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Journal Abstract Search

141 related items for PubMed ID: 26709268

  • 1. Clinical Utility of Bone Marrow Study in Gaucher Disease: A Case Report of Gaucher Disease Type 3 With Intractable Myoclonic Seizures.
    Rim JH, Baik M, Yoon SO, Heo K, Song J.
    Ann Lab Med; 2016 Mar; 36(2):177-9. PubMed ID: 26709268
    [No Abstract] [Full Text] [Related]

  • 2. Gaucher disease patient with myoclonus epilepsy and a novel mutation.
    Tajima A, Ohashi T, Hamano S, Higurashi N, Ida H.
    Pediatr Neurol; 2010 Jan; 42(1):65-8. PubMed ID: 20004867
    [Abstract] [Full Text] [Related]

  • 3. From Bone Marrow Necrosis to Gaucher Disease; A Long Way to Run.
    Erdem N, Çizmecioğlu A, Aydoğdu İ.
    Turk J Haematol; 2015 Dec; 32(4):373-4. PubMed ID: 26376635
    [No Abstract] [Full Text] [Related]

  • 4. Gaucher disease: successful treatment of myoclonic status epilepticus with levetiracetam.
    Vaca GF, Lenz T, Knight EM, Tuxhorn I.
    Epileptic Disord; 2012 Jun; 14(2):155-8. PubMed ID: 22569507
    [Abstract] [Full Text] [Related]

  • 5. Evolving features in type 3 Gaucher disease on long-term enzyme replacement therapy.
    Elstein D, Abrahamov A, Altarescu G, Zimran A.
    Blood Cells Mol Dis; 2013 Feb; 50(2):140. PubMed ID: 23085428
    [No Abstract] [Full Text] [Related]

  • 6. Metaphyseal undertubulation in gaucher disease: resolution at MRI in a patient undergoing enzyme replacement therapy.
    Kelman CG, Disler DG.
    J Comput Assist Tomogr; 2000 Feb; 24(1):173-5. PubMed ID: 10667678
    [Abstract] [Full Text] [Related]

  • 7. [Gaucher disease. A case report].
    Ortega Pérez M, Infante-Velásquez C, Maragoto-Rizo A, García-Ruiz G, Rodríguez E.
    Rev Neurol; 2000 Feb; 37(2):198-9. PubMed ID: 12938079
    [No Abstract] [Full Text] [Related]

  • 8. [Gaucher disease: MR evaluation of bone marrow features during treatment with enzyme replacement].
    Poll LW, vom Dahl S, Koch JA, Börner D, Willers R, Cohnen M, Jung G, Scherer A, Niederau C, Häussinger D, Mödder U.
    Rofo; 2001 Oct; 173(10):931-7. PubMed ID: 11588682
    [Abstract] [Full Text] [Related]

  • 9. Gaucher disease: A 10 year old girl with anemia and huge spelenomegaly (a case report).
    Davarian A, Mirbehbahani NB.
    Pak J Biol Sci; 2008 Apr 01; 11(7):1063-5. PubMed ID: 18810981
    [Abstract] [Full Text] [Related]

  • 10. Persistent bone disease in adult type 1 Gaucher disease despite increasing doses of enzyme replacement therapy.
    de Fost M, van Noesel CJ, Aerts JM, Maas M, Pöll RG, Hollak CE.
    Haematologica; 2008 Jul 01; 93(7):1119-20. PubMed ID: 18519519
    [No Abstract] [Full Text] [Related]

  • 11. Neurologic improvement in a type 3 Gaucher disease patient treated with imiglucerase/miglustat combination.
    Capablo JL, Franco R, de Cabezón AS, Alfonso P, Pocovi M, Giraldo P.
    Epilepsia; 2007 Jul 01; 48(7):1406-8. PubMed ID: 17433057
    [Abstract] [Full Text] [Related]

  • 12. Late-onset Myoclonic Seizure in a 78-year-old Woman with Gaucher Disease.
    Yamaguchi-Takegami N, Takahashi A, Mitsui J, Sugiyama Y, Chikada A, Porto KJL, Takegami N, Sakuishi K, Ishiura H, Yamada K, Shimizu J, Tsuji S, Toda T.
    Intern Med; 2024 Mar 15; 63(6):861-865. PubMed ID: 37558486
    [Abstract] [Full Text] [Related]

  • 13. Novel G377S (c.1246G>T) mutation associated with Gaucher disease type 1.
    Zhou Y, Kraemer RR, Peker D, Wakefield DN, de Idiaquez Bakula DA.
    Am J Hematol; 2013 Oct 15; 88(10):922-3. PubMed ID: 23828321
    [No Abstract] [Full Text] [Related]

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  • 15. Evaluation of treatment response to enzyme replacement therapy with Velaglucerase alfa in patients with Gaucher disease using whole-body magnetic resonance imaging.
    Laudemann K, Moos L, Mengel E, Lollert A, Hoffmann C, Brixius-Huth M, Wagner D, Düber C, Staatz G.
    Blood Cells Mol Dis; 2016 Mar 15; 57():35-41. PubMed ID: 26852653
    [Abstract] [Full Text] [Related]

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  • 18. Gaucher disease diagnosed in a 30-year-old black man.
    Nithya P, Constantine A, Roger V, Albert B.
    Clin Genet; 2008 Oct 15; 74(4):399-400. PubMed ID: 18637939
    [No Abstract] [Full Text] [Related]

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  • 20. Adult type 3 Gaucher disease as manifestation of R463C/Rec Nci I mutation: first reported case in the world literature.
    Chauhan V, Kumar RV, Mahesh DM, Kashyap R, Thakur S.
    J Assoc Physicians India; 2013 May 15; 61(5):346-8. PubMed ID: 24482953
    [Abstract] [Full Text] [Related]

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