H. Ergin
Ergin, Hacer.
Results 1-20 of 39 (Search time: 0.013 seconds).
Issue Date | Title | Author(s) | |
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1 | 2004 | Apert syndrome | Kılıç, İlknur.; Baykara, Y.; Semerci, Cavidan Nur. ; Ergin, Hacer. ; Tufan Şatıroğlu, N. Lale |
2 | 2007 | Brainstem evoked response audiometry and risk factors in premature infants | Kılıç, İlknur ; Karahan, Hakan; Kurt, Tülay; Ergin, Hacer ; Şahiner, Türker |
3 | 2019 | Caffeine prevents bilirubin-induced cytotoxicity in cultured newborn rat astrocytes | Deliktaş, Mehmet ; Ergin, Hacer ; Demiray, Aydın ; Akça, Hakan ; Özdemir, Özmert M.A. ; Özdemir, Mehmet Bülent |
4 | 2011 | Calcinosis cutis in a newborn with transient pseudohypoparathyroidism | Ergin, Hacer ; Karaca, Abdullah ; Ergin, Şeniz ; Çördük, Nergül ; Karabulut, N. |
5 | 1998 | Camptodactyly, myopia, and fibrosis of the medial rectus of the eye in two sibs born to consanguineous parents: Autosomal recessive entity? | Kılıç, İlknur ; Kılıç, B. Alper; Ergin, Hacer ; Aygün, M.G.; Akşit, M. Arif |
6 | 2003 | A case of hereditary angioedema with recurrent arthritis, erythema marginatum-like rash and chest pain | Ergin, Hacer ; Başkan, Merve; Akalın, Necdet; Gürses, Dolunay |
7 | 2006 | A case with proximal femoral focal deficiency (PFFD) and fibular A/hypoplasia (FA/H) associated with urogenital anomalies | Ergin, Hacer ; Semerci, Cavidan Nur; Bican, M.; Düzcan, Füsun ; Yagci, A.B.; Erdogan, K.M.; Tufan, Ahmet Çevik |
8 | 2010 | A causal relationship between UDP-glucuronosyltransferase 1A1 promoter polymorphism and idiopathic hyperbilirubinemia in Turkish newborns | Ergin, Hacer ; Bican, M.; Atalay, Ömer Erol |
9 | 1998 | Comparison of amoxicillin with second and third generation cephalosporins in the treatment of acute otitis media | Kara, Cüneyt Orhan ; Ozuer, M.Z.; Kilic, I.; Yalcin, A.N.; Ergin, H. |
10 | 2019 | Comparison of cut and intact cord milking regarding cerebral oxygenation, hemodynamic and hematological adaptation of term infants. | Orpak, Ümmühan Seda; Ergin, Hacer ; Çıralı, Ceren; Özdemir, Özmert MA ; Koşar Can, Özlem ; Çelik Ü |
11 | 2015 | Congenital brucellosis in a premature infant | Şahin, Özlem ; Ergin, H. ; Kucuktasci, K.; Öztekin, Ö. ; Özdemir, Ö.M.A. ; Akbulut, M. |
12 | 2010 | Congenital cystic adenomatoid malformation: Case report | Özdemir, Özmert Muhammet Ali ; Ergin, Hacer ; Karaca, A.; Koltuksuz, U.; Karabulut, N.; Yalçin, Nagihan |
13 | 2008 | Congenital lymphoedema, bronchiectasis and seizure: Case report | Semiz, Serap ; Dagdeviren, E.; Ergin, H. ; Kilic, I.; Kirac, S.; Cimbis, M.; Semiz, E. |
14 | 2004 | Çocukluk çağı yabancı cisim aspirasyonlarının değerlendirilmesi | Gürses, Dolunay ; Akçay, Ahmet ; Çakaloz, İnanç; Kılıç, İlknur ; Ergin, Hacer ; Kara, Cüneyt Orhan |
15 | 2005 | Denizli ilindeki çocukluk çağı zehirlenmeleri | Akçay, Ahmet ; Gürses, Dolunay ; Özdemir, Ayşegül; Kılıç, İlknur ; Ergin, Hacer |
16 | 1995 | Diffuse neonatal hemangiomatosis: A case report | Ergin, H. ; Karaduman, A.; Ekici, E.; Ergul, P.; Erdal, F. |
17 | 2010 | The EEC syndrome and SHFM: Report of two cases and mutation analysis of p63 gene | Ergin, Hacer ; Semerci Gündüz, Cavidan Nur ; Tugrul Karakuş, Y.; Scheffer, H.; Ergin, Şeniz ; Koltuksuz, U.; Meijer, R. |
18 | 2019 | The effects of bosentan on hyperoxia-induced lung injury in neonatal rats | Özdemir, Özmert M.A. ; Taban, Özgün ; Enli, Yaşar ; Bir, Ferda ; Şahin, Barbaros ; Ergin, Hacer |
19 | 2009 | Electrophysiological assessment of the brain function in term SGA infants | Özdemir, Özmert Muhammet Ali. ; Ergin, Hacer. ; Şahiner, Türker. |
20 | 2013 | Enalapril-induced acute retal failure and jugular venous thrombosis associated with a homozygous methylene tetrahydrofolate reductase A1298C polymorphisms in a newborn with central venous line: Case report | Ergin, H. ; Küçüktasçi, K.; Özdemir, O.M.A. ; Eliaçik, C.; Gürses, Dolunay ; Yüksel, S. ; Polat, A. |
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