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Biblioteca

MARC Lista (tabellare)
Neuromuscular disease : a case-based approach / / John H.J. Wokke, Peter A. van Doorn, Jessica E. Hoogendijk, and Marianne de Visser [[electronic resource]]
Neuromuscular disease : a case-based approach / / John H.J. Wokke, Peter A. van Doorn, Jessica E. Hoogendijk, and Marianne de Visser [[electronic resource]]
Autore Wokke John H. J. <1952->
Pubbl/distr/stampa Cambridge : , : Cambridge University Press, , 2013
Descrizione fisica 1 online resource (x, 171 pages) : digital, PDF file(s)
Disciplina 616.8
Collana Cambridge medicine
Soggetto topico Musculoskeletal system - Diseases
ISBN 1-107-23259-7
1-107-32638-9
1-107-33282-6
0-511-73590-1
1-107-33614-7
1-107-33219-2
1-107-33448-9
1-299-25739-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Introduction: approach to the patient -- Part I: Motor neurone diseases -- Case 1: Classical amyotrophic lateral sclerosis -- Case 2: ALS with frontotemporal dementia -- Case 3: Primary lateral sclerosis -- Case 4: Progressive muscular atrophy -- Case 5: Kennedy disease -- Case 6: Spinal muscular atrophy type III, Kugelberg-Welander disease -- Case 7: Post-polio syndrome -- Case 8: Spinal dural fistula -- Part II: Neuropathies -- Case 9: Charcot-Marie-Tooth disease type 1A -- Case 10: Hereditary neuropathy with liability to pressure palsy -- Case 11: Charcot-Marie-Tooth disease type 2A, mitofusinopathy -- Case 12: X-linked Charcot-Marie-Tooth disease -- Case 13: Hereditary sensory and autonomic neuropathy type 4 -- Case 14: Guillain-Barre syndrome -- Case 15: Miller-Fisher syndrome -- Case 16: Chronic inflammatory demyelinating polyneuropathy -- Case 17: Multifocal motor neuropathy -- Case 18: Peripheral nerve hyperexcitability syndrome, Morvan's syndrome -- Case 19: Vasculitic neuropathy -- Case 20: Neuropathy and ataxia caused by IgM gammopathy -- Case 21: Polyneuropathy, organomegaly, endocrinopathy, M-protein and skin changes -- Case 22: Subacute sensory paraneoplastic neuropathy and ganglionopathy -- Case 23: Neurolymphomatosis -- Case 24: Diabetic neuropathy -- Case 25: Alcohol neuropathy -- Case 26: HIV neuropathy -- Case 27: Lyme radiculoneuritis -- Case 28: Lepromatous neuropathy -- Case 29: Toxic iatrogenic neuropathy -- Case 30: Idiopathic neuralgic amyotrophy -- Case 31: Small nerve fibre neuropathy -- Case 32: Critical illness polyneuropathy -- Case 33: Chronic idiopathic axonal polyneuropathy -- Part III: Neuromuscular Junction Disorders -- Case 34: Classic myasthenia gravis -- Case 35: Myasthenia gravis with autoantibodies to MuSK -- Case 36: Lambert-Eaton myasthenic syndrome -- Case 37: Congenital myasthenic syndrome: slow channel syndrome -- Part IV: Myopathies -- Case 38: Becker muscular dystrophy -- Case 39: Caveolinopathy, including limb girdle muscular dystrophy type 1C -- Case 40: Limb girdle muscular dystrophy type 2A, calpainopathy -- Case 41: Limb girdle muscular dystrophy type 2I, fukutin-related protein deficiency -- Case 42: Emery-Dreifuss muscular dystrophy -- Case 43: Facio-scapulo-humeral dystrophy -- Case 44: Miyoshi myopathy, dysferlinopathy, limb girdle muscular dystrophy type 2B -- Case 45: Distal myopathy with rimmed vacuoles, hereditary inclusion body myopathy -- Case 46: Oculopharyngeal muscular dystrophy -- Case 47: A woman with a family history of muscle weakness and severe cardiac complaints, desminopathy -- Case 48: Late-onset congenital myopathy caused by a mutation in the RYR1 gene, central core disease -- Case 49: Bethlem myopathy -- Case 50: Myotonic dystrophy type 1, Curschmann-Steinert disease -- Case 51: Myotonic dystrophy type 2, proximal myotonic myopathy -- Case 52: Becker myotonia, chloride channelopathy -- Case 53: Glycogen storage disease type 2, Pompe disease -- Case 54: Glycogen storage disease type 5, McArdle disease -- Case 55: Mitochondrial disease: progressive ophthalmoplegia -- Case 56: Myositis -- Case 57: Sporadic inclusion body myositis -- Case 58: Sarcoid myopathy -- Case 59: Hypothyroid myopathy.
