153 related articles for article (PubMed ID: 27408432)
1. Familial Hemophagocytic Lymphohistiocytosis due to Mutation of UNC13D Gene.
Giri PP; Biswas N; Chakravarty S
Indian J Hematol Blood Transfus; 2016 Jun; 32(Suppl 1):344-6. PubMed ID: 27408432
[TBL] [Abstract][Full Text] [Related]
2. Familial Hemophagocytic Lymphohistiocytosis secondary to UNC13D mutation: a report of two cases.
Sadeghi P; Esslami GG; Rokni-Zadeh H; Changi-Ashtiani M; Mohsenipour R
BMC Pediatr; 2022 Nov; 22(1):667. PubMed ID: 36401200
[TBL] [Abstract][Full Text] [Related]
3. Hemophagocytic lymphohistiocytosis: a review inspired by the COVID-19 pandemic.
Soy M; Atagündüz P; Atagündüz I; Sucak GT
Rheumatol Int; 2021 Jan; 41(1):7-18. PubMed ID: 32588191
[TBL] [Abstract][Full Text] [Related]
4. Identification of a novel nonsense mutation in the UNC13D gene from a patient with hemophagocytic lymphohistiocytosis: a case report.
Hu X; Liu D; Jiang X; Gao B; Chen C
BMC Med Genet; 2018 May; 19(1):82. PubMed ID: 29783935
[TBL] [Abstract][Full Text] [Related]
5. Hemophagocytic Lymphohistiocytosis in Children: Pathogenesis and Treatment.
Ishii E
Front Pediatr; 2016; 4():47. PubMed ID: 27242976
[TBL] [Abstract][Full Text] [Related]
6. Case report: Cerebellar swelling and hydrocephalus in familial hemophagocytic lymphohistiocytosis.
Yoshida T; Moriya K; Oikawa K; Miura S; Asakura Y; Tanifuji S; Kusano S; Endo M; Akasaka M
Front Pediatr; 2022; 10():1051623. PubMed ID: 36589154
[TBL] [Abstract][Full Text] [Related]
7. Mutations of the hemophagocytic lymphohistiocytosis-associated gene UNC13D in a patient with systemic juvenile idiopathic arthritis.
Hazen MM; Woodward AL; Hofmann I; Degar BA; Grom A; Filipovich AH; Binstadt BA
Arthritis Rheum; 2008 Feb; 58(2):567-70. PubMed ID: 18240215
[TBL] [Abstract][Full Text] [Related]
8. The 253-kb inversion and deep intronic mutations in UNC13D are present in North American patients with familial hemophagocytic lymphohistiocytosis 3.
Qian Y; Johnson JA; Connor JA; Valencia CA; Barasa N; Schubert J; Husami A; Kissell D; Zhang G; Weirauch MT; Filipovich AH; Zhang K
Pediatr Blood Cancer; 2014 Jun; 61(6):1034-40. PubMed ID: 24470399
[TBL] [Abstract][Full Text] [Related]
9. Clinical, immunological and genetic findings in patients with UNC13D deficiency (FHL3): A systematic review.
Amirifar P; Ranjouri MR; Abolhassani H; Moeini Shad T; Almasi-Hashiani A; Azizi G; Moamer S; Aghamohammadi A; Yazdani R
Pediatr Allergy Immunol; 2021 Jan; 32(1):186-197. PubMed ID: 32679608
[TBL] [Abstract][Full Text] [Related]
10. Novel and atypical splicing mutation in a compound heterozygous UNC13D defect presenting in Familial Hemophagocytic Lymphohistiocytosis triggered by EBV infection.
