MARC details
| 000 -LEADER |
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| fixed length control field |
03996cam a2200265 4500 |
| 001 - CONTROL NUMBER |
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| control field |
9780124171275 |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION |
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| fixed length control field |
220107t2015 xxu||||| |||| 00| 0 eng d |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
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| International Standard Book Number |
9780124171275 |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
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| International Standard Book Number |
9780124170445 |
| 041 ## - LANGUAGE CODE |
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| Language code of text/sound track or separate title |
eng |
| 100 ## - MAIN ENTRY--PERSONAL NAME |
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| Personal name |
Darras, Basil T. |
| 245 #0 - TITLE STATEMENT |
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| Title |
Neuromuscular disorders of infancy, childhood, and adolescence: a clinician's approach |
| 250 ## - EDITION STATEMENT |
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| Edition statement |
2nd ed. |
| 260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT) |
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| Place of publication, distribution, etc. |
London : |
| Name of publisher, distributor, etc. |
Academic Press, |
| Date of publication, distribution, etc. |
2015 |
| 300 ## - PHYSICAL DESCRIPTION |
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| Extent |
1 online resource:illustrations (chiefly color) |
| 505 ## - FORMATTED CONTENTS NOTE |
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| Formatted contents note |
Introduction : historical perspectives -- Genetics of neuromuscular disorders -- Electromyography in pediatrics -- Muscle biopsy for diagnosis of neuromuscular and metabolic diseases -- Nerve biopsy -- Neonatal hypotonia -- Arthrogryposis -- Spinal muscular atrophies -- Juvenile amyotrophic lateral sclerosis -- Infectious or acquired motor neuron diseases -- The stiff-man syndrome in children and adolescents -- Radiculopathies and plexopathies -- Congenital and acquired facial palsies -- Mononeuropathies -- Overview of pediatric peripheral neuropathies -- Congenital and early infantile neuropathies -- Hereditary neuropathies in late childhood and adolescence -- Hereditary sensory and autonomic neuropathies -- Peripheral neuropathy in inherited metabolic disease -- Acute polyneuropathies -- Chronic inflammatory demyelinating polyradiculoneuropathy -- Neuropathies secondary to systemic disorders -- Toxic neuropathies -- Hansen's disease (leprosy) : leprous neuropathy -- Acquired presynaptic neuromuscular junction disorders : infant botulism and Lambert-Eaton myasthenic syndrome -- Congenital myasthenic syndromes -- Juvenile and neonatal myasthenia gravis -- Congenital and other structural myopathies -- Congenital muscular dystrophies -- Dystrophinopathies -- Clinical management of dystrophinopathies : a systematic approach -- Facioscapulohumeral dystrophy -- Distal myopathies -- Limb-girdle muscular dystrophies -- Emery-Dreifuss muscular dystrophy : nuclear envelopathies -- Myopathies of systemic disease -- Myotonic dystrophy -- Muscle channelopathies : myotonias and periodic paralyses -- Glycogen storage diseases of muscle -- Lipid storage myopathies due to fatty acid oxidation defects -- Mitochondrial encephalomyopathies -- Juvenile dermatomyositis and other inflammatory myopathies in children -- Neuromuscular problems of the critically ill neonate and child -- Intensive care management, including cardiorespiratory care -- Malignant hyperthermia : an inherited disorder of muscle calcium metabolism -- Disorders of the ocular motor cranial nerves and extraocular muscles -- Oromotor dysfunction in neuromuscular disorders : evaluation and treatment -- Complex regional pain syndromes i and ii (reflex sympathetic dystrophy, causalgia) -- Friedreich ataxia -- Dominantly inherited spinocerebellar syndromes -- Principles and practice of molecular therapies -- Orthopedic management -- Rehabilitation of the child with a neuromuscular disorder -- Outcome measures in neuromuscular diseases. |
| 520 ## - SUMMARY, ETC. |
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| Summary, etc. |
Neuromuscular disorders are diagnosed across the lifespan and create many challenges especially with infants, children and adolescents. This new edition of the definitive reference, edited by the established world renowned authorities on the science, diagnosis and treatment of neuromuscular disorders in childhood is a timely and needed resource for all clinicians and researchers studying neuromuscular disorders, especially in childhood. The Second Edition is completely revised to remain current with advances in the field and to insure this remains the standard reference for clinical neurologi. |
| 690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) |
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| Topical term or geographic name as entry element |
Neuromuscular diseases in children. |
| 690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) |
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| Topical term or geographic name as entry element |
Neuromuscular diseases. |
| 700 ## - ADDED ENTRY--PERSONAL NAME |
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| Personal name |
Jones, H.Royden |
| 700 ## - ADDED ENTRY--PERSONAL NAME |
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| Personal name |
Ryan, Monique M. |
| 700 ## - ADDED ENTRY--PERSONAL NAME |
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| Personal name |
De Vivo, Darryl C. |
| 856 ## - ELECTRONIC LOCATION AND ACCESS |
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| Uniform Resource Identifier |
<a href="https://go.openathens.net/redirector/nhs?url=https://www.clinicalkey.com/dura/browse/bookChapter/3-s2.0-C20130000771">https://go.openathens.net/redirector/nhs?url=https://www.clinicalkey.com/dura/browse/bookChapter/3-s2.0-C20130000771</a> |