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Muscular Dystrophy, Becker's -- 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, Childhood, Pseudohypertrophic -- 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 -- Congresses. : The Biochemistry of myasthenia gravis and muscular dystrophy / edited by G. G. Lunt and R. M. Marchbanks  1978 1
Muscular dystrophy -- Diagnosis : Muscular dystrophy : a concise guide / Raymond A. Huml, editor  2015 1
 

Muscular Dystrophy, Duchenne -- See Also Dystrophin


A muscle protein localized in surface membranes which is the product of the Duchenne/Becker muscular dystrophy gene. Individuals with Duchenne muscular dystrophy usually lack dystrophin completely while those with Becker muscular dystrophy have dystrophin of an altered size. It shares features with other cytoskeletal proteins such as SPECTRIN and alpha-actinin but the precise function of dystrophin is not clear. One possible role might be to preserve the integrity and alignment of the plasma membrane to the myofibrils during muscle contraction and relaxation. MW 400 kDa
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Muscular Dystrophy, Duchenne   7
 

Muscular Dystrophy, Duchenne and Becker Types -- 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, Duchenne-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, Duchenne -- diagnosis : Duchenne muscular dystrophy / Alan E.H. Emery, Francesco Muntoni, Rosaline Quinlivan  2015 1
Muscular Dystrophy, Duchenne -- genetics   3
Muscular Dystrophy, Duchenne -- history : Duchenne muscular dystrophy / Alan E.H. Emery, Francesco Muntoni, Rosaline Quinlivan  2015 1
Muscular Dystrophy, Duchenne -- psychology. : Occupational therapy and Duchenne muscular dystrophy / by Kate Stone ... [and others]  2007 1
Muscular Dystrophy, Duchenne -- psychology -- Case Reports : Occupational Therapy and Duchenne Muscular Dystrophy : Stone Duchenne  2007 1
Muscular Dystrophy, Duchenne -- therapy   6
Muscular Dystrophy, Duchenne -- therapy -- Case Reports : Occupational Therapy and Duchenne Muscular Dystrophy : Stone Duchenne  2007 1
 

Muscular Dystrophy, Duchenne 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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Muscular Dystrophy, Facioscapulohumeral : FSHD facioscapulohumeral muscular dystrophy : clinical medicine and molecular cell biology / edited by Meena Upadhyaya and David N Cooper  2004 1
Muscular Dystrophy, Facioscapulohumeral -- genetics : FSHD facioscapulohumeral muscular dystrophy : clinical medicine and molecular cell biology / edited by Meena Upadhyaya and David N Cooper  2004 1
Muscular dystrophy -- Genetic aspects. : Death gene / directed by Alan Erson  2002 1
Muscular dystrophy -- 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 dystrophy in children -- See Also the narrower term Duchenne muscular dystrophy


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Muscular dystrophy in children -- Patients.   2
Muscular dystrophy in children -- Popular works. : Muscular dystrophy in children : a guide for families / Irwin M. Siegel  1999 1
Muscular dystrophy -- Juvenile fiction. : See ya, Simon / David Hill  1995 1
Muscular dystrophy -- Molecular aspects : Molecular Mechanisms of Muscular Dystrophies  2006 1
Muscular dystrophy -- Molecular aspects -- Laboratory manuals : Muscular dystrophy : methods and protocols / edited by Katharine M.D. Bushby and Louise V.B. Anderson  2001 1
Muscular dystrophy -- Patients : Shorts RAI Film Festival 2021. The daring young girl on the flying trapeze / a film by Nina Ross ; produced by: Nancy Willis and Nina Ross  2020 1
Muscular dystrophy -- Popular works.   4
 

Muscular Dystrophy, Pseudohypertrophic -- 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, Pseudohypertrophic, Childhood -- 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 Pseudohypertrophic Progressive, 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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Muscular Dystrophy, Pseudohypertrophic Progressive, Duchenne 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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Muscular dystrophy -- Psychological aspects : Muscular dystrophy and other neuromuscular diseases : psychosocial issues / Leon I. Charash [and others], editors  2013 1
Muscular dystrophy -- Research.   2
Muscular dystrophy -- Research -- 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 dystrophy -- Social aspects : Muscular dystrophy and other neuromuscular diseases : psychosocial issues / Leon I. Charash [and others], editors  2013 1
Muscular dystrophy -- Treatment   3
 

Muscular Flaccidities -- See Muscle Hypotonia


A diminution of the skeletal muscle tone marked by a diminished resistance to passive stretching
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Muscular Flaccidity -- See Muscle Hypotonia


A diminution of the skeletal muscle tone marked by a diminished resistance to passive stretching
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Muscular Hypotonia -- See Muscle Hypotonia


A diminution of the skeletal muscle tone marked by a diminished resistance to passive stretching
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Muscular pain -- See Myalgia


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  Muscular rheumatism -- 2 Related Subjects   2
 

Muscular sense -- See Also Movement, Psychology of


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Muscular sense.   16
Muscular system.   3
Muscular system -- injuries -- Case Reports : Athletic and Orthopedic Injury Assessment : a Case Study Approach  2017 1
Muscular system -- Wounds and injuries -- Case studies : Athletic and Orthopedic Injury Assessment : a Case Study Approach  2017 1
 

Muscularis Mucosae -- See Mucous Membrane


An EPITHELIUM with MUCUS-secreting cells, such as GOBLET CELLS. It forms the lining of many body cavities, such as the DIGESTIVE TRACT, the RESPIRATORY TRACT, and the reproductive tract. Mucosa, rich in blood and lymph vessels, comprises an inner epithelium, a middle layer (lamina propria) of loose CONNECTIVE TISSUE, and an outer layer (muscularis mucosae) of SMOOTH MUSCLE CELLS that separates the mucosa from submucosa
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Musculature -- See Muscles



--individual muscles, e.g. Tensor tympani muscle; also subdivision Muscles under individual organs and regions of the body, e.g. Foot--Muscles; and headings beginning with the word Muscle
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Musculo-skeletal system -- See Musculoskeletal system


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