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488 related items for PubMed ID: 22605457

  • 21. 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, Inborn Errors Working Party of the EBMT.
    Haematologica; 2015 Jul; 100(7):978-88. PubMed ID: 26022711
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  • 22. Clinical aspects, immunologic assessment, and genetic analysis in Taiwanese children with hemophagocytic lymphohistiocytosis.
    Lee WI, Chen SH, Hung IJ, Yang CP, Jaing TH, Chen CJ, Li SP, Huang JL.
    Pediatr Infect Dis J; 2009 Jan; 28(1):30-4. PubMed ID: 19057461
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  • 24. Hemophagocytic lymphohistiocytosis associated with H1N1 virus infection and visceral leishmaniasis in a 4.5-month-old infant.
    Ay Y, Yildiz B, Unver H, Karapinar DY, Vardar F.
    Rev Soc Bras Med Trop; 2012 Jun; 45(3):407-9. PubMed ID: 22760147
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  • 25. Biotinidase deficiency and juvenile myelomonocytic leukemia in a Turkish infant of consanguineous parents.
    Yetgin S, Aytac S, Kalkanoglu S, Coskun T, Ortmann C, Kratz C, Niemeyer C.
    Pediatr Hematol Oncol; 2007 Sep; 24(6):453-5. PubMed ID: 17710663
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  • 30. Profound biotinidase deficiency in a child with predominantly spinal cord disease.
    Chedrawi AK, Ali A, Al Hassnan ZN, Faiyaz-Ul-Haque M, Wolf B.
    J Child Neurol; 2008 Sep; 23(9):1043-8. PubMed ID: 18645204
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  • 32. Cobalamin C disease presenting with hemophagocytic lymphohistiocytosis.
    Wu S, Gonzalez-Gomez I, Coates T, Yano S.
    Pediatr Hematol Oncol; 2005 Dec; 22(8):717-21. PubMed ID: 16251179
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  • 33. Biotinidase deficiency in childhood.
    Venkataraman V, Balaji P, Panigrahi D, Jamal R.
    Neurol India; 2013 Dec; 61(4):411-3. PubMed ID: 24005734
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  • 34. Analysis of mutations causing biotinidase deficiency.
    Pindolia K, Jordan M, Wolf B.
    Hum Mutat; 2010 Sep; 31(9):983-91. PubMed ID: 20556795
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  • 37. Hyperferritinemia as the diagnostic clue in life-threatening hemophagocytic lymphohistiocytosis.
    Kerzel S, Zemlin M, Kömhoff M, Klaus G, Maier RF.
    Klin Padiatr; 2009 Sep; 221(5):318-21. PubMed ID: 19199227
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