281 related articles for article (PubMed ID: 22129058)
1. Familial hemophagocytic lymphohistiocytosis and X-linked lymphoproliferative disease.
Marsh RA; Filipovich AH
Ann N Y Acad Sci; 2011 Nov; 1238():106-21. PubMed ID: 22129058
[TBL] [Abstract][Full Text] [Related]
2. Epstein-Barr virus-induced hemophagocytic lymphohistiocytosis and X-linked lymphoproliferative disease: a mimicker of sepsis in the pediatric intensive care unit.
Mischler M; Fleming GM; Shanley TP; Madden L; Levine J; Castle V; Filipovich AH; Cornell TT
Pediatrics; 2007 May; 119(5):e1212-8. PubMed ID: 17403820
[TBL] [Abstract][Full Text] [Related]
3. Familial hemophagocytic lymphohistiocytosis in the neonate.
Whaley BF
Adv Neonatal Care; 2011 Apr; 11(2):101-7. PubMed ID: 21730897
[TBL] [Abstract][Full Text] [Related]
4. [Progress of diagnosis and treatment of X-linked inhibitor of apoptosis deficiency].
Yang X; Kanegane H; Miyawaki T
Zhonghua Er Ke Za Zhi; 2012 Jun; 50(6):428-30. PubMed ID: 22931939
[No Abstract] [Full Text] [Related]
5. Hemophagocytic lymphohistiocytosis: advances in pathophysiology, diagnosis, and treatment.
Chandrakasan S; Filipovich AH
J Pediatr; 2013 Nov; 163(5):1253-9. PubMed ID: 23953723
[No Abstract] [Full Text] [Related]
6. XIAP deficiency: a unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease.
Marsh RA; Madden L; Kitchen BJ; Mody R; McClimon B; Jordan MB; Bleesing JJ; Zhang K; Filipovich AH
Blood; 2010 Aug; 116(7):1079-82. PubMed ID: 20489057
[TBL] [Abstract][Full Text] [Related]
7. X-linked Lymphoproliferative Disease Type 1 in a Patient With the p.Gly93Asp SH2D1A Gene Mutation and Hemophagocytic Lymphohistiocytosis.
de la Varga-Martínez R; Mora-López F; García-Cuesta D; Garrastazul-Sánchez MP; Quintero S; Rodríguez C; Sampalo A
J Pediatr Hematol Oncol; 2017 Nov; 39(8):e483-e485. PubMed ID: 28816794
[TBL] [Abstract][Full Text] [Related]
8. Clinical phenotype and functional analysis of a rare XIAP/BIRC4 mutation.
Vieth S; Ammann S; Schwarz K; Härtel C; Schultz C; Lehmberg K; Lauten M
Klin Padiatr; 2013 Nov; 225(6):343-6. PubMed ID: 24166087
[TBL] [Abstract][Full Text] [Related]
9. Fatal sibling cases of familial hemophagocytic lymphohistiocytosis (FHL) with MUNC13-4 mutations: case reports.
Nakao T; Shimizu T; Fukushima T; Saito M; Okamoto M; Sugiura M; Yamamoto K; Ueda I; Imashuku S; Kobayashi C; Koike K; Tsuchida M; Sumazaki R; Matsui A
Pediatr Hematol Oncol; 2008; 25(3):171-80. PubMed ID: 18432499
[TBL] [Abstract][Full Text] [Related]
10. Familial hemophagocytic lymphohistiocytosis in two brothers with X-linked agammaglobulinemia.
Schultz KA; Neglia JP; Smith AR; Ochs HD; Torgerson TR; Kumar A
Pediatr Blood Cancer; 2008 Aug; 51(2):293-5. PubMed ID: 18421721
[TBL] [Abstract][Full Text] [Related]
11. Prolonged course of familial hemophagocytic lymphohistiocytosis.
Steinberg O; Yacobovich J; Dgany O; Kodman Y; Livni G; Rachmel A; Stein J; Yaniv I; Tamary H
J Pediatr Hematol Oncol; 2006 Dec; 28(12):831-3. PubMed ID: 17164654
[TBL] [Abstract][Full Text] [Related]
12. Immunotherapy of familial hemophagocytic lymphohistiocytosis with antithymocyte globulins: a single-center retrospective report of 38 patients.
