Li Shelly (16 results)

Condition: New. 2011 paperback book, as shown. SIGNED BY THE AUTHOR. New book, clean, tight and unmarked with a crisp, clean cover.

Condition: New.

Paperback or Softback. Condition: New. Future Imperfect: Best of Wily Writers. Book.

Condition: As New. Unread book in perfect condition.

Condition: New. Print on Demand.

Condition: New.

Hardcover. Condition: new. Hardcover. This case-based book answers the questions people with myasthenia gravis ask most urgently, from the fear of progression in ocular disease to the possibility of life-threatening myasthenic crisis and the realities of lifelong management. Through real-world clinical scenarios, it traces the evolution of our understanding of myasthenia gravis, highlighting key historical milestones, shifting epidemiology, and the wide spectrum of typical and atypical presentations that define this complex disorder. This book comprehensively covers topics related to clinical aspects of diagnosing and treating myasthenia gravis. Each chapter unfolds as a clinical encounter, guiding readers through diagnostic reasoning at the bedside and in the laboratory, including antibody testing, electrodiagnostics, and common diagnostic pitfalls, and usage of proper treatment. The cases illuminate frequent mistakes that delay diagnosis or lead to ineffective treatment, while offering practical strategies to avoid them. Special attention is given to ocular myasthenia, generalized myasthenia with typical and atypical presentations, myasthenic crisis, seronegative disease, thymoma-associated myasthenia gravis, pregnancy planning, allowance and avoidance of medications that could trigger myasthenic exacerbation, and challenging overlaps with conditions such as diabetes, thyroid disease, and infection. Discussions on differentiation from disorders with similar presentations such as congenital myasthenic syndromes, Lambert-Eaton myasthenic syndrome and botulism are provided. From first symptoms to refractory disease and crisis management, this book provides a clear, concise experience-driven approach to treatment selection and adjustment. Traditional therapies and modern targeted agents are discussed alongside real patient outcomes, including the proper use of pyridostigmine, corticosteroids, non-steroidal immunosuppressive therapy, intravenous immunoglobulin, plasmapheresis, complement inhibitors, FcRn antagonists, B cell depletion therapy, and thymectomy. Designed for neuromuscular specialists, neurologists, trainees, and informed clinicians, this book serves as both a trusted guide and a clinical companion for navigating the full course of myasthenia gravis with confidence and clarity. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.…

Buch. Condition: Neu. Druck auf Anfrage Neuware - Printed after ordering - This case-based book answers the questions people with myasthenia gravis ask most urgently, from the fear of progression in ocular disease to the possibility of life-threatening myasthenic crisis and the realities of lifelong management. Through real-world clinical scenarios, it traces the evolution of our understanding of myasthenia gravis, highlighting key historical milestones, shifting epidemiology, and the wide spectrum of typical and atypical presentations that define this complex disorder. This book comprehensively covers topics related to clinical aspects of diagnosing and treating myasthenia gravis.Each chapter unfolds as a clinical encounter, guiding readers through diagnostic reasoning at the bedside and in the laboratory, including antibody testing, electrodiagnostics, and common diagnostic pitfalls, and usage of proper treatment. The cases illuminate frequent mistakes that delay diagnosis or lead to ineffective treatment, while offering practical strategies to avoid them. Special attention is given to ocular myasthenia, generalized myasthenia with typical and atypical presentations, myasthenic crisis, seronegative disease, thymoma-associated myasthenia gravis, pregnancy planning, allowance and avoidance of medications that could trigger myasthenic exacerbation, and challenging overlaps with conditions such as diabetes, thyroid disease, and infection. Discussions on differentiation from disorders with similar presentations such as congenital myasthenic syndromes, Lambert-Eaton myasthenic syndrome and botulism are provided.From first symptoms to refractory disease and crisis management, this book provides a clear, concise experience-driven approach to treatment selection and adjustment. Traditional therapies and modern targeted agents are discussed alongside real patient outcomes, including the proper use of pyridostigmine, corticosteroids, non-steroidal immunosuppressive therapy, intravenous immunoglobulin, plasmapheresis, complement inhibitors, FcRn antagonists, B cell depletion therapy, and thymectomy. Designed for neuromuscular specialists, neurologists, trainees, and informed clinicians, this book serves as both a trusted guide and a clinical companion for navigating the full course of myasthenia gravis with confidence and clarity.…