Record Nr. UNINA-9910465657903321
Wokke John H. J. <1952->  
Cambridge : , : Cambridge University Press, , 2013
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Neuromuscular disease : a case-based approach / / John H.J. Wokke, Peter A. van Doorn, Jessica E. Hoogendijk, and Marianne de Visser [[electronic resource]]
Neuromuscular disease : a case-based approach / / John H.J. Wokke, Peter A. van Doorn, Jessica E. Hoogendijk, and Marianne de Visser [[electronic resource]]
Autore Wokke John H. J. <1952->
Pubbl/distr/stampa Cambridge : , : Cambridge University Press, , 2013
Descrizione fisica 1 online resource (x, 171 pages) : digital, PDF file(s)
Disciplina 616.8
Collana Cambridge medicine
Soggetto topico Musculoskeletal system - Diseases
ISBN 1-107-23259-7
1-107-32638-9
1-107-33282-6
0-511-73590-1
1-107-33614-7
1-107-33219-2
1-107-33448-9
1-299-25739-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Introduction: approach to the patient -- Part I: Motor neurone diseases -- Case 1: Classical amyotrophic lateral sclerosis -- Case 2: ALS with frontotemporal dementia -- Case 3: Primary lateral sclerosis -- Case 4: Progressive muscular atrophy -- Case 5: Kennedy disease -- Case 6: Spinal muscular atrophy type III, Kugelberg-Welander disease -- Case 7: Post-polio syndrome -- Case 8: Spinal dural fistula -- Part II: Neuropathies -- Case 9: Charcot-Marie-Tooth disease type 1A -- Case 10: Hereditary neuropathy with liability to pressure palsy -- Case 11: Charcot-Marie-Tooth disease type 2A, mitofusinopathy -- Case 12: X-linked Charcot-Marie-Tooth disease -- Case 13: Hereditary sensory and autonomic neuropathy type 4 -- Case 14: Guillain-Barre syndrome -- Case 15: Miller-Fisher syndrome -- Case 16: Chronic inflammatory demyelinating polyneuropathy -- Case 17: Multifocal motor neuropathy -- Case 18: Peripheral nerve hyperexcitability syndrome, Morvan's syndrome -- Case 19: Vasculitic neuropathy -- Case 20: Neuropathy and ataxia caused by IgM gammopathy -- Case 21: Polyneuropathy, organomegaly, endocrinopathy, M-protein and skin changes -- Case 22: Subacute sensory paraneoplastic neuropathy and ganglionopathy -- Case 23: Neurolymphomatosis -- Case 24: Diabetic neuropathy -- Case 25: Alcohol neuropathy -- Case 26: HIV neuropathy -- Case 27: Lyme radiculoneuritis -- Case 28: Lepromatous neuropathy -- Case 29: Toxic iatrogenic neuropathy -- Case 30: Idiopathic neuralgic amyotrophy -- Case 31: Small nerve fibre neuropathy -- Case 32: Critical illness polyneuropathy -- Case 33: Chronic idiopathic axonal polyneuropathy -- Part III: Neuromuscular Junction Disorders -- Case 34: Classic myasthenia gravis -- Case 35: Myasthenia gravis with autoantibodies to MuSK -- Case 36: Lambert-Eaton myasthenic syndrome -- Case 37: Congenital myasthenic syndrome: slow channel syndrome -- Part IV: Myopathies -- Case 38: Becker muscular dystrophy -- Case 39: Caveolinopathy, including limb girdle muscular dystrophy type 1C -- Case 40: Limb girdle muscular dystrophy type 2A, calpainopathy -- Case 41: Limb girdle muscular dystrophy type 2I, fukutin-related protein deficiency -- Case 42: Emery-Dreifuss muscular dystrophy -- Case 43: Facio-scapulo-humeral dystrophy -- Case 44: Miyoshi myopathy, dysferlinopathy, limb girdle muscular dystrophy type 2B -- Case 45: Distal myopathy with rimmed vacuoles, hereditary inclusion body myopathy -- Case 46: Oculopharyngeal muscular dystrophy -- Case 47: A woman with a family history of muscle weakness and severe cardiac complaints, desminopathy -- Case 48: Late-onset congenital myopathy caused by a mutation in the RYR1 gene, central core disease -- Case 49: Bethlem myopathy -- Case 50: Myotonic dystrophy type 1, Curschmann-Steinert disease -- Case 51: Myotonic dystrophy type 2, proximal myotonic myopathy -- Case 52: Becker myotonia, chloride channelopathy -- Case 53: Glycogen storage disease type 2, Pompe disease -- Case 54: Glycogen storage disease type 5, McArdle disease -- Case 55: Mitochondrial disease: progressive ophthalmoplegia -- Case 56: Myositis -- Case 57: Sporadic inclusion body myositis -- Case 58: Sarcoid myopathy -- Case 59: Hypothyroid myopathy.
