Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Sırrı ÇAM"'
Autor:
Tahir Buran, Muhammet Burak Batır, Fethi Sırrı Çam, Elmas Kasap, Fatih Çöllü, Hamide Betül Gerik Çelebi, Mustafa Şahin
Publikováno v:
BMC Gastroenterology, Vol 23, Iss 1, Pp 1-10 (2023)
Abstract Background Ulcerative colitis (UC) is a chronic inflammatory bowel disease that develops due to the impaired immune response in genetically susceptible individuals, and its etiopathogenesis is not fully elucidated. IL-17 A is a cytokine that
Externí odkaz:
https://doaj.org/article/23725d0c5a9246c3b3c2f9016e508b94
Publikováno v:
Haseki Tıp Bülteni, Vol 58, Iss 2, Pp 208-210 (2020)
We present two siblings with elevated serum creatine kinase concentrations, developmental delay, muscle weakness, and contractures of the lower limbs. Cranial magnetic resonance imaging revealed diffuse white matter hyperintensity in both siblings. I
Externí odkaz:
https://doaj.org/article/74a26140879b43348bd0a57088c2afd3
Autor:
Hamıde Betul GERİK CELEBİ, Sırrı ÇAM
Publikováno v:
Kocatepe Tıp Dergisi. 24:184-189
OBJECTIVE: Skeletal dysplasias is a complex disease group characterized by disproportionate short stature and various orthopedic complications. X-Linked Spondyloepiphyseal Dysplasia Tarda is an X-linked inherited skeletal dysplasia accompanied by pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::537b6e6b3cd3a9f1ca49fb372bcccbe9
https://doi.org/10.18229/kocatepetip.1061617
https://doi.org/10.18229/kocatepetip.1061617
Publikováno v:
Journal of Surgery and Medicine. 7:245-248
Background/Aim: JAK2 is a gene that provides instructions for making a protein called Janus kinase 2, which is involved in the signaling process that regulates the growth and division of cells. Variations in the JAK2 gene have been associated with se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4ed09f37551e08e8662318f72bb6376
https://doi.org/10.28982/josam.7771
https://doi.org/10.28982/josam.7771
Publikováno v:
Psychiatry and Clinical Psychopharmacology, Vol 29, Iss 1, Pp 8-13 (2019)
BACKGROUND: Studies on the role of microRNAs (miRNA) in anxiety disorders are limited. We aimed to determine the availability of miRNAs as biomarkers in serum and to demonstrate the changes of miRNAs expression in patients with panic disorder (PD). M
Externí odkaz:
https://doaj.org/article/d3729faec5904d398332843ba5770aa4
Publikováno v:
Journal of Pediatric Emergency and Intensive Care Medicine, Vol 6, Iss 1, Pp 41-43 (2019)
Pyridoxine-dependent epilepsy (PDE) is a rare autosomal recessive encephalopathy due to mutations in the ALDH7A1 gene. Intractable seizures are the most frequent clinical form in the early infantile period. A case of a 4-month-old female patient pres
Externí odkaz:
https://doaj.org/article/9f79bd76d1594df2be4b1d4d04e8b539
Publikováno v:
Journal of Pediatric Research, Vol 5, Iss 4, Pp 225-227 (2018)
Severe congenital neutropenia is a hereditary disease characterized by a low number of neutrophils occurring from the first months of life leading to severe infections. It is rare but threatens life because of severe infections. For this reason, earl
Externí odkaz:
https://doaj.org/article/86f6afcde95a4bb9bbe2c2ee2924706a
Autor:
Seda Vatansever, Burak Ulkumen, Sırrı Çam, Burcu Artunc Ulkumen, Muhammet Burak Batir, Halil Gursoy Pala
Publikováno v:
Brazilian Journal of Otorhinolaryngology v.88 n.4 2022
Brazilian Journal of Otorhinolaryngology
Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial (ABORL-CCF)
instacron:ABORL-CCF
Brazilian Journal of Otorhinolaryngology
Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial (ABORL-CCF)
instacron:ABORL-CCF
Introduction Pregnancy rhinitis is a common sex hormone-related otorhinolaryngological disorder. There are some epidemiological and physiological studies on pregnancy rhinitis, but histopathological and biomolecular changes have not been studied thor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb4789d50552091812a595c16abbc0b3
https://doi.org/10.1016/j.bjorl.2020.06.015
https://doi.org/10.1016/j.bjorl.2020.06.015
Autor:
Hilmi BOLAT, Hamıde Betul GERİK CELEBİ, Gül ÜNSEL-BOLAT, Esra ÇOLAK GENİŞ, Özge DEMİRCAN, Sırrı ÇAM
Publikováno v:
Celal Bayar Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi. 9:305-309
Giriş ve Amaç: Gelişim geriliği (GG) ve entelektüel yetersizlik (EY) fenotipik ve genetik olarak heterojen bir grup hastalıktır. GG/EY olguların etiyolojisinde altta yatan önemli bir kısmını genetik nedenler oluşturmaktadır. Bu araştı
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52583e9d6ea22819d6a4296890d4efae
https://doi.org/10.34087/cbusbed.1063262
https://doi.org/10.34087/cbusbed.1063262
Autor:
F. Sırrı Çam
Publikováno v:
Moleküler Biyoloji ve Genetik ISBN: 9786258352481
Globally we are experiencing a unique period of progress and innovation in life sciences. This situation continues to change our way of life. At the beginning of the 21st century, biotechnology (including gene technology) is seen as the key technolog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cbaa52a4dc28c81dc386d2fe184e8516
https://doi.org/10.53478/tuba.978-625-8352-48-1.ch28
https://doi.org/10.53478/tuba.978-625-8352-48-1.ch28
