A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
Neurol 102:e209258, Lail,G.,et al, 2024
Telemedicine in Neurology
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Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture
Neurol 90:e172-e176, Roy, B. & Raynor, E., 2018
Palliative Care and Neurology
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The Limbic-Girdle Muscular Dystrophies
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Evidence-Based Path to Newborn Screening for Duchenne Muscular Dystrophy
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Transition to Adult Care for Children with Chronic Neurological Disorders
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New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
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Diagnosis and Etiology of Congenital Muscular Dystrophy
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Diagnostic Evaluation of Clinically Normal Subjects with Chronic hyperCKemia
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Case 35-2006: A Newborn Boy with Hypotonia
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Neurological and Neuromuscular Disease as a Risk Factor for Respiratory Failure in Children Hospitalized With Influenza Infection
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Clinical Relevance of Atrial Fibrillation/Flutter, Stroke, Pacemaker Implant, and Heart Failure in Emery-Dreifuss Muscular Dystrophy
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Clinical and Genetic Aspects of Distal Myopathies
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Congenital Muscular Dystrophy with Rigid Spine Syndrome:A Clinical, Pathological, Radiological, and Genetic Study
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Bent Spine Syndrome
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Cognitive Dysfunction as the Major Presenting Feature of Becker's Muscular Dystrophy
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Diagnosis of Merosin (Laminin-2) Deficient Congenital Muscular Dystrophy by Skin Biopsy
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Palliative Care in Neurology
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Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996
Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
Ann Neurol 40:782-791, Pegoraro,E.,et al, 1996
Brain Abnormalities in Duchenne Muscular Dystrophy:Phosphorus-31 Magnetic Resonance Spectroscopy & Neuropsych Study
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Facioscapulohumeral Muscular Dystrophy in Early Childhood
Arch Neurol 51:387-394, Brouwer,O.F.,et al, 1994
Clinicopath Conf
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Congenital Muscular Dystrophy
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Frequency of Cerebral Infarction in Patients with Inherited Neuromuscular Disease
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Facioscapulohumeral Dystrophy Associated with Hearing Loss & Coats Syndrome
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Myotonic Dystrophy, Mitral Valve Prolapse, and Cerebral Embolism
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Abnormal Iris Vasculature in Myotonic Dystrophy
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The Spectrum of Mild X-Linked Recessive Muscular Dystrophy
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