Record Nr. UNINA-9910792070903321
Wokke John H. J. <1952->  
Cambridge : , : Cambridge University Press, , 2013
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Neuromuscular disease : a case-based approach / / John H.J. Wokke, Peter A. van Doorn, Jessica E. Hoogendijk, and Marianne de Visser [[electronic resource]]
Neuromuscular disease : a case-based approach / / John H.J. Wokke, Peter A. van Doorn, Jessica E. Hoogendijk, and Marianne de Visser [[electronic resource]]
Autore Wokke John H. J. <1952->
Pubbl/distr/stampa Cambridge : , : Cambridge University Press, , 2013
Descrizione fisica 1 online resource (x, 171 pages) : digital, PDF file(s)
Disciplina 616.8
Collana Cambridge medicine
Soggetto topico Musculoskeletal system - Diseases
ISBN 1-107-23259-7
1-107-32638-9
1-107-33282-6
0-511-73590-1
1-107-33614-7
1-107-33219-2
1-107-33448-9
1-299-25739-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Introduction: approach to the patient -- Part I: Motor neurone diseases -- Case 1: Classical amyotrophic lateral sclerosis -- Case 2: ALS with frontotemporal dementia -- Case 3: Primary lateral sclerosis -- Case 4: Progressive muscular atrophy -- Case 5: Kennedy disease -- Case 6: Spinal muscular atrophy type III, Kugelberg-Welander disease -- Case 7: Post-polio syndrome -- Case 8: Spinal dural fistula -- Part II: Neuropathies -- Case 9: Charcot-Marie-Tooth disease type 1A -- Case 10: Hereditary neuropathy with liability to pressure palsy -- Case 11: Charcot-Marie-Tooth disease type 2A, mitofusinopathy -- Case 12: X-linked Charcot-Marie-Tooth disease -- Case 13: Hereditary sensory and autonomic neuropathy type 4 -- Case 14: Guillain-Barre syndrome -- Case 15: Miller-Fisher syndrome -- Case 16: Chronic inflammatory demyelinating polyneuropathy -- Case 17: Multifocal motor neuropathy -- Case 18: Peripheral nerve hyperexcitability syndrome, Morvan's syndrome -- Case 19: Vasculitic neuropathy -- Case 20: Neuropathy and ataxia caused by IgM gammopathy -- Case 21: Polyneuropathy, organomegaly, endocrinopathy, M-protein and skin changes -- Case 22: Subacute sensory paraneoplastic neuropathy and ganglionopathy -- Case 23: Neurolymphomatosis -- Case 24: Diabetic neuropathy -- Case 25: Alcohol neuropathy -- Case 26: HIV neuropathy -- Case 27: Lyme radiculoneuritis -- Case 28: Lepromatous neuropathy -- Case 29: Toxic iatrogenic neuropathy -- Case 30: Idiopathic neuralgic amyotrophy -- Case 31: Small nerve fibre neuropathy -- Case 32: Critical illness polyneuropathy -- Case 33: Chronic idiopathic axonal polyneuropathy -- Part III: Neuromuscular Junction Disorders -- Case 34: Classic myasthenia gravis -- Case 35: Myasthenia gravis with autoantibodies to MuSK -- Case 36: Lambert-Eaton myasthenic syndrome -- Case 37: Congenital myasthenic syndrome: slow channel syndrome -- Part IV: Myopathies -- Case 38: Becker muscular dystrophy -- Case 39: Caveolinopathy, including limb girdle muscular dystrophy type 1C -- Case 40: Limb girdle muscular dystrophy type 2A, calpainopathy -- Case 41: Limb girdle muscular dystrophy type 2I, fukutin-related protein deficiency -- Case 42: Emery-Dreifuss muscular dystrophy -- Case 43: Facio-scapulo-humeral dystrophy -- Case 44: Miyoshi myopathy, dysferlinopathy, limb girdle muscular dystrophy type 2B -- Case 45: Distal myopathy with rimmed vacuoles, hereditary inclusion body myopathy -- Case 46: Oculopharyngeal muscular dystrophy -- Case 47: A woman with a family history of muscle weakness and severe cardiac complaints, desminopathy -- Case 48: Late-onset congenital myopathy caused by a mutation in the RYR1 gene, central core disease -- Case 49: Bethlem myopathy -- Case 50: Myotonic dystrophy type 1, Curschmann-Steinert disease -- Case 51: Myotonic dystrophy type 2, proximal myotonic myopathy -- Case 52: Becker myotonia, chloride channelopathy -- Case 53: Glycogen storage disease type 2, Pompe disease -- Case 54: Glycogen storage disease type 5, McArdle disease -- Case 55: Mitochondrial disease: progressive ophthalmoplegia -- Case 56: Myositis -- Case 57: Sporadic inclusion body myositis -- Case 58: Sarcoid myopathy -- Case 59: Hypothyroid myopathy.
Record Nr. UNINA-9910820566003321
Wokke John H. J. <1952->  
Cambridge : , : Cambridge University Press, , 2013
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui