Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Emine İpek Ceylan"'
Autor:
Burak Deliloğlu, Özlem Tüfekçi, Funda Tüzün, Ayça Aykut, Emine İpek Ceylan, Asude Durmaz, Şebnem Yılmaz, Nuray Duman, Hasan Özkan, Hale Ören
Background. Hereditary bone marrow failure syndromes are a category of biologically different syndromes that can cause cytopenia in at least one hematopoietic cell lineage. Case. We present a 29-week-old male infant who had a low Apgar Score, advance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87a01de1225c165d8698f66f14bc6a95
https://avesis.deu.edu.tr/publication/details/6816b441-7341-4947-ae64-d00630bcbf33/oai
https://avesis.deu.edu.tr/publication/details/6816b441-7341-4947-ae64-d00630bcbf33/oai
Autor:
Sebile Kılavuz, Murat Basaranoglu, Serdar Epcacan, Derya Bako, Arife Ozer, Yasemin Nuran Donmez, Emine Ipek Ceylan, Ajlan Tukun, Serdar Ceylaner, Hadi Geylani, Halise Neslihan Onenli Mungan
Publikováno v:
Metabolic brain disease. 37(4)
Gaucher disease type 2 is the most progressive and the rarest form of Gaucher disease, defined as the acute neuronopathic type. We presented two GD2 patients who died before three months of age due to severe septicemia, respiratory and liver failure.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63bc9d576e437561e897c78c03b6f6ca
https://pubmed.ncbi.nlm.nih.gov/35254599
https://pubmed.ncbi.nlm.nih.gov/35254599
Autor:
Tahir Atik, Ayse Yagci, Melis Palamar, Hüseyin Onay, Emine Ipek Ceylan, Taner Akalin, Nergiz Ismayilova
Publikováno v:
European journal of ophthalmology. 32(1)
Purpose:To investigate vitamin D receptor polymorphisms in ocular surface squamous cell neoplasm and to evaluate the relationship between the identified polymorphisms and susceptibility to ocular s...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7864ee78bbf2e9e7ed412bc690c0366d
https://pubmed.ncbi.nlm.nih.gov/34269094
https://pubmed.ncbi.nlm.nih.gov/34269094