03.14. Department of Internal Medicine

Bibliometrics Email Alert

Card

Organization name
03.14. Department of Internal Medicine
Parent OrgUnit
Country
Turkey

OrgUnit's Researchers publications
(Dept/Workgroup Publication)

Refined By:
Author:  Sharafi, Parisa

Results 1-10 of 10 (Search time: 0.007 seconds).

Issue DateTitleAuthor(s)
11-Sep-2018Automated washing of long-term cryopreserved peripheral blood stem cells promotes cell viability and preserves CD34+ cell numbersAerts Kaya, Fatima; Koca, Gül; Sharafi, Parisa ; Sayla, Funda Çakmak; Uçkan-Çetinkaya, Duygu; Özdemir, Evren
2Feb-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 
32023Clinical 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 
42022Combined effects of bone morphogenetic protein-7 and mineral trioxide aggregate on the proliferation, migration, and differentiation of human dental pulp stem cellsEren, Selen Kucukkaya; Zirh, Elham Bahador; Zirh, Selim; Sharafi, Parisa ; Zeybek, Naciye Dilara
51-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 
62020Hastalık tedavisinde genetik yaklaşımlarSharafi, Parisa 
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 
93-Apr-2018Possible modifier genes in the variation of neurofibromatosis type 1 clinical phenotypesSharafi, Parisa ; Ayter, Şükriye 
102020Yapay Zekâ ve GenetikAyter, Şükriye ; Sharafi, Parisa