Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Mehmet FİDANBOY"'
Publikováno v:
PLoS ONE, Vol 6, Iss 9, p e25212 (2011)
Paclitaxel (Taxol®) is a widely used chemotherapeutic agent that has a major dose limiting side-effect of painful peripheral neuropathy. Currently there is no effective therapy for the prevention or treatment of chemotherapy-induced painful peripher
Externí odkaz:
https://doaj.org/article/ffc47506a3c843e1941dead0e5306154
Autor:
Halit Akbas, Naci Cine, Mahmut Erdemoglu, Ahmet Engin Atay, Selda Simsek, Aysegul Turkyilmaz, Mehmet Fidanboy
Publikováno v:
Case Reports in Obstetrics and Gynecology, Vol 2013 (2013)
Ring chromosomes are unusual abnormalities that are observed in prenatal diagnosis. A 23-year-old patient (gravida 1, para 0) referred for amniocentesis due to abnormal maternal serum screening result in the 16th week of second pregnancy. Cytogenetic
Externí odkaz:
https://doaj.org/article/d35fd26527444974863877d436d68107
Publikováno v:
Volume: 9, Issue: 2 206-218
Turkish Journal of Forestry Research
Ormancılık Araştırma Dergisi
Turkish Journal of Forestry Research
Ormancılık Araştırma Dergisi
Forest fires are one of the main problems that cause economic losses by threatening natural life and biological ecosystem by disrupting forestry activities. Fires can cause damage to the natural sources like vegetation, water and air, or completely e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::718eb1586a2195755a8ea8f2b89b9b34
https://doi.org/10.17568/ogmoad.1066557
https://doi.org/10.17568/ogmoad.1066557
Autor:
Emin Kapi, Mehmet Fidanboy, Selcuk Otcu, Cihan Akgul Ozmen, Mahmut Balkan, Turgay Budak, M. Nuri Özbek
Publikováno v:
Journal of Pediatric Genetics. :205-208
Trisomy 8 is a relatively rare chromosomal abnormality. The majority of cases present with the mosaic form. Regular trisomy 8 is usually lethal and frequently results in miscarriage, while those with "trisomy 8 mosaicism" are more likely to survive.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1fe30d5bca256d2f0dbf774dc99fa32
https://doi.org/10.3233/pge-2012-032
https://doi.org/10.3233/pge-2012-032
Publikováno v:
Journal of Pediatric Genetics. :239-242
We report a case with different chromosome Y abnormalities. Case was an 11-year-old boy, who was diagnosed with short stature, referred to laboratory of human medical genetics laboratory for genetic evaluation. Chromosomal analysis of the case was ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a021f895d9e8573c0f2e78a681ae2151
https://doi.org/10.3233/pge-12038
https://doi.org/10.3233/pge-12038
Autor:
Turgay Budak, Mahmut Balkan, Hilmi Isi, M. Nail Alp, Mehmet Fidanboy, Sevgi Kalkanli, Halit Akbas
Publikováno v:
Journal of Pediatric Genetics. :243-246
We report a case of complete tetraploidy in amniotic fluid culture obtained at 17 wk of pregnancy. Amniocentesis was performed in this pregnancy because of a high-risk maternal serum screening result and abnormal ultrasound findings. Amniotic fluid w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52a8f8e20f0403934d8f21c565912876
https://doi.org/10.3233/pge-12039
https://doi.org/10.3233/pge-12039
Autor:
Ayşegül Türkyılmaz, Talip Gül, Ali Özler, Mehmet Obut, Hatice Ender Soydinç, Muhammet Erdal Sak, Mehmet Sıddık Evsen, Mehmet Fidanboy, Mahmut Balkan
Publikováno v:
Turkish Journal of Obstetrics and Gynecology, Vol 10, Iss 2, Pp 67-71 (2013)
SUMMARY Objective: The aim of the present study is to evaluate etiologic factors in patients with recurrent pregnancy loss (RPL). Material and methods: The records of patients admitted to Obstetrics& Gynecology Clinic of Dicle University Medical Facu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39ef0f5292d64c6c831725b1e72fa4f4
https://doi.org/10.5505/tjod.2013.61587
https://doi.org/10.5505/tjod.2013.61587
Autor:
Mehmet Fidanboy, Turgay Budak, Abdullah Gedik, Ayşegül Türkyılmaz, Halit Akbas, Sevgi Kalkanli, Hilmi Isi, M N Alp, Selda Şimşek, Mahmut Balkan, Diclehan Oral
Publikováno v:
Genetics and Molecular Research. 9:1094-1103
We reviewed cytogenetic studies performed on 4216 patients who were referred to the Cytogenetics Unit at Dicle University Hospital, Diyarbair, Southeast Turkey, between 2000 and 2009. The cases were grouped according to the reason of referral for cyt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9717d1c1ad46e337b56e47304efd6b0
https://doi.org/10.4238/vol9-2gmr827
https://doi.org/10.4238/vol9-2gmr827
Autor:
Ahmet Engin Atay, Mahmut Erdemoglu, Naci Cine, Ayşegül Türkyılmaz, Selda Şimşek, Halit Akbas, Mehmet Fidanboy
Publikováno v:
Case Reports in Obstetrics and Gynecology, Vol 2013 (2013)
Case Reports in Obstetrics and Gynecology
Case Reports in Obstetrics and Gynecology
Ring chromosomes are unusual abnormalities that are observed in prenatal diagnosis. A 23-year-old patient (gravida 1, para 0) referred for amniocentesis due to abnormal maternal serum screening result in the 16th week of second pregnancy. Cytogenetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d0a2c50614c7b449704fdc11b27a128
https://doaj.org/article/d35fd26527444974863877d436d68107
https://doaj.org/article/d35fd26527444974863877d436d68107