Projects per year
Fingerprint Dive into the research topics where Duygu Selcen is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 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
Network
Recent external collaboration on country level. Dive into details by clicking on the dots.
Projects 1977 2016
Muscular Diseases
Research
Mutation
Proteins
Mentors
Congenital Myasthenic Syndromes
Muscular Diseases
Cholinergic Receptors
Electron Microscopy
Muscles
Research Output 1995 2019
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-e894Research 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-e1777Research 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