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Journal Abstract Search

130 related items for PubMed ID: 8422264

  • 21. Novel mutations in the EDAR gene in two Pakistani consanguineous families with autosomal recessive hypohidrotic ectodermal dysplasia.
    Naeem M, Muhammad D, Ahmad W.
    Br J Dermatol; 2005 Jul; 153(1):46-50. PubMed ID: 16029325
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  • 22. [Relationship between apolipoprotein E and apolipoprotein B polymorphisms in youths with coronary heart disease].
    Li S, Lei ZW, Chen Z, Lin D, Ke XS, Zhong YM, Wu SF.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Jun; 20(3):241-3. PubMed ID: 12778454
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  • 23. Absence of intestinal synthesis of apolipoprotein B-48 in two cases of abetalipoproteinemia.
    Levy E, Marcel YL, Milne RW, Grey VL, Roy CC.
    Gastroenterology; 1987 Nov; 93(5):1119-26. PubMed ID: 3653634
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  • 24. Postprandial lipid absorption in seven heterozygous carriers of deleterious variants of MTTP in two abetalipoproteinemic families.
    Di Filippo M, Varret M, Boehm V, Rabès JP, Ferkdadji L, Abramowitz L, Dumont S, Lenaerts C, Boileau C, Joly F, Schmitz J, Samson-Bouma ME, Bonnefont-Rousselot D.
    J Clin Lipidol; 2019 Nov; 13(1):201-212. PubMed ID: 30522860
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  • 28. Novel mutations in SAR1B and MTTP genes in Tunisian children with chylomicron retention disease and abetalipoproteinemia.
    Magnolo L, Najah M, Fancello T, Di Leo E, Pinotti E, Brini I, Gueddiche NM, Calandra S, Slimene NM, Tarugi P.
    Gene; 2013 Jan 01; 512(1):28-34. PubMed ID: 23043934
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  • 29. Apolipoprotein B gene DNA polymorphisms (EcoRI and MspI) and serum lipid levels in the Serbian healthy population: interaction of rare alleles and smoking and cholesterol levels.
    Glisić S, Savić I, Alavantić D.
    Genet Epidemiol; 1995 Jan 01; 12(5):499-508. PubMed ID: 8557182
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  • 30. Molecular characterization of Tunisian families with abetalipoproteinemia and identification of a novel mutation in MTTP gene.
    Najah M, Youssef SM, Yahia HM, Afef S, Awatef J, Saber H, Fadhel NM, Sassolas A, Naceur SM.
    Diagn Pathol; 2013 Apr 04; 8():54. PubMed ID: 23556456
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  • 34. Multilocus approach to cardiovascular risk.
    Pallaud C, Maurice M, Cheng S, Grow M, Aguillon D, Sass C, Siest G, Visvikis S.
    Scand J Clin Lab Invest Suppl; 1999 Apr 04; 230():168-76. PubMed ID: 10389215
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  • 35. Abetalipoproteinemia with an ApoB-100-lipoprotein(a) glycoprotein complex in plasma. Indication for an assembly defect.
    Menzel HJ, Dieplinger H, Lackner C, Hoppichler F, Lloyd JK, Muller DR, Labeur C, Talmud PJ, Utermann G.
    J Biol Chem; 1990 Jan 15; 265(2):981-6. PubMed ID: 2295628
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  • 36. A tale of 2 cousins: An atypical and a typical case of abetalipoproteinemia.
    Paquette M, Dufour R, Hegele RA, Baass A.
    J Clin Lipidol; 2016 Jan 15; 10(4):1030-1034. PubMed ID: 27578136
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