Hatice Karasoy

Hatice Karasoy

UNVERIFIED PROFILE

Are you Hatice Karasoy?   Register this Author

Register author
Hatice Karasoy

Hatice Karasoy

Publications by authors named "Hatice Karasoy"

Are you Hatice Karasoy?   Register this Author

13Publications

311Reads

11Profile Views

Vestibular impairment in chronic inflammatory demyelinating polyneuropathy.

J Neurol 2018 Feb 19;265(2):381-387. Epub 2017 Dec 19.

Department of Neurology, Royal Prince Alfred Hospital, Sydney, Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00415-017-8712-8DOI Listing
February 2018

Homozygous MYH7 R1820W mutation results in recessive myosin storage myopathy: scapuloperoneal and respiratory weakness with dilated cardiomyopathy.

Neuromuscul Disord 2015 Apr 26;25(4):340-4. Epub 2015 Jan 26.

Boğaziçi University, Department of Molecular Biology and Genetics, KP 301, Bebek, Istanbul 34342, Turkey. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.nmd.2015.01.007DOI Listing
April 2015

Myasthenia gravis and thymoma coexisting with myotonic dystrophy type 1.

Neuromuscul Disord 2014 Jan 11;24(1):40-2. Epub 2013 Sep 11.

Ege University School of Medicine, Neurology Department, Bornova Izmir, Turkey.

View Article

Download full-text PDF

Source
https://linkinghub.elsevier.com/retrieve/pii/S09608966130095
Publisher Site
http://dx.doi.org/10.1016/j.nmd.2013.09.001DOI Listing
January 2014

DNAJC6 is responsible for juvenile parkinsonism with phenotypic variability.

Parkinsonism Relat Disord 2013 Mar 2;19(3):320-4. Epub 2012 Dec 2.

Boğaziçi University, Department of Molecular Biology and Genetics, KP 301, Bebek, 34342 Istanbul, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.parkreldis.2012.11.006DOI Listing
March 2013

Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathy.

Hum Mutat 2012 Jun 4;33(6):949-59. Epub 2012 Apr 4.

Department of Translational Medicine and Neurogenetics, Institut de Génétique et de Biologie Moléculaire et Cellulaire, INSERM U964/CNRS UMR7104, University of Strasbourg, Collège de France, Illkirch, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/humu.22067DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3374402PMC
June 2012

Sydenham chorea and Hashimoto thyroiditis: an unusual association.

J Child Neurol 2010 Jun 29;25(6):757-8. Epub 2010 Mar 29.

Department of Neurology, Cumhuriyet University School of Medicine, Sivas, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/0883073809343721DOI Listing
June 2010

Zuclopenthixol-induced neuroleptic malignant syndrome in an adolescent girl.

Clin Toxicol (Phila) 2007 ;45(3):277-80

Department of Child Psychiatry, Ege University, School of Medicine, Izmir, Turkey.

View Article

Download full-text PDF

Source
http://www.tandfonline.com/doi/full/10.1080/1556365060103169
Publisher Site
http://dx.doi.org/10.1080/15563650601031692DOI Listing
May 2007

Atypical EEG findings in subacute sclerosing panencephalitis.

Clin Neurophysiol 2005 Aug;116(8):1762-7

Department of Neurology, Ege University School of Medicine, Bornova, 35100 Izmir, Turkey.

View Article

Download full-text PDF

Source
http://linkinghub.elsevier.com/retrieve/pii/S138824570500121
Publisher Site
http://dx.doi.org/10.1016/j.clinph.2005.03.026DOI Listing
August 2005

Deletion analysis and clinical correlations in patients with Xp21 linked muscular dystrophy.

Turk J Pediatr 2004 Oct-Dec;46(4):333-8

Department of Pediatrics, Dokuz Eylül University Faculty of Medicine, Izmir, Turkey.

View Article

Download full-text PDF

Source
April 2005

Identification of a locus for an autosomal recessive hyaline body myopathy at chromosome 3p22.2-p21.32.

Neuromuscul Disord 2004 Jan;14(1):4-9

Department of Molecular Biology and Genetics, Bogaziçi University, Bebek 34342, Istanbul, Turkey.

View Article

Download full-text PDF

Source
January 2004