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Management of Pituitary Tumors, an Issue of Neurosurgery Clinics
  • Language: en
  • Pages: 240

Management of Pituitary Tumors, an Issue of Neurosurgery Clinics

  • Type: Book
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  • Published: 2012-10-09
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  • Publisher: Saunders

This issue of the Neurosurgery Clinics of North America, Guest Edited by Drs. Manish Aghi and Lewis Blevins, is devoted to Management of Pituitary Tumors. Experts in the field have assembled to provide articles on Imaging of the pituitary and parasellar region; Management of Incidentally Found Nonfunctional Pituitary Tumors; Endoscopic Surgery for Pituitary Tumors; Prolactinomas - Medical versus Surgical Management; Neurosurgery for Cushing's Disease; Postoperative radiotherapy and stereotactic radiosurgery for pituitary tumors; Management options for persistent postoperative acromegaly; Medical management of persistent and recurrent Cushing's disease; Management of Large Aggressive Nonfunctional Pituitary Tumors - Experimental Medical Options when Surgery and Radiation Fail; Pituitary Carcinoma; Visual Outcomes after Surgery For Nonfunctional Adenomas Causing Visual Compromise; and Hypopituitarism and Central Diabetes Insipidus: Peri-Operative Diagnosis and Management.

Management of Pituitary Tumors, An Issue of Neurosurgery Clinics - E-Book
  • Language: en
  • Pages: 240

Management of Pituitary Tumors, An Issue of Neurosurgery Clinics - E-Book

This issue of the Neurosurgery Clinics of North America, Guest Edited by Drs. Manish Aghi and Lewis Blevins, is devoted to Management of Pituitary Tumors. Experts in the field have assembled to provide articles on Imaging of the pituitary and parasellar region; Management of Incidentally Found Nonfunctional Pituitary Tumors; Endoscopic Surgery for Pituitary Tumors; Prolactinomas – Medical versus Surgical Management; Neurosurgery for Cushing’s Disease; Postoperative radiotherapy and stereotactic radiosurgery for pituitary tumors; Management options for persistent postoperative acromegaly; Medical management of persistent and recurrent Cushing’s disease; Management of Large Aggressive Nonfunctional Pituitary Tumors – Experimental Medical Options when Surgery and Radiation Fail; Pituitary Carcinoma; Visual Outcomes after Surgery For Nonfunctional Adenomas Causing Visual Compromise; and Hypopituitarism and Central Diabetes Insipidus: Peri-Operative Diagnosis and Management.

Pituitary Adenoma, An Issue of Neurosurgery Clinics of North America
  • Language: en
  • Pages: 153

Pituitary Adenoma, An Issue of Neurosurgery Clinics of North America

This issue of Neurosurgery Clinics, Guest Edited by Drs. Manish K. Aghi and Lewis S. Blevins, will focus on Pituitary Adenoma. Topics include, but are not limited to, Molecular biology of nonfunctional and functional pituitary adenomas, Intraoperative Fluorescent Visualization of pituitary adenomas, Intraoperative MRI for pituitary adenomas, Pituitary Apoplexy, Management of giant pituitary adenomas, Management of Pituitary Adenomas Invading the Cavernous Sinus, Management of Recurrent Pituitary Adenomas, Medical Management of Cushing’s Disease, Medical Management of Acromegaly, Surgery for Pediatric Pituitary Adenomas, Visual Outcomes after Pituitary Surgery, Endocrine Outcomes after Pituitary Surgery, Sodium perturbations after pituitary surgery, and Sinonasal Quality of Life After Pituitary Surgery.

Acromegaly
  • Language: en
  • Pages: 300

Acromegaly

Reviewing the most current literature, this text is a guide to medical decision-making regarding the diagnosis and treatment of patients with acromegaly. The scope of the book is comprehensive, covering all relevant facets of acromegaly, beginning with a history of the disorder and a review of the somatotrophic axis. Etiology is then discussed, including growth hormone secreting pituitary adenomas and other neuroendocrine tumors. Subsequent chapters present imaging modalities and diagnosis via radiology and clinical findings, as well as comorbid symptoms such as sleep apnea, musculoskeletal considerations, cardiovascular disorders, cancer and diabetes. Both medical and surgical management chapters describe each in detail, including radiotherapy, transsphenoidal surgery, somatostatin analogues and dopamine agonists. Concluding chapters present long-term follow-up as well as an extended selected patient story detailing life with the disease. Bringing together the latest in endocrinologic and neurosurgical evidence and practice, Acromegaly will be the go-to resource for this challenging condition for years to come.

