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The distinct genetic pattern of ALS in Turkey and novel mutations.
Neurobiol Aging. 2015 Apr;36(4):1764.e9-1764.e18. doi: 10.1016/j.neurobiolaging.2014.12.032. Epub 2015 Jan 10.
Neurobiol Aging. 2015.
PMID: 25681989
Free PMC article.
FBXO7-R498X mutation: phenotypic variability from chorea to early onset parkinsonism within a family.
Gündüz A, Eken AG, Bilgiç B, Hanagasi HA, Bilgüvar K, Günel M, Başak AN, Ertan S.
Gündüz A, et al. Among authors: eken ag.
Parkinsonism Relat Disord. 2014 Nov;20(11):1253-6. doi: 10.1016/j.parkreldis.2014.07.016. Epub 2014 Aug 14.
Parkinsonism Relat Disord. 2014.
PMID: 25169713
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Coexistence of autosomal recessive spastic ataxia of Charlevoix Saguenay and spondyloepiphyseal dysplasia in a Turkish patient.
Kurt S, Kartal E, Aksoy D, Cevik B, Eken AG, Sahbaz I, Nazli Basak A.
Kurt S, et al. Among authors: eken ag.
J Neurol Sci. 2015 Oct 15;357(1-2):290-1. doi: 10.1016/j.jns.2015.06.050. Epub 2015 Jun 25.
J Neurol Sci. 2015.
PMID: 26142023
No abstract available.
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Two young sisters with spinocerebellar ataxia type 2 showing different clinical progression of disease.
Yiş U, Dirik E, Kurul SH, Eken AG, Başak AN.
Yiş U, et al. Among authors: eken ag.
Cerebellum. 2009 Jun;8(2):127-9. doi: 10.1007/s12311-008-0080-6. Epub 2008 Nov 21.
Cerebellum. 2009.
PMID: 19023636
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Bell's palsy and choreiform movements during peginterferon alpha and ribavirin therapy.
Barut S, Karaer H, Oksuz E, Eken AG, Basak AN.
Barut S, et al. Among authors: eken ag.
World J Gastroenterol. 2009 Aug 7;15(29):3694-6. doi: 10.3748/wjg.15.3694.
World J Gastroenterol. 2009.
PMID: 19653353
Free PMC article.
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Association of a synonymous SCN1B variant affecting splicing efficiency with Benign Familial Infantile Epilepsy (BFIE).
Usluer S, Kayserili MA, Eken AG, Yiş U, Leu C, Altmüller J, Thiele H, Nürnberg P, Sander T, Çağlayan SH.
Usluer S, et al. Among authors: eken ag.
Eur J Paediatr Neurol. 2017 Sep;21(5):773-782. doi: 10.1016/j.ejpn.2017.05.001. Epub 2017 May 13.
Eur J Paediatr Neurol. 2017.
PMID: 28566192
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