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Russia (Federation) -- Muscovy (Grand Duchy) : Ivan the Terrible in Russian historical memory since 1991 / Charles J. Halperin  2021 1
Muscripts, Latin -- Germany -- Bamberg -- History : Chronik des Hydatius. Fortführung der Spanischen Epitome  2019 1
Musculació. : Field-based tests for soccer players : methodological concerns and applications / Filipe Manuel Clemente, Rafael Oliveira, Rui Silva, Zeki Akyildiz, Halil Ibrahim Ceylan, Javier Raya González, Francisco Tomás González Fernández, Rui Araújo, Hugo Sarmento, Ricardo Lima, Bruno Silva, Sérgio Matos, Yung-Sheng Chen, José Afonso  2022 1
 

Muscular Atrophies -- See Muscular Atrophy


Derangement in size and number of muscle fibers occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessness, malnutrition, and particularly in denervation
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Muscular Atrophies, Neurogenic -- See Muscular Atrophy


Derangement in size and number of muscle fibers occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessness, malnutrition, and particularly in denervation
  1
 

Muscular Atrophies, Neurotrophic -- See Muscular Atrophy


Derangement in size and number of muscle fibers occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessness, malnutrition, and particularly in denervation
  1
 

Muscular Atrophies, Post-Poliomyelitis -- See Postpoliomyelitis Syndrome


A syndrome characterized by new neuromuscular symptoms that occur at least 15 years after clinical stability has been attained in patients with a prior history of symptomatic poliomyelitis. Clinical features include new muscular weakness and atrophy of the limbs, bulbar innervated musculature, and muscles of respiration, combined with excessive fatigue, joint pain, and reduced stamina. The process is marked by slow progression and periods of stabilization. (From Ann NY Acad Sci 1995 May 25;753:68-80)
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Muscular Atrophies, Postpoliomyelitis -- See Postpoliomyelitis Syndrome


A syndrome characterized by new neuromuscular symptoms that occur at least 15 years after clinical stability has been attained in patients with a prior history of symptomatic poliomyelitis. Clinical features include new muscular weakness and atrophy of the limbs, bulbar innervated musculature, and muscles of respiration, combined with excessive fatigue, joint pain, and reduced stamina. The process is marked by slow progression and periods of stabilization. (From Ann NY Acad Sci 1995 May 25;753:68-80)
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  Muscular atrophy -- 3 Related Subjects   3
Muscular atrophy.   7
Muscular atrophy -- Age factors : Clinical nutrition and aging : sarcopenia and muscle metabolism / edited by Chad Cox, PhD  2016 1
Muscular atrophy -- Diet therapy : Clinical nutrition and aging : sarcopenia and muscle metabolism / edited by Chad Cox, PhD  2016 1
Muscular Atrophy -- etiology   2
Muscular atrophy -- Exercise therapy : Propuesta de evaluación e intervención para pacientes hospitalizados con síndrome de desacondicionamiento físico (SDF) / Ft. Olga Cecilia Vargas Pinilla, Ft. Ana María Castro Montoy, Ft. Andrea Paola Vargas Guerrero  2016 1
Muscular atrophy in children -- Australia -- Biography : Mackenzie's Mission : how one family turned tragedy into hope and love / Rachael Casella, with Jonathan Casella  2020 1
 

Muscular Atrophy, Neurogenic -- See Muscular Atrophy


Derangement in size and number of muscle fibers occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessness, malnutrition, and particularly in denervation
  1
 

Muscular Atrophy, Neurotrophic -- See Muscular Atrophy


Derangement in size and number of muscle fibers occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessness, malnutrition, and particularly in denervation
  1
Muscular atrophy -- Patients -- United States -- Biography : Year of the tiger : an activist's life / Alice Wong  2022 1
 

Muscular Atrophy, Post-Poliomyelitis -- See Postpoliomyelitis Syndrome


A syndrome characterized by new neuromuscular symptoms that occur at least 15 years after clinical stability has been attained in patients with a prior history of symptomatic poliomyelitis. Clinical features include new muscular weakness and atrophy of the limbs, bulbar innervated musculature, and muscles of respiration, combined with excessive fatigue, joint pain, and reduced stamina. The process is marked by slow progression and periods of stabilization. (From Ann NY Acad Sci 1995 May 25;753:68-80)
  1
 

