The Impact of the COVID-19 Pandemic on Respiratory Syncytial Virus Infection in the Neonatal Period.

Autor: Akbay Ak S; Department of Neonatology, Ministry of Health, Dr. Behcet Uz Pediatric Diseases and Surgery Training and Research Hospital, Izmir, Türkiye., Soysal B; Department of Neonatology, Gazi Yasargil Training and Research Hospital, Diyarbakır, Türkiye., Yangın Ergon E; Department of Neonatology, Ministry of Health, Dr. Behcet Uz Pediatric Diseases and Surgery Training and Research Hospital, Izmir, Türkiye., Kalkanlı OH; Department of Neonatology, Ministry of Health, Dr. Behcet Uz Pediatric Diseases and Surgery Training and Research Hospital, Izmir, Türkiye., Ayhan Y; Department of Clinical Microbiology, Ministry of Health, Dr. Behcet Uz Pediatric Diseases and Surgery Training and Research Hospital, Izmir, Türkiye., Alkan Ozdemir S; Department of Neonatology, Ministry of Health, Dr. Behcet Uz Pediatric Diseases and Surgery Training and Research Hospital, Izmir, Türkiye., Calkavur S; Department of Neonatology, Ministry of Health, Dr. Behcet Uz Pediatric Diseases and Surgery Training and Research Hospital, Izmir, Türkiye., Gokmen Yıldırım T; Department of Neonatology, Ministry of Health, Dr. Behcet Uz Pediatric Diseases and Surgery Training and Research Hospital, Izmir, Türkiye.

Publikováno v: American journal of perinatology [Am J Perinatol] 2024 Sep; Vol. 41 (12), pp. 1706-1713. Date of Electronic Publication: 2024 Jan 25.

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Intravenous Immunoglobulin Use in Hemolytic Disease Due to ABO Incompatibility to Prevent Exchange Transfusion

Autor: Okulu E., Erdeve O., Kilic I., Olukman O., Calkavur S., Buyukkale G., Cetinkaya M.

Introduction: Intravenous immunoglobulin (IVIG) has been widely used to treat the hemolytic disease of the newborn (HDN). Although it has been shown that IVIG treatment reduces the duration of phototherapy and hospitalization, the use of IVIG in hemo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______9436::e240e839269caa6c97b2cf27b73e943b
https://hdl.handle.net/11454/79915

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encephalopathy: pyruvate carboxylase deficiency

Autor: Kose, MD, Colak, R, Ergon, EY, Kulali, F, Yildiz, M, Alkan, S, Atilgan, T, Aslan, F, Brown, R, Brown, G, Serdaroglu, E, Calkavur, S

Pyruvate carboxylase (PC) deficiency is a rare autosomal recessive disease and provides clinics in three essential phenotypes. Type B PC deficiency is characterized by lactic acidosis and hyperammonemia. We report a Turkish patient who was diagnosed

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3566::4d9061f14b7489c397fd0acce4359290