Moleküler Biyoloji ve Genetik

Kurt, S., Kartal, E., Aksoy, D., Cevik, B., Eken, A.G., Şahbaz, I., Basak, N., 'Coexistance of autosomal recessive spastic ataxia of Charlevoix Saguenay and spondyloepiphyseal dysplasia in a Turkish patient', European Journal of Neurology,  Meeting Abstract: PP4196, 21, 691-691, 2014.

Türkçe

Jiang, .ZH., Huang, S.W., Luo, H.Y., Akar, N., Basak, A.N.,et al. 'Assessment of HbF QTLs Affecting Disease Severity and Genetic Analysis in Patients Homozygous for Codon 8 (-AA) beta(0)-Thalassemia Mutation',Blood 124, 21, 2014.  

Türkçe

İskender, C., Eken, A.G., Özoğuz, A., Akimoto, C., Alstermark, H., Andersen, P.M., Başak, A.N., 'C9orf72 hexanucleotide repeat expansion in Turkish ALS patients', Journal of Neurology,  Meeting Abstract:EP4118, 261, S222-S222, 2014.

Türkçe

İskender, C., Eken, A.G., Özoğuz, A., Akimoto, C., Alstermark, H., Andersen, P.M., Başak, A.N., 'C9orf72 hexanucleotide repeat expansion in Turkish ALS patients', European Journal of Neurology,  Meeting Abstract: EP4118, 21, 328-328, 2014.

Türkçe

Suna Lahut, David Vadasz,Candan Depboylu, Vincent Ries,Martina Krenzer,Karin Stiasny-Kolster, A. Nazli Basak,Wolfgang H. Oertel , Georg Auburger, The PD-associated alpha-synuclein promoter Rep1 allele 2shows diminished frequency in restless legs syndrome , Neurogenetics, s10048-014-040, 10048-014, 2014

Türkçe

Gündüz A, Eken AG, Bilgiç B, Hanagasi HA, Bilgüvar K, Günel M, Başak AN, Ertan S , 'FBX07-R498X mutation: Phenotypic variability from chorea to early onset parkinsonism within a family',Parkinsonism & Related Disorders, 20, 11, 1253-1256, 2014

Türkçe

Zimon, M., Battaloğlu, E., Parman, Y., Erdem, S., Baets, J., De Vriendt, E., Atkınson, D., Almeida-Souza, L., Deconinck, T., Özes, B., Goossens, D., Çırak, S., Van Damme, P., Shboul, M., Voit, T., Van Maldergem, L., Dan, B., El-Khateeb, M.S., Guergueltcheva, V., Lopez-Laso, E., Goemans, N., Masri, A., Zuchner, S., Timmerman, V., Topaloğlu, H., De Jonghe, P., Jordanova, A., "Unraveling the Genetic Landscape of Autosomal Recessive Charcot-Marie-Tooth Neuropathies Using A Homozygosity Mapping Approach", Neurogenetics, 16, 1, 33-42, 2015.

Türkçe

Yüceyar, N., Ayhan, O., Karasoy, H., Tolun, A., "Homozygous MYH7 R1820W Mutation Results in Recessive Myosin Storage Myopathy: Scapuloperoneal and Respiratory Weakness With Dilated Cardiomyopathy", Neuromuscular Disorders, 25, 4, 340-344, 2015.

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