Info
- Utilizzare la checkbox di selezione a fianco di ciascun documento per attivare le funzionalità di stampa, invio email, download nei formati disponibili del (i) record.
Evaluation and treatment of myopathies / / edited by Robert C. Griggs, Emma Ciafaloni, Patrick F. Chinnery
| Evaluation and treatment of myopathies / / edited by Robert C. Griggs, Emma Ciafaloni, Patrick F. Chinnery |
| Edizione | [Second edition.] |
| Pubbl/distr/stampa | Oxford : , : Oxford University Press, , [2014] |
| Descrizione fisica | 1 online resource (387 p.) |
| Disciplina | 616.7/44 |
| Altri autori (Persone) | GriggsRobert C. <1939-> |
| Collana | Contemporary neurology series |
| Soggetto topico |
Muscles - Diseases - Treament
Muscles - Diseases - Diagnosis |
| Soggetto genere / forma | Electronic books. |
| ISBN |
0-19-933040-9
0-19-934886-3 0-19-987394-1 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Structure and function of normal muscle / Robert C. Griggs -- Evaluation of the patient with myopathy / Robert C. Griggs, Emma Ciafaloni -- Genetic evaluation of the patient and family / Gerald Pfeffer, Patrick F. Chinnery -- The muscular dystrophies / Emma Ciafaloni, Robert C. Griggs -- Myofibrillar myopathies / Duygu Selcen -- Congenital myopathies / Francesco Muntoni, Caroline Sewry, Heinz Jungbluth -- Metabolic myopathies / Gráinne S. Gorman, Patrick F. Chinnery -- Mitochondrial myopathy / Gerald Pfeffer, Patrick F. Chinnery -- Muscle channelopathies / Araya Puwanant, Robert C. Griggs -- Inflammatory myopathies / Anthony A. Amato, Andrew Mammen -- Muscle pain and fatigue / Michael R. Rose, Dr. Patrick Gordon -- Prevention and management of systemic complications of myopathies / Wendy M. King, Robert C. Griggs. |
| Record Nr. | UNINA-9910453667603321 |
| Oxford : , : Oxford University Press, , [2014] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Evaluation and treatment of myopathies / / edited by Robert C. Griggs, Emma Ciafaloni, Patrick F. Chinnery
| Evaluation and treatment of myopathies / / edited by Robert C. Griggs, Emma Ciafaloni, Patrick F. Chinnery |
| Edizione | [Second edition.] |
| Pubbl/distr/stampa | Oxford : , : Oxford University Press, , [2014] |
| Descrizione fisica | 1 online resource (387 p.) |
| Disciplina | 616.7/44 |
| Altri autori (Persone) | GriggsRobert C. <1939-> |
| Collana | Contemporary neurology series |
| Soggetto topico |
Muscles - Diseases - Treament
Muscles - Diseases - Diagnosis |
| ISBN |
0-19-933040-9
0-19-934886-3 0-19-987394-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Structure and function of normal muscle / Robert C. Griggs -- Evaluation of the patient with myopathy / Robert C. Griggs, Emma Ciafaloni -- Genetic evaluation of the patient and family / Gerald Pfeffer, Patrick F. Chinnery -- The muscular dystrophies / Emma Ciafaloni, Robert C. Griggs -- Myofibrillar myopathies / Duygu Selcen -- Congenital myopathies / Francesco Muntoni, Caroline Sewry, Heinz Jungbluth -- Metabolic myopathies / Gráinne S. Gorman, Patrick F. Chinnery -- Mitochondrial myopathy / Gerald Pfeffer, Patrick F. Chinnery -- Muscle channelopathies / Araya Puwanant, Robert C. Griggs -- Inflammatory myopathies / Anthony A. Amato, Andrew Mammen -- Muscle pain and fatigue / Michael R. Rose, Dr. Patrick Gordon -- Prevention and management of systemic complications of myopathies / Wendy M. King, Robert C. Griggs. |
