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DUYGU SELCEN, M.D.

M.D.

Neurology with Special Qualifications in Child Neurology Physician

NPI: 1376517169IndividualAccepts Medicare

Specialties, Licenses & Credentials

Neurology with Special Qualifications in Child Neurology PhysicianPrimary

Psychiatry & Neurology — Neurology with Special Qualifications in Child Neurology

Code: 2084N0402X

42357(MN)

CMS Specialties

PrimaryNEUROLOGY

Additional

PEDIATRIC MEDICINE

Education

OTHER

Class of 1988

Research & Publications (20)

Mutation in BAG3 causes severe dominant childhood muscular dystrophy.
PMID 19085932·Ann Neurol·2009
7-preclinical
The Z-disk diseases.
PMID 19181098·Adv Exp Med Biol·2008
6-review
Myofibrillar myopathies.
PMID 18769253·Curr Opin Neurol·2008
6-review
Dok-7 myasthenia: phenotypic and molecular genetic studies in 16 patients.
PMID 18626973·Ann Neurol·2008
8-other
Mutations in ZASP define a novel form of muscular dystrophy in humans.
PMID 15668942·Ann Neurol·2005
8-other
Are MuSK antibodies the primary cause of myasthenic symptoms?
PMID 15184594·Neurology·2004
8-other
Mutations in myotilin cause myofibrillar myopathy.
PMID 15111675·Neurology·2004
8-other
Myofibrillar myopathy: clinical, morphological and genetic studies in 63 patients.
PMID 14711882·Brain·2004
8-other
Myofibrillar myopathy caused by novel dominant negative alpha B-crystallin mutations.
PMID 14681890·Ann Neurol·2003
5-case
Familial cardioneuromyopathy with hyaline masses and nemaline rods: a novel phenotype.
PMID 11835379·Ann Neurol·2002
8-other
The earliest pathologic alterations in dysferlinopathy.
PMID 11402103·Neurology·2001
8-other
Myasthenic syndrome due to defects in rapsyn: Clinical and molecular findings in 39 patients.
PMID 19620612·Neurology·2009
8-other
A 49-year-old man with contractures, weakness, and cardiac arrhythmia.
PMID 19506227·Neurology·2009
5-case
Myofibrillar myopathy with limb-girdle phenotype in a Thai patient.
PMID 19253808·J Med Assoc Thai·2009
5-case
Further observations in congenital myasthenic syndromes.
PMID 18567859·Ann N Y Acad Sci·2008
6-review
A 46-year-old woman with severe weakness following acute respiratory distress syndrome.
PMID 17470757·Neurology·2007
5-case
Zaspopathy in a large classic late-onset distal myopathy family.
PMID 17337483·Brain·2007
8-other
Sporadic late onset nemaline myopathy.
PMID 16148261·Neurology·2005
8-other
Titinopathies: what happens when a big gene mutates in a big family?
PMID 15728278·Neurology·2005
7-preclinical
Rapsyn mutations in humans cause endplate acetylcholine-receptor deficiency and myasthenic syndrome.
PMID 11791205·Am J Hum Genet·2002
7-preclinical

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
200 1ST ST SW
ROCHESTER, MN 55905

Location

Practice Location

200 1ST ST SW, ROCHESTER, MN
(507) 284-2511

Quick Facts

NPI
1376517169
Entity Type
Individual
Gender
Female
Medicare
Accepted
Specialties
1
Locations
1
Years in Practice
38
Publications
20

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