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Journal Abstract Search

141 related items for PubMed ID: 7942949

  • 1. Ceredase dosing concerns for Gaucher's disease.
    Moscicki RA, van Heek J.
    Am J Med; 1994 Oct; 97(4):402-3. PubMed ID: 7942949
    [No Abstract] [Full Text] [Related]

  • 2. [Course of a case of Gaucher's disease type 1 treated over a year with glucocerebrosidase (Cérédase)].
    Belmatoug N, Azorin M, Huten D, de Villemeur TB, Carbon C.
    Rev Med Interne; 1993 Oct; 14(10):996. PubMed ID: 8009089
    [Abstract] [Full Text] [Related]

  • 3. Pulmonary involvement of Gaucher's disease in children: a common presentation in Saudi Arabia.
    Banjar H.
    Ann Trop Paediatr; 1998 Mar; 18(1):55-9. PubMed ID: 9692003
    [Abstract] [Full Text] [Related]

  • 4. [Enzyme therapy in children with severe forms of Gaucher's disease].
    Zeman J, Hrebícek M, Vepreková L, Kytnarová J, Houstková H, Malinová V, Hodanová K, Poupĕtová H, Ledvinová J, Hoza J.
    Cas Lek Cesk; 1997 Feb 05; 136(3):95-7. PubMed ID: 9221177
    [Abstract] [Full Text] [Related]

  • 5. Treatment of Gaucher's disease.
    Hollak CE, Aerts JM, van Oers MH.
    N Engl J Med; 1993 May 27; 328(21):1565-6; author reply 1567. PubMed ID: 8479498
    [No Abstract] [Full Text] [Related]

  • 6. Enzyme-replacement therapy for Gaucher's disease.
    N Engl J Med; 1991 Dec 19; 325(25):1809-11. PubMed ID: 1944489
    [No Abstract] [Full Text] [Related]

  • 7. Gaucher's disease: therapy by intravenous infusions of modified glucocerebrosidase.
    Beck M, Valadares ER, Lotz J.
    Clin Investig; 1993 Jan 19; 71(1):78. PubMed ID: 8453266
    [No Abstract] [Full Text] [Related]

  • 8. Treatment regimens in Gaucher's disease.
    Beutler E.
    Lancet; 1995 Aug 26; 346(8974):581-2. PubMed ID: 7658807
    [No Abstract] [Full Text] [Related]

  • 9. [Enzyme therapy of Gaucher's disease].
    Beck M.
    Dtsch Med Wochenschr; 1993 Jun 25; 118(25):964-5. PubMed ID: 8519225
    [No Abstract] [Full Text] [Related]

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  • 11. [Persistence of pulmonary lesions in a 6-year-old boy with type I Gaucher's disease treated by alglucerase since the age of 20 months].
    Versteegh C, Avni F, Cuvelier P, Ferster A.
    Arch Pediatr; 1998 Dec 25; 5(12):1341-3. PubMed ID: 9885741
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  • 13. Successful treatment of bone marrow failure in Gaucher's disease with low-dose modified glucocerebrosidase.
    Mistry PK, Davies S, Corfield A, Dixon AK, Cox TM.
    Q J Med; 1992 Jul 25; 83(303):541-6. PubMed ID: 1484931
    [Abstract] [Full Text] [Related]

  • 14. Neurological features in Gaucher's disease during enzyme replacement therapy.
    Ono H, Fujiwara M, Ito K, Ueda H, Mizoguchi N, Sakura N.
    Acta Paediatr; 2001 Feb 25; 90(2):229-31. PubMed ID: 11236058
    [Abstract] [Full Text] [Related]

  • 15. Plasma lipoprotein responses to enzyme-replacement in Gaucher's disease.
    Cenarro A, Pocovi M, Giraldo P, Garcia-Otin AL, Ordovas JM.
    Lancet; 1999 Feb 20; 353(9153):642-3. PubMed ID: 10030334
    [No Abstract] [Full Text] [Related]

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  • 17. Alglucerase for Gaucher's disease.
    Med Lett Drugs Ther; 1991 Aug 23; 33(851):82. PubMed ID: 1865852
    [No Abstract] [Full Text] [Related]

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  • 20. Velaglucerase (Vpriv) for Gaucher's disease.
    Med Lett Drugs Ther; 2010 May 03; 52(1337):36. PubMed ID: 20508578
    [No Abstract] [Full Text] [Related]

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