| Record Nr. | UNINA-9910791052903321 |
| Oxford : , : Oxford University Press, , [2014] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Evaluation and treatment of myopathies / / edited by Robert C. Griggs, Emma Ciafaloni, Patrick F. Chinnery
| Evaluation and treatment of myopathies / / edited by Robert C. Griggs, Emma Ciafaloni, Patrick F. Chinnery |
| Edizione | [Second edition.] |
| Pubbl/distr/stampa | Oxford : , : Oxford University Press, , [2014] |
| Descrizione fisica | 1 online resource (387 p.) |
| Disciplina | 616.7/44 |
| Altri autori (Persone) | GriggsRobert C. <1939-> |
| Collana | Contemporary neurology series |
| Soggetto topico |
Muscles - Diseases - Treament
Muscles - Diseases - Diagnosis |
| ISBN |
0-19-933040-9
0-19-934886-3 0-19-987394-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Structure and function of normal muscle / Robert C. Griggs -- Evaluation of the patient with myopathy / Robert C. Griggs, Emma Ciafaloni -- Genetic evaluation of the patient and family / Gerald Pfeffer, Patrick F. Chinnery -- The muscular dystrophies / Emma Ciafaloni, Robert C. Griggs -- Myofibrillar myopathies / Duygu Selcen -- Congenital myopathies / Francesco Muntoni, Caroline Sewry, Heinz Jungbluth -- Metabolic myopathies / Gráinne S. Gorman, Patrick F. Chinnery -- Mitochondrial myopathy / Gerald Pfeffer, Patrick F. Chinnery -- Muscle channelopathies / Araya Puwanant, Robert C. Griggs -- Inflammatory myopathies / Anthony A. Amato, Andrew Mammen -- Muscle pain and fatigue / Michael R. Rose, Dr. Patrick Gordon -- Prevention and management of systemic complications of myopathies / Wendy M. King, Robert C. Griggs. |
| Record Nr. | UNINA-9910810135703321 |
| Oxford : , : Oxford University Press, , [2014] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Neuromuscular case studies [[electronic resource] /] / Tulio E. Bertorini
| Neuromuscular case studies [[electronic resource] /] / Tulio E. Bertorini |
| Autore | Bertorini Tulio E |
| Edizione | [First edition] |
| Pubbl/distr/stampa | Philadelphia, : Butterworth-Heinemann, c2008 |
| Descrizione fisica | 1 online resource (xiv, 646 pages) : illustrations (some color) |
| Disciplina |
616.7/44
616.744 |
| Soggetto topico | Neuromuscular diseases |
| ISBN | 0-7020-3869-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Chapter 1 Neuromuscular Anatomy and Function -- Chapter 2 Neurological Evaluation and Ancillary Tests -- Chapter 3 Therapy in Neuromuscular Diseases -- Case 1 Carpal Tunnel Syndrome in an Elderly Woman Likely from Rheumatoid Arthritis and the Use of a Walker -- Case 2 A Uremic Patient with a Shunt-Related Ischemic Monomelic Neuropathy Later Diagnosed with Carpal Tunnel Syndrome from Beta-2 Microglobulin Accumulation -- Case 3 A Diabetic with Peripheral Neuropathy and Carpal Tunnel Syndrome Who Later Developed Dysautonomia -- Case 4 Martin Gruber and Anastomosis and Carpal Tunnel Syndrome -- Case 5 Traumatic Median Neuropathy at the Elbow Mimicking Anterior Interossei Syndrome -- Case 6 Pronator Teres Syndrome -- Case 7 Ulnar Entrapment at the Elbow -- Case 8 Ulnar Neuropathy at the Wrist from a Ganglion Cyst -- Case 9 Focal Myositis Causing Radial Neuropathy -- Case 10 Musculoskeletal Neuropathy from Compression During Positioning for Back Surgery -- Case 11 Acute Brachial Neuritis -- Case 12 