Cytogenetic results of amniocentesis materials: incidence of abnormal karyotypes in the Turkish collaborative study

Autor: M Yirmibes, Karaoguz, F, Bal, T, Yakut, N Ozturk, Ercelen, M A, Ergun, A Balci, Gokcen, A Asyali, Biri, Y, Kimya, B, Urman, M, Gultomruk, U, Egeli, S, Menevse

Publikováno v: Genetic counseling (Geneva, Switzerland). 17(2)

The experience on prenatal chromosome diagnosis of four Turkish centers participating in a collaborative study on 6041 genetic amniocentesis performed during a 4-8 years period were reviewed. 5887 (97.5%) patients had strong clinical indications for

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c8c4918400438e228ab1dc9372e94a01
https://pubmed.ncbi.nlm.nih.gov/16970041

Serum levels of malonyldialdehyde (MDA) and paraoxonase activities in patients with Behcet's disease

Autor: Isik, Birgul, Aytekin, Sema, Balci, Gokcen

Publikováno v: In Clinical Biochemistry 2009 42(4):345-345

Febrile ulceronecrotic Mucha-Habermann disease: a case report and a review of the literature

Autor: Sema Aytekin, Gokcen Balci, Ozgur Yagdiran Duzgun

Publikováno v: Aytekin, Sema; Balci, Gokcen; & Duzgun, Ozgur Yagdiran. (2005). Febrile ulceronecrotic Mucha-Habermann disease: A case report and a review of the literature. Dermatology Online Journal, 11(3). Retrieved from: http://www.escholarship.org/uc/item/6kp6f1j2

We report a case of febrile ulceronecrotic Mucha-Habermann disease (FUMHD) in a 27-year-old woman. After 20 days of a mild eruption, extensive polymorphous, papular and ulcerohemorrhagic skin lesions gradually developed, associated with intermittent

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fbebf9aae4fcc27f1f73e7996d8eccf
https://pubmed.ncbi.nlm.nih.gov/16409927