03. School of Medicine

Organization name
03. School of Medicine
City
Ankara
Country
Turkey

SubOrgUnits
(Taskgroup)

Results 1-20 of 35 (Search time: 0.002 seconds).

OrgUnit's Researchers publications
(Dept/Workgroup Publication)

Results 1-11 of 11 (Search time: 0.004 seconds).

Issue DateTitleAuthor(s)
1Feb-2018Clinical findings and mutation analysis of NF1 patients in TurkeyTerzi, Yunus Kasım; Balcı, Sibel Oğuzkan; Anlar, Banu; Varan, Ali; Evans, Sibel Ersoy; Sharafi, Parisa ; Ayter, Şükriye 
22023Clinical signs and genetic evaluation of patients with neurofibromatosis type 1 with and without optic pathway gliomas in a center in TurkeySharafi, Parisa ; Varan, Ali; Ersoy-Evans, Sibel; Ayter, Şükriye 
31-Jul-2018The effect of parental age on NF1 patients in TurkeyErsoy, Evans Sibel; Sharafi, Parisa ; Anlar, Banu; Varan, Ali; Yılmaz, Ömer Faruk; Turan, Mustafa ; Ayter, Şükriye 
42018Factors influencing the success of cord blood collection: A tertiary perinatal medicine center’s experienceTanaçan, Atakan; Yurdakul, Pınar ; Aktoz, Fatih; Örgül, Gökçen; Beksaç, Mehmet Sinan
5Nov-2017Flow Cytometric Aldehyde Dehydrogenase (ALDH) Assay Enables a Fast and Accurate Human Umblical Cord Blood Hematopoietic Stem Cell Assessment.Gencer, Emine Begüm; Yurdakul, Pınar ; Dalva, Klara; Beksaç, Meral
61-May-2018Heightened CXCR4 and CXCL12 expression in NF1-associated neurofibromasKaraosmanoğlu, Beren; Kocaefe, Çetin Y.; Söylemezoğlu, Figen; Anlar, Banu; Varan, Ali; Vargel, İbrahim; Ayter, Şükriye 
72019Lösemiler ve NF1 ile İlişkili Tümörlerde EVI2A ve EVI2B Genlerinin RolüAyter, Şükriye ; Sharafi, Parisa ; Anlar, Banu; Varan, Ali; Çetin, Mualla
8May-2017NF1 Gene Mutations are the Major Molecular Event in Neurofibromatosis-Noonan SyndromeSharafi, Parisa ; Anlar, Banu; Ayter, Şükriye 
9Oct-2013PhacomatosisAyter, Şükriye 
103-Apr-2018Possible modifier genes in the variation of neurofibromatosis type 1 clinical phenotypesSharafi, Parisa ; Ayter, Şükriye 
112020Yapay Zekâ ve GenetikAyter, Şükriye ; Sharafi, Parisa