Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Veysel Gök"'
Autor:
Firdevs AYDIN, Kemal DENİZ, Süreyya Burcu GÖRKEM, Veysel GÖK, Alper ÖZCAN, Ebru YILMAZ, Ekrem ÜNAL, Musa KARAKÜKÇÜ, Türkan PATIROĞLU, Mehmet Akif ÖZDEMİR, Can ACIPAYAM, Defne AY TUNCEL
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S31- (2021)
Objective: Rhabdoid tumors, which are rare in childhood, are aggressive cancers. It can be particularly seen in 3 different anatomical regions, mostly in the central nervous system, kidneys, and soft tissue in early childhood. In this study, it was a
Externí odkaz:
https://doaj.org/article/0154714528984f74b8b6314ef38cda86
Autor:
Meltem Erol, Özgül Yiğit, Oktay Adanır, Mehmet Toksöz, Halis Narin, Veysel Gök, Dilek Borakay, Murat Konya
Publikováno v:
Haseki Tıp Bülteni, Vol 52, Iss 2, Pp 116-119 (2014)
Hereditary multiple exostoses is an autosomal dominant disease with abnormal bone formation especially at the long bones. Osteochondromas, which occur in the course of the disease, can cause growth disturbances in affected children. Due to pressure e
Externí odkaz:
https://doaj.org/article/a6f9301120894620baf607c20412b275
Autor:
Turgut SEBER, Tuğba UYLAR SEBER, Elif AKTAŞ, Fatma Türkan MUTLU, Veysel GÖK, Şuayip KESKİN, Fatoş TEKELİOĞLU, Arzu TASDEMİR
Publikováno v:
Anatolian Current Medical Journal. 5:91-96
Aim: Lymphadenopathy (LAP) is one of the most common daily practice clinical findings in children. LAPs that involve more than one region and do not decrease with treatment are a significant cause of anxiety for clinicians and families. In this occur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d50e3210409bfab9b2338f136856df9
https://doi.org/10.38053/acmj.1240036
https://doi.org/10.38053/acmj.1240036
Autor:
Veysel Gök, Gülsüm Gümüş, Habibe Selver Durmuş, Ekrem Ünal, Hakan Gümüş, Musa Karakükcü, Ayşe Kaçar Bayram, Hüseyin Per
Publikováno v:
Trends in Pediatrics. 3:120-125
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::413f7c1da91eb1a01d1e3b3979f18a6d
https://doi.org/10.4274/tp.2022.29292
https://doi.org/10.4274/tp.2022.29292
Autor:
Şefika AKYOL, Deniz KOÇAK GÖL, Ebru YILMAZ, Zehra Filiz KARAMAN, Alper ÖZCAN, Ahmet KÜÇÜK, Veysel GÖK, Firdevs AYDIN, Huseyin PER, Musa KARAKÜKCÜ, Türkan PATIROĞLU, Mehmet Akif ÖZDEMİR, Ekrem ÜNAL
Publikováno v:
Journal of Translational and Practical Medicine. 1:85-88
Aim: Hemophilias are inherited bleeding disorders, in which the patients generally present with clinical complaints of hemarthrosis. Intracranial hemorrhage (ICH) is one of the severe bleeding types with the highest mortality and morbidity throughout
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea1f6d0169dc793721390e6618db13c9
https://doi.org/10.51271/jtpm-0024
https://doi.org/10.51271/jtpm-0024
Publikováno v:
Journal of Translational and Practical Medicine. :9-13
Aim: The enzyme of methylenetetrahydrofolate reductase (MTHFR) is fundamental for folate metabolism and has two common polymorphisms (C677T and A1298G). Methotrexate, which interrupts folate metabolism, is one of the backbone drugs of pediatric acute
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37e536f60e4e7cd952c45fa89bdb8b87
https://doi.org/10.51271/jtpm-0010
https://doi.org/10.51271/jtpm-0010
Autor:
Merve KARACA, Veysel GÖK, Ümmü ALAKUŞ SARI, Mehmet Akif DÜNDAR, Firdevs AYDIN, Alper ÖZCAN, Ebru YILMAZ, Mehmet CANPOLAT, Serdar CEYLANER, Fatih KARDAŞ, Musa KARAKUKCU, Ekrem ÜNAL
Publikováno v:
Journal of Translational and Practical Medicine. 1:65-67
Triosephosphate isomerase deficiency is an autosomal recessive disorder characterized by progressive neuromuscular degeneration, seizure, dystonia, weak muscles, cardiomyopathy, hemolytic anemia, and death in early childhood. In the glycolytic pathwa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e7bdb0941db8b1a975e0da2bf98c3fa
https://doi.org/10.51271/jtpm-0020
https://doi.org/10.51271/jtpm-0020
Autor:
Veysel Gök, Şerife Erdem, Yeşim Haliloğlu, Atıl Bişgin, Serkan Belkaya, Kemal Erdem Başaran, Mehmed Fatih Canatan, Alper Özcan, Ebru Yılmaz, Can Acıpayam, Musa Karakükcü, Halit Canatan, Hüseyin Per, Türkan Patıroğlu, Ahmet Eken, Ekrem Ünal
Publikováno v:
Genes and Immunity
Insufficient dietary folate intake, hereditary malabsorption, or defects in folate transport may lead to combined immunodeficiency (CID). Although loss of function mutations in the major intestinal folate transporter PCFT/SLC46A1 was shown to be asso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0edea6ed55d70a1217e8f6a063bc38e
https://avesis.erciyes.edu.tr/publication/details/cc9b5c39-00d9-4e3f-baef-1b60d6bf37fa/oai
https://avesis.erciyes.edu.tr/publication/details/cc9b5c39-00d9-4e3f-baef-1b60d6bf37fa/oai
Autor:
Veysel GÖK, Alper ÖZCAN, Ebru YILMAZ, Musa KARAKÜKCÜ, Türkan PATIROĞLU, Mehmet Akif ÖZDEMİR, Ekrem ÜNAL
Publikováno v:
Journal of Translational and Practical Medicine. 1
Background and aim: Acute lymphoblastic leukemia (ALL) is the most prevalent malignant disorder in childhood. CD40 is a member of the tumor necrosis factor (TNF) receptor family. Soluble CD40 (sCD40) was previously found to be associated with poor pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db49e608125952de93ea6177c61053f1
https://doi.org/10.51271/jtpm-0012
https://doi.org/10.51271/jtpm-0012
Autor:
Veysel GÖK, Ekrem ÜNAL
Publikováno v:
Volume: 5, Issue: 4 1199-1206
Journal of Health Sciences and Medicine
Journal of Health Sciences and Medicine
Hemophilia A, B are X-linked recessive bleeding disorder that typically results from a deficiency of clotting factor VIII (FVIII) and factor IX (FIX). The severity of the disease is determined according to the FVIII and FIX levels. Hemophilia A and B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d3cbfc755671db124f119b3449e89b9
https://dergipark.org.tr/tr/pub/jhsm/issue/71310/1108174
https://dergipark.org.tr/tr/pub/jhsm/issue/71310/1108174