Zobrazeno 1 - 10
of 33
pro vyhledávání: '"A, Karabent"'
Autor:
Ahmet Emre Aycan, Mehmet Ada, Yasemin Ozsurekci, Melda Celik, Mehmet Ceyhan, Nezahat Gürler, Eda Karadag Oncel, Ozan Altunta, Adnan Karabent, Venhar Gurbuz, Y ld z Camc o lu, Umut Akyol, Özlem Özgür, Emre Alhan
Publikováno v:
Journal of Vaccines & Vaccination.
Background: Acute otitis media (AOM) is one of the most common childhood diseases requiring antimicrobial prescription drugs in pre-school children. In this study, we sought to describe the bacterial etiology of pediatric cases of AOM in Turkey. Mate
Publikováno v:
American Journal of Hematology. 36:82-85
Antiplatelet antibodies were shown by the Handin and Stossel method in the sera of all 103 patients with acute idiopathic thrombocytopenic purpura (ITP) and in 100 cases following recovery from it. These antibodies were also shown in the sera of all
Publikováno v:
European Journal of Haematology. 41:95-95
Publikováno v:
Israel journal of medical sciences. 26(12)
Publikováno v:
American Journal of Hematology; 1991, Vol. 36 Issue 2, p82-85, 4p
Autor:
Diren, H., Kutluk, M., Karabent, A., Göçmen, A., Adalioglu, G., Kenanoglu, A., Diren, H B, Kutluk, M T, Göçmen, A, Adalioğlu, G, Kenanoğlu, A
Publikováno v:
Pediatric Radiology; Mar1986, Vol. 16 Issue 3, p231-234, 4p
Publikováno v:
European Journal of Haematology; May1989, Vol. 42 Issue 5, p431-435, 5p
Publikováno v:
Pediatric Radiology. 16:231-234
In this article a family with five members suffering from primary hypertrophic osteoarthropathy (PHO) is reported. Our cases are characterized by swollen and painful joints and clubbing of distal phalanges of hands and feet. The diagnosis made upon o
Publikováno v:
European journal of haematology. 42(5)
49 children with acute idiopathic thrombocytopenic purpura (ITP) were divided into non-treatment, oral prednisone (2 mg/kg), and high-dose intravenous methylprednisolone (HIVMP) treatment groups which consisted of 17, 16 and 16 children respectively.
Publikováno v:
European journal of pediatrics. 147(2)
We report a case of protein C deficiency which presented with purpura fulminans. The inheritance of protein C deficiency is discussed and the importance of warfarin (Coumadin) treatment in this conditions is emphasized.