<?xml version="1.0" encoding="UTF-8"?>
<mods xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns="http://www.loc.gov/mods/v3" version="3.1" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
  <titleInfo>
    <title>Neuromuscular disorders</title>
  </titleInfo>
  <name type="personal">
    <namePart>Amato, Anthony A.</namePart>
    <namePart type="date">1960-</namePart>
    <role>
      <roleTerm authority="marcrelator" type="text">creator</roleTerm>
    </role>
  </name>
  <name type="personal">
    <namePart>Russell, James Adams</namePart>
    <namePart type="date">1951-</namePart>
  </name>
  <typeOfResource>text</typeOfResource>
  <originInfo>
    <place>
      <placeTerm type="code" authority="marccountry">nyu</placeTerm>
    </place>
    <place>
      <placeTerm type="text">New York</placeTerm>
    </place>
    <publisher>McGraw-Hill Education Medical</publisher>
    <dateIssued>2016</dateIssued>
    <edition>Segunda edición</edition>
    <issuance>monographic</issuance>
  </originInfo>
  <language>
    <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
  </language>
  <physicalDescription>
    <form authority="marcform">print</form>
    <extent>viii, 948 páginas ilustraciones</extent>
  </physicalDescription>
  <abstract>Approach to patients with neuromuscular disease -- Testing in neuromuscular disease -- Muscle and nerve histopathology -- Principles of immunomodulating treatment -- The rehabilitation of neuromuscular diseases / Sabrina Paganoni and Erik Ensrud -- Amyotrophic lateral sclerosis -- Hereditary spastic paraparesis -- Spinal muscular atrophies -- Other motor neuron disorders -- Disorders of motor nerve hyperactivity -- Charcot-Marie-Tooth disease and related disorders -- Other hereditary neuropathies -- Guillain-Barré syndrome and related disorders -- Chronic inflammatory demyelinating polyradiculoneuropathy and related neuropathies -- Vasculitic neuropathies -- Neuropathies associated with systemic disease -- Neuropathies associated with infections -- Neuropathies related to nutritional deficiencies -- Neuropathies associated with malignancy -- Toxic neuropathies -- Neuropathies associated with endocrinopathies -- Idiopathic polyneuropathy -- Cervical and thoracic radiculopathies, brachial plexopathies, and mononeuropathies of the arm -- Focal neuropathies of the lower extremities : radiculopathies, plexopathies, and mononeuropathies -- Autoimmune myasthenia gravis -- Other disorders of neuromuscular transmission -- Muscular dystrophies -- Congenital myopathies -- Metabolic myopathies -- Mitochondrial disorders -- Myotonic dystrophies -- Nondystrophic myotonias and periodic paralysis -- Inflammatory myopathies -- Myopathies associated with systemic disease -- Toxic myopathies -- Neuromuscular mimics / Sabrina Paganoni and Erik Ensrud</abstract>
  <tableOfContents>Approach to patients with neuromuscular diseaseTesting in neuromuscular disease -- Muscle and nerve histopathology -- Principles of immunomodulating treatment -- The rehabilitation of neuromuscular diseases / Sabrina Paganoni and Erik Ensrud -- Amyotrophic lateral sclerosis -- Hereditary spastic paraparesis -- Spinal muscular atrophies -- Other motor neuron disorders -- Disorders of motor nerve hyperactivity -- Charcot-Marie-Tooth disease and related disorders -- Other hereditary neuropathies -- Guillain-Barré syndrome and related disorders -- Chronic inflammatory demyelinating polyradiculoneuropathy and related neuropathies -- Vasculitic neuropathies -- Neuropathies associated with systemic disease -- Neuropathies associated with infections -- Neuropathies related to nutritional deficiencies -- Neuropathies associated with malignancy -- Toxic neuropathies -- Neuropathies associated with endocrinopathies -- Idiopathic polyneuropathy -- Cervical and thoracic radiculopathies, brachial plexopathies, and mononeuropathies of the arm -- Focal neuropathies of the lower extremities : radiculopathies, plexopathies, and mononeuropathies -- Autoimmune myasthenia gravis -- Other disorders of neuromuscular transmission -- Muscular dystrophies -- Congenital myopathies -- Metabolic myopathies -- Mitochondrial disorders -- Myotonic dystrophies -- Nondystrophic myotonias and periodic paralysis -- Inflammatory myopathies -- Myopathies associated with systemic disease -- Toxic myopathies -- Neuromuscular mimics / Sabrina Paganoni and Erik Ensrud.</tableOfContents>
  <note type="statement of responsibility">Anthony A. Amato, MD, Vice-Chairman, Department of Neurology, Chief, Neuromuscular Divbision, Brigham and Women's Hospital, Boston, Massachusetts, Harvard Medical School, Boston, Massachusetts, James A. Russell, DO, FAAN, Vice Chairman, Department of Neurology, Lahey Hospital &amp; Medical Center, Director, ALS Clinic, Lahey Hospital &amp; Medical Center, Chairman, Ethics Center, Lahey Hospital &amp; Medical Center, Clinical Professor of Neurology, Tufts University School of Medicine, Boston, Massachusetts</note>
  <note>Texto en inglés</note>
  <subject authority="">
    <topic>Enfermedades neuromusculares</topic>
    <topic>Diagnostíco</topic>
  </subject>
  <subject authority="">
    <topic>Diagnóstico diferencial</topic>
  </subject>
  <subject authority="">
    <topic>Técnicas y procedimientos diagnósticos</topic>
  </subject>
  <subject authority="">
    <topic>Ortopedia</topic>
  </subject>
  <subject authority="">
    <topic>Rehabilitación</topic>
  </subject>
  <classification authority="nlm">WE 550</classification>
  <relatedItem>
    <titleInfo>
      <title>Neuromuscular disorders</title>
    </titleInfo>
  </relatedItem>
  <identifier type="isbn">9780071752503 (2a.Ed.)</identifier>
  <identifier type="isbn" invalid="yes"/>
  <identifier type="lccn">2015008911</identifier>
  <recordInfo>
    <recordContentSource authority="marcorg">Co-BoUCM</recordContentSource>
    <recordCreationDate encoding="marc">171020</recordCreationDate>
    <recordChangeDate encoding="iso8601">20180313061229.0</recordChangeDate>
    <recordIdentifier>on1004273955</recordIdentifier>
    <languageOfCataloging>
      <languageTerm authority="iso639-2b" type="code">ger</languageTerm>
    </languageOfCataloging>
  </recordInfo>
</mods>
