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Neuromuscular case studies
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Bertorini, Tulio E.
Neuromuscular case studies
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Neuromuscular case studiesTulio E. Bertorini.
作者:
Bertorini, Tulio E.
出版者:
Philadelphia :Butterworth-Heinemann,c2008.
面頁冊數:
xiv, 646 p. :ill. (some col.) ;29 cm.
標題:
Neuromuscular diseasesCongresses.
電子資源:
An electronic book accessible through the World Wide Web; click for information
ISBN:
9780750673327
Neuromuscular case studies
Bertorini, Tulio E.
Neuromuscular case studies
[electronic resource] /Tulio E. Bertorini. - 1st ed. - Philadelphia :Butterworth-Heinemann,c2008. - xiv, 646 p. :ill. (some col.) ;29 cm.
Includes bibliographical references and index.
Chapter 1 Neuromuscular Anatomy and Function -- Chapter 2Neurological Evaluation and Ancillary Tests -- Chapter 3Therapy in Neuromuscular Diseases -- Case 1Carpal Tunnel Syndrome in an Elderly Woman Likely from Rheumatoid Arthritis and the Use of a Walker -- Case 2A Uremic Patient with a Shunt-Related Ischemic Monomelic Neuropathy Later Diagnosed with Carpal Tunnel Syndrome from Beta-2 Microglobulin Accumulation -- Case 3A Diabetic with Peripheral Neuropathy and Carpal Tunnel Syndrome Who Later Developed Dysautonomia -- Case 4Martin Gruber and Anastomosis and Carpal Tunnel Syndrome -- Case 5Traumatic Median Neuropathy at the Elbow Mimicking Anterior Interossei Syndrome -- Case 6Pronator Teres Syndrome -- Case 7Ulnar Entrapment at the Elbow -- Case 8Ulnar Neuropathy at the Wrist from a Ganglion Cyst -- Case 9Focal Myositis Causing Radial Neuropathy -- Case 10Musculoskeletal Neuropathy from Compression During Positioning for Back Surgery -- Case 11Acute Brachial Neuritis -- Case 12Lower Trunk Plexopathy and Horner b2 ss Syndrome from Lymphoma -- Case 13 Radiation Plexopathy -- Case 14Suprascapular Neuropathy -- Case 15C6 Radiculopathy with Motor Deficits from Herpes Zoster -- Case 16C5 Radiculopathy from a Ruptured Disc -- Case 17C7 Radiculopathy from a Herniated Disc -- Case 18L4 Radiculopathy from a Disc Herniation and Peroneal Entrapment -- Case 19S1 Radiculopathy -- Case 20L5 Radiculopathy and an Accessory Peroneal Nerve -- Case 21L2 Radiculopathy from Tumor Invasion -- Case 22Demylinating Lumbosacral Radiculoneuropathy in a Diabetic -- Case 23Cauda Equina Syndrome from Spinal Stenosis -- Case 24Sciatic Neurofibroma Mimicking Tarsal Tunnel Syndrome -- Case 25Femoral Neuropathy from a Hematoma from Angiography -- Case 26Carcinomatous Lumbosacral Plexopathy -- Case 27Meralgia Paresthetica -- Case 28Lumbosacral Ependymoma Mimicking a Motor Neuron Disease -- Case 29Acute Facial Neuropathy -- Case 30Neurosarcoidosis Presenting with Bilateral Vi and Vii Nerve Palsies -- Case 31A Patient with Als Presenting with Head Drop -- Case 32Man in the Barrel Syndrome -- Case 33Benign Focal Amyotrophy or Monomelic Amyotrophy -- Case 34Post-Myelopathy Amyotrophy -- Case 35Tethered Cord Syndrome Causing Muscle Pseudohypertrophy from Partial Denervation -- Case 36Kennedy b2 ss Disease -- Case 37Machado-Joseph Disease -- Case 38Infantile Spinal Muscular Atrophy -- Case 39Guillain Bar�r Syndrome with Central Demyelination -- Case 40Acute Inflammatory Polyneuropathy in an HIV Positive Person -- Case 41Miller Fisher Syndrome -- Case 42Ciguatera Poisoning -- Case 43Acute Quadriplegic Polyneuropathy from Porphyria -- Case 44Critical Illness Myopathy -- Case 45Pernicious Anemia Presenting with Hand Numbness in a Patient with Cervical Spondylosis -- Case 46Pernicious Anemia Manifesting with Weakness and Abnormal Gait -- Case 47Chronic Inflammatory Demyelinating Polyneuropathy -- Case 48Chronic Inflammatory Demyelinating Polyneuropathy with -- Asymmetric Presentation in a Patient with a Monoclonal Gammopathy -- Case 49Purely Motor Chronic Inflammatory Demyelinating Polyneuropathy -- Case 50Subacute Inflammatory Demyelinating Polyneuropathy in a Diabetic -- Case 51Demyelinating Neuropathy Associated with MAG Antibodies -- Case 52Hereditary Demyelinating Polyneuropathy with Multiple Sclerosis -- Case 53Inflammatory Polyneuropathy after Bariatric Surgery -- Case 54Diabetic Amyotrophy -- Case 55Diabetic Amyotrophy/Mononeuritis Multiplex in the Upper Extremities -- Case 56Diabetic Muscle Infarct -- Case 57Uremic Neuropathy -- Case 58(A) Demyelinating Charcot-Marie-Tooth Disease (B) Axonal Charcot-Marie-Tooth Disease -- Case 59Hereditary Polyneuropathy with Liability to Pressure Palsy Presenting with Bilateral Median Neuropathy after Snow Skiing -- Case 60Hereditary Neuropathy with Liability to Pressure Palsy Presenting with a Footdrop -- Case 61Mononeuritis Multiplex from Vasculitic Neuropathy -- Case 62Vasculitic Neuropathy from Rheumatoid Arthritis -- Case 63Wegener b2 ss Granulomatosis and Peripheral Neuropathy -- Case 64Neurolymphomatosis Presenting with Mononeuritis Multiplex -- Case 65Paraneoplastic Ganglioneuritis -- Case 66Familial Amyloid Neuropathy -- Case 67Amiodarone Neuropathy -- Case 68Myasthenia Gravis Presenting with Difficulty Swallowing -- Case 69Familial Myasthenia Gravis with Recurrence after Thymectomy -- Case 70Eaton Lambert Myasthenic Syndrome Secondary to Small Cell Carcinoma of the Lung -- Case 71Eaton Lambert Myasthenic Syndrome in a Patient with Hypothyroidism and Later Uterine Carcinoma -- Case 72Slow Channel Congenital Myasthenic Syndrome -- Case 73Hypokalemic Periodic Paralysis -- Case 73Thyrotoxic Periodic Paralysis -- Case 74Becker b2 ss Muscular Dystrophy Presenting with Large Muscles -- Case 75A Manifest Carrier of Muscular Dystrophy -- Case 76Distal Muscular Dystrophy from Dysferlin Deficiency -- Case 77Oculopharyngeal Muscular Dystrophy -- Case 78Facioscapulohumeral Muscular Dystrophy -- Case 79Merosin Deficient Congenital Muscular Dystrophy -- Case 80Central Core Disease Manifesting with Progressive Weakness in an Adult -- Case 81Mitochondrial Disease Manifests as Progressive External Ophthalmoplegia Mimicking Myasthenia Gravis -- Case 82Mitochondrial Myopathy with Prominent Neck Lipoma -- Case 83Rhabdomyolysis in a Patient with Myophosphorylase Deficiency -- Case 84Adult Onset Acid Maltase Deficiency -- Case 85Myoglobinuria from a Viral Infection as the First Manifestation of Carnitine Palmitoyltransferase (Cpt) Deficiency in An Adult -- Case 86Proximal Weakness from Beta-2 Microglobulin Accumulation in a Uremic Patient -- Case 87Hypothyroid Myopathy -- Case 88Hypoparathyroid Myopathy -- Case 89Dermatomyositis in a Mother and Her Son -- Case 90Polymyositis and Myoadenylate Deaminase Deficiency (Double Trouble?) -- Case 91Inclusion Body Myositis -- Case 92Inclusion Body Myositis in a Young HIV Positive Person -- Case 93Eosinophilic Fascitis -- Case 94Bent Spine Syndrome -- Case 95A Case of Stiff Person Syndrome and Myasthenia Gravis -- Case 96Cramp Fasciculation Syndrome from a Chronic, Predominantly Motor Neuronopathy -- Case 97Myotonic Congenita -- Case 98Schwartz-Jampel Syndrome -- Case 99Tetany -- Case 100Proximal Myotonic Myopathy -- Case 101 Acquired Rippling Muscle Disease.
