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196 related items for PubMed ID: 22395213

  • 1. Hemophagocytic lymphohistiocytosis can mimic the superior vena cava syndrome.
    Park M, Choi JW, Park HJ, Kim HJ, Hi Son M, Yoon JH, Kim SJ, Park WS, Park BK.
    J Pediatr Hematol Oncol; 2012 May; 34(4):e152-4. PubMed ID: 22395213
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 3. [Anaplastic large cell lymphoma associated with hemophagocytic lymphohistiocytosis: a case report and review of the literature].
    Balwierz W, Czogała M, Czepko E.
    Przegl Lek; 2010 Jul; 67(6):436-8. PubMed ID: 21344777
    [Abstract] [Full Text] [Related]

  • 4. Hemophagocytic lymphohistiocytosis: an update on diagnosis and pathogenesis.
    Rosado FG, Kim AS.
    Am J Clin Pathol; 2013 Jun; 139(6):713-27. PubMed ID: 23690113
    [Abstract] [Full Text] [Related]

  • 5. Hemophagocytic lymphohistiocytosis: when the immune system runs amok.
    Janka G.
    Klin Padiatr; 2009 Sep; 221(5):278-85. PubMed ID: 19707989
    [Abstract] [Full Text] [Related]

  • 6. A case report of hemophagocytic lymphohistiocytosis (HLH).
    Rajadhyaksha A, Sonawale A, Agrawal A, Ahire K, Kawale J.
    J Assoc Physicians India; 2014 Jul; 62(7):637-41. PubMed ID: 25672045
    [Abstract] [Full Text] [Related]

  • 7. Hemophagocytic lymphohistiocytosis and Kawasaki disease: combined manifestation and differential diagnosis.
    Titze U, Janka G, Schneider EM, Prall F, Haffner D, Classen CF.
    Pediatr Blood Cancer; 2009 Sep; 53(3):493-5. PubMed ID: 19434728
    [Abstract] [Full Text] [Related]

  • 8. [Analysis of clinical phenotype and genetic mutations of a pedigree of familial hemophagocytic lymphohistiocytosis].
    Sun S, Guo X, Zhu Y, Yang X, Li Q, Gao J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):570-3. PubMed ID: 25297583
    [Abstract] [Full Text] [Related]

  • 9. [Sinus histiocytosis with massive lymphadenopathy with complete occlusion of the superior and inferior vena cava].
    Runde J, Ebbecke H, Kurlemann G, Frosch M, Schuierer G.
    Klin Padiatr; 1997 Oct; 209(1):39-42. PubMed ID: 9121077
    [Abstract] [Full Text] [Related]

  • 10. Management of superior vena cava syndrome by internal jugular to femoral vein bypass.
    Dhaliwal RS, Das D, Luthra S, Singh J, Mehta S, Singh H.
    Ann Thorac Surg; 2006 Jul; 82(1):310-2. PubMed ID: 16798237
    [Abstract] [Full Text] [Related]

  • 11. Remission and relapse of hemophagocytic lymphohistiocytosis in a patient harboring a PRF1 homozygous mutation: a case report.
    Huang Z, Wang Y, Xie Z, Shen K.
    J Pediatr Hematol Oncol; 2014 Jan; 36(1):e5-8. PubMed ID: 23073044
    [Abstract] [Full Text] [Related]

  • 12. Myelofibrosis in a patient with familial hemophagocytic lymphohistiocytosis.
    Friedman GK, Hammers Y, Reddy V, Pressey JG.
    Pediatr Blood Cancer; 2008 Jun; 50(6):1260-2. PubMed ID: 18253962
    [Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. Hemophagocytic lymphohistiocytosis at initiation of kawasaki disease and their differential diagnosis.
    Chen Y, Shang S, Zhang C, Liu T, Yang Z, Tang Y.
    Pediatr Hematol Oncol; 2010 Apr; 27(3):244-9. PubMed ID: 20367269
    [Abstract] [Full Text] [Related]

  • 15. Rare cause of Hemophagocytic Lymphohistiocytosis due to mutation in PRF1 and SH2D1A genes in two children - a case report with a review.
    Sheth J, Patel A, Shah R, Bhavsar R, Trivedi S, Sheth F.
    BMC Pediatr; 2019 Mar 08; 19(1):73. PubMed ID: 30849948
    [Abstract] [Full Text] [Related]

  • 16. Familial hemophagocytic lymphohistiocytosis type 3 diagnosed at school age: a case report.
    Manno EC, Salfa I, Palma P, Bertaina A, Lombardi A, Moretta F, Coniglio ML, Sieni E, Aricò M, Finocchi A.
    J Pediatr Hematol Oncol; 2014 Mar 08; 36(2):e128-30. PubMed ID: 23669735
    [Abstract] [Full Text] [Related]

  • 17. Hemophagocytic syndrome in a 4-month-old infant with biotinidase deficiency.
    Kardas F, Patiroglu T, Unal E, Chiang SC, Bryceson YT, Kendirci M.
    Pediatr Blood Cancer; 2012 Jul 15; 59(1):191-3. PubMed ID: 22605457
    [Abstract] [Full Text] [Related]

  • 18. Fatal hemophagocytic lymphohistiocytosis in X-linked chronic granulomatous disease associated with a perforin gene variant.
    van Montfrans JM, Rudd E, van de Corput L, Henter JI, Nikkels P, Wulffraat N, Boelens JJ.
    Pediatr Blood Cancer; 2009 Apr 15; 52(4):527-9. PubMed ID: 19058215
    [Abstract] [Full Text] [Related]

  • 19. Fatal hemophagocytic syndrome in a patient with a previously well-controlled asymptomatic HIV infection after EBV reactivation.
    Thoden J, Rieg S, Venhoff N, Wennekes V, Schmitt-Graeff A, Wagner D, Kern WV.
    J Infect; 2012 Jan 15; 64(1):110-2. PubMed ID: 21888928
    [Abstract] [Full Text] [Related]

  • 20. 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 Jan 15; 22(3):281-5. PubMed ID: 22029169
    [Abstract] [Full Text] [Related]

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