Cardiovascular and Metabolic Comorbidities in Pituitary Disorders
  • Language: en
  • Pages: 108

Cardiovascular and Metabolic Comorbidities in Pituitary Disorders

Pituitary disorders may be associated with an increased risk of cardiovascular and metabolic complications and, in consequence, increased mortality. Excessive secretion of pituitary hormones provokes functional and systemic abnormalities which can be manifested by cardiovascular complications such as eg. arterial hypertension, heart failure, arrhythmia, as through metabolic disturbances, including obesity and diabetes. Subclinical effects of pituitary diseases, such as cardiac and vascular dysfunction, also modifies prognosis but due to its asymptomatic course are frequently diagnosed with significant time delay. Even successful surgery and pharmacological treatment of pituitary disorders do...

New Horizons in Tumor Microenvironment Biology and Therapy: Implications for New Therapies Vol. II
  • Language: en
  • Pages: 254
Meningioma: From Basic Research to Clinical Translational Study
  • Language: en
  • Pages: 409

Meningioma: From Basic Research to Clinical Translational Study

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The Evidence for Neurosurgery
  • Language: en
  • Pages: 602

The Evidence for Neurosurgery

This textbook aims to examine some of the most controversial areas of neurological surgery by applying the current evidence to illuminate our understanding of the pathophysiology of each disease and the outcomes from surgical and non-surgical treatments. The Evidence for Neurosurgery is a textbook that will challenge current dogmas in many instances, provide an organized framework for understanding where current evidence can be applied clinically, and illustrate where gaps in the evidence exist and how these deficiencies may be filled in the future. In the first chapter, "Clinical Evidence", the reader will gain an understanding of the levels of clinical evidence and will learn what types of study designs are appropriate and in which situations. The textbook is then divided into six sections: Spine, Vascular, Tumor, Pediatrics, Functional, and Trauma.

Tumors of the Central Nervous System, Volume 7
  • Language: en
  • Pages: 368

Tumors of the Central Nervous System, Volume 7

Various aspects, including diagnosis, therapy, and prognosis, of two brain tumors (meningioma and schwannoma) , of brain tumors are discussed in this volume. Insights on the understanding of molecular pathways involved in brain tumor biology are explained. For example, the role of E-cadherin gene instability, carbonic anhydrase 11, urokinase plasminogen activator, and Wnt signaling is discussed in detail. Such information will lead to the development of effective aniicancer drugs. The role of molecular genetics and epigenetic mechanisms in schwannomas is explained. Also, is explained the role of cyclin D1 in vestibular schwannoma. The determination of subtypes of meningiomas using perfusion ...

Tumors of the Central Nervous System, Volume 11
  • Language: en
  • Pages: 396

Tumors of the Central Nervous System, Volume 11

Like the ten preceding volumes in the series Tumors of the Central Nervous System, this book is distinguished for its comprehensive approach, its distinguished roster of some 93 contributors representing 8 different countries and its embrace of leading-edge technology and methods. Volume 11: Imaging, Glioma and Glioblastoma, Stereotactic Radiotherapy, Spinal Cord Tumors, Meningioma, and Schwannomas concentrates on the diagnosis, prognosis and therapy of four types of tumors, namely Glioblastoma, Meningioma, Schwannoma and Spinal Tumors. The book offers an in-depth survey of a range of new technologies and their applications to tumor diagnosis, treatment and therapy assessment. The contributors explain in thorough detail a range of current and newly developed imaging methods, including molecular imaging and PET scan. Also covered is molecular profiling of brain tumors to select therapy in clinical trials of brain tumors. Discussion includes a review of such surgical treatments as resection and the application of non-invasive stereotactic radiosurgery for treating high-risk patients with brain metastasis. Additional discussion is devoted to tumor seeding.