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[Cardiomyopathy in hereditary muscular dystrophies].
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Hereditary muscular diseases and symptoms from the gastrointestinal tract.
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Clinical and genetic characteristics of childhood-onset myotonic dystrophy.
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Differences in the pattern of cognitive impairments between juvenile and adult onset myotonic dystrophy type 1.
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Diagnosis and Treatment of Mitochondrial Myopathies.
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Psychosocial Management of the Patient With Duchenne Muscular Dystrophy.
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[Osteoarthropathies and Myopathies associated with Disorders of the Thyroid Endocrine System].
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Prenatal, Neonatal, and Early Childhood Features in Congenital Myotonic Dystrophy.
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Cognitive profile in Duchenne muscular dystrophy boys without intellectual disability: The role of executive functions.
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Cognitive impairment, clinical severity and MRI changes in MELAS syndrome.
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Diagnostic work-up in steroid myopathy.
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