particularly unusual bodies, big and small--as an overlooked yet crucial marker that informs human identity and culture. Exploring miniaturism, giganticism, obesity, and the lived experiences of actual big and small people, Vallone boldly addresses the uncomfortable implications of using physical measures to judge normalcy, goodness, gender identity, and beauty. This wide-ranging work surveys the lives and contexts of both real and imagined persons with extraordinary bodies from the seventeenth century to the present day through close examinations of art, literature, folklore, and cultural practices, as well as scientific and pseudo-scientific discourses. Generously illustrated and written in a lively and accessible style, Vallone's provocative study encourages readers to look with care at extraordinary bodies and the cultures that created, depicted, loved, and dominated them.

Arachnoid Cysts
  • Language: en
  • Pages: 388

Arachnoid Cysts

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.

Malcolm Lowry's
  • Language: en
  • Pages: 436

Malcolm Lowry's "La Mordida"

Although Malcolm Lowry (1909-1957) published only two novels--Ultramarine and Under the Volcano--in his lifetime, numerous other works, most of which have since been edited for publication, were in various stages of composition at his death. La Mordida, the longest and most significant of the manuscripts that have not been previously published, is a draft of a novel based on Lowry's visit to Mexico in 1945-46, which ended in the arrest and deportation of Lowry and his wife following a nightmarish run-in with corrupt immigration authorities. On its most immediate level, the title La Mordida--which means "the little bite," Mexican slang for the small bribe that officials are apt to demand in o...

Medizingeschichte in Schlaglichtern
  • Language: de
  • Pages: 382

Medizingeschichte in Schlaglichtern

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Die Erforschung der
  • Language: de
  • Pages: 556
Gliomas del Encéfalo
  • Language: es
  • Pages: 683

Gliomas del Encéfalo

None

What is NOONAN SYNDROME ? Causes, Treatment and More.
  • Language: en
  • Pages: 44

What is NOONAN SYNDROME ? Causes, Treatment and More.

What is NOONAN SYNDROME ? Causes, Treatment and More. Noonan syndrome is a genetically inherited disease with heterogeneous, phenotypic manifestations that can change with age. Gene mutations involve the RAAS/MAPK (mitogen-activated protein kinase) signalling pathway. The patient presentation can range from mild to severe. Thus, The most consistent features are wide-set eyes, low-set ears, short stature, and pulmonic stenosis. Noonan syndrome is typically inherited in an autosomal dominant manner. Diagnostic criteria have been developed to aid in the diagnosis of Noonan syndrome. Noonan syndrome is typically a clinical diagnosis. Thus, it is strived in this E-Booklet to describe the Aetiology, Prevalence, Diagnosis, Management, Outlook, and Complications of Noonan syndrome along with plenty of ILLUSTRATIONS for better understanding the entity. Dr. H. K. Saboowala. M.B.(Bom) .M.R.S.H.(London