Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ahmet İbrahim KURTOĞLU"'
Autor:
Hacer Yapıcıoğlu, Ahmet İbrahim Kurtoğlu, Şeref Selçuk Kılıç, Çiğdem Akcabay, Ferda Özlü, Şerif Hamitoğlu, Nejat Narlı, Mehmet Satar
Publikováno v:
Cukurova Medical Journal, Vol 46, Iss 3, Pp 1309-1314 (2021)
Konjenital batın ön duvarı defektleri nadir görülen yapısal anomalilerdir. Bu olguların ve eşlik eden anomalilerin erken saptanması, bebeklerin doğumdan sonra yatırılarak izleminin ve bakımlarının erken başlanması prognozu etkilemekt
Externí odkaz:
https://doaj.org/article/cc0728e54e734d66a3e953efd670cc0f
Autor:
Nejat Narli, Şerif Hamitoğlu, Hacer Yapicioğlu, Mehmet Satar, Çiğdem Akcabay, Ahmet İbrahim Kurtoğlu, Ferda Özlü, Şeref Selçuk Kılıç
Publikováno v:
Cukurova Medical Journal. 46:1309-1314
Konjenital batın ön duvarı defektleri nadir görülen yapısal anomalilerdir. Bu olguların ve eşlik eden anomalilerin erken saptanması, bebeklerin doğumdan sonra yatırılarak izleminin ve bakımlarının erken başlanması prognozu etkilemekt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca2f5c6959f120cca52107da6cb3dbb9
https://doi.org/10.17826/cumj.908437
https://doi.org/10.17826/cumj.908437
Autor:
Mustafa ÖZDEMİR, Tugay TEPE, Şerif HAMİTOĞLU, Ahmet İbrahim KURTOĞLU, Ferda ÖZLÜ, Hacer YAPICIOĞLU
Publikováno v:
Volume: 10, Issue: 3 401-404
Abant Tıp Dergisi
Abant Tıp Dergisi
Dandy-Walker malformasyonu, serebellar vermis agenezisi veya hipoplazisi, 4. ventrikülün kistik dilatasyonu ve posterior fossa genişlemesi ile karakterize nadir bir konjenital malformasyondur. Hastaların yaklaşık %70-90’ında postnatal hidros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9980d0f036225574de7d74b6c33d6125
https://dergipark.org.tr/tr/pub/abantmedj/issue/66135/950391
https://dergipark.org.tr/tr/pub/abantmedj/issue/66135/950391
Autor:
Atil Bisgin, Ferda Özlü, Hacer Yapıcıoğlu Yıldızdaş, Neslihan Önenli Mungan, Ahmet İbrahim Kurtoğlu, Mehmet Satar
Publikováno v:
Turk Arch Pediatr
Molybdenum cofactor deficiency is a rare neurometabolic disease that is usually characterized by seizures, abnormal muscle tonus, developmental delay and poor nutrition, and is seen soon after birth. Pyloric stenosis causes serious vomiting in the fi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43956416195956c8a77b259d5bbbf88b
https://doi.org/10.14744/turkpediatriars.2020.57984
https://doi.org/10.14744/turkpediatriars.2020.57984
Publikováno v:
Turkish Journal of Parasitology. 37:135-138
Blastocystis hominis (B. hominis) is a parasite that often causes gastrointestinal symptoms in patients with immune deficiency and has a controversial pathogenicity in healthy people, although some symptoms are reported outside of the gastrointestina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55735aa72eabd904eb3c61196e30b385
https://doi.org/10.5152/tpd.2013.29
https://doi.org/10.5152/tpd.2013.29
Autor:
Murat, Tutanç, Ibrahim, Silfeler, Tümay, Ozgür, Vicdan Köksaldı, Motor, Ahmet Ibrahim, Kurtoğlu
Publikováno v:
Turkiye parazitolojii dergisi. 37(2)
Blastocystis hominis (B. hominis) is a parasite that often causes gastrointestinal symptoms in patients with immune deficiency and has a controversial pathogenicity in healthy people, although some symptoms are reported outside of the gastrointestina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4b5ac87a937a47e43be72c7d48765c5b
https://pubmed.ncbi.nlm.nih.gov/23955912
https://pubmed.ncbi.nlm.nih.gov/23955912
Publikováno v:
Medicine Science, Vol 9, Iss 1, Pp 241-5 (2020)
Familial Mediterranean fever (FMF) is a hereditary disease characterized by recurrent attacks of fever, peritonitis, pleuritis and/or synovitis. In this study, we retrospectively evaluated demographic, clinical findings, and genetic features in 149 c
Externí odkaz:
https://doaj.org/article/d44d9cab119e4de9b7c27c7f8baf31be