Feza Deymeer - Concepedia

Author

Feza Deymeer

Istanbul University ORCID

Also Known As

Bürki, F., Deymeer, Feza, F Deymeer, F. DEYMEER, F. Deymeer, FEZA DEYMEER, Feza DEYMEER, Feza Deymeer

159

Publications

3.8K

Citations

H-Index

137

Concepts

All Affiliations

Istanbul University Bakırköy Psychiatric Hospital Boğaziçi University Hacettepe University Universität Ulm

About

Feza Deymeer is an author at Istanbul University specializing in medicine, genetics, and autoimmune disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	23	34	2.5K
2	Health Sciences	5	5	90
3	Allergy	3	3	245
4	Public Health	2	2	44
5	Applied Physiology	2	2	49

Feza Deymeer

Publications

3.5K

Citations

H-Index

Page 1

	Year	Citations
Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome Nikki Plaster, Rabi Tawil, Martin Tristani‐Firouzi, Cell Episodic Electrical PhenotypesDevelopmental BiologyGenetic DisorderGeneticsPhysiology	2001	991
A comprehensive analysis of the epidemiology and clinical characteristics of anti-LRP4 in myasthenia gravis Paraskevi Zisimopoulou, Panagiota Evangelakou, John Tzartos, Journal of Autoimmunity Autoimmune DiseaseMedicinePathologyComprehensive AnalysisDermatology	2013	317
Clinical comparison of anti-MuSK- vs anti-AChR-positive and seronegative myasthenia gravis Feza Deymeer, Özlem Güngör–Tunçer, Vuslat Yılmaz, Neurology Muscle FunctionAllergyAutoimmune DiseaseSkeletal MusclePhysiology	2007	166
Oculopharyngodistal myopathy is a distinct entity Hacer Durmuş, Steven H. Laval, Feza Deymeer, Neurology	2011	84
MuSK autoantibodies in myasthenia gravis detected by cell based assay — A multinational study Anastasios Tsonis, Paraskevi Zisimopoulou, Konstantinos Lazaridis, Journal of Neuroimmunology Autoimmune DiseaseMusk AutoantibodiesImmunologyPathologyAutoimmunity	2015	79
Titin antibodies in “seronegative” myasthenia gravis — A new role for an old antigen Christos Stergiou, Konstantinos Lazaridis, Vasiliki Zouvelou, Journal of Neuroimmunology New RoleAutoimmune DiseaseImmunologyPathologyAutoimmunity	2016	71
Novel muscle chloride channel mutations and their effects on heterozygous carriers. Volker Mailänder, R Heine, Feza Deymeer, PubMed	1996	68
Proof of a non-functional muscle chloride channel in recessive myotonia congenita (Becker) by detection of a 4 base pair deletion R Heine, Alfred L. George, Ursula Pika, Human Molecular Genetics	1994	67
GFPT1-myasthenia Duygu Selcen, Xin‐Ming Shen, Margherita Milone, Neurology	2013	65
Natural history of SMA IIIb Feza Deymeer, Yeşim Parman, Mehveş Poda Neurology	2008	61

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