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Journal Abstract Search

346 related items for PubMed ID: 18074390

  • 1. A teenage boy with late onset hemophagocytic lymphohistiocytosis with predominant neurologic disease and perforin deficiency.
    Beaty AD, Weller C, Levy B, Vogler C, Ferguson WS, Bicknese A, Knutsen AP.
    Pediatr Blood Cancer; 2008 May; 50(5):1070-2. PubMed ID: 18074390
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  • 2. A neurologic presentation of familial hemophagocytic lymphohistiocytosis which mimicked septic emboli to the brain.
    Turtzo LC, Lin DD, Hartung H, Barker PB, Arceci R, Yohay K.
    J Child Neurol; 2007 Jul; 22(7):863-8. PubMed ID: 17715280
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  • 3. Hemophagocytic lymphohistiocytosis with isolated central nervous system reactivation and optic nerve involvement.
    Chong KW, Lee JH, Choong CT, Paeds MM, Chan DW, Fortier MV, Chan MY.
    J Child Neurol; 2012 Oct; 27(10):1336-9. PubMed ID: 22378674
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  • 4. Pathology of the liver in familial hemophagocytic lymphohistiocytosis.
    Chen JH, Fleming MD, Pinkus GS, Pinkus JL, Nichols KE, Mo JQ, Perez-Atayde AR.
    Am J Surg Pathol; 2010 Jun; 34(6):852-67. PubMed ID: 20442642
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  • 5. Familial hemophagocytic lymphohistiocytosis in a 6-week-old male infant.
    Jakovljević G, Kardum-Skelin I, Rogosić S, Culić S, Stepan J, Gagro A, Skarić I, Mikecin L, Bonevski A, Barisić I, Nakić M.
    Coll Antropol; 2010 Jun; 34(2):631-4. PubMed ID: 20698142
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  • 6. Central nervous system involvement in a case of familial hemophagocytic lymphohistiocytosis with perforin mutation.
    Akbayram S, Akgun C, Dogan M, Caksen H, Okur H, Oner AF.
    Genet Couns; 2011 Jun; 22(3):281-5. PubMed ID: 22029169
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  • 8. Neonatal hemophagocytic lymphohistiocytosis--case report.
    Roganović J, Kvenić B, Jonjić N, Seili-Bekafigo I, Kardum-Skelin I.
    Coll Antropol; 2010 Mar; 34(1):285-90. PubMed ID: 20432763
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  • 9. Late-onset cases of familial hemophagocytic lymphohistiocytosis with missense perforin gene mutations.
    Ueda I, Kurokawa Y, Koike K, Ito S, Sakata A, Matsumora T, Fukushima T, Morimoto A, Ishii E, Imashuku S.
    Am J Hematol; 2007 Jun; 82(6):427-32. PubMed ID: 17266056
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  • 10. Familial hemophagocytic lymphohistiocytosis in an adult patient homozygous for A91V in the perforin gene, with tuberculosis infection.
    Mancebo E, Allende LM, Guzmán M, Paz-Artal E, Gil J, Urrea-Moreno R, Fernández-Cruz E, Gayà A, Calvo J, Arbós A, Durán MA, Canet R, Balanzat J, Udina MA, Vercher FJ.
    Haematologica; 2006 Sep; 91(9):1257-60. PubMed ID: 16956828
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  • 14. Central nervous system involvement in Turkish children with primary hemophagocytic lymphohistiocytosis.
    Gurgey A, Aytac S, Balta G, Oguz KK, Gumruk F.
    J Child Neurol; 2008 Nov; 23(11):1293-9. PubMed ID: 18984839
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  • 15. Primary necrotizing lymphocytic central nervous system vasculitis due to perforin deficiency in a four-year-old girl.
    Moshous D, Feyen O, Lankisch P, Schwarz K, Schaper J, Schneider M, Dilloo D, Laws HJ, Schwahn BC, Niehues T.
    Arthritis Rheum; 2007 Mar; 56(3):995-9. PubMed ID: 17328077
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  • 16. 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
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  • 17. 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
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  • 19. Necrotizing epiglottitis and hemophagocytic lymphohistiocytosis.
    Kong MS, Engel SH, Zalzal GH, Preciado D.
    Int J Pediatr Otorhinolaryngol; 2009 Jan; 73(1):119-25. PubMed ID: 19062109
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