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Journal Abstract Search

66 related items for PubMed ID: 2586376

  • 1. [Genetically determined hepatosplenomegaly. A discussion by gastroenterologists in Freiburg].
    von Klaus Haag B, Ringwald G, Strittmatter B, Glatt E, Hellerich U.
    Med Klin (Munich); 1989 Oct 15; 84(10):499-502. PubMed ID: 2586376
    [No Abstract] [Full Text] [Related]

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  • 3. [Enzyme replacement therapy for Gaucher disease introduced in late adulthood].
    Juhász P, Tóth B, Maródi L, Erdos M.
    Orv Hetil; 2012 Feb 19; 153(7):264-70. PubMed ID: 22318527
    [Abstract] [Full Text] [Related]

  • 4. [Diagnostic image (215). A woman with abdominal pain and hepatosplenomegaly].
    Kwee WS, Wirtz JJ.
    Ned Tijdschr Geneeskd; 2004 Nov 13; 148(46):2273. PubMed ID: 15584542
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  • 6. [Differential diagnosis of diseases accompanied by development of the hepatolienal syndrome].
    Lytkin MI, Mishchenko AS, Simonov VV.
    Klin Med (Mosk); 1971 Feb 13; 49(2):59-64. PubMed ID: 5001026
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  • 7. A new variant neuropathic type of Gaucher's disease characterized by hydrocephalus, corneal opacities, deformed toes, and fibrous thickening of spleen and liver capsules.
    Inui K, Yanagihara K, Otani K, Suzuki Y, Akagi M, Nakayama M, Ida H, Okada S.
    J Pediatr; 2001 Jan 13; 138(1):137-9. PubMed ID: 11148530
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  • 9. A familial disorder characterized by hepatosplenomegaly presenting as "preleukemia".
    Holimon JL, Madge GE.
    Va Med Mon (1918); 1971 Dec 13; 98(12):644-8. PubMed ID: 5129122
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  • 10. [A boy with hepatosplenomegaly].
    Rev Clin Esp; 1991 Mar 13; 188(4):206-13. PubMed ID: 1784748
    [No Abstract] [Full Text] [Related]

  • 11. Gaucher disease and β-thalassemia: A rare coinheritance.
    Makis A, Tzoufi M, Pappa E, Kyrochristos I, Zikou A, Xydis V, Argyropoulou MI, Chaliasos N.
    Blood Cells Mol Dis; 2017 Jun 13; 65():35-37. PubMed ID: 28458077
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  • 12. [Male with hepato-splenomegaly, pancytopenia, and pain in the left thigh].
    Cabezas Agrícola JM, Otero Antón E, Rodríguez López I, Forteza Vila J, Barrio Gómez E.
    Rev Clin Esp; 1996 Nov 13; 196(11):785-6. PubMed ID: 9132844
    [No Abstract] [Full Text] [Related]

  • 13. The clinical course of untreated Gaucher disease in 22 patients over 10 years: hematological and skeletal manifestations.
    Piran S, Roberts A, Patterson MA, Amato D.
    Blood Cells Mol Dis; 2009 Nov 13; 43(3):289-93. PubMed ID: 19793665
    [Abstract] [Full Text] [Related]

  • 14. [Niemann-Pick disease in adults in hepato-spleno-pulmonary form].
    Bourel M, Sabouraud O, Chevrel ML, Ferrand B, Lenoir P, Morel H, Badiche A.
    Sem Hop; 1968 May 08; 44(22):1499-508. PubMed ID: 4302768
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  • 15. Clinical and enzyme studies in Gaucher disease.
    Kaur M, Kabra M, Kher A, Naik G, Bharucha BA, Verma IC.
    Indian Pediatr; 1996 Sep 08; 33(9):735-8. PubMed ID: 9057400
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  • 16. [New aspects of Osler's disease].
    Stinner G.
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1966 Sep 08; 86(3):249-57. PubMed ID: 4167663
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  • 19. A 16-year-old girl with epistaxis and hepatosplenomegaly.
    Woods M, Greenes D.
    Curr Opin Pediatr; 1995 Dec 08; 7(6):733-9. PubMed ID: 8776027
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  • 20. [Gaucher disease type I diagnosed at 63 years old presenting with thrombocytopenia].
    Kawahara S, Kato A, Oshimi K, Ida H.
    Rinsho Ketsueki; 2008 May 08; 49(5):335-9. PubMed ID: 18572811
    [Abstract] [Full Text] [Related]

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