• Türkçe
    • English
  • English 
    • Türkçe
    • English
  • Login
Search 
  •   DSpace Home
  • Search
  •   DSpace Home
  • Search
JavaScript is disabled for your browser. Some features of this site may not work without it.

Search

xmlui.mirage2.discovery.showAdvancedFiltersxmlui.mirage2.discovery.hideAdvancedFilters

Filters

Use filters to refine the search results.

Now showing items 1-2 of 2

  • Sort Options:
  • Relevance
  • Title Asc
  • Title Desc
  • Issue Date Asc
  • Issue Date Desc
  • Results Per Page:
  • 5
  • 10
  • 20
  • 40
  • 60
  • 80
  • 100

Unraveling The Genetic Landscape Of Autosomal Recessive Charcot-Marie-Tooth Neuropathies Using A Homozygosity Mapping Approach 

Zimon, Magdalena; Battaloglu, Esra; Parman, Yesim; Erdem, Sevim; Baets, Jonathan; De Vriendt, Els; Atkinson, Derek; Almeida-Souza, Leonardo; Deconinck, Tine; Ozes, Burcak; Goossens, Dirk; Cirak, Sebahattin; Van Damme, Philip; Shboul, Mohammad; Voit, Thomas; Van Maldergem, Lionel; Dan, Bernard; El-Khateeb, Mohammed S.; Guergueltcheva, Velina; Lopez-Laso, Eduardo; Goemans, Nathalie; Masri, Amira; Zuechner, Stephan; Timmerman, Vincent; Topaloglu, Haluk; De Jonghe, Peter; Jordanova, Albena (Springer, 2015)
Autosomal recessive forms of Charcot-Marie-Tooth disease (ARCMT) are rare but severe disorders of the peripheral nervous system. Their molecular basis is poorly understood due to the extensive genetic and clinical ...

The Distinct Genetic Pattern of ALS in Turkey and Novel Mutations 

Ozoguz, Aslihan; Uyan, Ozgun; Birdal, Gunes; Iskender, Ceren; Kartal, Ece; Lahut, Suna; Omur, Ozgur; Agim, Zeynep Sena; Eken, Asli Gundogdu; Sen, Nesli Ece; Kavak, Pinar; Saygi, Ceren; Sapp, Peter C.; Keagle, Pamela; Parman, Yesim; Tan, Ersin; Koc, Filiz; Deymeer, Feza; Oflazer, Piraye; Hanagasi, Hasmet; Gurvit, Hakan; Bilgic, Basar; Durmus, Hacer; Ertas, Mustafa; Kotan, Dilcan; Akalin, Mehmet Ali; Gulluoglu, Halil; Zarifoglu, Mehmet; Aysal, Fikret; Dosolu, Nilgun; Bilguvar, Kaya; Gunel, Murat; Keskin, Ozlem; Akgun, Tahsin; Ozcelik, Hilmi; Landers, John E.; Brown, Robert H.; Basak, A. Nazli (Elsevier Science Inc, 2015)
The frequency of amyotrophic lateral sclerosis (ALS) mutations has been extensively investigated in several populations; however, a systematic analysis in Turkish cases has not been reported so far. In this study, we ...
Hacettepe Üniversitesi Kütüphaneleri
Açık Erişim Birimi
Beytepe Kütüphanesi | Tel: (90 - 312) 297 6585-117 || Sağlık Bilimleri Kütüphanesi | Tel: (90 - 312) 305 1067
Bizi Takip Edebilirsiniz: Facebook | Twitter | Youtube | Instagram
Web sayfası:www.library.hacettepe.edu.tr | E-posta:openaccess@hacettepe.edu.tr
Sayfanın çıktısını almak için lütfen tıklayınız.
Contact Us | Send Feedback



DSpace software copyright © 2002-2016  DuraSpace
Theme by 
Atmire NV
 

 


DSpace@Hacettepe
huk openaire onayı
by OpenAIRE

About HUAES
Open Access PolicyGuidesSubcriptionsContact

livechat

sherpa/romeo

Browse

All of DSpaceCommunities & CollectionsBy Issue DateAuthorsTitlesSubjectsTypeDepartmentPublisherLanguageRightsIndexing SourceFundingxmlui.ArtifactBrowser.Navigation.browse_subtype

My Account

LoginRegister

Discover

Author
Parman, Yesim (2)
Agim, Zeynep Sena (1)Akalin, Mehmet Ali (1)Akgun, Tahsin (1)Almeida-Souza, Leonardo (1)Atkinson, Derek (1)Aysal, Fikret (1)Baets, Jonathan (1)Basak, A. Nazli (1)Battaloglu, Esra (1)... View MoreSubject
Neurosciences & Neurology (2)
Genetics & Heredity (1)Geriatrics & Gerontology (1)... View MoreDate Issued
2015 (2)
Has File(s)Yes (2)

DSpace software copyright © 2002-2016  DuraSpace
Theme by 
Atmire NV