Alsina L; Colobran R; de Sevilla MF; Català A; Viñas L; Ricart S; Plaza AM; Lois S; Juan M; Pujol-Borrell R; Martinez-Gallo M
Clin Immunol; 2014 Aug; 153(2):292-7. PubMed ID: 24825797
[TBL] [Abstract][Full Text] [Related]
11. COVID-19-associated cytokine storm syndrome and diagnostic principles: an old and new Issue.
Yongzhi X
Emerg Microbes Infect; 2021 Dec; 10(1):266-276. PubMed ID: 33522893
[TBL] [Abstract][Full Text] [Related]
12. Characterization of a large UNC13D gene duplication in a patient with familial hemophagocytic lymphohistiocytosis type 3.
Hiejima E; Shibata H; Yasumi T; Shimodera S; Hori M; Izawa K; Kawai T; Matsuoka M; Kojima Y; Ohara A; Nishikomori R; Ohara O; Heike T
Clin Immunol; 2018 Jun; 191():63-66. PubMed ID: 29596912
[TBL] [Abstract][Full Text] [Related]
13. Screening the PRF1, UNC13D, STX11, SH2D1A, XIAP, and ITK gene mutations in Chinese children with Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis.
Zhizhuo H; Junmei X; Yuelin S; Qiang Q; Chunyan L; Zhengde X; Kunling S
Pediatr Blood Cancer; 2012 Mar; 58(3):410-4. PubMed ID: 21674762
[TBL] [Abstract][Full Text] [Related]
14. Familial hemophagocytic lymphohistiocytosis in a neonate: Case report and literature review.
Yang Y; Luo Z; Yuan T
Medicine (Baltimore); 2021 Nov; 100(47):e27786. PubMed ID: 34964741
[TBL] [Abstract][Full Text] [Related]
15. RF1 Gene Mutation in Familial Hemophagocytic Lymphohistiocytosis 2: A Family Report and Literature Review.
Shi Y; Qiao Z; Bi X; Zhang C; Fu J; Jia Y; Yang G
Pharmgenomics Pers Med; 2021; 14():1637-1645. PubMed ID: 34938098
[TBL] [Abstract][Full Text] [Related]
16. Germline Compound Heterozygous Variants Identified in the
Dantas VM; Valle CT; de Oliveira RP; Bezerra MTAL; do Amaral CT; Brandão RAS; Cerqueira Maia JM; Petta TB
Front Pediatr; 2021; 9():633996. PubMed ID: 34249802
[TBL] [Abstract][Full Text] [Related]
17. A case report of novel mutation in PRF1 gene, which causes familial autosomal recessive hemophagocytic lymphohistiocytosis.
Bordbar MR; Modarresi F; Farazi Fard MA; Dastsooz H; Shakib Azad N; Faghihi MA
BMC Med Genet; 2017 May; 18(1):49. PubMed ID: 28468610
[TBL] [Abstract][Full Text] [Related]
18. Characterization of a novel splicing mutation in UNC13D gene through amplicon sequencing: a case report on HLH.
Liu D; Hu X; Jiang X; Gao B; Wan C; Chen C
BMC Med Genet; 2017 Nov; 18(1):135. PubMed ID: 29157204
[TBL] [Abstract][Full Text] [Related]
19. UNC13D is the predominant causative gene with recurrent splicing mutations in Korean patients with familial hemophagocytic lymphohistiocytosis.
Yoon HS; Kim HJ; Yoo KH; Sung KW; Koo HH; Kang HJ; Shin HY; Ahn HS; Kim JY; Lim YT; Bae KW; Lee KO; Shin JS; Lee ST; Chung HS; Kim SH; Park CJ; Chi HS; Im HJ; Seo JJ
Haematologica; 2010 Apr; 95(4):622-6. PubMed ID: 20015888
[TBL] [Abstract][Full Text] [Related]
20. Detection of a novel gross deletion in the UNC13D gene ends the diagnostic odyssey for a family with familial hemophagocytic lymphohistiocytosis 3.
Nagaraj CB; Brightman DS; Rea H; Wakefield E; Harkavy NVG; Dyer L; Zhang W
BMC Pediatr; 2024 Jan; 24(1):34. PubMed ID: 38212754
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