Mahlaoui N; Ouachée-Chardin M; de Saint Basile G; Neven B; Picard C; Blanche S; Fischer A
Pediatrics; 2007 Sep; 120(3):e622-8. PubMed ID: 17698967
[TBL] [Abstract][Full Text] [Related]
13. [Genetic defects and pathogenesis of hemophagocytic syndrome].
Ishii E
Rinsho Ketsueki; 2006 Oct; 47(10):1340-52. PubMed ID: 17094573
[No Abstract] [Full Text] [Related]
14. The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesis.
Bode SF; Ammann S; Al-Herz W; Bataneant M; Dvorak CC; Gehring S; Gennery A; Gilmour KC; Gonzalez-Granado LI; Groß-Wieltsch U; Ifversen M; Lingman-Framme J; Matthes-Martin S; Mesters R; Meyts I; van Montfrans JM; Pachlopnik Schmid J; Pai SY; Soler-Palacin P; Schuermann U; Schuster V; Seidel MG; Speckmann C; Stepensky P; Sykora KW; Tesi B; Vraetz T; Waruiru C; Bryceson YT; Moshous D; Lehmberg K; Jordan MB; Ehl S;
Haematologica; 2015 Jul; 100(7):978-88. PubMed ID: 26022711
[TBL] [Abstract][Full Text] [Related]
15. [Research advances in molecular genetics and treatment of familial hemophagocytic lymphohistiocytosis].
Lv XQ; Hu J
Zhongguo Dang Dai Er Ke Za Zhi; 2013 Nov; 15(11):965-9. PubMed ID: 24229589
[TBL] [Abstract][Full Text] [Related]
16. Novel mutations in TNFRSF7/CD27: Clinical, immunologic, and genetic characterization of human CD27 deficiency.
Alkhairy OK; Perez-Becker R; Driessen GJ; Abolhassani H; van Montfrans J; Borte S; Choo S; Wang N; Tesselaar K; Fang M; Bienemann K; Boztug K; Daneva A; Mechinaud F; Wiesel T; Becker C; Dückers G; Siepermann K; van Zelm MC; Rezaei N; van der Burg M; Aghamohammadi A; Seidel MG; Niehues T; Hammarström L
J Allergy Clin Immunol; 2015 Sep; 136(3):703-712.e10. PubMed ID: 25843314
[TBL] [Abstract][Full Text] [Related]
17. Hemophagocytic lymphohistiocytosis and related disorders.
Filipovich AH
Curr Opin Allergy Clin Immunol; 2006 Dec; 6(6):410-5. PubMed ID: 17088644
[TBL] [Abstract][Full Text] [Related]
18. Successful stem cell transplant with antibody-based conditioning for XIAP deficiency with refractory hemophagocytic lymphohistiocytosis.
Worth AJ; Nikolajeva O; Chiesa R; Rao K; Veys P; Amrolia PJ
Blood; 2013 Jun; 121(24):4966-8. PubMed ID: 23766462
[No Abstract] [Full Text] [Related]
19. Usual and Unusual Manifestations of Familial Hemophagocytic Lymphohistiocytosis and Langerhans Cell Histiocytosis.
Erker C; Harker-Murray P; Talano JA
Pediatr Clin North Am; 2017 Feb; 64(1):91-109. PubMed ID: 27894453
[TBL] [Abstract][Full Text] [Related]
20. Hemophagocytic lymphohistiocytosis after lung transplant: report of 2 cases and a literature review.
Diaz-Guzman E; Dong B; Hobbs SB; Kesler MV; Hayes D
Exp Clin Transplant; 2011 Jun; 9(3):217-22. PubMed ID: 21649574
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]