A Polymorphism in the IL-5 Gene is Associated with Inhibitor Development in Severe Hemophilia A Patients von Fidancı, Inanç Değer, Zülfikar, Bülent, Kavaklı, Kaan, Ar, M Cem, Kılınç, Yurdanur, Başlar, Zafer, Cağlayan, Server Hande

Volltext

An association analysis at 2q36 reveals a new candidate susceptibility gene for juvenile absence epilepsy and/or absence seizures associated with generalized tonic–clonic seizures... von Yalçin, Özlem, Baykan, Betül, Ağan, Kadriye, Yapici, Zuhal, Yalçin, Destina, Dizdarer, Gülşen, Türkdoğan, Dilşad, Özkara, Çiğdem, Ünalp, Aycan, Uludüz, Derya, Gül, Günay, Kuşcu, Demet, Ayta, Semih, Tutkavul, Kemal, Çomu, Sinan, Tatli, Burak, Meral, Cihan, Bebek, Nerses, Çağlayan, Server Hande

Volltext

An association analysis at 2q36 reveals a new candidate susceptibility gene for juvenile absence epilepsy and/or absence seizures associated with generalized tonic-clonic seizures:... von Yalçin, Özlem, Baykan, Betül, Ağan, Kadriye, Yapici, Zuhal, Yalçin, Destina, Dizdarer, Gülşen, Türkdoğan, Dilşad, Özkara, Çiğdem, Ünalp, Aycan, Uludüz, Derya, Gül, Günay, Kuşcu, Demet, Ayta, Semih, Tutkavul, Kemal, Çomu, Sinan, Tatli, Burak, Meral, Cihan, Bebek, Nerses, Çağlayan, Server Hande

Volltext

Lafora Disease: Molecular Etiology von Server Caglayan, Hande

Volltext

De novo 8p23.1 deletion in a patient with absence epilepsy von Akcakaya, Nihan Hande, Capan, Özlem Yalcin, Schulz, Herbert, Sander, Thomas, Caglayan, Server Hande, Yapıcı, Zuhal

Volltext

A Polymorphism in the IL-5 Gene is Associated with Inhibitor Development in Severe Hemophilia A Patients/Agir Hemofili A Hastalarinda Inhibitör Gelisimi ile IL-5 Genindeki Bir Poli... von Fidanci, Inanç Deger, Zülfikar, Bülent, Kavakli, Kaan, Ar, M Cem, Kilinç, Yurdanur, Baslar, Zafer, Çaglayan, Server Hande

Volltext