H. Ergin
Ergin, Hacer.
Results 1-20 of 22 (Search time: 0.008 seconds).
Issue Date | Title | Author(s) | |
---|---|---|---|
1 | 2020 | Acquired lung cysts in a premature neonate with congenital cytomegalovirus infection | Özdemir, Özmert Muhammet Ali ; Çıralı, C. ; Ergin, Hacer ; Çetin, Ebru Nevin ; Kara, A. |
2 | 2013 | Alcohol intoxication in newborn: A case report | Özdemir, Özmert Muhammet Ali ; Küçüktaşçı, Kazım ; Şahin, Özlem ; Akpınar, Alper ; Ergin, Hacer |
3 | 2004 | Apert syndrome | Kılıç, İlknur.; Baykara, Y.; Semerci, Cavidan Nur. ; Ergin, Hacer. ; Tufan Şatıroğlu, N. Lale |
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 | 2015 | Congenital brucellosis in a premature infant | Şahin, Özlem ; Ergin, H. ; Kucuktasci, K.; Öztekin, Ö. ; Özdemir, Ö.M.A. ; Akbulut, M. |
9 | 2010 | Congenital cystic adenomatoid malformation: Case report | Özdemir, Özmert Muhammet Ali ; Ergin, Hacer ; Karaca, A.; Koltuksuz, U.; Karabulut, N.; Yalçin, Nagihan |
10 | 2008 | Congenital lymphoedema, bronchiectasis and seizure: Case report | Semiz, Serap ; Dagdeviren, E.; Ergin, H. ; Kilic, I.; Kirac, S.; Cimbis, M.; Semiz, E. |
11 | 2022 | Congenital Penile Lymphedema in a Preterm Newborn | Sönmez Demir G. ; Özdemir Ö.M.A. ; Ergin H. |
12 | 1995 | Diffuse neonatal hemangiomatosis: A case report | Ergin, H. ; Karaduman, A.; Ekici, E.; Ergul, P.; Erdal, F. |
13 | 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. |
14 | 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. |
15 | 2004 | Femoral-facial syndrome with hemifacial microsomia and hypoglossia | Düzcan, F.; Ergin, H. ; Perçin, E.F.; Tepeli, E.; Erkula, G. |
16 | 2006 | Macrodactyly and proteus syndrome | Özdemir, Özmert Muhammet Ali ; Ergin, Hacer ; Sözeri-Özdemir, Ayşegül |
17 | 1997 | Netherton's syndrome and neonatal hypernatremia: A case report | Ergin, Hacer ; Kiliç, I.; Tekinalp, G. |
18 | 2015 | A Newborn with Congenital Mixed Phenotype Acute Leukemia After In Vitro Fertilization | Ergin, Hacer. ; Özdemir, Özmert Muhamet Ali ; Karaca, A.; Türk, Nilay Şen ; Düzcan, F.; Ergin, Ş.; Kazanci, E. |
19 | 2008 | A newborn with positive antiglobulin test whose mother took methyldopa in pregnancy | Özdemir, Özmert Muhammet Ali. ; Ergin, Hacer. ; İnce, Tülay. |
20 | 2000 | Paraurethral cysts in newborn: A case report and review of literature | Herek, Özkan ; Ergin, Hacer ; Karaduman, Dolunay; Çetin, O.; Akşit, Mehmet Arif |
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