New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
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Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
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Clinicopathologic Conference, Hypocalcemic Myopathy Due to Hypoparathyroidism
NEJM 388:1513-1520, Case 12-2023, 2023
Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
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Underappreciated Statin-Induced Myopathic Weakness Causes Disability
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Erroneous Diagnosis Corrected After 28 Years
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Neurologic Aspects of Inflammatory Bowel Disease
Neurol 45:416-421, Lossos,A.,et al, 1995
Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995
Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995
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Small Cell CA (of lung) with Lambert-Eaton Myasthenic Syndr, Case 32-1994, NEJM 331:528-5354., , 1994
Sudden Onset of Profound Weakness in a Toddler
J Pediatr 122:663-667, Carraccio,C.,et al, 1993
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Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989
Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
Neurol 38:573-580, Mohire,M.D.,et al, 1988
The Lambert-Eaton Myasthenic Syndrome, A Review of 50 Cases
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Neurotoxic Effects of Organophosphorus Insecticides:An Intermediate Syndrome
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Central Core Disease, Clinical Features in 13 Patients
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Clin. Path. Conference
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Inclusion Body Myositis
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A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings
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Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
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Rigid Spine Syndrome:A Type I Fiber Myopathy
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Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
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