Lower Trunk Plexopathy and Horner's Syndrome from Lymphoma -- Case 13 Radiation Plexopathy -- Case 14 Suprascapular Neuropathy -- Case 15 C6 Radiculopathy with Motor Deficits from Herpes Zoster -- Case 16 C5 Radiculopathy from a Ruptured Disc -- Case 17 C7 Radiculopathy from a Herniated Disc -- Case 18 L4 Radiculopathy from a Disc Herniation and Peroneal Entrapment -- Case 19 S1 Radiculopathy -- Case 20 L5 Radiculopathy and an Accessory Peroneal Nerve -- Case 21 L2 Radiculopathy from Tumor Invasion -- Case 22 Demylinating Lumbosacral Radiculoneuropathy in a Diabetic -- Case 23 Cauda Equina Syndrome from Spinal Stenosis -- Case 24 Sciatic Neurofibroma Mimicking Tarsal Tunnel Syndrome -- Case 25 Femoral Neuropathy from a Hematoma from Angiography -- Case 26 Carcinomatous Lumbosacral Plexopathy -- Case 27 Meralgia Paresthetica -- Case 28 Lumbosacral Ependymoma Mimicking a Motor Neuron Disease -- Case 29 Acute Facial Neuropathy -- Case 30 Neurosarcoidosis Presenting with Bilateral Vi and Vii Nerve Palsies -- Case 31 A Patient with Als Presenting with Head Drop -- Case 32 Man in the Barrel Syndrome -- Case 33 Benign Focal Amyotrophy or Monomelic Amyotrophy -- Case 34 Post-Myelopathy Amyotrophy -- Case 35 Tethered Cord Syndrome Causing Muscle Pseudohypertrophy from Partial Denervation -- Case 36 Kennedy₂s Disease -- Case 37 Machado-Joseph Disease -- Case 38 Infantile Spinal Muscular Atrophy -- Case 39 Guillain Barř Syndrome with Central Demyelination -- Case 40 Acute Inflammatory Polyneuropathy in an HIV Positive Person -- Case 41 Miller Fisher Syndrome -- Case 42 Ciguatera Poisoning -- Case 43 Acute Quadriplegic Polyneuropathy from Porphyria -- Case 44 Critical Illness Myopathy -- Case 45 Pernicious Anemia Presenting with Hand Numbness in a Patient with Cervical Spondylosis -- Case 46 Pernicious Anemia Manifesting with Weakness and Abnormal Gait -- Case 47 Chronic Inflammatory Demyelinating Polyneuropathy -- Case 48 Chronic Inflammatory Demyelinating Polyneuropathy with Asymmetric Presentation in a Patient with a Monoclonal Gammopathy -- Case 49 Purely Motor Chronic Inflammatory Demyelinating Polyneuropathy -- Case 50 Subacute Inflammatory Demyelinating Polyneuropathy in a Diabetic -- Case 51 Demyelinating Neuropathy Associated with MAG Antibodies -- Case 52 Hereditary Demyelinating Polyneuropathy with Multiple Sclerosis -- Case 53 Inflammatory Polyneuropathy after Bariatric Surgery -- Case 54 Diabetic Amyotrophy -- Case 55 Diabetic Amyotrophy/Mononeuritis Multiplex in the Upper Extremities -- Case 56 Diabetic Muscle Infarct -- Case 57 Uremic Neuropathy -- Case 58 (A) Demyelinating Charcot-Marie-Tooth Disease (B) Axonal Charcot-Marie-Tooth Disease -- Case 59 Hereditary Polyneuropathy with Liability to Pressure Palsy Presenting with Bilateral Median Neuropathy after Snow Skiing -- Case 60 Hereditary Neuropathy with Liability to Pressure Palsy Presenting with a Footdrop -- Case 61 Mononeuritis Multiplex from Vasculitic Neuropathy -- Case 62 Vasculitic Neuropathy from Rheumatoid Arthritis -- Case 63 Wegener's Granulomatosis and Peripheral Neuropathy -- Case 64 Neurolymphomatosis Presenting with Mononeuritis Multiplex -- Case 65 Paraneoplastic Ganglioneuritis -- Case 66 Familial Amyloid Neuropathy -- Case 67 Amiodarone Neuropathy -- Case 68 Myasthenia Gravis Presenting with Difficulty Swallowing -- Case 69 