In this unique book, Dr. Bertorini guides you through more than 100 cases that demonstrate the diagnosis and management of a wide range of common and rare neuromuscular disorders. No other reference boasts such a large array of clinical studies devoted to all areas of this broad topic! Each case study reviews the etiologies, pathogenesis, differential diagnosis, and management of a particular disorder, helping you not only recognize its presentation, but also determine a diagnosis and the best treatment plans for your patients. You b2 sll also find expert guidance on the basic mechanisms of neuromuscular disorders, clinical examination, and diagnostic tests b7 sincluding EMG, muscle biopsy, genetic testing, and more. More than 100 detailed case studies explore both common and rare neuromuscular disorders and the treatment protocols for each, equipping you with the knowledge you need to confidently manage any challenge. Each case includes a summary of important points or highlights of the study. Case studies are arranged either by complaint or by diagnosis so that you can successfully manage your patients with or without an initial diagnosis. Comprehensive coverage of EMGs and nerve conduction studies and other diagnostic tests, including muscle and nerve biopsies and genetic testing, helps you accurately diagnose nerve, muscle, and neuromuscular transmission disorders. Detailed discussions of treatment plans and commonly used drugs enhance your management of autoimmune disorders, painful neuropathy, dysautonomia, and other neuromuscular disorders. A reader-friendly format takes you step by step through the diagnosis and treatment of neuromuscular disorders, from the basic anatomy and physiology of the nerve and muscle through to clinical evaluation, diagnostic testing, and therapy. More than 350 high-quality illustrations, including full-color patient photographs, biopsies, and EMG tracings, make complex concepts easier to understand and apply.
Electronic reproduction.
Amsterdam :
Elsevier Science & Technology,
2009.
Mode of access: World Wide Web.
ISBN: 9780750673327
Source: 17105:17105Elsevier Science & Technologyhttp://www.sciencedirect.comSubjects--Topical Terms:
402495
Neuromuscular diseases
--Congresses.Index Terms--Genre/Form:
214472
Electronic books.
LC Class. No.: RC925.5 / .B435 2008
Dewey Class. No.: 616.7/44
National Library of Medicine Call No.: 2008 H-448
Neuromuscular case studies
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Chapter 1 Neuromuscular Anatomy and Function -- Chapter 2Neurological Evaluation and Ancillary Tests -- Chapter 3Therapy in Neuromuscular Diseases -- Case 1Carpal Tunnel Syndrome in an Elderly Woman Likely from Rheumatoid Arthritis and the Use of a Walker -- Case 2A Uremic Patient with a Shunt-Related Ischemic Monomelic Neuropathy Later Diagnosed with Carpal Tunnel Syndrome from Beta-2 Microglobulin Accumulation -- Case 3A Diabetic with Peripheral Neuropathy and Carpal Tunnel Syndrome Who Later Developed Dysautonomia -- Case 4Martin Gruber and Anastomosis and Carpal Tunnel Syndrome -- Case 5Traumatic Median Neuropathy at the Elbow Mimicking Anterior Interossei Syndrome -- Case 6Pronator Teres Syndrome -- Case 7Ulnar Entrapment at the Elbow -- Case 8Ulnar Neuropathy at the Wrist from a Ganglion Cyst -- Case 9Focal Myositis Causing Radial Neuropathy -- Case 10Musculoskeletal Neuropathy from Compression During Positioning for Back Surgery -- Case 11Acute Brachial Neuritis -- Case 12Lower Trunk Plexopathy and Horner b2 ss Syndrome from Lymphoma -- Case 13 Radiation Plexopathy -- Case 14Suprascapular Neuropathy -- Case 15C6 Radiculopathy with Motor Deficits from Herpes Zoster -- Case 16C5 Radiculopathy from a Ruptured Disc -- Case 17C7 Radiculopathy from a Herniated Disc -- Case 18L4 Radiculopathy from a Disc Herniation and Peroneal Entrapment -- Case 19S1 Radiculopathy -- Case 20L5 Radiculopathy and an Accessory Peroneal Nerve -- Case 21L2 Radiculopathy from Tumor Invasion -- Case 22Demylinating Lumbosacral Radiculoneuropathy in a Diabetic -- Case 23Cauda Equina Syndrome from Spinal Stenosis -- Case 24Sciatic Neurofibroma Mimicking Tarsal Tunnel Syndrome -- Case 25Femoral Neuropathy from a Hematoma from Angiography -- Case 26Carcinomatous Lumbosacral Plexopathy -- Case 27Meralgia Paresthetica -- Case 28Lumbosacral Ependymoma Mimicking a Motor Neuron Disease -- Case 29Acute Facial Neuropathy -- Case 30Neurosarcoidosis Presenting with Bilateral Vi and Vii Nerve Palsies -- Case 31A Patient with Als Presenting with Head Drop -- Case 32Man in the Barrel Syndrome -- Case 33Benign Focal Amyotrophy or Monomelic Amyotrophy -- Case 34Post-Myelopathy Amyotrophy -- Case 35Tethered Cord Syndrome Causing Muscle Pseudohypertrophy from Partial Denervation -- Case 36Kennedy b2 ss Disease -- Case 37Machado-Joseph Disease -- Case 38Infantile Spinal Muscular Atrophy -- Case 39Guillain Bar�r Syndrome with Central Demyelination -- Case 40Acute Inflammatory Polyneuropathy in an HIV Positive Person -- Case 41Miller Fisher Syndrome -- Case 42Ciguatera Poisoning -- Case 43Acute Quadriplegic Polyneuropathy from Porphyria -- Case 44Critical Illness Myopathy -- Case 45Pernicious Anemia Presenting with Hand Numbness in a Patient with Cervical Spondylosis -- Case 46Pernicious Anemia Manifesting with Weakness and Abnormal Gait -- Case 47Chronic Inflammatory Demyelinating Polyneuropathy -- Case 48Chronic Inflammatory Demyelinating Polyneuropathy with -- Asymmetric Presentation in a Patient with a Monoclonal Gammopathy -- Case 49Purely Motor Chronic Inflammatory Demyelinating Polyneuropathy -- Case 50Subacute Inflammatory Demyelinating Polyneuropathy in a Diabetic -- Case 51Demyelinating Neuropathy Associated with MAG Antibodies -- Case 52Hereditary Demyelinating Polyneuropathy with Multiple Sclerosis -- Case 53Inflammatory Polyneuropathy after Bariatric Surgery -- Case 54Diabetic Amyotrophy -- Case 55Diabetic Amyotrophy/Mononeuritis Multiplex in the Upper Extremities -- Case 56Diabetic Muscle Infarct -- Case 57Uremic Neuropathy -- Case 58(A) Demyelinating Charcot-Marie-Tooth Disease (B) Axonal Charcot-Marie-Tooth Disease -- Case 59Hereditary Polyneuropathy with Liability to Pressure Palsy Presenting with Bilateral Median Neuropathy after Snow Skiing -- Case 60Hereditary Neuropathy with Liability to Pressure Palsy Presenting with a Footdrop -- Case 61Mononeuritis Multiplex from Vasculitic Neuropathy -- Case 62Vasculitic Neuropathy from Rheumatoid Arthritis -- Case 63Wegener b2 ss Granulomatosis and Peripheral Neuropathy -- Case 64Neurolymphomatosis Presenting with Mononeuritis Multiplex -- Case 65Paraneoplastic Ganglioneuritis -- Case 66Familial Amyloid Neuropathy -- Case 67Amiodarone Neuropathy -- Case 68Myasthenia Gravis Presenting with Difficulty Swallowing -- Case 69Familial Myasthenia Gravis with Recurrence after Thymectomy -- Case 70Eaton Lambert Myasthenic Syndrome Secondary to Small Cell Carcinoma of the Lung -- Case 71Eaton Lambert Myasthenic Syndrome in a Patient with Hypothyroidism and Later Uterine Carcinoma -- Case 72Slow Channel Congenital Myasthenic Syndrome -- Case 73Hypokalemic Periodic Paralysis -- Case 73Thyrotoxic Periodic Paralysis -- Case 74Becker b2 ss Muscular Dystrophy Presenting with Large Muscles -- Case 75A Manifest Carrier of Muscular Dystrophy -- Case 76Distal Muscular Dystrophy from Dysferlin