Gürgey A - Search Results

1

Spectrum, and clinical and functional implications of UNC13D mutations in familial haemophagocytic lymphohistiocytosis.

Rudd E, Bryceson YT, Zheng C, Edner J, Wood SM, Ramme K, Gavhed S, Gürgey A, Hellebostad M, Bechensteen AG, Ljunggren HG, Fadeel B, Nordenskjöld M, Henter JI. Rudd E, et al. Among authors: gurgey a. J Med Genet. 2008 Mar;45(3):134-41. doi: 10.1136/jmg.2007.054288. Epub 2007 Nov 9. J Med Genet. 2008. PMID: 17993578

2

Sequence analysis of the granulysin and granzyme B genes in familial hemophagocytic lymphohistiocytosis.

Ericson KG, Fadeel B, Andersson M, Gudmundsson GH, Gürgey A, Yalman N, Janka G, Nordenskjöld M, Henter JI. Ericson KG, et al. Among authors: gurgey a. Hum Genet. 2003 Jan;112(1):98-9. doi: 10.1007/s00439-002-0841-0. Epub 2002 Oct 11. Hum Genet. 2003. PMID: 12483306

3

Characterization of PRF1, STX11 and UNC13D genotype-phenotype correlations in familial hemophagocytic lymphohistiocytosis.

Horne A, Ramme KG, Rudd E, Zheng C, Wali Y, al-Lamki Z, Gürgey A, Yalman N, Nordenskjöld M, Henter JI. Horne A, et al. Among authors: gurgey a. Br J Haematol. 2008 Oct;143(1):75-83. doi: 10.1111/j.1365-2141.2008.07315.x. Epub 2008 Aug 15. Br J Haematol. 2008. PMID: 18710388 Free article.

4

Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis.

Göransdotter Ericson K, Fadeel B, Nilsson-Ardnor S, Söderhäll C, Samuelsson A, Janka G, Schneider M, Gürgey A, Yalman N, Révész T, Egeler R, Jahnukainen K, Storm-Mathiesen I, Haraldsson A, Poole J, de Saint Basile G, Nordenskjöld M, Henter J. Göransdotter Ericson K, et al. Among authors: gurgey a. Am J Hum Genet. 2001 Mar;68(3):590-7. doi: 10.1086/318796. Epub 2001 Feb 6. Am J Hum Genet. 2001. PMID: 11179007 Free PMC article.

5

Spectrum and clinical implications of syntaxin 11 gene mutations in familial haemophagocytic lymphohistiocytosis: association with disease-free remissions and haematopoietic malignancies.

Rudd E, Göransdotter Ericson K, Zheng C, Uysal Z, Ozkan A, Gürgey A, Fadeel B, Nordenskjöld M, Henter JI. Rudd E, et al. Among authors: gurgey a. J Med Genet. 2006 Apr;43(4):e14. doi: 10.1136/jmg.2005.035253. J Med Genet. 2006. PMID: 16582076 Free PMC article.

6

Clinical and molecular aspects of Turkish familial hemophagocytic lymphohistiocytosis patients with perforin mutations.

Okur H, Balta G, Akarsu N, Oner A, Patiroglu T, Bay A, Sayli T, Unal S, Gurgey A. Okur H, et al. Among authors: gurgey a. Leuk Res. 2008 Jun;32(6):972-5. doi: 10.1016/j.leukres.2007.11.033. Epub 2008 Jan 10. Leuk Res. 2008. PMID: 18190960

7

Structural and functional analysis of perforin mutations in association with clinical data of familial hemophagocytic lymphohistiocytosis type 2 (FHL2) patients.

An O, Gursoy A, Gurgey A, Keskin O. An O, et al. Among authors: gurgey a. Protein Sci. 2013 Jun;22(6):823-39. doi: 10.1002/pro.2265. Protein Sci. 2013. PMID: 23592409 Free PMC article.

8

Defective UNC13D gene-associated familial hemophagocytic lymphohistiocytosis triggered by visceral leishmaniasis: a diagnostic challenge.

Balta G, Azik FM, Gurgey A. Balta G, et al. Among authors: gurgey a. J Pediatr Hematol Oncol. 2014 Jan;36(1):e42-5. doi: 10.1097/MPH.0b013e31829b7f22. J Pediatr Hematol Oncol. 2014. PMID: 23774160

9

Association of nonimmune hydrops fetalis with familial hemophagocytic lymphohistiocytosis in identical twin neonates with perforin His222Arg (c665A>G) mutation.

Balta G, Topcuoglu S, Gursoy T, Gurgey A, Ovali F. Balta G, et al. Among authors: gurgey a. J Pediatr Hematol Oncol. 2013 Nov;35(8):e332-4. doi: 10.1097/MPH.0b013e31827078c6. J Pediatr Hematol Oncol. 2013. PMID: 23073042

10

Assessment of clinical and laboratory presentations of familial hemophagocytic lymphohistiocytosis patients with homozygous W374X mutation.

Balta G, Okur H, Unal S, Yarali N, Gunes AM, Unal S, Turker M, Guler E, Ertem M, Albayrak M, Patiroglu T, Gurgey A. Balta G, et al. Among authors: gurgey a. Leuk Res. 2010 Aug;34(8):1012-7. doi: 10.1016/j.leukres.2010.02.002. Epub 2010 Mar 1. Leuk Res. 2010. PMID: 20197201

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