about
Clinical and genetic characterization of manifesting carriers of DMD mutationsNonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene.A mutation causes MuSK reduced sensitivity to agrin and congenital myasthenia.Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort.Hereditary inclusion body myopathy in Persian Jews: a case report from Iran.Intravascular T-cell lymphoma: A rare, poorly characterized entity with cytotoxic phenotype.Anti-3-hydroxy-3-methylglutaryl-coenzyme a reductase autoantibody-positive necrotizing autoimmune myopathy with dermatomyositis-like eruption.Diagnostic challenges in POEMS syndrome presenting with polyneuropathy: A case series.Giant congenital melanocytic nevus with neurofibroma-like changes and spina bifida occulta
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description
onderzoeker
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researcher ORCID ID = 0000-0001-5788-8619
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Payam Soltanzadeh
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Payam Soltanzadeh
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Payam Soltanzadeh
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Payam Soltanzadeh
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Payam Soltanzadeh
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Payam Soltanzadeh
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Payam Soltanzadeh
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Payam Soltanzadeh
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Payam Soltanzadeh
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Payam Soltanzadeh
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0000-0001-5788-8619