Familial Myasthenia Gravis with Recurrence after Thymectomy -- Case 70 Eaton Lambert Myasthenic Syndrome Secondary to Small Cell Carcinoma of the Lung -- Case 71 Eaton Lambert Myasthenic Syndrome in a Patient with Hypothyroidism and Later Uterine Carcinoma -- Case 72 Slow Channel Congenital Myasthenic Syndrome -- Case 73 Hypokalemic Periodic Paralysis -- Case 73 Thyrotoxic Periodic Paralysis -- Case 74 Becker's Muscular Dystrophy Presenting with Large Muscles -- Case 75 A Manifest Carrier of Muscular Dystrophy -- Case 76 Distal Muscular Dystrophy from Dysferlin Deficiency -- Case 77 Oculopharyngeal Muscular Dystrophy -- Case 78 Facioscapulohumeral Muscular Dystrophy -- Case 79 Merosin Deficient Congenital Muscular Dystrophy -- Case 80 Central Core Disease Manifesting with Progressive Weakness in an Adult -- Case 81 Mitochondrial Disease Manifests as Progressive External Ophthalmoplegia Mimicking Myasthenia Gravis -- Case 82 Mitochondrial Myopathy with Prominent Neck Lipoma -- Case 83 Rhabdomyolysis in a Patient with Myophosphorylase Deficiency -- Case 84 Adult Onset Acid Maltase Deficiency -- Case 85 Myoglobinuria from a Viral Infection as the First Manifestation of Carnitine Palmitoyltransferase (Cpt) Deficiency in An Adult -- Case 86 Proximal Weakness from Beta-2 Microglobulin Accumulation in a Uremic Patient -- Case 87 Hypothyroid Myopathy -- Case 88 Hypoparathyroid Myopathy -- Case 89 Dermatomyositis in a Mother and Her Son -- Case 90 Polymyositis and Myoadenylate Deaminase Deficiency (Double Trouble?) -- Case 91 Inclusion Body Myositis -- Case 92 Inclusion Body Myositis in a Young HIV Positive Person -- Case 93 Eosinophilic Fascitis -- Case 94 Bent Spine Syndrome -- Case 95 A Case of Stiff Person Syndrome and Myasthenia Gravis -- Case 96 Cramp Fasciculation Syndrome from a Chronic, Predominantly Motor Neuronopathy -- Case 97 Myotonic Congenita -- Case 98 Schwartz-Jampel Syndrome -- Case 99 Tetany -- Case 100 Proximal Myotonic Myopathy -- Case 101 Acquired Rippling Muscle Disease. |
| Record Nr. | UNISA-996212361603316 |
Bertorini Tulio E
|
||
| Philadelphia, : Butterworth-Heinemann, c2008 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
| ||
Neuromuscular disorders [[electronic resource] /] / edited by Rabi N. Tawil, Shannon Venance
| Neuromuscular disorders [[electronic resource] /] / edited by Rabi N. Tawil, Shannon Venance |
| Pubbl/distr/stampa | Chichester, West Sussex, UK, : Wiley-Blackwell, 2011 |
| Descrizione fisica | 1 online resource (285 p.) |
| Disciplina | 616.7/44 |
| Altri autori (Persone) |
TawilRabi N
VenanceShannon Lee <1959-> |
| Collana | Neurology in practice |
| Soggetto topico |
Neuromuscular diseases
Musculoskeletal system - Diseases |
| ISBN |
1-119-97331-7
1-283-27410-8 9786613274106 1-119-97333-3 1-119-97330-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Neuromuscular Disorders; Contents; Contributor List; Acknowledgment; Series Preface; Preface; 1: Neuromuscular Diseases: Approach to Clinical Diagnosis; Part I: Myopathies; 2: Approach to Diseases of Muscle; 3: Inflammatory Myopathies; 4: Toxic Myopathies; 5: Metabolic Myopathies; 6: Mitochondrial Myopathies; 7: Dystrophinopathies; 8: Limb-Girdle Dystrophies; 9: Facioscapulohumeral Dystrophy; 10: Myotonic Dystrophies; 11: Oculopharyngeal Muscular Dystrophy; 12: Distal Myopathies; 13: Muscle Channelopathies; 14: Congenital Myopathies; Part II: Disorders of the Neuromuscular Junction