Muscular Atrophy, Postpoliomyelitis -- See Postpoliomyelitis Syndrome


A syndrome characterized by new neuromuscular symptoms that occur at least 15 years after clinical stability has been attained in patients with a prior history of symptomatic poliomyelitis. Clinical features include new muscular weakness and atrophy of the limbs, bulbar innervated musculature, and muscles of respiration, combined with excessive fatigue, joint pain, and reduced stamina. The process is marked by slow progression and periods of stabilization. (From Ann NY Acad Sci 1995 May 25;753:68-80)
  1
Muscular atrophy -- Prevention : Clinical nutrition and aging : sarcopenia and muscle metabolism / edited by Chad Cox, PhD  2016 1
Muscular Atrophy, Spinal   2
Muscular Atrophy, Spinal -- therapy : Exon skipping and inclusion therapies : methods and protocols / edited by Toshifumi Yokota, Rika Maruyama  2018 1
Muscular atrophy -- Treatment : Clinical nutrition and aging : sarcopenia and muscle metabolism / edited by Chad Cox, PhD  2016 1
muscular Christianity. : How football began : a global history of how the world's football codes were born / Tony Collins  2018 1
 

Muscular Contraction -- See Muscle Contraction


A process leading to shortening and/or development of tension in muscle tissue. Muscle contraction occurs by a sliding filament mechanism whereby actin filaments slide inward among the myosin filaments
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Muscular Contractions -- See Muscle Contraction


A process leading to shortening and/or development of tension in muscle tissue. Muscle contraction occurs by a sliding filament mechanism whereby actin filaments slide inward among the myosin filaments
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Muscular coordination -- See Motor ability


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Muscular Disease -- See Muscular Diseases


Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE
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Muscular Diseases   22
Muscular Diseases -- diagnosis   4
Muscular Diseases -- diagnostic imaging : Musculoskeletal ultrasound : the essentials / W.W. Gibbon  1996 1
Muscular Diseases -- genetics : Muscle Disease : Pathology and Genetics / edited by Hans H. Goebel, Caroline A. Sewry, Roy O. Weller  2013 1
Muscular Diseases -- nursing. : The skeletal system and the muscular system / edited by Janet T.E. Riddle ; with contributions from Kathleen B. Nicoll, Isabella I. Rowantree  1989 1
Muscular Diseases -- pathology   3
Muscular Diseases -- therapy.   5
 

Muscular Disorder, Atrophic -- See Muscular Disorders, Atrophic


Disorders characterized by an abnormal reduction in muscle volume due to a decrease in the size or number of muscle fibers. Atrophy may result from diseases intrinsic to muscle tissue (e.g., MUSCULAR DYSTROPHY) or secondary to PERIPHERAL NERVOUS SYSTEM DISEASES that impair innervation to muscle tissue (e.g., MUSCULAR ATROPHY, SPINAL)
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Muscular Disorders, Atrophic -- See Also Muscular Atrophy


Derangement in size and number of muscle fibers occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessness, malnutrition, and particularly in denervation
  1
Muscular Disorders, Atrophic -- therapy : The plasticity of skeletal muscle : from molecular mechanism to clinical applications / Kunihiro Sakuma, editor  2017 1
 

Muscular dystrophies -- See Muscular dystrophy


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Muscular Dystrophies   4
Muscular Dystrophies -- diagnosis : Muscular dystrophy : methods and protocols / edited by Katharine M.D. Bushby and Louise V.B. Anderson  2001 1
Muscular Dystrophies -- genetics   4
Muscular Dystrophies -- history. : The history of a genetic disease : Duchenne muscular dystrophy or Meryon's disease / Alan E. H. Emery & Marcia L. H. Emery  1995 1
Muscular Dystrophies -- prevention & control : Handbook of sampling methods for arthropods in agriculture / edited by Larry P. Pedigo and G. David Buntin  1994 1
 

Muscular Dystrophy -- See Muscular Dystrophies


A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS
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Muscular dystrophy.   13
Muscular dystrophy -- Animal models -- Congresses. : The Biochemistry of myasthenia gravis and muscular dystrophy / edited by G. G. Lunt and R. M. Marchbanks  1978 1
 

Muscular Dystrophy, Becker -- See Muscular Dystrophy, Duchenne


An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcolemma. Muscle fibers undergo a process that features degeneration and regeneration. Clinical manifestations include proximal weakness in the first few years of life, pseudohypertrophy, cardiomyopathy (see MYOCARDIAL DISEASES), and an increased incidence of impaired mentation. Becker muscular dystrophy is a closely related condition featuring a later onset of disease (usually adolescence) and a slowly progressive course. (Adams et al., Principles of Neurology, 6th ed, p1415)
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Muscular Dystrophy, Becker Type -- See Muscular Dystrophy, Duchenne


An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcolemma. Muscle fibers undergo a process that features degeneration and regeneration. Clinical manifestations include proximal weakness in the first few years of life, pseudohypertrophy, cardiomyopathy (see MYOCARDIAL DISEASES), and an increased incidence of impaired mentation. Becker muscular dystrophy is a closely related condition featuring a later onset of disease (usually adolescence) and a slowly progressive course. (Adams et al., Principles of Neurology, 6th ed, p1415)
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