Literature DB >> 25147377

fHLH: becoming a blended family.

Carl E Allen1, Kenneth L McClain1.   

Abstract

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Year:  2014        PMID： 25147377      PMCID： PMC4141507          DOI： 10.1182/blood-2014-06-582791

Source DB:  PubMed          Journal:  Blood        ISSN： 0006-4971            Impact factor:   22.113


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  7 in total

Review 1.  Pathophysiology and spectrum of diseases caused by defects in lymphocyte cytotoxicity.

Authors:  Marie Meeths; Samuel C C Chiang; Alexandra Löfstedt; Martha-Lena Müller; Bianca Tesi; Jan-Inge Henter; Yenan T Bryceson
Journal:  Exp Cell Res       Date:  2014-03-28       Impact factor: 3.905

2.  HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis.

Authors:  Jan-Inge Henter; Annacarin Horne; Maurizio Aricó; R Maarten Egeler; Alexandra H Filipovich; Shinsaku Imashuku; Stephan Ladisch; Ken McClain; David Webb; Jacek Winiarski; Gritta Janka
Journal:  Pediatr Blood Cancer       Date:  2007-02       Impact factor: 3.167

Review 3.  Hemophagocytic lymphohistiocytosis: advances in pathophysiology, diagnosis, and treatment.

Authors:  Shanmuganathan Chandrakasan; Alexandra H Filipovich
Journal:  J Pediatr       Date:  2013-08-15       Impact factor: 4.406

4.  Hypomorphic mutations in PRF1, MUNC13-4, and STXBP2 are associated with adult-onset familial HLH.

Authors:  Kejian Zhang; Michael B Jordan; Rebecca A Marsh; Judith A Johnson; Diane Kissell; Jarek Meller; Joyce Villanueva; Kimberly A Risma; Qian Wei; Peter S Klein; Alexandra H Filipovich
Journal:  Blood       Date:  2011-08-31       Impact factor: 22.113

Review 5.  How I treat hemophagocytic lymphohistiocytosis.

Authors:  Michael B Jordan; Carl E Allen; Sheila Weitzman; Alexandra H Filipovich; Kenneth L McClain
Journal:  Blood       Date:  2011-08-09       Impact factor: 22.113

6.  Synergistic defects of different molecules in the cytotoxic pathway lead to clinical familial hemophagocytic lymphohistiocytosis.

Authors:  Kejian Zhang; Shanmuganathan Chandrakasan; Heather Chapman; C Alexander Valencia; Ammar Husami; Diane Kissell; Judith A Johnson; Alexandra H Filipovich
Journal:  Blood       Date:  2014-06-10       Impact factor: 22.113

7.  Macrophage activation syndrome in patients with systemic juvenile idiopathic arthritis is associated with MUNC13-4 polymorphisms.

Authors:  Kejian Zhang; Jennifer Biroschak; David N Glass; Susan D Thompson; Terri Finkel; Murray H Passo; Bryce A Binstadt; Alexandra Filipovich; Alexei A Grom
Journal:  Arthritis Rheum       Date:  2008-09
  7 in total
  3 in total

1.  Type 5 Familial Hemophagocytic Lymphohistiocytosis in a Seven-year-old Girl Post Second Bone Marrow Transplantation with Failure to Thrive: STXBP2 Novel Mutation.

Authors:  Abdullah Baothman; Hani Almalki; Khalid Abumelha; Abobaker Alshegifi; Abdulrahman Baashar
Journal:  Cureus       Date:  2019-11-27

2.  Exome sequencing detected an extremely rare case of foetal onset familial haemophagocytic lymphohistiocytosis type 5 presenting with hydrops foetalis.

Authors:  V Thadchanamoorthy; M T R Jayatunga; Kavinda Dayasiri; E Jasinge; M L M Jinnah; C Pereira; V Skrahina; Markandu Thirukumar
Journal:  BMC Med Genomics       Date:  2021-02-16       Impact factor: 3.063

Review 3.  Immune cartography of macrophage activation syndrome in the COVID-19 era.

Authors:  Dennis McGonagle; Athimalaipet V Ramanan; Charlie Bridgewood
Journal:  Nat Rev Rheumatol       Date:  2021-02-05       Impact factor: 32.286
  3 in total

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