Yayıncı "GALENOS YAYINCILIK" Scopus İndeksli Yayınlar Koleksiyonu için listeleme
Toplam kayıt 9, listelenen: 1-9
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Active management of the third stage of labor: A brief overview of key issues
(GALENOS YAYINCILIK, 2018)Postpartum hemorrhage is a potentially life-threatening, albeit preventable, condition that persists as a leading cause of maternal death. It occurs mostly during the third stage of labor, and active management of the third ... -
Bullous Pyoderma Gangrenosum in a Patient with Acute Myelogenous Leukemia as a Pathergic Reaction after Bone Marrow Biopsy
(GALENOS YAYINCILIK, 2017)… -
Could Neutrophil CD64 Expression Be Used as a Diagnostic Parameter of Bacteremia in Patients with Febrile Neutropenia?
(GALENOS YAYINCILIK, 2017)Objective: The aim of this study is to investigate if neutrophil CD64 expression in febrile neutropenia patients could be used as an early indicator of bacteremia. Materials and Methods: All consecutive patients older than ... -
Intradiploic Hematoma in a Hemophilic Patient: Hemophilic Pseudotumor of Calvarium
(GALENOS YAYINCILIK, 2017)… -
Liver Transplantation in a Patient with Acquired Dysfibrinogenemia Who Presented with Subdural Hematoma: A Case Report
(GALENOS YAYINCILIK, 2017)… -
Micronuclei frequencies in lymphocytes and cervical cells of women with polycystic ovarian syndrome
(GALENOS YAYINCILIK, 2017)Objective: The aim of this study was to determine micronucleus (MN) frequencies in exfoliated cervical cells and peripheral blood lymphocytes of women with polycystic ovarian syndrome (PCOS). Materials and Methods: Fifteen ... -
Newborn Screening for Congenital Hypothyroidism
(GALENOS YAYINCILIK, 2013)Newborn screening (NS) for congenital hypothyroidism (CH) is one of the major achievements in preventive medicine. Most neonates born with CH have normal appearance and no detectable physical signs. Hypothyroidism in the ... -
A Novel ATP6V0A2 Mutation Causing Recessive Cutis Laxa with Unusual Manifestations of Bleeding Diathesis and Defective Wound Healing
(GALENOS YAYINCILIK, 2019)Objective: Autosomal recessive cutis laxa type IIA (ARCL2A) is a rare congenital disorder characterized by loose arid elastic skin, growth and developmental delay, and skeletal anomalies. It is caused by biallelic mutations ... -
Successful Treatment of Disseminated Fusariosis with the Combination of Voriconazole and Liposomal Amphotericin B
(GALENOS YAYINCILIK, 2016)…