Hardcover. Condition: new. Hardcover. This case-based book answers the questions people with myasthenia gravis ask most urgently, from the fear of progression in ocular disease to the possibility of life-threatening myasthenic crisis and the realities of lifelong management. Through real-world clinical scenarios, it traces the evolution of our understanding of myasthenia gravis, highlighting key historical milestones, shifting epidemiology, and the wide spectrum of typical and atypical presentations that define this complex disorder. This book comprehensively covers topics related to clinical aspects of diagnosing and treating myasthenia gravis. Each chapter unfolds as a clinical encounter, guiding readers through diagnostic reasoning at the bedside and in the laboratory, including antibody testing, electrodiagnostics, and common diagnostic pitfalls, and usage of proper treatment. The cases illuminate frequent mistakes that delay diagnosis or lead to ineffective treatment, while offering practical strategies to avoid them. Special attention is given to ocular myasthenia, generalized myasthenia with typical and atypical presentations, myasthenic crisis, seronegative disease, thymoma-associated myasthenia gravis, pregnancy planning, allowance and avoidance of medications that could trigger myasthenic exacerbation, and challenging overlaps with conditions such as diabetes, thyroid disease, and infection. Discussions on differentiation from disorders with similar presentations such as congenital myasthenic syndromes, Lambert-Eaton myasthenic syndrome and botulism are provided. From first symptoms to refractory disease and crisis management, this book provides a clear, concise experience-driven approach to treatment selection and adjustment. Traditional therapies and modern targeted agents are discussed alongside real patient outcomes, including the proper use of pyridostigmine, corticosteroids, non-steroidal immunosuppressive therapy, intravenous immunoglobulin, plasmapheresis, complement inhibitors, FcRn antagonists, B cell depletion therapy, and thymectomy. Designed for neuromuscular specialists, neurologists, trainees, and informed clinicians, this book serves as both a trusted guide and a clinical companion for navigating the full course of myasthenia gravis with confidence and clarity. Shipping may be from our Sydney, NSW warehouse or from our UK or US warehouse, depending on stock availability.…

Hardback. Condition: New.

Paperback. Condition: Good. No Jacket. Pages can have notes/highlighting. Spine may show signs of wear. ~ ThriftBooks: Read More, Spend Less.

Hardback. Condition: New.

Paperback / softback. Condition: New. This item is printed on demand. New copy - Usually dispatched within 5-9 working days.

paperback. Condition: New. Language:Chinese.Paperback. Pub Date: 2015-4-1 Pages: 301 Publisher: Machinery Industry Press daily organ most frequently used what is? The answer is that our brains. (Even during sleep your brain also is active) What a day is the most neglected organ? The answer is our brains. (You'll immediately eye astringent eye drops. brain tired you would not know it?) Riding a boat behind. The brain is the same. if you do not engage in active practice. day by day it becomes silly to let you see your jo.…

Buch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -This case-based book answers the questions people with myasthenia gravis ask most urgently, from the fear of progression in ocular disease to the possibility of life-threatening myasthenic crisis and the realities of lifelong management. Through real-world clinical scenarios, it traces the evolution of our understanding of myasthenia gravis, highlighting key historical milestones, shifting epidemiology, and the wide spectrum of typical and atypical presentations that define this complex disorder. This book comprehensively covers topics related to clinical aspects of diagnosing and treating myasthenia gravis.Each chapter unfolds as a clinical encounter, guiding readers through diagnostic reasoning at the bedside and in the laboratory, including antibody testing, electrodiagnostics, and common diagnostic pitfalls, and usage of proper treatment. The cases illuminate frequent mistakes that delay diagnosis or lead to ineffective treatment, while offering practical strategies to avoid them. Special attention is given to ocular myasthenia, generalized myasthenia with typical and atypical presentations, myasthenic crisis, seronegative disease, thymoma-associated myasthenia gravis, pregnancy planning, allowance and avoidance of medications that could trigger myasthenic exacerbation, and challenging overlaps with conditions such as diabetes, thyroid disease, and infection. Discussions on differentiation from disorders with similar presentations such as congenital myasthenic syndromes, Lambert-Eaton myasthenic syndrome and botulism are provided.From first symptoms to refractory disease and crisis management, this book provides a clear, concise experience-driven approach to treatment selection and adjustment. Traditional therapies and modern targeted agents are discussed alongside real patient outcomes, including the proper use of pyridostigmine, corticosteroids, non-steroidal immunosuppressive therapy, intravenous immunoglobulin, plasmapheresis, complement inhibitors, FcRn antagonists, B cell depletion therapy, and thymectomy. Designed for neuromuscular specialists, neurologists, trainees, and informed clinicians, this book serves as both a trusted guide and a clinical companion for navigating the full course of myasthenia gravis with confidence and clarity. 245 pp. Englisch.…

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