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Duygu Selcen, MD

  • 3475 Citations
  • 33 Scopus h-Index
1977 …2019
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  • 3 Similar Profiles
Congenital Myasthenic Syndromes Medicine & Life Sciences
Mutation Medicine & Life Sciences
Muscle Weakness Medicine & Life Sciences
Muscles Medicine & Life Sciences
Muscular Dystrophies Medicine & Life Sciences
Muscular Diseases Medicine & Life Sciences
Desmin Medicine & Life Sciences
Distal Myopathies Medicine & Life Sciences

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Projects 1977 2016

Congenital Myasthenic Syndromes

Engel, A. G. & Selcen, D.

Project: Research project

Investigation of Myofibillar Myopathies

Selcen, D.

National Institutes of Health

12/15/04 → 11/30/09

Project: Research project

Muscular Diseases
Research
Mutation
Proteins
Mentors

ELECTRON MICROSCOPY OF MYOPATHIES

Engel, A. G. & Selcen, D.

National Institutes of Health

5/1/77 → 4/30/16

Project: Research project

Congenital Myasthenic Syndromes
Muscular Diseases
Cholinergic Receptors
Electron Microscopy
Muscles

Research Output 1995 2019

  • 3475 Citations
  • 33 Scopus h-Index
  • 74 Article
  • 3 Chapter
  • 1 Book
  • 1 Conference contribution
1 Citation (Scopus)

A homozygous mutation in GMPPB leads to centronuclear myopathy with combined pre- and postsynaptic defects of neuromuscular transmission

Nicolau, S., Liewluck, T., Shen, X. M., Selcen, D., Engel, A. G. & Milone, M., Aug 1 2019, In : Neuromuscular Disorders. 29, 8, p. 614-617 4 p.

Research output: Contribution to journal › Article

Congenital Myasthenic Syndromes
Congenital Structural Myopathies
Mutation
Muscular Dystrophies
Muscle Weakness

Idiopathic inflammatory myopathy: Interrater variability in muscle biopsy reading

Olivier, P. A., De Paepe, B., Aronica, E., Berfelo, F., Colman, R., Amato, A., Dimitri, D., Gallardo, E., Gherardi, R., Goebel, H. H., Hilton-Jones, D., Hofer, M., Holton, J., Schrøder, H. D., Selcen, D., Stenzel, W., de Visser, M. & De Bleecker, J. L., Aug 27 2019, In : Neurology. 93, 9, p. e889-e894

Research output: Contribution to journal › Article

Myositis
Reading
Biopsy
Muscles
Connective Tissue

Slow-channel myasthenia due to novel mutation in M2 domain of AChR delta subunit

Shen, X. M., Milone, M., Wang, H. L., Banwell, B., Selcen, D., Sine, S. M. & Engel, A. G., Oct 1 2019, In : Annals of Clinical and Translational Neurology. 6, 10, p. 2066-2078 13 p.

Research output: Contribution to journal › Article

Open Access
Congenital Myasthenic Syndromes
Hydrophobic and Hydrophilic Interactions
Terminology
Activation Analysis
Bungarotoxins
3 Citations (Scopus)

Congenital myasthenic syndromes in adult neurology clinic: A long road to diagnosis and therapy

Kao, J. C., Milone, M., Selcen, D., Shen, X. M., Engel, A. G. & Liewluck, T., Nov 6 2018, In : Neurology. 91, 19, p. e1770-e1777

Research output: Contribution to journal › Article

Congenital Myasthenic Syndromes
Neurology
Therapeutics
Diagnostic Errors
Thymectomy
1 Citation (Scopus)

Novel Homozygous Variant in TTC19 Causing Mitochondrial Complex III Deficiency with Recurrent Stroke-Like Episodes: Expanding the Phenotype

Conboy, E., Selcen, D., Brodsky, M. C., Gavrilova, R. M. & Lan Ho, M., Jul 1 2018, In : Seminars in Pediatric Neurology. 26, p. 16-20 5 p.

Research output: Contribution to journal › Article

Lactic Acid
Stroke
Exome
Phenotype
Consanguinity