Granulocytic sarcoma after stem cell transplantation in a child with biphenotypic leukemia

Autor: Kaya, Z., Koçak, Ü, Meryem Albayrak, Gürsel, T., Akyürek, N., Oktar, S. Ö

Publikováno v: Scopus-Elsevier
Turkish Journal of Hematology, Vol 26, Iss 03, Pp 151-153 (2009)

Granulocytic sarcoma is an extramedullary tumor composed of leukemic blasts. Isolated granulocytic sarcoma has rarely been reported in children with leukemia undergoing allogeneic stem cell transplantation. We report a case of isolated granulocytic s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::78dfe9284d496142ec3c5e923754a3da
https://pubmed.ncbi.nlm.nih.gov/27265499

Supernumerary Nipples in Children with Hematologic Disorders.

Autor: Aslan, D.¹ (AUTHOR) drdahutf@ixir.com, Gürsel, T.¹ (AUTHOR), Kaya, Z.¹ (AUTHOR)

Publikováno v: Pediatric Hematology & Oncology. Jul2004, Vol. 21 Issue 5, p461-463. 3p.

Fatal Epstein-Barr virus infection in a case of familial hemophagocytic lymphohistiocytosis with syntaxin-11 mutation

Autor: Meryem Albayrak, Kaya, Z., Yilmaz-Keskin, E., Stadt, U. Z., Koçak, Ü, Gürsel, T.

Publikováno v: Scopus-Elsevier

Familial hemophagocytic lymphohistiocytosis (FHL) is a fatal disease of early infancy caused by defective natural killer cell activity and is characterized by fever, organomegaly, pancytopenia, and coagulopathy. Disease-causing mutations have been fo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1e399308b765acc364a600e2ad5bba95
https://avesis.gazi.edu.tr/publication/details/54a89343-f86b-4631-a397-64aabe1bf8d7/oai

Evaluation of clinical characteristics, diagnosis and management in childhood immune thrombocytopenic purpura: a single center's experience

Autor: Koçak, Ü, Aral, Y. Z., Kaya, Z., Öztürk, G., Gürsel, T.

Publikováno v: Scopus-Elsevier

purpura (ITP) are controversial. We reviewed the files of 162 children with ITP to evaluate clinical characteristics, response to treatment and outcome. History of antecedent infection, vaccination and serologic evidence for acute viral infection wer

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::9c969b799a644a927ebaff90b6a6197d
https://avesis.gazi.edu.tr/publication/details/d76296c0-8e5b-4431-afaf-b7f10418544e/oai

A novel von Willebrand disease causing mutation (Arg273Trp) in the von Willebrand factor propeptide that results in defective multimerization and secretion

Autor: Allen, S., Abuzenedah, A.M., Hinks, J., Blaggs, J.L., Gürsel, T., Ingerslev, Jørgen, Goodeve, A.C., Peake, I.R.and, Daly, M.E.

Publikováno v: Allen, S, Abuzenedah, A M, Hinks, J, Blaggs, J L, Gürsel, T, Ingerslev, J, Goodeve, A C, Peake, I R A & Daly, M E 2000, ' A novel von Willebrand disease causing mutation (Arg273Trp) in the von Willebrand factor propeptide that results in defective multimerization and secretion ', Blood, bind 96, s. 560-568 .

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pure_au_____::31fb8c718207a1cac2c69dd7658ef9cd
https://pure.au.dk/portal/da/publications/a-novel-von-willebrand-disease-causing-mutation-arg273trp-in-the-von-willebrand-factor-propeptide-that-results-in-defective-multimerization-and-secretion(09aeecd0-b59e-11da-bee9-02004c4f4f50).html