Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Ozdemir, OMA"'
We report a preterm newborn diagnosed as having congenital cytomegalovirus infection who developed lung cysts during her clinical follow-up. The lung cysts were shown in chest X-ray, and confirmed by thoracic computed tomography. A few weeks after st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::34b676b81db0c4e8704a68f562455548
Objective: Unconjugated bilirubin (UCB) may cause neurotoxicity in preterm neonates due to immaturity of UGT1A1 leading to bilirubin accumulation in the brain. Caffeine used in the treatment of apnea of prematurity was reported to decrease mechanical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::472bc9e3f6525bf7436de51ce25339d7
Autor:
Dincer, T, Yorgancioglu-Budak, G, Olmez, A, Er, I, Dodurga, Y, Ozdemir, OMA, Toraman, B, Yildirim, A, Sabir, N, Akarsu, NA, Semerci, CN, Kalay, E
Microcephalic primordial dwarfism (MPD) is a group of autosomal recessive inherited single-gene disorders with intrauterine and postnatal global growth failure. Seckel syndrome is the most common form of the MPD. Ten genes are known with Seckel syndr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::9efeab2a3cf1afb86f4af45083c76ce5
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/23672
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/23672
Caffey disease is a rare condition of early infancy, characterized by soft tissue swelling, bone lesions, and hyperirritability. Its typical radiological finding is periosteal new bone formation. It can be sporadic or inherited in an autosomal domina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::53ba8f72f0624cdafcfab4c3011bf56c
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/22915
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/22915
Neonatal Bartter syndrome (NBS) is a rare autosomal recessive renal tubular disorder. This disease is characterized by hypokalemia, hypochloremia, and metabolic alkalosis that is often associated with failure to thrive and recurrent episodes of dehyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::0be709b7d80003b74637b8813a65f111
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/22994
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/22994
Septic arthritis is encountered very rarely during the neonatal period and its diagnosis can delay because of atypical symptoms, thus it may lead to serious sequelae. The sequale can be prevented by early diagnosis and concomitant treatment. In neona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::149df96bfe5e1f0965064959434f2a24
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/23318
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/23318
Endotracheal intubation is a common daily procedure used for sustaining life in premature and term neonates in the neonatal intensive care unit. This procedure can be associated with some iatrogenic complications. One of these complications is ingest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::72f20a2cd556818521317fdb8e92f6f7
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/15451
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/15451
Autor:
Ergin, H, Ozdemir, OMA, Karaca, A, Sen Turk, N, Duzcan, F, Ergin, S, Kazanci, E, Vergin, C, Erbay, A
Congenital leukemia is a rare disease. The majority of cases of this disease are acute myelogenous leukemia (AML). Congenital acute lymphoblastic leukemia (ALL) is rare and most often is of B cell lineage. Rarely, some cases have been designated biph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::c1b95df19f33796b7dd71f1deb47d157
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/22372
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/22372
Autor:
Dogan, M, Firinci, F, Balci, YI, Gurses, D, Polat, A, Ozdemir, OMA, Enli, Y, Akbulut, M, Sahin, B
Doxorubicin is an anthracycline group antibiotic and has long been used as an antineoplastic agent. The most important side effect that limits the usage of doxorubicin is cardiotoxicity, which is observed at cumulative doses. We investigated the prot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::0b2c52a9e18a76f2fefc79f946c7e1ac
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/22129
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/22129
Neonatal Bartter syndrome (BS) is an inherited renal tubular disorder characterized with normal blood pressure, hypokalemia, hypochloremic metabolic alkalosis, hyperreninemia and increased urinary loss of sodium, potassium and chloride. In this disor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::f79c1dd84d81a71337e76baa93c81611
https://doi.org/10.4274/jpr.14633
https://doi.org/10.4274/jpr.14633