Karasoy H - Search Results

1

Electrophysiological evaluation of oropharyngeal swallowing in myotonic dystrophy.

Ertekin C, Yüceyar N, Aydoğdu, Karasoy H. Ertekin C, et al. Among authors: karasoy h. J Neurol Neurosurg Psychiatry. 2001 Mar;70(3):363-71. doi: 10.1136/jnnp.70.3.363. J Neurol Neurosurg Psychiatry. 2001. PMID: 11181860 Free PMC article.

2

Myasthenia gravis and thymoma coexisting with myotonic dystrophy type 1.

Ekmekci O, Karasoy H, Bademkiran F, Akkus DE, Yuceyar N. Ekmekci O, et al. Among authors: karasoy h. Neuromuscul Disord. 2014 Jan;24(1):40-2. doi: 10.1016/j.nmd.2013.09.001. Epub 2013 Sep 11. Neuromuscul Disord. 2014. PMID: 24291332 Free article.

3

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

Yüceyar N, Ayhan Ö, Karasoy H, Tolun A. Yüceyar N, et al. Among authors: karasoy h. Neuromuscul Disord. 2015 Apr;25(4):340-4. doi: 10.1016/j.nmd.2015.01.007. Epub 2015 Jan 26. Neuromuscul Disord. 2015. PMID: 25666907

4

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

Onengüt S, Uğur SA, Karasoy H, Yüceyar N, Tolun A. Onengüt S, et al. Among authors: karasoy h. Neuromuscul Disord. 2004 Jan;14(1):4-9. doi: 10.1016/s0960-8966(03)00163-9. Neuromuscul Disord. 2004. PMID: 14659406

5

Vestibular impairment in Charcot-Marie-Tooth disease.

Akdal G, Koçoğlu K, Tanrıverdizade T, Bora E, Bademkıran F, Yüceyar AN, Ekmekçi Ö, Şengün İŞ, Karasoy H. Akdal G, et al. Among authors: karasoy h. J Neurol. 2021 Feb;268(2):526-531. doi: 10.1007/s00415-020-10186-x. Epub 2020 Aug 30. J Neurol. 2021. PMID: 32862243

6

Atypical EEG findings in subacute sclerosing panencephalitis.

Ekmekci O, Karasoy H, Gökçay A, Ulkü A. Ekmekci O, et al. Among authors: karasoy h. Clin Neurophysiol. 2005 Aug;116(8):1762-7. doi: 10.1016/j.clinph.2005.03.026. Clin Neurophysiol. 2005. PMID: 15982925

7

Proton MR spectroscopy in Rett syndrome.

Gökcay A, Kitis O, Ekmekci O, Karasoy H, Sener RN. Gökcay A, et al. Among authors: karasoy h. Comput Med Imaging Graph. 2002 Jul-Aug;26(4):271-5. doi: 10.1016/s0895-6111(02)00016-2. Comput Med Imaging Graph. 2002. PMID: 12074922 Review.

8

DNAJC6 is responsible for juvenile parkinsonism with phenotypic variability.

Köroğlu Ç, Baysal L, Cetinkaya M, Karasoy H, Tolun A. Köroğlu Ç, et al. Among authors: karasoy h. Parkinsonism Relat Disord. 2013 Mar;19(3):320-4. doi: 10.1016/j.parkreldis.2012.11.006. Epub 2012 Dec 2. Parkinsonism Relat Disord. 2013. PMID: 23211418

9

Vestibular impairment in chronic inflammatory demyelinating polyneuropathy.

Akdal G, Tanrıverdizade T, Şengün İ, Bademkıran F, Koçoğlu K, Yüceyar AN, Ekmekçi Ö, Karasoy H, Halmágyi GM. Akdal G, et al. Among authors: karasoy h. J Neurol. 2018 Feb;265(2):381-387. doi: 10.1007/s00415-017-8712-8. Epub 2017 Dec 19. J Neurol. 2018. PMID: 29260355

10

A database for screening and registering late onset Pompe disease in Turkey.

Gokyigit MC, Ekmekci H, Durmus H, Karlı N, Koseoglu E, Aysal F, Kotan D, Ali A, Koytak PK, Karasoy H, Yaman A, Sengun İS, Sayin R, Tiftikcioglu BI, Soysal A, Tutkavul K, Bayrak AO, Kısabay A, Elci MA, Yayla V, Yılmaz İA, Ozdamar SE, Erdogan C, Tasdemir N, Serdaroglu Oflazer P; Turkish Study Group for Late Onset Pompe Disease. Gokyigit MC, et al. Among authors: karasoy h. Neuromuscul Disord. 2018 Mar;28(3):262-267. doi: 10.1016/j.nmd.2017.12.008. Epub 2017 Dec 20. Neuromuscul Disord. 2018. PMID: 29395671

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