Deficiency -- Case 77Oculopharyngeal Muscular Dystrophy -- Case 78Facioscapulohumeral Muscular Dystrophy -- Case 79Merosin Deficient Congenital Muscular Dystrophy -- Case 80Central Core Disease Manifesting with Progressive Weakness in an Adult -- Case 81Mitochondrial Disease Manifests as Progressive External Ophthalmoplegia Mimicking Myasthenia Gravis -- Case 82Mitochondrial Myopathy with Prominent Neck Lipoma -- Case 83Rhabdomyolysis in a Patient with Myophosphorylase Deficiency -- Case 84Adult Onset Acid Maltase Deficiency -- Case 85Myoglobinuria from a Viral Infection as the First Manifestation of Carnitine Palmitoyltransferase (Cpt) Deficiency in An Adult -- Case 86Proximal Weakness from Beta-2 Microglobulin Accumulation in a Uremic Patient -- Case 87Hypothyroid Myopathy -- Case 88Hypoparathyroid Myopathy -- Case 89Dermatomyositis in a Mother and Her Son -- Case 90Polymyositis and Myoadenylate Deaminase Deficiency (Double Trouble?) -- Case 91Inclusion Body Myositis -- Case 92Inclusion Body Myositis in a Young HIV Positive Person -- Case 93Eosinophilic Fascitis -- Case 94Bent Spine Syndrome -- Case 95A Case of Stiff Person Syndrome and Myasthenia Gravis -- Case 96Cramp Fasciculation Syndrome from a Chronic, Predominantly Motor Neuronopathy -- Case 97Myotonic Congenita -- Case 98Schwartz-Jampel Syndrome -- Case 99Tetany -- Case 100Proximal Myotonic Myopathy -- Case 101 Acquired Rippling Muscle Disease.
520
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In this unique book, Dr. Bertorini guides you through more than 100 cases that demonstrate the diagnosis and management of a wide range of common and rare neuromuscular disorders. No other reference boasts such a large array of clinical studies devoted to all areas of this broad topic! Each case study reviews the etiologies, pathogenesis, differential diagnosis, and management of a particular disorder, helping you not only recognize its presentation, but also determine a diagnosis and the best treatment plans for your patients. You b2 sll also find expert guidance on the basic mechanisms of neuromuscular disorders, clinical examination, and diagnostic tests b7 sincluding EMG, muscle biopsy, genetic testing, and more. More than 100 detailed case studies explore both common and rare neuromuscular disorders and the treatment protocols for each, equipping you with the knowledge you need to confidently manage any challenge. Each case includes a summary of important points or highlights of the study. Case studies are arranged either by complaint or by diagnosis so that you can successfully manage your patients with or without an initial diagnosis. Comprehensive coverage of EMGs and nerve conduction studies and other diagnostic tests, including muscle and nerve biopsies and genetic testing, helps you accurately diagnose nerve, muscle, and neuromuscular transmission disorders. Detailed discussions of treatment plans and commonly used drugs enhance your management of autoimmune disorders, painful neuropathy, dysautonomia, and other neuromuscular disorders. A reader-friendly format takes you step by step through the diagnosis and treatment of neuromuscular disorders, from the basic anatomy and physiology of the nerve and muscle through to clinical evaluation, diagnostic testing, and therapy. More than 350 high-quality illustrations, including full-color patient photographs, biopsies, and EMG tracings, make complex concepts easier to understand and apply.
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2009.
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Title from title screen (viewed on Dec. 9, 2009).
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