X-Linked Emery-Dreifuss Muscular Dystrophy Can Be Diagnosed from Skin Biopsy or Blood Sample
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Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture
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LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine
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Cardiomyopathy May Be the Only Clinical Manifestation in Female Carriers of Duchenne Muscular Dystrophy
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Mosaic Express of Dystrophin in Carriers of Becker's Muscular Dyst & X-Linked Synd of Myalgia & Cramps
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Dystrophinopathy in Isolated Cases of Myopathy in Females
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Detection of Duchenne and Becker MD Carriers by Quant Multiplex Polymerase Chain Reaction
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The Frequency of Patients with Dystrophic Abnormalities in a Limb-Girdle Patient Population
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Direct Diagnosis of Carriers of Duchenne & Becker Muscular Dystrophy by Amplification of Lymphocyte RNA
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Mosaic Expression of Dystrophic in Symptomatic Carriers of Duchenne's Muscular Dystrophy
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DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
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Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
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Gene Studies in Newborn Males with Duchenne Muscular Dystrophy Detected by Neonatal Screening
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Prenatal Diagnosis & Detection of Carriers with DNA Probes in Duchenne's Muscular Dystrophy
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Prenatal Diagnosis & Carrier Detection of Duchenne Muscular Dystrophy with Closely Linked RFLPs
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Duchenne Muscular Dystrophy:Carrier Detection by Ultrasound & Computerised Tomography
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The Female Carrier of Duchenne Muscular Dystrophy
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Progressive Muscle Disease in a Young Woman With Family History of Duchenne's Muscular Dystrophy
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Electrocardiogram Abnormalities in Carriers of Duchenne Muscular Dystrophy
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Carrier Detection in Duchenne Muscular Dystrophy
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Serum LDH-5 in Carriers of Duchenne Muscular Dystrophy
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Deformed Erythrocytes in Muscular Dystrophies
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Systemic Membrane Defect in the Proximal Muscular Dystrophies
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Carrier Detection in Duchenne Muscular Dystrophy
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A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
Neurol 102:e209258, Lail,G.,et al, 2024
Cancer Risk in Patients with Muscular Dystrophy and Myotonic Dystrophy
Neurol 103:e209883, Maya-Gonzalez,C.,et al, 2024
Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
NEJM 388:2379-2387, Case 19-2023, 2023
Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
UptoDate 2022 Jan, Darras, B.T., 2022
Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021
Telemedicine in Neurology
Neurol 94:30-38,16, Hatcher-Martin, J.M.,et al, 2020
"Boule Du Biceps" in Dysferlinopathy
Neurol 94:83-84, El Sherif, R.,et al, 2020