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Retinoblastoma constitutes a global disease that burdens many families all over the world. This book highlights the essential basic information needed by every ophthalmologist and covers all aspects of this tumor: history, genetics, epidemiology, clinical features, diagnosis, imaging, management, and prognosis. The book includes basic knowledge, but is also designed to discuss current treatment modalities showing improved survival compared to the past. A whole chapter is dedicated to histopathological features and the American Joint Commission on Cancer staging system, with the aim of having it internationally used in all countries to improve outcomes and for research purposes. Readers will find the book enjoyable, comprehensive, and easy to understand.
September 07-08, 2017 Paris, France Key Topics : Psychology Case Reports, Case Reports on Neurology, Ophthalmology Case Reports, Dentistry Case Reports, Cardiology Case Reports, Pulmonology Case Reports, Gastroenterology Case Reports, Diabetes Case Reports, Obstetrics and Gynaecology Case Reports, Epidemiology Case Reports, Surgical Case Reports, Case Reports on Paediatrics, Case Reports on Public Health, Dermatology Case Reports, Emergency Medicine and Critical Care Case Reports, Forensic and Legal Medicine Case reports, Internal Medicine Case Reports, Orthopaedics & Rheumatology Case Reports, Pharmacology and Therapeutics Case Reports, Women’s Health Case Reports, Radiology Case Reports, Anaesthesiology Case Reports, Pathology- Anatomic & Clinical Case Reports, Sexual Health Case Reports, Case Reports in Cancer Science, Case Reports in Clinical Pathology, Geriatric Medicine Case Reports, Veterinary Case Reports, Vascular and Endovascular Surgery,
Neurofibromatosis, one of the most common genetic disorders, is a group of three conditions—Neurofibromatosis 1, Neurofibromatosis 2 and Schwannomatosis—that share some clinical features, such as the presence of cranial and spinal nerve sheet tumors. However, they differ in type of genetic disorder, age of clinical onset, manifestations, management and prognosis. Due to multisystem involvement, a multidisciplinary treatment approach that includes research is ideal. This book provides a systematic, comprehensive and updated outline of Neurofibromatosis. It is a useful reference for clinicians, researchers and students.
Frontiers in Oncology is delighted to present the Methods in series of article collections. Methods in Surgical Oncology will publish high-quality methodical studies on key topics in the field. It aims to highlight recent advances in the field, whilst emphasizing important directions and new possibilities for future inquiries. The Methods in Surgical Oncology collection aims to highlight the latest experimental techniques and methods used to investigate fundamental questions in Surgical Oncology. Review Articles or Opinion Articles on methodologies or applications including the advantages and limitations of each are welcome. This Research Topic includes technologies and up-to-date methods which help aim to help advance science.
Retinoblastoma constitutes a global disease that burdens many families all over the world. This book highlights the essential basic information needed by every ophthalmologist and covers all aspects of this tumor: history, genetics, epidemiology, clinical features, diagnosis, imaging, management, and prognosis. The book includes basic knowledge, but is also designed to discuss current treatment modalities showing improved survival compared to the past. A whole chapter is dedicated to histopathological features and the American Joint Commission on Cancer staging system, with the aim of having it internationally used in all countries to improve outcomes and for research purposes. Readers will find the book enjoyable, comprehensive, and easy to understand.
Kniha přináší souhrnné údaje o genetickém poradenství, molekulárních metodách, o nejčastějších nádorových syndromech a jejich molekulárních příčinách, jejich klinickém sledování a prevenci, ale i přehledné údaje o méně častých až vzácných onemocněních.
The author of this instructive volume is in the direct line of missionary pioneers to the Moslem world. He follows Raymond Lull, Henry Martyn, Ion Keith-Falconer, and Bishop French, and, with his friend and comrade the Rev. James Cantine, now stands in the shining line of succession at the close of a decade of patient and brave service at that lonely outpost on the shores of the Persian Gulf. Others have followed in their footsteps, until the Arabian Mission, the adopted child of the Reformed Church in America, is at present a compact and resolute group of men and women at the gates of Arabia, waiting on God's will, and intent first of all upon fulfilling in the spirit of obedience to the Master the duty assigned them.
Al-Mefty's Meningiomas, Second Edition is the definitive guide to meningioma diagnosis, treatment, and surgery, and reflects over a decade of major advances in the diagnosis and management of both intracranial and spinal meningiomas since the first edition was published.The text begins with important information on anatomy, pathology, and epidemiology, followed by clinical and preoperative considerations. The expert authors then provide detailed descriptions of state-of-the-art surgical approaches listed by anatomical site and special operative considerations for intracranial meningiomas. The book closes with incisive discussion of breakthroughs in radiosurgery, radiotherapy and chemotherapy...
Now thoroughly revised, this Second Edition text focuses on a case-based learning approach that features decision-making information presented in algorithmic format. Sections covered are the anatomy of the orbit, pathophysiologic and anatomic principles in classifying, diagnosing and investigating orbital disease, diseases of the orbit, and the management of those diseases. New topics include orbital ultrasound, gamma scanning, magnetic resonance imaging, incidence of lesions by location, management of complex vascular lesions, granulomatous inflammations of the orbit, and orbital atrophy. A conceptual model is presented and a new classification scheme discussed. Several chapters have been updated and illustrations are plentiful.