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List of works by Payam Soltanzadeh

A mutation causes MuSK reduced sensitivity to agrin and congenital myasthenia.

scientific article

Anti-3-hydroxy-3-methylglutaryl-coenzyme a reductase autoantibody-positive necrotizing autoimmune myopathy with dermatomyositis-like eruption

scientific article published on 18 January 2018

Clinical and genetic characterization of manifesting carriers of DMD mutations

scientific article

Diagnostic challenges in POEMS syndrome presenting with polyneuropathy: A case series

scientific article published on 11 May 2017

Giant congenital melanocytic nevus with neurofibroma-like changes and spina bifida occulta

scientific article published on 01 November 2006

Hereditary inclusion body myopathy in Persian Jews: a case report from Iran.

scientific article published on 10 July 2013

Intravascular T-cell lymphoma: A rare, poorly characterized entity with cytotoxic phenotype.

scientific article

Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort

scientific article

Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene

scientific article

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