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408 related items for PubMed ID: 17542869

  • 1. Familial homozygous hypercholesterolemia: report of two patients and review of the literature.
    Sethuraman G, Sugandhan S, Sharma G, Chandramohan K, Chandra NC, Dash SS, Komal A, Sharma VK.
    Pediatr Dermatol; 2007; 24(3):230-4. PubMed ID: 17542869
    [Abstract] [Full Text] [Related]

  • 2. Severe xanthomatosis in heterozygous familial hypercholesterolemia.
    Aljenedil S, Ruel I, Watters K, Genest J.
    J Clin Lipidol; 2018; 12(4):872-877. PubMed ID: 29778561
    [Abstract] [Full Text] [Related]

  • 3. Autosomal recessive hypercholesterolemia in three sisters with phenotypic homozygous familial hypercholesterolemia: diagnostic and therapeutic procedures.
    Thomas HP, Vogt A, Wilund KR, Schliesser C, Steinhagen-Thiessen E, Kassner U.
    Ther Apher Dial; 2004 Aug; 8(4):275-80. PubMed ID: 15274677
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  • 4. Skin manifestations in familial heterozygous hypercholesterolemia.
    Pietroleonardo L, Ruzicka T.
    Acta Dermatovenerol Alp Pannonica Adriat; 2009 Dec; 18(4):183-7. PubMed ID: 20043058
    [Abstract] [Full Text] [Related]

  • 5. Unusual xanthomas in a young patient with heterozygous familial hypercholesterolemia and type III hyperlipoproteinemia.
    Feussner G, Dobmeyer J, Nissen H, Hansen TS.
    Am J Med Genet; 1996 Oct 16; 65(2):149-54. PubMed ID: 8911609
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  • 6. A xanthomatosis-susceptibility gene may exist in a Syrian family with familial hypercholesterolemia.
    Vergopoulos A, Bajari T, Jouma M, Knoblauch H, Aydin A, Bähring S, Mueller-Myhsok B, Dresel A, Joubran R, Luft FC, Schuster H.
    Eur J Hum Genet; 1997 Oct 16; 5(5):315-23. PubMed ID: 9412789
    [Abstract] [Full Text] [Related]

  • 7. The challenge produced by familial homozygous hypercholesterolemia when treating premature coronary arterial disease in the young.
    Shankarappa RK, Moorthy N, Bhat SP, Dwarakaprasad R, Nanjappa MC.
    Cardiol Young; 2009 Jun 16; 19(3):257-63. PubMed ID: 19344536
    [Abstract] [Full Text] [Related]

  • 8. Low-density lipoprotein apheresis using double filtration plasmapheresis: 27-month use in a child with homozygous familial hypercholesterolemia.
    Fernández-Fuertes LF, Tapia Martín M, Nieves Plá I, Novoa Mogollón FJ, Díaz Cremades J.
    Ther Apher Dial; 2010 Oct 16; 14(5):484-5. PubMed ID: 21175548
    [No Abstract] [Full Text] [Related]

  • 9. Low-density lipoprotein apheresis in children with familial hypercholesterolemia: follow-up to 21 years.
    Palcoux JB, Atassi-Dumont M, Lefevre P, Hequet O, Schlienger JL, Brignon P, Roussel B.
    Ther Apher Dial; 2008 Jun 16; 12(3):195-201. PubMed ID: 18503695
    [Abstract] [Full Text] [Related]

  • 10. Preemptive liver transplantation in a child with familial hypercholesterolemia.
    Maiorana A, Nobili V, Calandra S, Francalanci P, Bernabei S, El Hachem M, Monti L, Gennari F, Torre G, de Ville de Goyet J, Bartuli A.
    Pediatr Transplant; 2011 Mar 16; 15(2):E25-9. PubMed ID: 20846238
    [Abstract] [Full Text] [Related]

  • 11. [Clinical manifestations of familial hypercholesterolemia].
    Ivanović-Krstić B, Kalimanovska-Ostrić D, Cvetković-Matić D, Simić D, Djukić P, Nikcević Dj.
    Srp Arh Celok Lek; 2000 Mar 16; 128(3-4):110-5. PubMed ID: 10932620
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  • 14. Case report-Rapid regression of xanthomas under lipoprotein apheresis in a boy with homozygous familial hypercholesterolemia.
    Katzmann J, Schürfeld C, März W, Laufs U.
    J Clin Lipidol; 2018 Mar 16; 12(4):868-871. PubMed ID: 29866529
    [Abstract] [Full Text] [Related]

  • 15. [Homozygous familial hypercholesterolemia: development and a case illustration].
    Choukri M, Laaroussi N, Taheri H, Chabraoui L.
    Ann Biol Clin (Paris); 2013 Mar 16; 71(1):99-103. PubMed ID: 23396432
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  • 17. Liver transplantation in a subject with familial hypercholesterolemia carrying the homozygous p.W577R LDL-receptor gene mutation.
    Schmidt HH, Tietge UJ, Buettner J, Barg-Hock H, Offner G, Schweitzer S, Dedoussis GV, Rodeck B, Kallfelz HC, Schlitt HJ, Oldhafer K, Klempnauer J.
    Clin Transplant; 2008 Mar 16; 22(2):180-4. PubMed ID: 18339137
    [Abstract] [Full Text] [Related]

  • 18. Overexpression of the CXCL3 gene in response to oxidized low-density lipoprotein is associated with the presence of tendon xanthomas in familial hypercholesterolemia.
    Martín-Fuentes P, Civeira F, Solanas-Barca M, García-Otín AL, Jarauta E, Cenarro A.
    Biochem Cell Biol; 2009 Jun 16; 87(3):493-8. PubMed ID: 19448742
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  • 20. Differential diagnosis of tendon tumors: xanthomas caused by hyperlipidemia in children.
    Reichwaldt I, Zustin J, Wenke K, Ridderbusch I.
    J Pediatr Surg; 2010 Oct 16; 45(10):e9-12. PubMed ID: 20920708
    [Abstract] [Full Text] [Related]

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