15: Approach to Diseases of the Neuromuscular Junction16: Myasthenia Gravis; 17: Botulism; 18: Lambert-Eaton Myasthenic Syndrome; 19: Congenital Myasthenic Syndromes; Part III: Disorders of Peripheral Nerve; 20: Approach to Diagnosis of Peripheral Nerve Disease; 21: Hereditary Motor Sensory Neuropathies (Charcot-Marie-Tooth Disease); 22: Diabetic Neuropathies; 23: Toxic and Metabolic Neuropathies; 24: Acute Inflammatory Demyelinating Neuropathies and Variants; 25: Chronic Immune-mediated Demyelinating Polyneuropathies; 26: Vasculitic Neuropathies; 27: Paraneoplastic Neuropathies 28: Brachial and Lumbosacral PlexopathiesPart IV: Disorders of Motor Neurons; 29: Approach to Diseases of the Motor Neurons; 30: Spinal Muscular Atrophy; 31: Amyotrophic Lateral Sclerosis; 32: Neuromuscular Disorders in the Intensive Care Unit; Index; colour plate |
| Record Nr. | UNINA-9910139599603321 |
| Chichester, West Sussex, UK, : Wiley-Blackwell, 2011 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Neuromuscular disorders / / edited by Rabi N. Tawil, Shannon Venance
| Neuromuscular disorders / / edited by Rabi N. Tawil, Shannon Venance |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | Chichester, West Sussex, UK, : Wiley-Blackwell, 2011 |
| Descrizione fisica | 1 online resource (285 p.) |
| Disciplina | 616.7/44 |
| Altri autori (Persone) |
TawilRabi N
VenanceShannon Lee <1959-> |
| Collana | Neurology in practice |
| Soggetto topico |
Neuromuscular diseases
Musculoskeletal system - Diseases |
| ISBN |
9786613274106
9781119973317 1119973317 9781283274104 1283274108 9781119973331 1119973333 9781119973300 1119973309 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Neuromuscular Disorders; Contents; Contributor List; Acknowledgment; Series Preface; Preface; 1: Neuromuscular Diseases: Approach to Clinical Diagnosis; Part I: Myopathies; 2: Approach to Diseases of Muscle; 3: Inflammatory Myopathies; 4: Toxic Myopathies; 5: Metabolic Myopathies; 6: Mitochondrial Myopathies; 7: Dystrophinopathies; 8: Limb-Girdle Dystrophies; 9: Facioscapulohumeral Dystrophy; 10: Myotonic Dystrophies; 11: Oculopharyngeal Muscular Dystrophy; 12: Distal Myopathies; 13: Muscle Channelopathies; 14: Congenital Myopathies; Part II: Disorders of the Neuromuscular Junction
15: Approach to Diseases of the Neuromuscular Junction16: Myasthenia Gravis; 17: Botulism; 18: Lambert-Eaton Myasthenic Syndrome; 19: Congenital Myasthenic Syndromes; Part III: Disorders of Peripheral Nerve; 20: Approach to Diagnosis of Peripheral Nerve Disease; 21: Hereditary Motor Sensory Neuropathies (Charcot-Marie-Tooth Disease); 22: Diabetic Neuropathies; 23: Toxic and Metabolic Neuropathies; 24: Acute Inflammatory Demyelinating Neuropathies and Variants; 25: Chronic Immune-mediated Demyelinating Polyneuropathies; 26: Vasculitic Neuropathies; 27: Paraneoplastic Neuropathies 28: Brachial and Lumbosacral PlexopathiesPart IV: Disorders of Motor Neurons; 29: Approach to Diseases of the Motor Neurons; 30: Spinal Muscular Atrophy; 31: Amyotrophic Lateral Sclerosis; 32: Neuromuscular Disorders in the Intensive Care Unit; Index; colour plate |
| Record Nr. | UNINA-9910821845003321 |
| Chichester, West Sussex, UK, : Wiley-Blackwell, 2011 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||