Associate Professor, Pediatrics, Mayo Medical School

Neurology

Duygu Selcen is an expert in the field of Neurology. He went to Wayne State University School of Medicine. Wayne State University School of Medicine is ranked 63 in research and 85 in primary care medicine He received awards:"Regional Top Doctor". Dr. Duygu Selcen is a published doctor and has 39 publications published. The lastest was: 'Multiple sclerosis in childhood: report of 16 cases.'

Publications

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• Editorial by concerned physicians: Unintended effect of the orphan drug act on the potential cost of 3,4-diaminopyridine.
• Congenital myasthenic syndromes: pathogenesis, diagnosis, and treatment.
• Evidence-based guideline summary: Diagnosis and treatment of limb-girdle and distal dystrophies: Report of the Guideline Development Subcommittee of the American Acade...
• Safety and yield of muscle biopsy in pediatric patients in the modern era.
• Anesthesia and Duchenne or Becker Muscular dystrophy: review of 117 anesthetic exposures.
• New horizons for congenital myasthenic syndromes.
• Reducing bodies and myofibrillar myopathy features in FHL1 Muscular dystrophy.
• Beneficial effects of albuterol in congenital endplate acetylcholinesterase deficiency and Dok-7 myasthenia.
• Myofibrillar myopathies.
• A 49-year-old woman with progressive shortness of breath.
• Infantile Muscular dystrophy in Canadian aboriginals is an ?B-crystallinopathy.
• Myasthenic syndrome caused by plectinopathy.
• Confirmation that abnormal desmin accumulation and migration are due to a desmin gene mutation in a familial cardiomyopathy and distal myopathy.
• What have we learned from the congenital myasthenic syndromes.
• Myasthenic syndrome due to defects in rapsyn: Clinical and molecular findings in 39 patients.
• A 49-year-old man with contractures, weakness, and cardiac arrhythmia.
• Myofibrillar myopathy with limb-girdle phenotype in a Thai patient.
• The Z-disk diseases.
• Mutation in BAG3 causes severe dominant childhood Muscular dystrophy.
• Dok-7 myasthenia: phenotypic and molecular genetic studies in 16 patients.
• Further observations in congenital myasthenic syndromes.
• A 46-year-old woman with severe weakness following acute respiratory distress syndrome.
• Zaspopathy in a large classic late-onset distal myopathy family.
• Sporadic late onset nemaline myopathy.
• Titinopathies: what happens when a big gene mutates in a big family?
• Mutations in ZASP define a novel form of Muscular dystrophy in humans.
• Are MuSK antibodies the primary cause of myasthenic symptoms?
• Mutations in myotilin cause myofibrillar myopathy.
• Myofibrillar myopathy: clinical, morphological and genetic studies in 63 patients.
• Myofibrillar myopathy caused by novel dominant negative alpha B-crystallin mutations.
• Familial cardioneuromyopathy with hyaline masses and nemaline rods: a novel phenotype.
• Rapsyn mutations in humans cause endplate acetylcholine-receptor deficiency and myasthenic syndrome.
• The earliest pathologic alterations in dysferlinopathy.
• Myopathy with muscle spindle excess: A new congenital neuroMuscular syndrome?
• Otocerebral anomalies associated with topical tretinoin use.
• High-dose intravenous immunoglobulin therapy in juvenile myasthenia gravis.
• Multiple sclerosis in childhood: report of 16 cases.
• Mucormycosis in a diabetic child and its treatment with fluconazole: a case report.

Schools

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• Hurley Med Center

• Mayo Clinic Rochester

• Wayne St University Chldns Hospital Of Mich

Conditions Treated

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• Gait Abnormality
• Muscular Dystrophy (MD)
• Spinal Muscular Atrophy (SMA)
• Syncope

Doctors Specialties

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• Neuromusculoskeletal Medicine
• Neurology

Accepted Insurances

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• Choice Plus POS II
• Blue Card PPO
• Blue Cross Blue Shield of Illinois PPO
• Blue Cross Accord
• Cigna PPO
• Great West Healthcare-Cigna PPO
• Open Access Plus
• Choice Care PPO
• MultiPlan PPO
• PHCS Network PPO
• Choice Plus POS
• Options PPO

Awards

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• Regional Top Doctor

Education

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• Wayne State University School of Medicine

Hospital

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• Mayo Clinic - Rochester, Minnesota

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