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Journal Abstract Search

444 related items for PubMed ID: 9412789

  • 21. [Three-year-old boy--a homozygote for familiar hypercholesterolemia].
    Dumić M, Uroic AS, Francetić I, Puretić Z, Matisić D, Kes P, Mikecin M, Reiner Z.
    Lijec Vjesn; 2007 May; 129(5):130-3. PubMed ID: 17695192
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  • 22. Tendon xanthomas in familial hypercholesterolemia are associated with cardiovascular risk independently of the low-density lipoprotein receptor gene mutation.
    Civeira F, Castillo S, Alonso R, Meriño-Ibarra E, Cenarro A, Artied M, Martín-Fuentes P, Ros E, Pocoví M, Mata P, Spanish Familial Hypercholesterolemia Group.
    Arterioscler Thromb Vasc Biol; 2005 Sep; 25(9):1960-5. PubMed ID: 16020744
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  • 25. A novel type of familial hypercholesterolemia: double heterozygous mutations in LDL receptor and LDL receptor adaptor protein 1 gene.
    Tada H, Kawashiri MA, Ohtani R, Noguchi T, Nakanishi C, Konno T, Hayashi K, Nohara A, Inazu A, Kobayashi J, Mabuchi H, Yamagishi M.
    Atherosclerosis; 2011 Dec; 219(2):663-6. PubMed ID: 21872251
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  • 27. Identification of two novel LDL receptor gene defects in French-Canadian pediatric population: mutational analysis and biochemical studies.
    Assouline L, Leitersdorf E, Lambert M, Reshef A, Feoli-Fonseca JC, Levy E.
    Hum Mutat; 1997 Dec; 9(6):555-62. PubMed ID: 9195230
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  • 28. 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 Dec; 24(3):230-4. PubMed ID: 17542869
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  • 29. Genetics and kinetics of familial hypercholesterolemia, with the special focus on FH-(Marburg) p.W556R.
    Soufi M, Kurt B, Schweer H, Sattler AM, Klaus G, Zschocke J, Schaefer JR.
    Atheroscler Suppl; 2009 Dec 29; 10(5):5-11. PubMed ID: 20129366
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  • 31. Analysis of the Afrikaner mutation in exon 9 of the low-density lipoprotein receptor gene in a large Dutch kindred suffering from familial hypercholesterolaemia.
    Defesche JC, Lansberg PJ, Reymer PW, Lamping RJ, Kastelein JJ.
    Neth J Med; 1993 Feb 29; 42(1-2):53-60. PubMed ID: 8446226
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  • 34. Concentrations of the atherogenic Lp(a) are elevated in FH.
    Lingenhel A, Kraft HG, Kotze M, Peeters AV, Kronenberg F, Kruse R, Utermann G.
    Eur J Hum Genet; 1998 Jan 29; 6(1):50-60. PubMed ID: 9781014
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  • 36. Autosomal recessive hypercholesterolaemia: normalization of plasma LDL cholesterol by ezetimibe in combination with statin treatment.
    Lind S, Olsson AG, Eriksson M, Rudling M, Eggertsen G, Angelin B.
    J Intern Med; 2004 Nov 29; 256(5):406-12. PubMed ID: 15485476
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  • 37. First case report of familial hypercholesterolemia in an Omani family due to novel mutation in the low-density lipoprotein receptor gene.
    Al-Hinai AT, Al-Abri A, Al-Dhuhli H, Al-Waili K, Al-Sabti H, Al-Yaarubi S, Al-Hashmi K, Banerjee Y, Al-Zakwani I, Al-Rasadi K.
    Angiology; 2013 May 29; 64(4):287-92. PubMed ID: 23162007
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  • 38. Identification of a recurrent insertion mutation in the LDLR gene in a Pakistani family with autosomal dominant hypercholesterolemia.
    Ajmal M, Ahmed W, Sadeque A, Ali SH, Bokhari SH, Ahmed N, Qamar R.
    Mol Biol Rep; 2010 Dec 29; 37(8):3869-75. PubMed ID: 20217239
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  • 40. HDL cholesterol levels in patients with molecularly defined familial hypercholesterolemia.
    Miltiadous G, Cariolou MA, Elisaf M.
    Ann Clin Lab Sci; 2002 Dec 29; 32(1):50-4. PubMed ID: 11848618
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