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PUBMED FOR HANDHELDS

Journal Abstract Search

134 related items for PubMed ID: 28458077

  • 1.
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  • 3. Coinheritance of Gaucher disease and α-thalassemia resulting in confusion between two inherited hematologic diseases.
    Miri-Moghaddam E, Velayati A, Naderi M, Tayebi N, Sidransky E.
    Blood Cells Mol Dis; 2011 Jan 15; 46(1):88-91. PubMed ID: 20846888
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  • 5. Enzyme Replacement Therapy in a Gaucher Family.
    Erdem N, Buran T, Berber I, Aydogdu I.
    J Natl Med Assoc; 2018 Aug 15; 110(4):330-333. PubMed ID: 30126557
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  • 6. 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 15; 138(1):137-9. PubMed ID: 11148530
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  • 7. Gaucher disease: progressive mesenteric and mediastinal lymphadenopathy despite enzyme therapy.
    Burrow TA, Cohen MB, Bokulic R, Deutsch G, Choudhary A, Falcone RA, Grabowski GA.
    J Pediatr; 2007 Feb 15; 150(2):202-6. PubMed ID: 17236903
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  • 8. Novel heterozygous c.798C>G and c.1040T>G mutations in the GBA1 gene are associated with a severe phenotype of Gaucher disease type 1.
    Machaczka M, Klimkowska M.
    Ann Hematol; 2014 Oct 15; 93(10):1787-9. PubMed ID: 24577513
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  • 9. Does enzyme replacement therapy enhance brain-derived neurotrophic factor expression in Gaucher disease?
    Agilli M, Ekinci S, Fidan G.
    J Neuroimmunol; 2015 Feb 15; 279():39. PubMed ID: 25669998
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  • 11. [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
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  • 12. 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
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  • 13. [A case of adult Gaucher disease].
    Werling K, Lengyel G, Vallent K, Zalatnai A, Burger M, Laky J.
    Orv Hetil; 1992 Oct 11; 133(41):2631-4. PubMed ID: 1408099
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  • 14. A patient with type 2 Gaucher's disease with respiratory disease.
    Shebani E, Johannesson M, Strömberg B, Roomans GM.
    J Pediatr; 2003 Feb 11; 142(2):209-10. PubMed ID: 12584549
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  • 15. Adult Gaucher disease in southern Tunisia: report of three cases.
    Ben Rhouma F, Kallel F, Kefi R, Cherif W, Nagara M, Azaiez H, Jedidi I, Elloumi M, Abdelhak S, Mseddi S.
    Diagn Pathol; 2012 Jan 10; 7():4. PubMed ID: 22233685
    [Abstract] [Full Text] [Related]

  • 16. Co-inheritance of novel ATRX gene mutation and globin (α & β) gene mutations in transfusion dependent beta-thalassemia patients.
    Al-Nafie AN, Borgio JF, AbdulAzeez S, Al-Suliman AM, Qaw FS, Naserullah ZA, Al-Jarrash S, Al-Madan MS, Al-Ali RA, AlKhalifah MA, Al-Muhanna F, Steinberg MH, Al-Ali AK.
    Blood Cells Mol Dis; 2015 Jun 10; 55(1):27-9. PubMed ID: 25976463
    [Abstract] [Full Text] [Related]

  • 17. A 16-year-old girl with epistaxis and hepatosplenomegaly.
    Woods M, Greenes D.
    Curr Opin Pediatr; 1995 Dec 10; 7(6):733-9. PubMed ID: 8776027
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  • 18. Characteristics of type I Gaucher disease associated with persistent thrombocytopenia after treatment with imiglucerase for 4-5 years.
    Hollak CE, Belmatoug N, Cole JA, Vom Dahl S, Deegan PB, Goldblatt J, Rosenbloom B, van Dussen L, Tylki-Szymańska A, Weinreb NJ, Zimran A, Cappellini MD.
    Br J Haematol; 2012 Aug 10; 158(4):528-38. PubMed ID: 22640238
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  • 19. Imaging findings in pediatric type 1 Gaucher disease: what the clinician needs to know.
    Green BA, Alexander AA, Hill PR, Lowe LH.
    J Pediatr Hematol Oncol; 2011 May 10; 33(4):301-5. PubMed ID: 21464762
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  • 20. Gaucher disease.
    Mignot C, Gelot A, De Villemeur TB.
    Handb Clin Neurol; 2013 May 10; 113():1709-15. PubMed ID: 23622393
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