Institutional Repository
    • Türkçe
    • English
  • English 
    • Türkçe
    • English
  • Login
Search 
  •   University of Economics & Technology Repository
  • Akademik Arşiv / Institutional Repository
  • Tıp Fakültesi / Faculty of Medicine
  • Temel Tıp Bilimleri Bölümü / Department of Basic Medical Sciences
  • Search
  •   University of Economics & Technology Repository
  • Akademik Arşiv / Institutional Repository
  • Tıp Fakültesi / Faculty of Medicine
  • Temel Tıp Bilimleri Bölümü / Department of Basic Medical Sciences
  • Search
JavaScript is disabled for your browser. Some features of this site may not work without it.

Search

Show Advanced FiltersHide Advanced Filters

Filters

Use filters to refine the search results.

Now showing items 1-4 of 4

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

Clinical findings and mutation analysis of NF1 patients in Turkey 

Terzi, Yunus Kasım; Oğuzkan-Balcı, Sibel; Anlar, Banu; Varan, Ali; Ersoy-Evans, Sibel; Sharafi, Parisa; Ayter, Şükriye (Elsevier B.V., 2018-02)
Neurofibromatosis type 1 (NF1) is an autosomal dominant disease that is caused by mutations of the NF1 gene. NF1 is clinically characterized by neurofibromas, pigmentation anomalies, and an increased risk of malignant ...
Thumbnail

Possible modifier genes in the variation of neurofibromatosis type 1 clinical phenotypes 

Sharafi, Parisa; Ayter, Şükriye (Taylor and Francis Ltd, 2018-04-03)
Neurofibromatosis type 1 (NF1) is the most common neurogenetic disorder worldwide, caused by mutations in the (NF1) gene. Although NF1 is a single-gene disorder with autosomal-dominant inheritance, its clinical expression ...
Thumbnail

The effect of parental age on NF1 patients in Turkey 

Ersoy-Evans, Sibel; Sharafi, Parisa; Anlar, Banu; Varan, Ali; Yılmaz, Ömer Faruk; Turan, Mustafa; Ayter, Şükriye (Springer Verlag, 2018-07-01)
Neurofibromatosis type 1 (NF1) is the most common neurogenetic disorder worldwide, and its clinical presentations are highly variable. NF1 is caused by mutations in the NF1 gene, and 50% of NF1 cases are sporadic, which ...
Thumbnail

Heightened CXCR4 and CXCL12 expression in NF1-associated neurofibromas 

Karaosmanoglu, Beren; Kocaefe, Çetin Y.; Söylemezoğlu, Figen; Anlar, Banu; Varan, Ali; Vargel, İbrahim; Ayter, Şükriye (Springer Berlin Heidelberg, 2018-05-01)
Neurofibromatosis type 1 (NF1) is the most common neurogenetic disorder worldwide, and its clinical presentations are highly variable. NF1 is caused by mutations in the NF1 gene, and 50% of NF1 cases are sporadic, which ...

DSpace software copyright © 2002-2016  DuraSpace
Contact Us | Send Feedback
Theme by 
Atmire NV
 

 

Browse

All of RepositoryCommunities & CollectionsBy Issue DateAuthorsTitlesSubjectsBy Submit DateBy TypeKapsamWOSScopusPubMedTR-DizinAvrupa Birliği Destekli Yayın SayısıTÜBİTAK Destekli Yayın SayısıDilErişimThis CollectionBy Issue DateAuthorsTitlesSubjectsBy Submit DateBy TypeKapsamWOSScopusPubMedTR-DizinAvrupa Birliği Destekli Yayın SayısıTÜBİTAK Destekli Yayın SayısıDilErişim

My Account

LoginRegister

Discover

Author
Ayter, Şükriye (4)
Anlar, Banu (3)Sharafi, Parisa (3)Varan, Ali (3)Ersoy-Evans, Sibel (2)Karaosmanoglu, Beren (1)Kocaefe, Çetin Y. (1)Oğuzkan-Balcı, Sibel (1)Söylemezoğlu, Figen (1)Terzi, Yunus Kasım (1)... View MoreSubjectNeurofibromatosis type 1 (4)Plexiform neurofibroma (2)Advanced maternal age (1)Advanced paternal age (1)Clinical variability (1)CXCL12 (1)CXCR4 (1)Genotype-phenotype relation (1)Genotype–phenotype correlation (1)Modifier genes (1)... View MoreDate Issued
2018 (4)
Has File(s)No (3)Yes (1)Typearticle (4)CoverageMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı (4)WOSWOS:000419720600015 (1)WOS:000429793400012 (1)WOS:000434269300002 (1)WOS:000435437400005 (1)Scopus2-s2.0-85034096433 (1)2-s2.0-85038925361 (1)2-s2.0-85042064609 (1)2-s2.0-85048232895 (1)PubMedPMID:29143198 (1)Dileng (4)Erişiminfo:eu-repo/semantics/closedAccess (3)info:eu-repo/semantics/openAccess (1)

DSpace software copyright © 2002-2016  DuraSpace
Contact Us | Send Feedback
Theme by 
Atmire NV
 

 


Creative Commons License
Institutional Repository by TOBB ETU Institutional Repository is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License..

Institutional Repository:



TOBB ETU için Devinim Yazılım Eğitim Danışmanlık tarafından özelleştirilerek kurulmuştur.