F
Feza Deymeer
Researcher at Istanbul University
Publications - 102
Citations - 3937
Feza Deymeer is an academic researcher from Istanbul University. The author has contributed to research in topics: Myasthenia gravis & Antibody. The author has an hindex of 27, co-authored 100 publications receiving 3602 citations.
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Journal ArticleDOI
Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome
Nikki M. Plaster,Rabi Tawil,Martin Tristani-Firouzi,Sonia Canún,Saïd Bendahhou,Akiko Tsunoda,Matthew R. Donaldson,Susan T. Iannaccone,Ewout R. Brunt,Richard J. Barohn,Richard J. Barohn,John Wesley Clark,Feza Deymeer,Alfred L. George,Frank A. Fish,Angelika F. Hahn,Alexandru Nitu,Coşkun Özdemir,Piraye Serdaroglu,S. H. Subramony,Gil I. Wolfe,Ying-Hui Fu,Louis J. Ptáček +22 more
TL;DR: In this paper, the authors have mapped an Andersen's locus to chromosome 17q23 near the inward rectifying potassium channel gene KCNJ2.1, which was found to play an important role in developmental signaling.
Journal Article
Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's Syndrome
Nikki M. Plaster,Rabi Tawil,Martin Tristani-Firouzi,Sonia Canún,Saïd Bendahhou,A Soemori,Donaldson,Susan T. Iannaccone,Ewout R. Brunt,Richard J. Barohn,J Clark,Feza Deymeer,Alfred L. George,Angelika F. Hahn,A Nitu,Piraye Serdaroglu,S. H. Subramony,Gil I. Wolfe,Ying-Hui Fu,Louis J. Ptáček +19 more
TL;DR: Findings suggest that Kir2.1 plays an important role in developmental signaling in addition to its previously recognized function in controlling cell excitability in skeletal muscle and heart.
Journal ArticleDOI
A comprehensive analysis of the epidemiology and clinical characteristics of anti-LRP4 in myasthenia gravis
Paraskevi Zisimopoulou,Panagiota Evangelakou,John Tzartos,Konstantinos Lazaridis,Vasiliki Zouvelou,Renato Mantegazza,Carlo Antozzi,Francesca Andreetta,Amelia Evoli,Feza Deymeer,Güher Saruhan-Direskeneli,Hacer Durmus,Talma Brenner,A. Vaknin,Sonia Berrih-Aknin,M. Frenkian Cuvelier,T. Stojkovic,M. DeBaets,Mario Losen,Pilar Martinez-Martinez,Kleopas A. Kleopa,Eleni Zamba-Papanicolaou,Tassos C. Kyriakides,Anna Kostera-Pruszczyk,Piotr Szczudlik,Beata Szyluk,Dragana Lavrnic,Ivana Basta,Stojan Peric,Chantal M. E. Tallaksen,Angelina H. Maniaol,Socrates J. Tzartos,Socrates J. Tzartos +32 more
TL;DR: A cell based assay (CBA) based on human LRP4 expressing HEK293 cells is developed, for the reliable and efficient detection of LRP 4 antibodies, which showed similar responses to published responses of AChR-MG rather than to MuSK-MG patients.
Journal ArticleDOI
Clinical comparison of anti-MuSK-vs anti-AChR-positive and seronegative myasthenia gravis
Feza Deymeer,Ozlem Gungor-Tuncer,Vuslat Yilmaz,Yesim Parman,Piraye Serdaroglu,Coşkun Özdemir,Angela Vincent,Güher Saruhan-Direskeneli +7 more
TL;DR: The seronegative group was in between the anti-MuSK positive and theAnti-AChR positive groups, being closer to the latter, with regard to the severity of the disease.
Journal ArticleDOI
The distinct genetic pattern of ALS in Turkey and novel mutations.
Aslihan Ozoguz,Özgün Uyan,Güneş Birdal,Ceren Iskender,Ece Kartal,Suna Lahut,Özgür Ömür,Zeynep Sena Agim,Aslı Gündoğdu Eken,Nesli-Ece Sen,Pinar Kavak,Ceren Saygı,Peter C. Sapp,Pamela Keagle,Yesim Parman,Ersin Tan,Filiz Koç,Feza Deymeer,Piraye Oflazer,Hasmet Hanagasi,Hakan Gurvit,Başar Bilgiç,Hacer Durmus,Mustafa Ertas,Dilcan Kotan,Mehmet Ali Akalin,Halil Güllüoğlu,Mehmet Zarifoglu,Fikret Aysal,Nilgün Döşoğlu,Kaya Bilguvar,Murat Gunel,Ozlem Keskin,Tahsin Akgün,Hilmi Ozcelik,John Landers,Robert H. Brown,A. Nazli Basak +37 more
TL;DR: Exome sequencing revealed mutations in OPTN, SPG11, DJ1, PLEKHG5, SYNE1, TRPM7, and SQSTM1 genes, many of them novel.